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Aliases & Descriptions for TP53 gene
(According to
1 HGNC ,
2 Entrez Gene ,
3 UniProtKB/Swiss-Prot ,
4 UniProtKB/TrEMBL , 5 OMIM , 6 GeneLoc
, and/or 7 Ensembl ,
8 miRBase )About This Section
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User Feedback Aliases & Descriptions tumor protein p531 2 transformation-related protein 532 LFS11 2 5 FLJ929432 p531 2 p53 tumor suppressor2 Phosphoprotein p532 3 p53 transformation suppressor2 P533 5 Tumor suppressor p533 p53 antigen2 Antigen NY-CO-133 TRP532
Search outside databases for aliases for TP53 genePrevious GC identifers: GC17P008026 GC17M008311 GC17M007514 GC17M007772 GC17M007512
Summaries for TP53 gene (According to Entrez Gene ,
Tocris Bioscience ,
Wikipedia's
Gene Wiki ,
UniProtKB/Swiss-Prot ,
and/or
UniProtKB/TrEMBL )
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User Feedback Entrez Gene summary for TP53 : This gene encodes tumor protein p53, which responds to diverse cellular stresses to regulate target genes that induce cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. p53 protein is expressed at low level in normal cells and at a high level in a variety of transformed cell lines, where it's believed to contribute to transformation and malignancy. p53 is a DNA-binding protein containing transcription activation, DNA-binding, and oligomerization domains. It is postulated to bind to a p53-binding site and activate expression of downstream genes that inhibit growth and/or invasion, and thus function as a tumor suppressor. Mutants of p53 that frequently occur in a number of different human cancers fail to bind the consensus DNA binding site, and hence cause the loss of tumor suppressor activity. Alterations of this gene occur not only as somatic mutations in human malignancies, but also as germline mutations in some cancer-prone families with Li-Fraumeni syndrome. Multiple p53 variants due to alternative promoters and multiple alternative splicing have been found. These variants encode distinct isoforms, which can regulate p53 transcriptional activity. (provided by RefSeq) UniProtKB/Swiss-Prot: P53_HUMAN, P04637 Function : Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on thephysiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression. Implicated in Notch signaling cross-over summary
for TP53 : p53 (aka TP53) is a transcription factor whose protein levels and post-translational modification state alterin response to cellular stress (such as DNA damage, hypoxia, spindle damage). Activation of p53 beginsthrough a number of mechanisms including phosphorylation by ATM, ATR, Chk1 and MAPKs. MDM2 is a ubiquitnligase that binds p53 and targets p53 for proteasomal degradation. Phosphorylation, p14ARF and USP7 preventMDM2-p53 interactions, leading to an increase in stable p53 tetramers in the cytoplasm. Furthermodifications such as methylation and acetylation lead to an increase in p53 binding to gene specificresponse elements. p53 regulates a large number of genes (>100 genes) that control a number of key tumorsuppressing functions such as cell cycle arrest, DNA repair, senescence and apoptosis. Whilst the activationof p53 often leads to apoptosis, p53 inactivation facilitates tumor progression. Gene Wiki entry for TP53 (P53)
Genomic Views for TP53 gene
(According to
GeneLoc and/or
HGNC , and/or
Entrez Gene (NCBI build 37) ,
and/or miRBase ,
Genomic Views according to
UCSC and
Ensembl (release 56) ,
Regulatory elements and Epigenetics data according to
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User Feedback Regulatory elements: SABiosciences Regulatory transcription factor binding sites in the TP53 gene upstream (promoter) region :C/EBPbeta AhR p53 MIF-1 Sp1 RFX1 E2F-5 E2F-4 E2F-2 E2F-1 Epigenetics: SABiosciences Methyl-Profiler DNA Methylation qPCR Primer Assays for TP53: MePH21488-1A Genomic Location: Genomic View : UCSC Golden Path with GeneCards custom track Entrez Gene cytogenetic band: 17p13.1 Ensembl cytogenetic band: 17p13.1 HGNC cytogenetic band: 17p13.1 TP53 Gene in genomic location: bands according to Ensembl, locations according to
(and/or Entrez Gene and/or Ensembl if different) GeneLoc gene densities for chromosome 17 GeneLoc Exon Structure
GeneLoc location for GC17M007565: view genomic region
(about GC identifiers )
Start:
7,565,257 bp from pter
End:
7,590,863 bp from pter
Size:
25,607 bases
Orientation:
minus strand
RefSeq DNA sequence: NC_000017.10 NT_010718.16 Proteins for TP53 gene
(According to
1 UniProtKB ,
and/or Ensembl ,
Phosphorylation sites according to 2 Phosphosite ,
RefSeq according to NCBI ,
PDB rendering according to OCA and/or Proteopedia ,
Recombinant Proteins
from
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Enzo Life Sciences ,
Abnova ,
OriGene ,
Novus Biologicals , and/or
Sino Biological ,
Biochemical Assays by
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Cell Signaling Technology , and/or
Enzo Life Sciences ,
Ontologies according to Gene
Ontology Consortium 01 May 2010 and
Entrez Gene ,
Antibodies by
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Cell Signaling Technology ,
Abnova ,
OriGene ,
Novus Biologicals , and/or
Epitomics )
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User Feedback UniProtKB/Swiss-Prot: P53_HUMAN, P04637 (See
protein sequence )Recommended Name: Cellular tumor antigen p53 Size : 393 amino acids; 43653 Da
Cofactor : Binds 1 zinc ion per subunit
Subunit : Interacts with AXIN1. Probably part of a complex consisting of TP53, HIPK2 and AXIN1 (By similarity). BindsDNA as a homotetramer. Interacts with histone acetyltransferases EP300 and methyltransferases HRMT1L2 and CARM1, and recruits them to promoters. In vitro, the interaction of TP53 with cancer-associated/HPV (E6) viral proteins leads to ubiquitination and degradation of TP53 giving a possible model for cell growth regulation. This complex formation requires an additional factor, E6-AP, which stably associates with TP53 in the presence of E6. Interacts (via C-terminus) with TAF1; when TAF1 is part of the TFIID complex. Interacts with ING4; this interaction may be indirect. Found in a complex with CABLES1 and TP73. Interacts with HIPK1, HIPK2, and P53DINP1. Interacts with WWOX. May interact with HCV core protein. Interacts with USP7 and SYVN1. Interacts with HSP90AB1. Interacts with CHD8; leading to recruit histone H1 and prevent transactivation activity (By similarity). Interacts with ARMC10, BANP, CDKN2AIP and E4F1. Interacts with YWHAZ; the interaction enhances TP53 transcriptional activity. Phosphorylation of YWHAZ on 'Ser-58' inhibits this interaction. Interacts (via DNA-binding domain) with MAML1 (via N-terminus). Interacts with MKRN1. Directly interacts with FBXO42; leading to ubiquination and degradation of TP53. Interacts (phosphorylated at Ser-15 by ATM) with the phosphatase PP2A-PPP2R5C holoenzyme; regulates stress-induced TP53-dependent inhibition of cell proliferation. Interacts with PPP2R2A
Subcellular location : Cytoplasm. Nucleus. Endoplasmic reticulum. Note=Interaction with BANP promotes nuclearlocalization
PDB structures from and Proteopedia : 1A1U (3D)
 1AIE (3D)
 1C26 (3D)
 1DT7 (3D)
 1GZH (3D)
 1H26 (3D)
 1HS5 (3D)
 1JSP (3D)
 1KZY (3D)
 1MA3 (3D)
 1OLG (3D)
 1OLH (3D)
 1PES (3D)
 1PET (3D)
 1SAE (3D)
 1SAF (3D)
 1SAH (3D)
 1SAJ (3D)
 1SAK (3D)
 1SAL (3D)
 1TSR (3D)
 1TUP (3D)
 1UOL (3D)
 1XQH (3D)
 1YC5 (3D)
 1YCQ (3D)
 1YCR (3D)
 1YCS (3D)
 2AC0 (3D)
 2ADY (3D)
 2AHI (3D)
 2ATA (3D)
 2B3G (3D)
 2BIM (3D)
 2BIN (3D)
 2BIO (3D)
 2BIP (3D)
 2BIQ (3D)
 2F1X (3D)
 2FEJ (3D)
 2FOJ (3D)
 2FOO (3D)
 2GS0 (3D)
 2H1L (3D)
 2H2D (3D)
 2H2F (3D)
 2H4F (3D)
 2H4H (3D)
 2H4J (3D)
 2H59 (3D)
 2J0Z (3D)
 2J10 (3D)
 2J11 (3D)
 2J1W (3D)
 2J1X (3D)
 2J1Y (3D)
 2J1Z (3D)
 2J20 (3D)
 2J21 (3D)
 2K8F (3D)
 2OCJ (3D)
 2PCX (3D)
 2QVQ (3D)
 2QXA (3D)
 2QXB (3D)
 2QXC (3D)
 2VUK (3D)
 2WGX (3D)
 2X0U (3D)
 2X0V (3D)
 2X0W (3D)
 2Z5S (3D)
 2Z5T (3D)
 3D05 (3D)
 3D06 (3D)
 3D07 (3D)
 3D08 (3D)
 3D09 (3D)
 3D0A (3D)
 3DAB (3D)
 3DAC (3D)
 3KMD (3D)
 3SAK (3D)
 
Secondary accessions : Q15086 Q15087 Q15088 Q16535 Q16807 Q16808 Q16809 Q16810 Q16811 Q16848 Q86UG1Q8J016 Q99659 Q9BTM4 Q9HAQ8 Q9NP68 Q9NPJ2 Q9NZD0 Q9UBI2 Q9UQ61 Alternative splicing : 2 isoforms : P04637-1 P04637-2 Post-translational modifications:
Acetylated. Acetylation of Lys-382 by CREBBP enhances transcriptional activity. Deacetylation of Lys-382 by SIRT1 impairs its ability to induce proapoptotic program and modulate cell senescence1
Phosphorylation on Ser residues mediates transcriptional activation. Phosphorylated by HIPK1 (By similarity). Phosphorylation at Ser-9 by HIPK4 increases repression activity on BIRC5 promoter. Phosphorylated on Thr-18 by VRK1, which may prevent the interaction with MDM2. Phosphorylated on Thr-55 by TAF1, which promotes MDM2-mediated degradation. Phosphorylated on Ser-46 by HIPK2 upon UV irradiation. Phosphorylation on Ser-46 is required for acetylation by CREBBP. Phosphorylated on Ser-392 following UV but not gamma irradiation. Phosphorylated upon DNA damage, probably by ATM or ATR. Phosphorylated on Ser-15 upon ultraviolet irradiation; which is enhanced by interaction with BANP1
Dephosphorylated by PP2A-PPP2R5C holoenzyme at Thr-55. SV40 small T antigen inhibits the dephosphorylation by the AC form of PP2A1
May be O-glycosylated in the C-terminal basic region. Studied in EB-1 cell line1
Ubiquitinated by SYVN1, which leads to proteasomal degradation. Ubiquitinated by MKRN1 at Lys-291 and Lys-292, which leads to proteasomal degradation. Ubiquitinated by MDM2. Deubiquitinated by USP10, leading to stabilize it1
Monomethylated at Lys-372 by SETD7, leading to stabilization and increased transcriptional activation. Monomethylated at Lys-370 by SMYD2, leading to decreased DNA-binding activity and subsequent transcriptional regulation activity. Lys-372 monomethylation prevents interaction with SMYD2 and subsequent monomethylation at Lys-3701
Sumoylated by SUMO11
Demethylation of di-methylated Lys-370 by KDM1A prevents interaction with TP53BP1 and represses TP53-mediated transcriptional activation1
View phosphorylation sites using PhosphoSite 2
REFSEQ proteins (7 alternative transcripts):
NP_000537.3 NP_001119584.1 NP_001119585.1 NP_001119586.1 NP_001119587.1 NP_001119588.1 NP_001119589.1 ENSEMBL proteins: ENSP00000394195 ENSP00000352610 ENSP00000391127 ENSP00000402130 ENSP00000398846 ENSP00000379735 ENSP00000269305 ENSP00000391478 ENSP00000410739 Human Recombinant Proteins 5/14 Gene Ontology (GO) cellular component terms (GO ID links to tree view) (see all 14
):
About this table
TP53 for ontologies About GeneDecksing Antibodies for TP53: Millipore Mono- and Polyclonal Antibodies for the study of TP53 Sigma-Aldrich Antibody Arrays and Antibodies for TP53 R&D Systems Antibodies for TP53 (p53) Cell Signaling Technology (CST) Antibodies for TP53   (p53) Monoclonal and Polyclonal Antibodies from Abnova (TP53 ) Origene Antibodies (see all 15 ): TP53 Novus Biologicals Antibodies for TP53 Epitomics antibodies for TP53
Assays for TP53: Millipore Kits and Assays for the Analysis of TP53 Sigma-Aldrich ELISAs for TP53 R&D Systems ELISAs for TP53 (p53) Cell Signaling Technology (CST) Sandwich ELISA Kits for TP53 (p53) Enzo Life Sciences assays for TP53
Protein
Domains/ Families for TP53 gene(According to InterPro , ProtoNet ,
UniProtKB , and/or BLOCKS ,
Sets of similar genes according to GeneDecks )
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TP53 for domains About GeneDecksing 5/7 InterPro domains/families (see all 7
):
Graphical View of Domain Structure for InterPro Entry P04637 ProtoNet protein and cluster: P04637
1 Blocks protein family : IPB010991 p53 UniProtKB/Swiss-Prot: P53_HUMAN, P04637 Domain : The nuclear export signal acts as a transcriptional repression domainSimilarity : Belongs to the p53 family
Gene Function for TP53 gene
(According to MGI May 08 2010, UniProtKB ,
IUBMB ,and/or Genatlas ,
shRNA from
OriGene ,
Sigma-Aldrich , RNAi from
Millipore ,
Abnova ,
siRNAs from
Applied Biosystems ,
Sigma-Aldrich , Clones from
Millipore ,
Sigma-Aldrich ,
OriGene ,
Sino Biological ,
Ontologies according to Gene Ontology Consortium 01 May 2010 via
Entrez Gene .)
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User Feedback UniProtKB/Swiss-Prot: P53_HUMAN, P04637 Function : Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on thephysiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression. Implicated in Notch signaling cross-over
Genatlas biochemistry entry for TP53 :tumor suppressor protein p53 required for G1 growth arrest by WAF1 (CDKN1A),following DNA damage or induction of apoptosis,also regulating a G2 checkpoint through cyclin B1,transcriptional activator through acetylation of transactivation site by CREBBP binding MDM2 resulting in transcriptional silencing and ubiquitin/proteasome dependent degradation of p53,activated by conjugation to UBL1 (SUMO1),putative up-regulated c-MYC target gene,putative teratologic suppressor gene and modulator of TFIIH (GTF2H),associated in nucleotide excision repair,activated by ATM in association with 14.3.3 proteins (YWHA*),tumor suppressor gene (see TSG17A),mutated in cancers such as pancreas and endometrial carcinomas,in Barrett's adenocarcinoma (and esophageal squamous cell carcinoma),in hepatocellular carcinoma with poor prognosis 5/17 Gene Ontology (GO) molecular function terms (GO ID links to tree view) (see all 17
):
About this table
TP53 for ontologies About GeneDecksing Animal Models: 15/30 MGI mutant phenotypes (inferred from 46 alleles ) (MGI details for Trp53) (see all 30
):
TP53 for phenotypes About GeneDecksing Pathways & Interactions for TP53 gene
(Pathways according to
Millipore ,
Cell Signaling Technology ,
Sigma-Aldrich ,
Applied Biosystems GeneAssist ,
KEGG
and/or UniProtKB ,
(map by GeneGo ),
Sets of similar genes according to GeneDecks ,
Proteins Network according to
SABiosciences ,
Interactions according to 1 UniProtKB ,
2 MINT , and/or
3 STRING ,
with links to IntAct and
Ensembl ,
Ontologies according to Gene Ontology Consortium 01 May 2010 via
Entrez Gene) .
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TP53 for pathways About GeneDecksing 5/16 Millipore Pathways for TP53 (see all 16
)5/39 Sigma-Aldrich "Your Favorite Gene" Pathways for TP53 (Your Favorite Gene powered by Ingenuity) (see all 39
)5/48 GeneAssist Pathways for TP53 (see all 48
)5
Cell Signaling Technology (CST) Pathways for TP53:
5/21 Kegg Pathways (Kegg details for TP53) (see all 21
): SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for TP53 5/252 Interacting proteins for TP53 (ENSP00000269305 3 P04637 1 , 2 ) via UniProtKB, MINT, and/or STRING (see all 252
) Interactant Interaction Details GeneCard External ID(s) MDM2 Q00987 1 , 2 STRING: ENSP00000258149 EBI-366083,EBI-389668 MINT-6540920 MINT-6665330 MINT-4793511 MINT-4793467 MINT-6823775 MINT-7013943 MINT-4049616 MINT-4054304 MINT-6540905 MINT-6540889 MINT-68742 MINT-7013780 MINT-56681 MINT-58468 MINT-7013791 MINT-68743 MINT-7013956 MINT-6540807 MINT-4545014 MINT-4049631 MINT-6540776 MINT-6801380 MINT-58465 MINT-7013688 MINT-7013802 MINT-6540796 MINT-4303990 EBI-366083,EBI-389668 MINT-6540920 MINT-6665330 MINT-4793511 MINT-4793467 MINT-6823775 MINT-7013943 MINT-4049616 MINT-4054304 MINT-6540905 MINT-6540889 MINT-68742 MINT-7013780 MINT-56681 MINT-58468 MINT-7013791 MINT-68743 MINT-7013956 MINT-6540807 MINT-4545014 MINT-4049631 MINT-6540776 MINT-6801380 MINT-58465 MINT-7013688 MINT-7013802 MINT-6540796 MINT-4303990 UBC P62988 1 , 2 STRING: ENSP00000344818 EBI-366083,EBI-413034 MINT-7220023 MINT-4051326 MINT-4304004 MINT-4054804 MINT-4304143 MINT-6801380 MINT-6615153 MINT-6541035 MINT-7299234 MINT-7298704 MINT-6799774 MINT-7013815 MINT-4052207 MINT-7219995 MINT-5114741 MDM4 O15151 1 , 2 STRING: ENSP00000356151 EBI-366083,EBI-398437 MINT-7291988 MINT-7292025 MINT-7291962 MINT-2517887 MINT-7291975 EBI-366083,EBI-398437 MINT-7291988 MINT-7292025 MINT-7291962 MINT-2517887 MINT-7291975 USP7 Q93009 1 , 2 STRING: ENSP00000371310 EBI-366083,EBI-302474 MINT-4304022 MINT-14904 MINT-15878 MINT-15877 MINT-15876 EBI-366083,EBI-302474 MINT-4304022 MINT-14904 MINT-15878 MINT-15877 MINT-15876 EP300 Q09472 1 , 2 STRING: ENSP00000263253 EBI-366083,EBI-447295 MINT-69507 MINT-2830826 MINT-7263630 MINT-6628507 EBI-366083,EBI-447295 MINT-69507 MINT-2830826 MINT-7263630 MINT-6628507
About this table 5/61 Gene Ontology (GO) biological process terms (GO ID links to tree view) (see all 61
):
GO ID Qualified GO term Evidence PubMed IDs GO:0000060 protein import into nucleus, translocation
IEA -- GO:0000122 negative regulation of transcription from RNA polymerase II promoter
IEA -- GO:0001701 in utero embryonic development
IEA -- GO:0001756 somitogenesis
-- -- GO:0001836 release of cytochrome c from mitochondria
IEA --
About this table
TP53 for ontologies About GeneDecksing
Drugs & Compounds for TP53 gene (Chemical Compounds according to UniProtKB , Enzo Life Sciences ,
Sigma-Aldrich , Tocris Bioscience , and/or
Novoseek and Drugs according to
Enzo Life Sciences and/or
PharmGKB )
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TP53 for compounds About GeneDecksing
Enzo Life Sciences drugs & compounds for TP53
Compounds for TP53 available from Tocris Bioscience About this table 10/1766 Novoseek chemical compound relationships for TP53 gene (see all 1766
)
Compound
Score
Articles
PubMed IDs for Articles with Shared Sentences (# sentences)
bcl2
100.00
415
9651943 (7), 18470731 (6), 11712682 (6), 8693593 (5) (see all 100 )
bpde
31.56
118
16244358 (10), 7586197 (7), 17630511 (7), 10786695 (6) (see all 47 )
leptomycin b
31.25
63
18784437 (7), 12539224 (6), 14662026 (5), 9819415 (4) (see all 33 )
roscovitine
19.70
70
18846503 (6), 17384267 (5), 11577989 (5), 11423970 (5) (see all 27 )
273h
16.87
23
11917017 (6), 19351493 (3), 8649776 (2), 17636407 (2) (see all 12 )
9-hydroxyellipticine
15.59
21
11724337 (5), 10652599 (5), 9883907 (4), 10737712 (4) (see all 5 )
cd437
15.07
35
11103825 (6), 10383141 (5), 11956107 (4), 10327056 (4) (see all 13 )
cisplatin
13.79
1112
9811465 (9), 15113856 (9), 12492119 (9), 17291459 (8) (see all 100 )
camptothecin
11.57
150
10536167 (6), 9815856 (5), 19445707 (5), 9673414 (4) (see all 95 )
advexin
11.45
9
19086841 (3), 16856803 (2), 12749760 (2), 20021420 (1) (see all 5 )
About this table 2 PharmGKB drug compound relationships for TP53 gene About this table
Transcripts for TP53 gene(GenBank/EMBL/DDBJ Accessions according to
Unigene
(Build 223 Homo sapiens; Apr 2 2010) or GenBank , RefSeq according to Entrez Gene ,
DOTS (version 10), and/or
AceView ,
non coding RNAs according to
RNAdb ,
ESTs according to GeneTide ,
exon structure from GeneLoc ,
alternative splicing isoforms according to ASD and/or
ECgene ,
RNAi Products from
Millipore and/or
Abnova ,
siRNAs from Applied Biosystems ,
Sigma-Aldrich ,
shRNA from
Sigma-Aldrich ,
OriGene ,
microRNA from SABiosciences ,
Tagged/untagged cDNA clones from
OriGene ,
Primers from
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SABiosciences , Expression Assays from Applied Biosystems )About This Section
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User Feedback Assays: Applied Biosystems TaqMan® Gene Expression Assays: NM_000546 NM_001126112 NM_001126113 NM_001126114 NM_001126115 NM_001126116 NM_001126117 Clones: Origene GFP tagged cDNA clones in CMV expression vector (see all 7 ): TP53 Origene Myc/DDK tagged cDNA clones in CMV expression vector (see all 7 ): TP53 Origene untagged cDNA clones in CMV expression vector (see all 7 ): TP53
Primers: Origene genome-wide validated SYBR primer pairs: TP53 SABiosciences RT2 qPCR Primer Assay for TP53: PPH00213A
REFSEQ mRNAs for TP53 gene (7 alternative transcripts): NM_000546.4 NM_001126112.1 NM_001126113.1 NM_001126114.1 NM_001126115.1 NM_001126116.1 NM_001126117.1
Additional cDNA sequence: AB082923.1 AF052180.1 AF307851.1 AK223026.1 AK225838.1 AK297462.1 AK297927.1 AK303277.1 AK312568.1 AM076970.1 AM076971.1 AM076972.1 AY429684.1 AY627884.1 BC003596.1 BT019622.1 CR608294.1 CR624912.1 DQ186648.1 DQ186649.1 DQ186650.1 DQ186651.1 DQ186652.1 DQ191317.1 DQ263704.1 DQ286964.1 DQ401704.1 DQ485152.1 DQ648883.1 DQ648884.1 DQ648885.1 DQ648886.1 DQ648887.1 EF101867.1 EF101868.1 EF101869.1 FJ207420.1 M14694.1 M14695.1 S66666.1 X01405.1 X02469.1 X60010.1 X60011.1 X60012.1 X60013.1 X60014.1 X60015.1 X60016.1 X60017.1 X60018.1 X60019.1 X60020.1
18 DOTS entries : DT.92469229 DT.100788714 DT.120961435 DT.100788713 DT.75152217 DT.40283865 DT.95274968 DT.100712946
DT.120961349 DT.100788719 DT.40120491 DT.120961395 DT.100788715 DT.92010563 DT.120961350 DT.120961391 DT.120961408 DT.99987012 24/112 AceView cDNA sequences (see all 112
):
CR608294 AY627884 AW865736 BX952582 X60012 CA432254 AA662570 CR624912 AI539544 BE886147 BQ057682 X60018 BQ066009 S66666 AA358870 X60016 BU673953 AA291539 AA379547 BU174921 CK904490 X02469 AL530477 AF307851 1 RNAdb entry of non coding RNAs:
LIT1750
highest scoring ESTs for TP53 :X02469 AA171861 AA296373 AB082923 AF307851 AU076984 AU120569 AU121050 AU129655 AU131952 Unigene Cluster for TP53:
Tumor protein p53 Hs.654481 [show with all ESTs ] Unigene Representative Sequence: NM_001126114 GeneLoc Exon Structure 5/9 Alternative Splicing Database (ASD) splice patterns (SP) for TP53 (see all 9
) ExUns: 1a · 1b ^ 2 ^ 3 ^ 4 ^ 5a · 5b ^ 6 ^ 7 ^ 8 ^ 9a · 9b ^ 10a · 10b ^ 11 ^ 12a · 12b · 12c SP1 :           -           -     -   -           SP2 :                     -                 SP3 :                     -     -             SP4 :                     -     -   -           SP5 :                         -   -          
About this scheme ECgene alternative splicing isoforms for TP53 9 Ensembl transcripts including schematic representations : ENST00000414315
ENST00000359597
ENST00000420246
ENST00000419024
ENST00000455263
ENST00000396473
ENST00000269305
ENST00000445888
ENST00000413465
Expression for TP53 gene
(Experimental results according to
1 GeneNote
and GNF BioGPS ,
probe sets-to-genes annotations according to
2 GeneAnnot ,
3 GeneTide ,
Sets of similar genes according to GeneDecks ,
Electronic Northern calculations according to data from
UniGene (Build 223 Homo sapiens),
SAGE tags according to
CGAP ,
plus additional links to
SOURCE , and/or
GNF
BioGPS , and/or
EXPOLDB , and/or
UniProtKB ,
Expression Assays from
Applied Biosystems ,
Primers from
OriGene and/or
SABiosciences
)
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User Feedback TP53 expression in normal and diseased human tissues Applied Biosystems TaqMan ® Gene Expression Assays for TP53 1 / 2 / 3
7 probe-sets matching TP53 gene
Affymetrix probe-set
Array
GeneAnnot data
GeneNote data
GeneTide data
# genes
Sensitivity
Specificity
Correlation
Length
Gb_Accession
Consensus
Uniqueness
Score
Rank
1974_s_at2 , 3
U95-A
1
1.00
1.00
0.82
0.88
X02469
1.00
1.00
1.00
1
1939_at2 , 3
U95-A
1
0.94
1.00
0.74
1.29
M22898
0.20
1.00
0.72
1
31618_at2 , 3
U95-A
1
0.75
1.00
0.54
0.84
S66666
0.60
1.00
0.82
1
211300_s_at2 , 3
U133-A
1
1.00
1.00
--
--
K03199
0.80
1.00
0.91
1
201746_at2 , 3
U133-A
1
1.00
1.00
--
--
NM_000546
0.60
1.00
0.82
1
211300_s_at2
U133Plus2
1
1.00
1.00
--
--
--
--
--
--
--
201746_at2
U133Plus2
1
1.00
1.00
--
--
--
--
--
--
--
About this table
TP53 for expression About GeneDecksing Data from
Genenote  
(Publications) and GNF BioGPS About these images About these images CGAP SAGE TAG: TTTTGTAGAG SOURCE GeneReport for Unigene cluster: Hs.654481 Expression variation in blood from EXPOLDB for TP53
Primers: Origene genome-wide validated SYBR primer pairs: TP53 SABiosciences RT2 qPCR Primer Assay for TP53: PPH00213A
Orthologs for TP53 gene
(Orthologs according to
1,2 HomoloGene (2 older version, for species not in 1 newer version),
3 euGenes ,
4 SGD
and/or
5 MGI May 08 2010,
with possible further links to
Flybase
and/or
WormBase ,
Gene Trees according to Ensembl )
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Orthologs for TP53 gene from 5/8 species (see all 8
)
About this table Species with no ortholog for TP53 ENSEMBL Gene Tree for TP53 Paralogs for TP53 gene (Paralogs according to 1 HomoloGene and 2 Ensembl , Pseudogenes according to 3 Pseudogene.org )About This Section
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User Feedback Paralogs for TP53 gene TP73 2 TP63 2
TP53 for paralogs About GeneDecksing
Genomic Variants for TP53 gene (SNPs according to the
1 NCBI SNP Database ,
2 Ensembl ,
3 PupaSUITE , and
UniProtKB ,
Linkage Disequilibrium by HapMap ,
Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants ,
Genotyping Reagents from
Applied Biosystems )
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HapMap Linkage Disequilibrium images for TP53 (up to first 250kb)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions) Database of Genomic Variants (DGV) variations for TP53: --
Disorders & Mutations for TP53 gene
(in which this Gene is Involved, According to
OMIM, UniProtKB ,
Novoseek , PharmGKB ,
Genatlas , GeneTests ,
Blood group antigen gene mutations by BGMUT ,
LSDB, HGMD, GAD ,
HuGE Navigator ,
BCGD,
and/or TGDB .)
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TP53 for disorders About GeneDecksing
OMIM: 191170 disorders : 114500 151623 114550 259500 260500 161550 260350 202300 114480 UniProtKB/Swiss-Prot: P53_HUMAN, P04637
TP53 is found in increased amounts in a wide variety of transformed cells. TP53 is frequently mutated or inactivated in about 60% of cancers Defects in TP53 are involved in esophageal squamous cell carcinoma (ESCC) [MIM:133239]. ESCC is a tumor of the esophagus Defects in TP53 are a cause of Li-Fraumeni syndrome (LFS) [MIM:151623]. LFS is an autosomal dominant familial cancer syndrome that in its classic form is defined by the existence of a proband affected by a sarcoma before 45 years with a first degree relative affected by any tumor before 45 years and another first degree relative with any tumor before 45 years or a sarcoma at any age. Other clinical definitions for LFS have been proposed (PubMed:8118819 and PubMed:8718514) and called Li-Fraumeni like syndrome (LFL). In these families affected relatives develop a diverse set of malignancies at unusually early ages. Four types of cancers account for 80% of tumors occurring in TP53 germline mutation carriers: breast cancers, soft tissue and bone sarcomas, brain tumors (astrocytomas) and adrenocortical carcinomas. Less frequent tumors include choroid plexus carcinoma or papilloma before the age of 15, rhabdomyosarcoma before the age of 5, leukemia, Wilms tumor, malignant phyllodes tumor, colorectal and gastric cancers Defects in TP53 may be associated with nasopharyngeal carcinoma [MIM:161550]; also known as nasopharyngeal cancer Defects in TP53 are found in Barrett metaplasia; also known as Barrett esophagus. It is a condition in which the normally stratified squamous epithelium of the lower esophagus is replaced by a metaplastic columnar epithelium. The condition develops as a complication in approximately 10% of patients with chronic gastroesophageal reflux disease and predisposes to the development of esophageal adenocarcinoma Defects in TP53 are involved in head and neck squamous cell carcinomas (HNSCC) [MIM:275355]; also known as squamous cell carcinoma of the head and neck Defects in TP53 are involved in oral squamous cell carcinoma (OSCC). Cigarette smoke is a prime mutagenic agent in cancer of the aerodigestive tract Defects in TP53 are a cause of lung cancer [MIM:211980] Defects in TP53 are a cause of choroid plexus papilloma [MIM:260500]. Choroid plexus papilloma is a slow-growing benign tumor of the choroid plexus that often invades the leptomeninges. In children it is usually in a lateral ventricle but in adults it is more often in the fourth ventricle. Hydrocephalus is common, either from obstruction or from tumor secretion of cerebrospinal fluid. If it undergoes malignant transformation it is called a choroid plexus carcinoma. Primary choroid plexus tumors are rare and usually occur in early childhood Defects in TP53 are a cause of one form of hereditary adrenocortical carcinoma (ADCC) [MIM:202300]. ADCC is a rare childhood tumor, representing about 0.4% of childhood tumors, with a high incidence of associated tumors. ADCC occurs with increased frequency in patients with the Beckwith-Wiedemann syndrome [MIM:130650] and is a component tumor in Li-Fraumeni syndrome [MIM:151623]
10/2562 Novoseek disease relationships for TP53 gene (see all 2562
)
Disease
Score
Articles
PubMed IDs for Articles with Shared Sentences (# sentences)
astrocytoma
100.00
463
19428789 (9), 10063271 (9), 9839169 (8), 8293408 (7) (see all 100 )
bladder cancer
100.00
917
11690548 (7), 7869472 (6), 17982131 (6), 12629332 (6) (see all 100 )
squamous cell carcinoma
100.00
2049
12610510 (10), 9127380 (9), 15390206 (9), 9388973 (7) (see all 100 )
colorectal cancer
100.00
1716
9587516 (8), 16416012 (8), 19954513 (7), 15958644 (7) (see all 100 )
glioblastoma
100.00
545
9839169 (8), 19706164 (7), 9166509 (6), 18462472 (6) (see all 100 )
retinoblastoma
100.00
982
9367711 (8), 9186339 (8), 7850321 (8), 10792093 (8) (see all 100 )
li-fraumeni syndrome
100.00
486
8649766 (9), 19834951 (7), 11245491 (6), 9703430 (5) (see all 100 )
tumor progression
100.00
725
19638963 (4), 18425359 (4), 16247444 (4), 12907609 (4) (see all 100 )
escc
100.00
408
19730383 (8), 17060721 (7), 16271069 (6), 16230424 (6) (see all 100 )
growth arrest
100.00
919
8756351 (6), 8183918 (5), 9314841 (4), 8754845 (4) (see all 100 )
About this table 5 PharmGKB disease relationships for TP53 gene About this table GeneTests: TP53 Li-Fraumeni Syndrome Locus Specific Mutation Databases: TP53 Human Gene Mutation Database : TP53 Genetic Association Database: TP53 Human Genome Epidemiology Navigator: TP53 (898 documents) Tumor Gene Database : TP53 Breast Cancer Gene Database : TP53
Medical News for TP53 gene (Possibly Related Articles in
Doctor's Guide )
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Publications for TP53 gene (in
PubMed .
Associations of this gene to articles via
1 Novoseek ,
2 HGNC ,
3 Entrez Gene ,
4 UniProtKB/Swiss-Prot ,
5 UniProtKB/TrEMBL ,
6 GAD , and/or
7 PharmGKB )
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User Feedback 10/17856 PubMed articles for TP53 gene (see all 17856
): Isolation and characterization of a human p53 cDNA clone: expression of the human p53 gene. (PubMed id 6396087) 2, 3 , 4 Matlashewski G....Benchimol S. (1984) Differential regulation of p53 and p21 by MKRN1 E3 ligase controls cell cycle arrest and apoptosis. (PubMed id 19536131) 1, 3 , 4 Lee E.-W.... Song J. (2009) The role of P53 and MDM2 polymorphisms in the risk of esophageal squamous cell carcinoma. (PubMed id 16230424) 1, 3 , 6 Hong Y....Lin D. (2005) [p53 gene codon 72 polymorphism and susceptibility to keloid] (PubMed id 16128105) 1, 3 , 6 Zhuo Y....Zhao Y.Z. (2005) The p53 codon 72 polymorphism in Thai nasopharyngeal carcinoma. (PubMed id 12893432) 1, 3 , 6 Tiwawech D....Ishida T. (2003) Differential effect of ik3-1/cables on p53- and p73-induced cell death. (PubMed id 11706030) 1, 3 , 4 Tsuji K.... Matsuoka M. (2002) p53 alterations in human squamous cell carcinomas and carcinoma cell lines. (PubMed id 7682763) 1, 3 , 4 Caamano J.... Klein-Szanto A.J.P. (1993) p53 codon 72 and MDM2 SNP309 polymorphisms and age of colorectal cancer onset in Lynch syndrome. (PubMed id 16203772) 1, 3 , 6 Sotamaa K....de la Chapelle A. (2005) Gene-gene and gene-environmental interactions of p53, p21, and IRF-1 polymorphisms in Korean women with cervix cancer. (PubMed id 14764039) 1, 3 , 6 Lee J.E....Park J.S. (2004) [Association of p53 gene polymorphism with susceptibility to ovarian cancer] (PubMed id 15634502) 1, 3 , 6 Kang S....Li Y. (2004)
Search for TP53 gene
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AND OR
Aliases
TP53 (Gene Symbol) tumor protein p53 LFS1 p53 Phosphoprotein p53 P53 p53 antigen TRP53 transformation-related protein 53 FLJ92943 p53 tumor suppressor p53 transformation suppressor Tumor suppressor p53 Antigen NY-CO-13
Disorders
anal condyloma xeroderma pigmentosum group a varicocele salivary gland carcinoma t(11; 14)(q13; q32) skin ulcer clonal evolution giant porokeratosis h pylori infection lichen sclerosus lymphoma splenic granulocytic sarcoma braf gene mutation adrenal carcinoma polyp benign malignant basal cell tumor colorectal adenocarcinoma posterior capsule opacification endometrial cancer, stage lesion; aortic unbalanced translocation primary cutaneous large t-cell lymphoma papillary microcarcinoma photodamaged skin bilateral retinoblastoma hidradenoma human mammary carcinoma htlv-i pituitary carcinoma gliosarcoma skin metastases adenoviral infection pulmonary capillary hemangiomatosis b-cell lymphoma recurrent pancreatic endocrine tumor acute generalized exanthematous pustulosis ulcerative jejunitis ovarian cancer stage iii hypertension malignant androgen independent prostate cancer plaque psoriasis restriction site polymorphism sclerosis; systemic hepatitis viral ovarian serous carcinoma trisomy 12 refractory cll arthritis, collagen-induced choline deficiencies metastasis spiradenoma seckel syndrome cardiac tumor chagas disease lentigo maligna benign laryngeal neoplasm vasculitis chronic glomerulonephritis leishmaniasis visceral oesophageal squamous cell carcinoma stage iii colorectal cancer dukes c anal squamous cell carcinoma recurrent nasopharyngeal carcinoma minimal deviation melanoma adenovirus infection esophageal adenocarcinoma granulosa cell tumor hypoplasia medullary thymoma carcinoid tumor pulmonary endometrial intraepithelial neoplasia occlusion; vessel gene abnormality malignant germ cell tumor occupational cancer ovarian granulosa cell tumor diabetic polyneuropathies adult-onset still disease cystitis interstitial BCC invasive breast cancer ovarian cancer stage recessive dystrophic epidermolysis bullosa multiple endocrine neoplasia type 2 ciliary body melanoma dystrophies fatty liver ovarian serous cystadenoma coronary restenosis breast-ovarian cancer brain disease infertility mixed thymoma breast cancer stage iiib NF1 urinary tract tumor inflammatory disease duodenal adenocarcinoma chromosome 12 trisomy breast cancer hypercholesterolemia refractory cancer follicular tumor keratocystic odontogenic tumor tumor promotion cervical intraepithelial neoplasia adult glioblastoma atrophic oral lichen planus carcinoma; nasopharyngeal adenoid; cyst ebv infection metachromatic leukodystrophies nonfunctioning pituitary adenoma brainstem glioblastoma intraepithelial carcinoma hyperglycemia leukoplakia oral mucosa anemia elastofibroma cervical cancer cancer other hypertrophic obstructive cardiomyopathies bone marrow toxicity pelvic cancer 8 trisomy prostatic adenocarcinoma multifocal osteosarcoma lichen planus hepatoblastoma plane wart colitis disseminated cancer atypical adenomatous hyperplasia gynecologic cancer replication error secondary mds osteoblastic osteosarcoma chronic dermatitis angina stable adenoma; basal cell aftereffect parotid tumor cholangioma genetic syndrome viral pathogenesis din 1a intracranial tumor hypersensitivity reaction type hidradenocarcinoma pharyngeal carcinoma squamous cell sezary syndrome hyperplasia; parathyroid sarcoid granuloma t-all immature teratoma infection; mycoplasma cloacogenic carcinoma dysplasia; ectodermal borderline ovarian tumor granulomatosis; wegener complicated pregnancy biliary tract cancer vin i granular cell tumor serous carcinoma porocarcinoma liposarcoma; pleomorphic metastatic ovarian carcinoma gastric carcinoid c-cell hyperplasia granuloma pyogenic differentiated vulvar intraepithelial neoplasia atypical choroid plexus papilloma borderline neoplasm pancreatic adenosquamous carcinoma egfr protein overexpression pleural mesothelioma papillomavirus infection chromosomal mutation demented LL leukemia l1210 hepatitis a hyperthyroidism chronic neutrophilic leukemia obstruction virus; bronchitis gastric mucosal atrophy sweat gland tumor pancreatic adenocarcinoma resectable hyperestrogenism nevi hepatitis viral infections diffuse type carcinoma precancerous lesions chronic idiopathic thrombocytopenic purpura histiocytic sarcoma melanosis coli fibrous histiocytoma duodenal tumor prostate cancer recurrent chronic gastritis high-grade lymphoma hashimoto thyroiditis celiac disease cyst; radicular lewis lung carcinoma malignant glioma hiv disease progression gliofibroma lipoma sarcoma; spindle cell hyperdiploidy connective tissue disease monosomy 5 turcot syndrome infarct hypersensitivity pneumonitis gliosis estrogen deficiency myelolipoma STIC bladder neck ocular defect smoldering multiple myeloma cervical cancer squamous cell arteriosclerosis acinic cell carcinoma primary lymphoma, brain axillary metastases colorectal mucinous adenocarcinoma macroglobulinemia; waldenstrom renal failure acute ischemic chromophobe cell renal carcinoma small intestinal adenocarcinoma collecting duct carcinoma eosinophilia bronchiolization benign follicular tumor radiation-induced dna damage retinal tumor CAD renal oncocytoma solitary kidney persistent infection conjunctival melanoma complications; postoperative superficial spreading melanoma dysplastic nevi pleomorphic rhabdomyosarcoma dementia sinonasal carcinoma structural chromosomal alterations microsatellite instability MDS cerebrotendinous xanthomatosis temperature-sensitive mutation vulvar dystrophy teratocarcinoma melanoma metastatic autoimmunities gastric adenoma diabetes; type 2 ganglioneuroblastoma, nodular parvovirus b19 infection ganglioneuroblastoma seminoma human papilloma virus infection undifferentiated gastric carcinoma basal cell hyperplasia fracture pathological neurological disorder scleroderma replication error phenotype primary liposarcoma papillary serous endometrial carcinoma alzheimer disease 2 translocation; trisomy 18 atypical endometrial hyperplasia cancer recurrence grade iii meningioma change; cognitive sarcoma microglandular adenosis disease; ischemic heart carotid atherosclerosis necrosis; tubular genomic instabilities histiocytic necrotizing lymphadenitis iatrogenic kaposi sarcoma chromosome instability syndrome encephalomyelitis malignant mixed mullerian tumor invasive carcinoma her-2 positive breast cancer chronic inflammatory disease unilateral breast cancer bacterial infection liposarcoma graft dysfunction acute myelomonocytic leukemia mesonephric hyperplasia ovarian leiomyosarcoma colorectal polyp bk virus infection calcification carcinoid hairy cell leukemia squamous cell carcinoma differentiated aberrant dna methylation absence status malignant ovarian germ cell tumor atypical intraductal hyperplasia mitochondrial damage pleural metastasis tumorigenicity radiation-induced recombination endometrial intraepithelial carcinoma eyelid tumor spongiform encephalomyelopathy adenocarcinoma metastatic extensive stage small cell lung cancer ocular tumor clear cell ependymoma t-cell neoplasm allelic imbalance leukemia lymphoid secretory carcinoma spindle cell haemangioendothelioma ovarian tumor splenic marginal zone lymphoma mesangial proliferation casp8, asp302his polymyositis androgenetic alopecia cartilaginous tumor renal tumor autoimmune neutropenia cystitis gastric intestinal type adenocarcinoma lymphocytic infiltrate herpes simplex immunopathology childhood lymphoma numerical chromosomal abnormalities neurodegenerative disease hypopharyngeal carcinoma bladder adenocarcinoma eccrine poroma inflammatory myofibroblastic tumor lip cancer cystadenocarcinoma epithelioid hemangioma TTD sebaceous hyperplasia ovarian cancer ALL pterygium chondromatosis atherogenesis solid carcinoma KA fibrosis liver adenocarcinoid tumor endometrioid tumor tumor virus infection hypopharyngeal squamous cell carcinoma papillary urothelial neoplasm sebaceous carcinoma sclc mental retardation ovarian cystadenoma cell injury growth delay familial wilms tumor progressive supranuclear palsies strongyloides stercoralis infection li-fraumeni syndrome active chronic inflammation papillomatosis malignant eyelid tumor infection; salmonella calcifying odontogenic cyst salivary gland adenocarcinoma dermatomyositis lung carcinoma recurrent adamantinomatous craniopharyngioma hepatobiliary disease gastric malt lymphoma bloom syndrome breast cancer recurrent ovarian endometriosis tonsillar cancer stillbirth retinal damage gastritis warthin tumor well-differentiated thymic carcinoma sporadic gastric adenocarcinoma malignant brenner tumor adult fibrosarcoma metastatic pancreatic cancer brainstem astrocytoma leukemogenesis ampullary adenocarcinoma cholecystitis neovasculature choriocarcinoma primary varicose veins peritoneal carcinomatosis mammary paget disease erythroleukemia triple-negative invasive breast carcinoma peutz-jegher syndrome cystic neoplasm hyperparathyroidism secondary juvenile polyp damage; renal mycosis fungoides epithelial skin tumor acute infection adult medulloblastoma bone loss carcinosarcoma abnormal spermatogenesis bilin somatic mutation shock panin benign salivary gland tumor pneumoniae dominant-negative mutant colorectal cancer hnscc eec syndrome hypertension papillary transitional cell carcinoma colonic disease bladder cancer recurrent pleomorphic xanthoastrocytoma myxoid leiomyosarcoma adenoma malignum malignant conversion transitional cell tumor huntington disease pick disease inflammatory joint disease choroid plexus carcinoma keloids chromosomal gain mesenchymal tumor cervical small cell carcinoma second malignancies severe dysplasia fetal hypoxia post-angioplasty low grade b-cell lymphoma disease; inflammatory bowel reactive hyperplasia human immunodeficiency virus myocarditis neuroendocrine carcinoma pleural thickening neuroblastic tumor n-myc gene amplification lymphoepithelioma-like carcinoma vascular malformation anaplastic meningioma trisomy 7 cutaneous lymphoproliferative disorder pelvic tumor rectal villous adenoma thymic lymphoma metastatic prostate cancer tumors, radiation-induced basal cell ameloblastoma oral disease recurrent carcinoma therapy-related aml oncogene activation congenital fibrosarcoma tuberous sclerosis 1 perianal bowens disease brain tumor malignant adenomyoepithelioma adenoma thyroid aids-related non-hodgkin lymphoma central nervous system hemangioblastoma meningioma, radiation-induced bleeding breakthrough polyp; vocal cord giant cell tumor carcinoma endometrial stage i nsclc lesion; vascular vascular disease occlusive chromosome mutation chronic myelomonocytic leukemia mediastinal seminoma tumor necrosis brain syndrome germinal epithelial inclusion cyst endocrine cancer follicular ameloblastoma actinic cheilitis ataxia polyp ulcer gallbladder adenoma vitamin excess stage ii nsclc glaucoma open-angle colorectal cancer stage ii hepatis peliosis enteropathy-type t-cell lymphoma cns tumor chronic leukemia adenomatoid tumor urothelial dysplasia cyclin d1 mrna overexpression ischemia; spinal cord renal ischemia pseudoglioma oesophageal stage iii nsclc failure; renal inguinal lymph node metastasis carcinogenesis, radiation simple endometrial hyperplasia RMS dysfunction; myocardial leukocytosis childhood choroid plexus carcinoma endometrioid carcinoma fibrosarcomas malignant chromosomal instabilities comedo carcinoma tumor escape nasal cancer testicular choriocarcinoma hypocellular lymphoma, small cleaved-cell, follicular endemic disease HL embryopathies salivary duct carcinoma ganglioneuroma cholangitis atypical meningioma mesothelioma fab m0 syndrome, zollinger-ellison shwachman-diamond syndrome gastritis h pylori lupus nephritis undifferentiated ovarian carcinoma dna virus infection respiratory papillomatosis atrial myxoma endometrial metaplasia lymphadenitis leukemia; lymphoblastic, acute (burkitt) skin carcinogenesis malignant insulinoma foot disease chromosomal deletion oral infection ovarian carcinosarcoma squamous cell carcinoma lung AA Treacher Collins syndrome pancreatic serous cystadenoma tumor hemorrhage biliary obstruction verrucous carcinoma alveolitis sarcomatoid renal cell carcinoma coronary atherosclerosis adenoma villous moderate epithelial dysplasia gastric hyperplasia binucleate cell neck cancer squamous cell inflammation trichilemmal carcinoma malignant mixed tumor lymphoid hyperplasia urothelial neoplasm borderline ovarian serous tumor liposarcoma recurrent hepatic hemangioma bowen disease pancreatic adenocarcinoma glioblastoma biphasic mesothelioma rectal cancer stage iii achondroplasia adenosarcoma anemia megaloblastic bladder cancer primary brain tumor cardiac rupture chromosome trisomy increased growth osteoarthritis laryngeal carcinoma moderate dysplasia angiogenic switch dna crosslink esophagitis reflux ileal pouch mixed cellularity vaginal carcinoma telomere shortening primary demyelination breast tumor hepatoid adenocarcinoma invasive ductal carcinoma alveolar soft part sarcoma metastatic uremia pineocytoma neural tumor precancerous condition papillary squamous cell carcinoma hnpcc inverted urothelial papilloma prostate cancer stage d ocular melanoma pinguecula cardia familial alzheimer disease retroviral infection invasive bladder transitional cell carcinoma adcc angiofibroma infertility male vitamin a deficiencies hyperparathyroidism primary large breast thrombophilia choledochal cyst esophageal cancer warburg effect genetic disorder syringocystadenoma papilliferum duodenal ulcer arthritis BSG high-grade squamous intraepithelial lesion hypopharyngeal tumor secondary glioblastoma lung tumor adrenal disease myelofibrosis anterior tongue tumor papillary adenocarcinoma pediatric glioblastoma multiforme gastrinoma atherosclerosis extramammary paget disease metaplasia discoid lupus erythematosus canarypox invasive; mole neuroblastoma gastroschisis porokeratosis, disseminated superficial actinic, 2 colorectal signet ring cell carcinoma cholecystitis chronic mesial temporal sclerosis cancer regression composite lymphoma heterotopia pancreatitis dna replication damage breast tubular adenoma base pair mismatches intestinal metaplasia smokers lung stage iiia nsclc b; hemophilia pelvic endometriosis benign lymphoepithelial lesion ovarian germ cell tumor clear cell chondrosarcoma autistic anemia refractory primary glioblastoma diffuse; lymphoma, mixed cell type inverted schneiderian papilloma NF2 stage i nsclc glioblastoma multiforme testis cancer lissencephalies tic oral mucosal disorder lip squamous cell carcinoma pin-1 common tumor low grade b-cell non-hodgkins lymphoma non-alcoholic steatohepatitis peritoneal mesothelioma gastric hamartoma metastatic carcinoma pediatric ependymoma acute myocardial ischemia cerebral malaria tumor initiation viremia tubular adenocarcinoma condyloma acuminatum colon cancer stage ii nbccs leukemia plasma cell acinar cell tumor acute ischemia intraepidermal carcinoma deficiency; vanadium primary leiomyosarcoma collagen vascular disease bone sarcoma encephalitis ampullary tumor hepatocarcinogenesis atypical hyperplasia fetal resorption tumor stage mycosis fungoides distortion keratoses laryngeal papilloma hereditary hemochromatosis extensive disease eczema esophageal squamous papilloma oropharyngeal cancer benign meningioma carcinoma transitional cell vascular proliferation subependymoma effusion blastoma nk cell leukemia sweat gland carcinoma mdm2 gene amplification hyperkeratosis focal necrosis hellp syndrome little disease hereditary ovarian carcinoma neuroendocrine tumor CLL breast cancer metastatic leukemia, transient steatosis renal angiomyolipoma dlbcl verrucous penile carcinoma medulloblastoma breast phyllodes tumor amyloid deposition malignant solid tumor xeroderma pigmentosum, complementation group e hormone-refractory prostate cancer canalicular adenoma autoimmune hepatitis acute myeloid leukemia sinonasal papilloma childhood liver cancer complete mole focal nodular hyperplasia fibrolamellar hepatocellular carcinoma rectal cancer dukes b2 alcoholism neurofibroma NPC biliary stricture craniopharyngioma cardiac carcinoma undifferentiated neuroblastoma porokeratosis palmaris et plantaris disseminata sebaceous adenoma bloody stool lipofuscin accumulation juvenile idiopathic arthritis ovary; polycystic (syndrome) malignant triton tumor cutaneous vascular tumor neoplastic process urothelial papilloma oral lichen planus aneurysm aortic edentulous rectal adenoma nf2 gene mutation refractory tumor microcephalies transitional cell metaplasia colorectal cancer stage iv trophoblastic tumor cronkhite-canada syndrome vin ii vulvar pagets disease latent infection myositis; ossificans glucose tolerance impaired biliary disease hepatitis c virus-related hepatocellular carcinoma generalized aggressive periodontitis dysplasia lysosomal storage disorders anaplastic astrocytoma disease, tay-sachs edema aml1 mutation extra-adrenal pheochromocytoma plexiform neurofibroma branchial cleft cyst gastrointestinal cancer relapsed neuroblastoma laryngeal polyp insertion mutation combined type sclc thyroid lymphoma adult diffuse large b-cell lymphoma balkan endemic nephropathy cheilitis malignant mammary phyllodes tumor syringoma growth arrest ependymoma osteonecrosis brain hypoxia ischemia alveolar soft part sarcoma verrucous oral leukoplakia hamartomatous polyp cardiac rhabdomyosarcoma cribriform carcinoma brain tumor protoplasmic astrocytoma carcinoma; thymic multiple endocrine neoplasia type 1 meningeal hemangiopericytoma leukemia secondary breast cancer, familial hypersensitivity disorder tumor embolus leukemia stem cell parkinsonism adenoma; hepatocellular renal dysplasia fibrillary astrocytoma precancerous skin lesion osteoid osteoma superinfection atherosclerotic plaque large cell neuroendocrine carcinoma ovarian hyperstimulation RA brca2 mutation fsgs microinvasive carcinoma erythroplakia duodenal polyp leukemia; monoblastic eye cancer oropharyngeal squamous cell carcinoma klatskin tumor glucagonoma pancreatic cancer benign ameloblastoma nonseminomatous germ cell tumor cutaneous squamous cell carcinoma vestibular schwannoma hematotoxicity MFH malignant solitary fibrous tumor pleomorphic cell sarcoma SCC small intestinal carcinoma localized disease sialoblastoma leukemia prolymphocytic juvenile pilocytic astrocytoma grade i astrocytoma cryptorchidism medullary breast carcinoma cyclin d1 protein overexpression hereditary cancer syndrome porokeratosis tumor angiogenesis adult t-cell leukemia testicular intraepithelial neoplasia proliferative breast disease central nervous system diffuse large b-cell lymphoma malignant stromal tumor gynecologic tumor conjunctival squamous cell carcinoma subependymal giant cell astrocytoma cancer differentiated moderately advanced cancer mgus maffucci syndrome tumor vasculature alopecia areata ovarian disease condyloma proliferating trichilemmal cyst peritoneal cancer alcoholic cirrhosis deficiency; zinc supratentorial pnet glomerulosclerosis oligoastrocytoma endometrial endometrioid adenocarcinoma kras gene mutation soft tissue tumor diffuse astrocytoma dukes a colorectal carcinoma low-grade cin dwarf corneal infection cholestasis chronic metastatic prostatic adenocarcinoma lesion; skin cervical cancer stage ib dermatitis choriomeningitis lymphocytic immunoblastic lymphoma endometrial undifferentiated carcinoma oligodendroglioma desmoplastic infantile astrocytoma bilateral cancer cerebellar liponeurocytoma monosomy 7 neck metastasis ovarian endometrioid carcinoma neurodegeneration rectal cancer recurrent multiple cancer, primary dedifferentiated liposarcoma osteosarcoma; small cell intraductal papillary-mucinous adenoma skeletal malformation retinopathies cervical leukoplakia ovarian yolk sac tumor brainstem glioma cardiac hypertrophy autoimmune response benign pheochromocytoma soft tissue lesion squamous cell carcinoma differentiated moderately hematological disorders human papillomavirus mucosal disease ubiquinone dehydrogenase bone metastases hepatic necrosis disorder myeloproliferative ovarian cancer, familial synovial sarcoma comedo poorly differentiated colorectal adenocarcinoma malignant lipomatous tumor dyskeratosis congenita fallopian tube adenocarcinoma thyroid disease mucocele cholestasis intrahepatic aneuploid bronchioloalveolar carcinoma interstitial pneumonia papillary urothelial carcinoma lung cancer 1 premalignant lesion bronchial adenocarcinoma endocervical adenocarcinoma hurthle cell neoplasm stage iv melanoma metaplastic carcinoma lesion; primary brain infarction mass phenotype ecl cell carcinoid cervical cancer stage iii large cell carcinoma thrombus colon cancer stage iii localized osteosarcoma insulinoma homogeneously staining region endometrial tumor psoriasis friend leukemia sex cord-stromal tumor dupuytren t cell deficiency adenomatous polyposis coli sialadenitis lymph node metastasis adenoma tubular sbla syndrome idiopathic pulmonary fibrosis desmoplasia acute biphenotypic leukemia silicotics helicobacter pylori gastritis hilar cholangiocarcinoma protein deregulation pancreatic exocrine tumor middle cerebral artery occlusion submandibular gland tumor well differentiated chondrosarcoma skull base chordoma gastrointestinal tumor chemoradiation invasive prostate carcinoma acute lymphoblastic leukemia chronic hepatitis acute graft-versus-host disease low-grade lymphoma endometrial stromal sarcoma keratoacanthoma clear cell tumor trisomy 17 plasma membrane alteration teratoma chronic hepatitis b primary cutaneous amyloidosis multiple system atrophies childhood central nervous system primitive neuroectodermal tumor type ii endometrial carcinoma fragile x syndrome multiple myeloma hepatobiliary tumor common acute lymphoblastic leukemia chronic lung disease lupus cutaneous spiradenocarcinoma fibromatosis; retroperitoneal high-risk cancer epidermoid carcinoma, nasopharyngeal ovarian mucinous tumor non-small cell carcinoma chromosome fragment rheumatic disease hepatitis b virus-related hepatocellular carcinoma corticotroph adenoma epithelioid hemangioendothelioma penile tumor endometrium; postmenopausal DSAP lung cancer systemic disease AML isochromosome 17q intestinal adenoma brain metastases SCID lymphadenopathies elastosis psoriasis vulgaris colon adenocarcinoma group b cockayne syndrome parathyroid tumor diabetic nephropathies malignant cylindroma rectal cancer cyst; inclusion embryonal rhabdomyosarcoma oral cancer hepatitis pharyngeal cancer tuberous sclerosis complex malignant smooth muscle tumor adenomatous nodule dysplastic oral leukoplakia deletion abnormality achalasia cardiovascular disease mixed oligoastrocytoma endometrial polyp benign glaucoma morphologic alteration flt3 internal tandem duplication lobular hyperplasia vascular malformation cerebral b-cell prolymphocytic leukemia fraxa normal tension glaucoma hormone replacement obese blast crisis tumor ulceration ectrodactyly brain damage (perinatal) MADD primary cutaneous lymphoma fibrosis pulmonary deficiency; immune cutaneous lupus erythematosus cytopenia desmoplastic trichoepithelioma recurrent adrenocortical carcinoma giant cell glioblastoma benign sweat gland tumor hyperplastic polyp guttate psoriasis disease; lung chronic myeloid leukemia partial mole congenital mesoblastic nephroma clear cell endometrial carcinoma skin toxicity intestinal cancer endometrial hyperplasia plasmacytoma cervical carcinoma, invasive cns lymphoma unknown primary tumor open eye hemangioendothelioma fatal outcome spot, white residual tumor pleural empyema cellular leiomyoma liver mass parathyroid carcinoma choroid plexus papilloma carcinoma; endocrine intestinal dysplasia occlusion; vascular demyelinating disease ovarian cancer stage i skin pigmented paragangliomas 3 malignant primary brain tumor hypertrophic actinic keratosis brain pathology dcis, comedo type adenomatosis anaplastic ependymoma acute renal failure fibrous histiocytoma malignant mucinous tumor carcinoma; hurthle cell penile squamous cell carcinoma growth alteration peritoneal metastases bronchial tumour murine encephalomyelitis rubella cystadenoma mucinous ovarian atrophy myoepithelioma ovarian cystic teratoma gastrointestinal disease adult soft tissue sarcoma primary sclerosing cholangitis papillary tumor recurrent cholesteatoma multiple cancer germinoma benign prostate hyperplasia macronucleus b-all cerebral arteriovenous malformation minimal residual disease squamous cell carcinoma intestinal tumor central neurocytoma intestinal lymphoma angelman syndrome gist, malignant invasive melanoma adenofibroma fuch endothelial dystrophy cyst; epithelial gerd pancreatic mucinous cystic neoplasm splice-site mutation partial obstruction adenoma cerebral cavernous malformations gene genetic abnormality bile duct stenosis aml progression hypoplasia; limb sporadic breast cancer cholesteatoma middle ear lincl signet-ring cell carcinoma chronic lymphoma limb malformation vertical transmission biphasic pulmonary blastoma terminal disease prostate cancer stage c benign skin tumor gastric tumor epilepticus; status colorectal serrated adenoma bladder cancer stage microinvasive squamous cell carcinoma ameloblastoma increased drug resistance misalignment hydropic change inflammatory breast cancer adenocarcinoma mucoepidermoid carcinoma leukemia, adult acute bronchopulmonary dysplasia leukoplakia rectal adenocarcinoma cin iii ependymoma benign neck tumor meningioma; transitional bannayan-riley-ruvalcaba syndrome poag malnutrition, protein-energy mammary tumorigenesis cerebellar pilocytic astrocytoma cin i norrie disease actinic porokeratosis ovarian serous tumor fibroadenoma high-grade cin gastric dysplasia myxoma; odontogenic uterine leiomyosarcoma ppar-gamma rearrangement basal squamous cell carcinoma intramuscular myxoma uterine cancer single tumor drug abuse intravenous chordoma penile intraepithelial neoplasia gastric polyp nuclear accumulation goiter supraglottic squamous cell carcinoma NECs influenza chronic lung injuries thyroid cancer (follicular cell) gestational trophoblastic disease testicular seminoma cdkn1a, ser31arg colonic dysplasia laryngeal papillomatosis dedifferentiated chondrosarcoma retinal neovascularization enteropathy anal cancer triton tumor superficial bladder cancer b virus infection beckwith-wiedemann syndrome breast mouse tenosynovial giant cell tumor malformation arthritis reactive flat adenoma epilepsies primary effusion lymphoma tp53 gene inactivation cecal carcinoma actinic keratosis polysomy mlh1, hypermethylation nonsense mutation nasal polyp anterior myocardial infarction hypoglycemia b-cell malignancy, low-grade meningitis pneumococcal adult astrocytic tumour lymphocytosis olfactory neuroblastoma gastric mucosal lesion papillary cystitis pancreatoblastoma polydactylies deficiency; niacin progressive multifocal leukoencephalopathies spindle cell tumor low-grade glioma abdominal aortic aneurysm duct ectasia gastric cancer stage iii tongue tumor adult hepatocellular carcinoma prostate cancer stage b primary acquired melanosis cns malignancy adenocarcinoma endometrial hereditary melanoma impaired wound healing aortic atherosclerosis multifocal dysplasia drinking; habitual prostate tumor leukemia; lymphoma chromosomal rearrangement brain sarcoma gastrointestinal lymphoma fibroadenoma phyllodes b-cell lymphoma low-grade dcis intratubular embryonal carcinoma diffuse hyperplasia aging; premature arthritis psoriatic borderline epithelial tumor benign epithelial tumor adrenal metastases pediatric solid tumor fibromatoses benign colorectal neoplasm active chronic hepatitis dilatations nodular sclerosis escc ovarian epithelial tumor medullary thyroid carcinoma disorder; growth lupus erythematosus systemic squamous hyperplasia cervical carcinoma stage iib spitz nevus damage liver polycythemia growth suppression mesothelial hyperplasia gravis; myasthenia microphthalmia benign prostatic hypertrophy fgfr4, gly388arg recurrent meningioma adenocarcinoma lung atypical carcinoid tumor biliary papillomatosis barrett epithelium malignant myoepithelioma glottic squamous cell carcinoma anaplastic large cell lymphoma invasive thymoma infarction; myocardial vulvar tumor structural chromosome aberration aids-related malignancies chromosomal aberration neurofibrillary tangle colonic adenoma childhood medulloblastoma philadelphia chromosome microphakia burkitt lymphoma jet lag asbestosis cml progression gastric cancer recurrent metastatic pancreatic adenocarcinoma farber disease large cell lung carcinoma mucosal inflammation chronic phase cml glioma cancer gene mutation sporadic burkitt lymphoma anaplastic oligoastrocytoma carcinoma; renal cell cll variants angioimmunoblastic t-cell lymphoma primary central nervous system lymphoma reticuloendotheliosis papillary serous carcinoma non-neoplastic disease lung sarcoma infrequent tumor granular cell carcinoma liposarcoma; myxoid metastatic renal cell carcinoma delayed graft function histiocytosis; langerhans cell derivative chromosome synchronous bilateral breast carcinoma metastatic gastric cancer parasympathetic paraganglioma low-grade fibromyxoid sarcoma cushing disease pelvic organ prolapse oa hip encephalopathies leukemia myeloid polymorphic light eruption granuloma glomerulonephritis dentigerous; tumor high grade cervical intraepithelial neoplasia von willebrand delivery preterm gallbladder adenocarcinoma viral shedding brca1 mutation solitary fibrous tumor adenoid cystic carcinoma childhood leukemia preneoplastic condition pancreatic ductal adenocarcinoma retroperitoneal leiomyosarcoma malignant state bowenoid actinic keratosis msi-l borderline ovarian epithelial neoplasm infection respiratory cylindrical cell papilloma xeroderma pigmentosum group c glandular odontogenic cyst apoptotic dna damage desmoplastic infantile ganglioglioma cell cycle deregulation mosaicism oa knee sacrococcygeal teratoma lymphoid malignancy inverted nasal papilloma cystadenoma serous low-grade squamous intraepithelial lesion ductal hyperplasia monomorphic adenoma wound, healed invasive lobular carcinoma acute cholecystitis pituitary adenoma, non-secreting physiological stress myxoma mitochondrial dna depletion colorectal adenoma oral cavity squamous cell carcinoma carotid occlusion breast cancer stage ii n-ras gene mutation lobular carcinoma tp53, lys292ile intestinal adenocarcinoma pheochromocytoma maxillary sinus carcinoma fibrosarcoma sinonasal undifferentiated carcinoma mesodermal mixed tumor congenital cystic adenomatoid malformation pulmonary blastoma ataxia telangiectasia gene deregulation peutz-jeghers haemangioma sclerosing urogenital cancer telangiectasia skin tumor hyperplasia benign brenner tumor adnexal neoplasm clonal immunoglobulin gene rearrangement underdevelopment xeroderma pigmentosum group d leukemia hydatidiform mole mixed germ cell tumor compensatory hypertrophy bronchitis chronic gastric ulcer spinal muscular atrophy nuclear alteration atypical fibroxanthoma huriez syndrome variable number tandem repeat polycystic kidney disease carcinoma gallbladder ITP angiomyolipoma nonproliferative fibrocystic change cardiomyopathies atopic dermatitis monoclonal immunoglobulin heavy chain gene rearrangement invasive growth egfr gene amplification bilateral diffuse uveal melanocytic proliferation hutchinson-gilford progeria syndrome deficiency; protein focal acute inflammation undifferentiated osteosarcoma benign nevi psoriatic plaque klippel-feil syndrome bone marrow tumor familial cancer degeneration retinal infection viral urological cancer sclerosis ovarian mucinous carcinoma iugr glomerular disease recurrent pterygium vascular hypoxia chronic esophagitis asthma spontaneous rupture papilloma skin bone marrow metastases brenner tumor obstructive uropathy jaundice cardiovascular risk factor bcl-2 translocation adult solid tumor abuse; tobacco intraductal breast neoplasm malnutrition proteinuria tuberculosis chemical carcinogenesis immunodeficiency clear cell carcinoma latent virus infection deficiency; iron hypersensitivities warts pttg overexpression exencephalies small intestinal gist paranasal sinus carcinoma duodenal adenoma prolactinoma paranasal sinus tumor serous effusion uterine carcinosarcoma lead line fixation; vocal cord crohn overlap syndrome basaloid carcinoma chronic hepatitis c cyst; dentigerous vulvar intraepithelial neoplasia laryngeal squamous cell carcinoma myxosarcoma adenomatous hyperplasia chronic hepatitis, b virus AD pathological angiogenesis lymph node cancer restenosis atypical alveolar hyperplasia epidermolysis cancer family syndrome small noncleaved cell lymphoma recurrent thymoma pediatric brain tumor cryptorchidism unilateral fundic gland polyp hemochromatosis keratinizing squamous cell carcinoma infectious chromosomal loss therapy-related acute myeloid leukemia hematopoetic islet cell carcinoma ferms megaesophagus bronchogenic carcinoma monosomy 3 benign ovarian tumor breast papillomatosis outbursts endometrioma tumor morphology reactive lymphoid hyperplasia brain death gliomatosis cerebri adenosquamous lung carcinoma cholesterol polyp hypertrophy; ventricular; left oncocytic adenoma type i endometrial adenocarcinoma ovarian cyst dermoid small intestine tumor estrogenic effect jc virus infection chromosomal duplication histiocytoma stage i malignant cutaneous melanoma male breast tumor prion disease esophageal dysplasia epithelial proliferation leiomyoma extrahepatic bile duct carcinoma reflux localized cancer cervical squamous cell carcinoma carcinoma ex pleomorphic adenoma superficial basal cell carcinoma merkel cell carcinoma intratubular germ cell neoplasia anal canal carcinoma c-myc translocation thymic hypoplasia strongyloidiasis degenerative disease copper deficiency lymphoma, t-cell piles neoplastic transformation 18 trisomy infection induced morphea colon cancer hepatosplenic t-cell lymphoma astrocytoma intestinal infection contralateral breast cancer thyroid cancer PBC abortion (spontaneous) albino chronic viral hepatitis omental metastasis influenza a virus infection tubal metaplasia ards conjunctival intraepithelial neoplasia salmonella typhimurium infection immaturity adrenocortical carcinoma clear cell sarcoma liver dysfunction undifferentiated carcinoma adenomatoid odontogenic tumor chronic superficial gastritis atrophy; thymus hereditary multiple exostoses central osteosarcoma infectious mononucleosis MPS I brcax gingival overgrowth sebaceoma leiomyosarcoma vascular disease 15 trisomy ovarian small cell carcinoma mediastinal teratoma immune tolerance epithelial-myoepithelial carcinoma hereditary pancreatitis sepsis adult aml ischemia retinal bullous pemphigoid transient ischemia papillary adenoma differentiated thyroid carcinoma cns lesion hepatic angiosarcoma intraductal proliferative lesion atrophic endometrium neuroblastoma stage polymorphic b-cell lymphoma squamous intraepithelial lesion nuclear aggregate cerebral infarction gastric cardia adenocarcinoma epilepsy temporal lobe fibroma arrhythmia cysts intradermal nevi pleomorphic adenoma adnexal carcinoma nasopharyngeal tumor extravasation innate immune response atrophic gastritis p16 gene inactivation gvhd cutaneous leishmaniasis astrocytoma, low grade deficiency; folate gastric cancer barrett esophagus non-invasive thymoma melanoma chronic ulcer dermatofibroma tumor progression ovarian cancer recurrent cardiac event severe epithelial dysplasia hairy leukoplakia nodular hidradenoma coxsackievirus carcinoma endometrial recurrent high-grade prostatic intraepithelial neoplasia botryoid sarcoma genital lichen sclerosus eruption linear porokeratosis bullosa; epidermolysis lung adenoma leydig cell tumor cytopathic effect neurofibromatosis carcinoma sarcoma apocrine metaplasia aggressive behavior bronchial dysplasia meningioma malignant blue nevus choroidal melanoma basal cell carcinoma sclerosing type pancreatic tumor high grade vulvar intraepithelial neoplasia breast disease aat deficiency pleomorphic carcinoma nodular tumor osteochondroma erythema multiforme mucinous cystadenocarcinoma acanthosis dysfunction; gland spermatocytic seminoma down syndrome focal hyperplasia brain stem tumor liposarcoma; round cell molluscum contagiosum colitis ulcerative adenoma tubulovillous inflammatory atypia parathyroid adenoma phyllodes tumor dcis grade 3 lymphoma malt primary tumor ovarian serous cystadenocarcinoma break, double-strand dna rhabdomyosarcoma disseminated superficial porokeratosis cyst benign testosterone deficiency SMS acute promyelocytic leukemia male genital warts cholelithiasis mild epithelial dysplasia MS cardiomyopathy dilated pediatric tumor breast cancer stage i malignant chondroblastoma arterial restenosis metastatic squamous cell carcinoma schistosomiasis japonica somatotroph adenoma nephrotoxic serum nephritis lymphocytic infiltration chromophobe tumor bile duct carcinoma endocrine tumor shigellosis vulvar carcinoma amoebic colitis aids-related lymphoma microglandular hyperplasia myelopathies cytoplasmic accumulation hyperparathyroidism cyclin e protein overexpression diabetes mellitus atypical adenoma dyspepsia cancer, radiation-induced myeloblastoma pterygia pigmented villonodular synovitis pregnancy early anal intraepithelial neoplasia carditis crescentic glomerulonephritis pneumoconiosis oncocytic tumor unicystic ameloblastoma ureteral cancer adnexal tumor mibelli cerebral hypoxia anaplastic ganglioglioma syndrome; turner lymphangiosis carcinomatosa melanocytic hyperplasia dermatofibrosarcoma protuberans metaplasia; squamous cell wilms tumor, favorable histology primary hyperplasia yolk sac tumor disomies, uniparental limb-mammary syndrome dcis acute coronary syndrome anterior tongue squamous cell carcinoma nephritis environmental carcinogenesis dystrophy; myotonic acute myocardial infarction cardiac angiosarcoma SAH limited stage sclc peyronie disease hypoxic crohns ileocolitis oral submucous fibrosis cellular stress posterior tongue tumor macroprolactinoma cholestasis multiple abnormalities carcinoma; odontogenic brain; ischemic lacrimal gland tumor benign breast tumor hypercalcemia carcinoma common bile duct acute pancreatitis polyposis limited cutaneous systemic sclerosis rna virus infection tonsillar squamous cell carcinoma fibroepithelial polyp pediatric supratentorial neoplasm fascination neural tube defect ependymoblastoma chondroblastoma prostate cancer lymphomatoid papulosis perianal pagets disease adjuvant arthritis cushing syndrome disease; heart corneal neovascularization intermediate-grade dcis warm ischemia demyelination goiter nodular adenocarcinoma lung stage i cholesteatoma penile carcinoma gemistocytic astrocytoma vasospasm grade 1 follicular lymphoma invasive bladder cancer epidermal hyperplasia mucosa associated lymphoid tissue transient cerebral ischemia bowenoid papulosis hmps1 paraganglioma atypical cell class i; histocompatibility complex gastric disease renal disease progressive her-2 gene amplification vin iii pyothorax-associated lymphoma cerebral astrocytoma cavitation cerebral vasospasm anaplastic thyroid carcinoma chromosome fragility disorder, late-onset adrenal tumor preneoplastic change cartilage; ossification cutaneous melanocytic neoplasm juvenile polyposis transitional cell hyperplasia cholera anal tumor basaloid squamous cell carcinoma vitiligo minimal lesion bovine leukemia hypothyroid herpes gastrointestinal neuroendocrine tumor extramedullary plasmacytoma malignant pleural effusion relapse pineal parenchymal tumor pancreatic cancer stage gastric non-hodgkin lymphoma neurofibrosarcoma thymoma cystic fibrosis supratentorial glioblastoma meibomian gland carcinoma encephalitis, tick-borne crohn colitis rheumatoid vasculitis diabetes mellitus insulin-dependent failure heart malignant rhabdoid tumor ovarian clear cell adenocarcinoma lymphoma leukemia, myeloid, ph1-negative fused fingers von brunns nests enterochromaffin-like cell carcinoid tumor colon sarcoma myopathies cognitive impairment thymic epithelial tumor cancer induction neuroendocrine cell cancer derailment 5q deletion degenerative endoreduplication necrosis acidosis renal dysgenesis persistent hyperplastic primary vitreous juvenile myelomonocytic leukemia thyroiditis vertebral anomalies chondrosarcoma lung, sequestration adenoacanthoma clear cell adenoma acute leukemia epithelial tumor disease; wilsons osteoblastoma parainfluenza osteosarcoma trisomy 3 koilocytosis prostate cancer stage cmv infection hemangioblastoma massive necrosis desmoid tumor cardiac dilatation msi-h psammoma pituitary tumor intraductal papillary adenocarcinoma ovarian sarcoma cardiac death; sudden atypical medullary carcinoma viral leukemia atherosclerotic occlusive disease ewing sarcoma benign tumor hpv-related endocervical adenocarcinoma carcinoid; goblet cell mucopolysaccharidosis helicobacter infection lewy body disease interstitial fibrosis arterial embolization peritonitis invasive micropapillary breast carcinoma papilloma genotoxic stress myxofibrosarcoma gastric gist cystic disease epithelioid mesothelioma lung melanoma papillary thyroid microcarcinoma oligodendroglial tumor laryngeal cancer recurrent accessory organ hemangiopericytoma dermatofibrosarcoma stromal tumor skin; appendage autoimmune disease cervical cancer stage arteritis; giant cell zinc excess dysgerminoma emphysema culture shock mitochondrial dna deletion cancer occult mitochondrial alteration choroid plexus tumor granular cell ameloblastoma breast sarcoma recurrent miscarriage adult syndrome hemorrhage intracerebral malignant ovarian serous tumor differentiating neuroblastoma idiopathic ulcerative colitis anemia; fanconi CHF epidermodysplasia verruciformis coagulative necrosis esophageal small cell carcinoma scrotal cancer leukemia, t-cell dermatomyositis; juvenile intracranial meningioma membranes; retention gingival carcinoma nervous system tumor fibrohistiocytic tumor richter syndrome mpnst parapsoriasis ameloblastic fibrosarcoma GCTs transgenic model hemangioma coronary occlusion dysplastic nevus syndrome adenosis brain lesion fetal adenocarcinoma limb defect uterine tumor permissiveness trichoepithelioma disorder; metabolic cleft palate photosensitized mast cell tumor chondroblastic osteosarcoma schistosomiasis follicular carcinoma congenital nevus anastomosis polycythemia vera pediatric cns tumor enzyme inhibition insulin resistance early gastric cancer familial hypercholesterolemia multifocal micronodular pneumocyte hyperplasia nerve sheath tumor dengue resection cavity null cell adenoma hyperplastic nodule transmissible canine venereal tumor ovarian metastases death fetal undifferentiated sarcoma xeroderma pigmentosum group e endometrial cancer lymphoproliferative disorder teratogenic effect adenosis sclerosing radiation syndrome intrahepatic cholangiocarcinoma follicular lymphoma dysfunction; placental tumor growth essential thrombocythemia appendiceal adenocarcinoma salivary gland tumor NHL ureteral obstruction cancer ovarian low malignant potential tumor gastric lymphoma embryonal carcinoma cutaneous melanoma fallopian tube carcinoma benign fibrohistiocytic tumor basal cell carcinoma adenocarcinoma differentiated moderately therapy-related myelodysplastic syndrome vascular tumor cell transformation vulvar lichen sclerosus lung disease granulomatous vulvar condyloma testicular torsion pnets intestinal type adenocarcinoma inflammatory cell infiltration periosteal osteosarcoma monosomies cerebellar medulloblastoma mixed glioma papillary carcinoma osteosarcoma; telangiectatic poorly differentiated thyroid carcinoma ppoma vulvar squamous cell carcinoma testicular germ cell tumor proliferative inflammation breast melanoma epithelial hyperplasia pigmentosum; xeroderma pseudoepitheliomatous hyperplasia spinal cord tumor superficial gastritis central giant cell granuloma ppnet breast cancer stage iii ampullary carcinoma werner syndrome conventional chondrosarcoma airway obstruction parotid cancer HCC ganglioglioma cystitis glandularis pancreatic ductal carcinoma hematologic malignancies barrett adenocarcinoma spinocerebellar ataxia type 1 burkitt-like lymphoma chronic renal failure chromatid break hemoglobinopathies pleurisy; tuberculous bile duct stricture disease graves acute megakaryoblastic leukemia ischemic stroke xenograft model chronic hyperplastic candidosis bullous keratopathy autoimmune TTP retroperitoneal liposarcoma stricture anemia aplastic malignant pleural mesothelioma raeb-t breast cancer stage supraglottic carcinoma inflammatory response acute disease pulmonary sclerosing hemangioma articular cartilage; degeneration squamous cell tumor blast leukemia adenomatous polyp multiple organ dysfunction syndrome retinoblastoma enchondroma mantle cell lymphoma amyotrophic lateral sclerosis, familial neuroepithelial tumor ischemia digeorge syndrome carcinoma poorly differentiated cervical lesion schizophrenia apocrine adenocarcinoma primary angiosarcoma adenocarcinoma gastric metastasizing leiomyoma hyperpigmentation functional disorder disease; hodgkin ptld urothelial hyperplasia adenoma liver pinealoblastoma break, single-strand dna hepatitis b effusion pleural atm gene mutation leukemia monocytic malignant mesothelioma malignant mastocytosis pediatric osteosarcoma recurrent tumor indolent lymphoma adrenocortical tumor lichen simplex chronicus mammary adenocarcinoma gastric lesion human herpesvirus 6 infection malignant sweat gland tumor acromegaly familial disease well differentiated liposarcoma typical carcinoid laryngeal neuroendocrine tumor enchondromatosis diabetic hyperglycemia gestational choriocarcinoma ALS mastocytoma colonic polyp tetraploidy liver adenocarcinoma human parvovirus skin cancer diphtheria malignant pheochromocytoma chondrosarcoma mesenchymal chronic infection hae iii stroke cancer differentiated poorly trisomies diffuse alveolar damage liver metastases apocrine carcinoma chronic liver disease xeroderma pigmentosum group b measle hot spots grade i vin ovarian adenocarcinoma atrophy muscle lymphoma, peripheral t-cell tongue carcinoma stage i hypogonadism adenomyosis pregnancy loss gingivitis vaccinia virus infection cutaneous lymphoma cancer relapse germline mutation intestinal gastric metaplasia ameloblastic fibroma squamous cell carcinoma tongue differentiated retinoblastoma pulmonary toxicity multiple tumors COPD melanoma recurrent HCL pancreatic acinar cell carcinoma chronic myocarditis oral papilloma gene fusion malignant disease disease; liver affect alteration cirrhosis (liver) malignant phyllodes tumor classic kaposi sarcoma atypical dysplasia chondroma childhood myelodysplastic syndrome hamartoma penile bowenoid papulosis mutagenic process dysfunction ovarian gastric adenosquamous carcinoma tabagism immunosuppression fibrous dysplasia colorectal cancer metastatic aortic stenosis serrated adenoma hepatitis c chronic disease genetic hypertension juvenile astrocytoma hyperprolactinemia glomus tumor grade 3 follicular lymphoma candidiasis chemical gastritis blister sarcoma metastatic lymphatic vessel tumor hepatotoxicity moderately differentiated neuroendocrine carcinoma fibrous tumor barkers reovirus infection atheroma; aortic preaxial polydactyly benign thymoma uveal melanoma cholangiocarcinoma lrchl lymphoma (non-hodgkins) paracoccidioidomycosis cin ii papillary hyperplasia CML stomatitis LHON pancreatic disease salivary gland pleomorphic adenoma goiter; multinodular; toxic carcinoma intestinal chronic inflammation gastrointestinal carcinoid tumor bile duct tumor hypertrophic scar chronic myeloproliferative disorder pneumoperitoneum lymphatic metastasis role playing placental disease myelodysplastic syndrome paget disease cutaneous t-cell lymphoma pleuropulmonary blastoma stage iii nasopharyngeal carcinoma polysomy 17 adenocarcinoma endometrial stage i delayed-type hypersensitivity smooth muscle tumor pulmonary granuloma histiocytosis; malignant motor deficit sarcoidosis sicca aseptic loosening thrombosis supratentorial tumor fasciitis; nodular Nbs childhood cancer colon tumor bacterial meningitis radiation leukemia polyp tubulovillous disease; protein adenosquamous carcinoma aldosteronism primary uterine sarcoma mdm2 gene mutation bone tumor addiction; drug adenocarcinoma differentiated poorly disease parkinsons posterior fossa neoplasm tongue cancer glomangiosarcoma cyst; odontogenic lung; mesothelioma high-grade sarcoma microcystic adnexal carcinoma interstitial lung disease alveolar rhabdomyosarcoma glottic carcinoma mature teratoma high grade b-cell lymphoma colitis; radiation microcalcification dfna5 solid tumor myeloid hyperplasia primary disease encapsulated thymoma leukoplakia oral schwannoma cerebral ischemia amelanotic melanoma breast papilloma metastatic basal cell carcinoma BL dna repair deficiency intraosseous ameloblastoma anaplastic oligodendroglioma spindle cell carcinoma von hippel-lindau disease odontogenic tumor endometriosis residual cancer aids-related kaposi sarcoma squamous papilloma anaplasia acute radiation colitis corneal tumor lung metastases primary adrenocortical nodular hyperplasia c-kit mutation cyclin d1 gene amplification hemangioma; infantile lymphangioleiomyomatosis gastric hyperplastic polyp antral carcinoma hypodiploidy aneurysm adenoma; pituitary slow acetylator cervical cancer recurrent oncogenesis intraepithelial prostatic neoplasia silicosis gonadoblastoma lung neuroendocrine tumor cervical adenocarcinoma atrophies basal cell tumour follicular large cell lymphoma primary peritoneal carcinoma ameloblastoma; malignant pseudotumor lymphosarcoma oral paracoccidioidomycosis nasopharyngeal juvenile angiofibroma bladder transitional cell carcinoma endothelial dysfunction embryonal tumor hypotensive carcinoma papillary thyroid posterior mediastinum carcinogenicity pancreatic exocrine cancer angiosarcoma bizarre leiomyoma desmoplastic cystadenoma iga nephropathies metastatic malignant melanoma mammary ductal carcinoma diabetic nephropathy type i stump chronic cervicitis hypertrophies anal warts common variable immunodeficiencies colorectal tumor stasis hyperplastic dystrophy autoimmune thyroid disease duodenal cancer nucleolar enlargement polysomy 3 GISTs adenomyoma active; myocarditis squamous metaplasia narcosis bilateral breast cancer effluvium; telogen adenoid basal carcinoma cockayne syndrome clastogenesis monosomy 17 nodular melanoma oral erythroplakia stress urinary incontinence extranodal lymphoma classical hodgkin lymphoma dna adduct formation pilocytic astrocytoma malignant transformation leg ulcer kaposi sarcoma medial degeneration b-cell neoplasm metastatic bladder cancer apocrine breast carcinoma cortical thymoma desmoplastic melanoma persistent lymphocytosis plasma cell dyscrasia synovial chondromatosis multiple meningioma mixed acinar-endocrine carcinoma small intestinal adenoma cervical squamous intraepithelial lesion esophagitis cancer cell growth germ cell tumor tumor; wilms neck cancer bovine lymphosarcoma endometrial polyp equine sarcoid ehrlich ascites tumor bone lesion keratocyst developmental disorder heavy chain alpha fulminant hepatitis failure liver tetrasomy carcinoma hepatocellular vascular degeneration salivary gland adenoid cystic carcinoma lymphoid tumor disease; skin gingival hyperplasia men2b dysplasia; epithelial cancer, treatment-related lung cancer stage i anaplastic lymphoma craniofacial abnormalities primary achalasia mild; cognitive impairment cowden syndrome benign thyroid tumor cutaneous myxoma brain glioblastoma aggressive non-hodgkin lymphoma chronic active hepatitis b double minutes mutagenic effect mucinous carcinoma pancytopenia growth failure cataract anencephaly atypical follicular adenoma placental site trophoblastic tumor malignant melanocytic lesion barrett metaplasia adrenocortical adenoma burn scar involvement, cns c-myc gene amplification thymic tumor dementia vascular peritoneal effusion GMs uv mutagenesis nephropathies cystic hyperplasia metastatic osteosarcoma iron overload triploidy synovitis
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ATLAS Chromosomes in Cancer entry for TP53 Genetics and Cytogenetics in Oncology and Haematology IARC TP53 mutation database http://www-p53.iarc.fr/ p53 web site at the Institut Curie http://p53.free.fr/ GeneReviews http://www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/TP53 NIEHS-SNPs http://egp.gs.washington.edu/data/tp53/ SHMPD http://shmpd.bii.a-star.edu.sg/gene.php?genestart=A&genename=TP53 Wikipedia http://en.wikipedia.org/wiki/P53
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Tocris compounds for TP53
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Aliases for TP53
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