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Aliases & Descriptions for TP53
(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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Aliases FLJ92943 2 LFS1 1 , 2 , 5 P53 3 , 5 TRP53 2 p53 1 , 2
Descriptions Antigen NY-CO-13 3 Phosphoprotein p53 2 , 3 Tumor suppressor p53 3 p53 antigen 2 p53 transformation suppressor 2 p53 tumor suppressor 2 transformation-related protein 53 2 tumor protein p53 2
Search outside databases for aliases for TP53 genePrevious GC identifers: GC17P008026 GC17M008311 GC17M007514 GC17M007772
Summaries for TP53 (According to Entrez Gene ,
Wikipedia's
Gene Wiki ,
UniProtKB/Swiss-Prot ,
and/or
UniProtKB/TrEMBL )
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EntrezGene summary for TP53 : This gene encodes tumor protein p53, which responds to diverse cellular stresses to regulate targetgenes 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 oftransformed cell lines, where it's believed to contribute to transformation and malignancy.p53 is a DNA-binding protein containing transcription activation, DNA-binding, and oligomerizationdomains. It is postulated to bind to a p53-binding site and activate expression of downstreamgenes that inhibit growth and/or invasion, and thus function as a tumor suppressor. Mutants of p53that frequently occur in a number of different human cancers fail to bind the consensus DNAbinding site, and hence cause the loss of tumor suppressor activity. Alterations of this geneoccur not only as somatic mutations in human malignancies, but also as germline mutations in somecancer-prone families with Li-Fraumeni syndrome. Multiple p53 variants due to alternativepromoters and multiple alternative splicing have been found. These variants encode distinctisoforms, 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 apoptosisdepending on the physiological circumstances and cell type. Involved in cell cycle regulation as atrans-activator that acts to negatively regulate cell division by controlling a set of genesrequired 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
Gene Wiki entry for TP53 (P53)
Genomic Location for TP53
(According to
GeneLoc and/or
HGNC , and/or
Entrez Gene (NCBI build 36) ,
and/or miRBase ,
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Ensembl ,
Transcription factor binding sites according to
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Genomic View : UCSC Golden Path with GeneCards custom track Transcription factor binding sites upstream to the TP53 gene 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 GC17M007512:
(about GC identifiers )
Start:
7,512,445 bp from pter
End:
7,531,642 bp from pter
Size:
19,198 bases
Orientation:
minus strand
RefSeq DNA sequence: NC_000017.9 NT_010718.15 Proteins for TP53
(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 Invitrogen ,
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Enzo Life Sciences ,
Abnova ,
OriGene and/or,
Abcam ,
Biochemical Assays by
Invitrogen ,
Millipore ,
R&D Systems ,
Cell Signaling Technology , and/or
Enzo Life Sciences ,
Ontologies according to Gene
Ontology Consortium 01 Apr 2009 and
Entrez Gene ,
Antibodies by Invitrogen ,
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Cell Signaling Technology ,
Abcam ,
Abnova , and/or
Novus Biologicals )
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UniProtKB/Swiss-Prot: P53_HUMAN, P04637 (See
protein sequence )Recommended Name: Cellular tumor antigen p53 Size : 393 amino acids; 43712 Da
Cofactor : Binds 1 zinc ion per subunit
Subunit : Interacts with AXIN1. Probably part of a complex consisting of TP53, HIPK2 and AXIN1 (Bysimilarity). Binds DNA as a homotetramer. Interacts with histone acetyltransferases EP300 andmethyltransferases HRMT1L2 and CARM1, and recruits them to promoters. In vitro, the interaction ofTP53 with cancer-associated/HPV (E6) viral proteins leads to ubiquitination and degradation ofTP53 giving a possible model for cell growth regulation. This complex formation requires anadditional factor, E6-AP, which stably associates with TP53 in the presence of E6. Interacts (viaC-terminus) with TAF1; when TAF1 is part of the TFIID complex. Interacts with ING4; thisinteraction 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 USP7and SYVN1. Interacts with HSP90AB1. Interacts with CHD8; leading to recruit histone H1 and preventtransactivation activity (By similarity). Interacts with ARMC10, BANP, CDKN2AIP and E4F1.Interacts with YWHAZ; the interaction enhances P53 transcriptional activity. Phosphorylation ofYWHAZ on 'Ser-58' inhibits this interaction. Interacts (via DNA-binding domain) with MAML1 (viaN-terminus)
Subcellular location : Cytoplasm. Nucleus. Endoplasmic reticulum. Note=Interaction with BANPpromotes nuclear localization
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)
 2Z5S (3D)
 2Z5T (3D)
 3D05 (3D)
 3D06 (3D)
 3D07 (3D)
 3D08 (3D)
 3D09 (3D)
 3D0A (3D)
 3DAB (3D)
 3DAC (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 ofLys-382 by SIRT1 impairs its ability to induce proapoptotic program and modulate cell senescence1
Phosphorylation on Ser residues mediates transcriptional activation. Phosphorylated by HIPK1 (Bysimilarity). 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 onThr-55 by TAF1, which promotes MDM2-mediated degradation. Phosphorylated on Ser-46 by HIPK2 uponUV irradiation. Phosphorylation on Ser-46 is required for acetylation by CREBBP. Phosphorylated onSer-392 following UV but not gamma irradiation. Phosphorylated upon DNA damage, probably by ATM orATR. Phosphorylated on Ser-15 upon ultraviolet irradiation; which is enhanced by interaction withBANP1
Dephosphorylated by PP2A. SV40 small T antigen inhibits the dephosphorylation by the AC form ofPP2A1
May be O-glycosylated in the C-terminal basic region. Studied in EB-1 cell line1
Ubiquitinated by SYVN1, which leads to proteasomal degradation1
Monomethylated at Lys-372 by SETD7, leading to stabilize it and increase transcriptionalactivation. Monomethylated at Lys-370 by SMYD2, leading to decrease DNA-binding activity andsubsequent transcriptional regulation activity. Lys-372 monomethylation prevents the interactionwith SMYD2 and subsequenct monomethylation at Lys-3701
Sumoylated by SUMO11
Demethylation of di-methylated Lys-370 by KDM1/LSD1 prevents interaction with TP53BP1 and repressesTP53-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: ENSP00000379735 ENSP00000352610 ENSP00000269305 Human Recombinant Proteins               OriGene Purified Recombinant Human Protein: TP53 5/11 Gene Ontology (GO) cellular component terms (links to tree view) (see all 11
):
About this table Antibodies for TP53: Assays for TP53:
Protein
Domains/ Families for TP53(According to InterPro , ProtoNet ,
UniProtKB , and/or BLOCKS ,
Sets of similar genes according to GeneDecks )
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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
(According to MGI Jun 06 2009, UniProtKB ,
IUBMB ,and/or Genatlas ,
shRNA from
OriGene ,
Sigma-Aldrich , RNAi from
Sigma-Aldrich ,
RNAi Products ,
Clones , and
Q-PCR Products
from Invitrogen ,
Millipore ,
OriGene , and/or
Abnova ,
siRNAs from
Applied Biosystems ,
SYBR primers from OriGene ,
Cell-based Assays from Millipore ,
Ontologies according to Gene Ontology Consortium 01 Apr 2009 via
Entrez Gene .)
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Inhib. RNA: Invitrogen RNAi Products for gene knock-down (TP53 ) Millipore RNAi Products for the Analysis of TP53 Gene knock-down Abnova Chimera RNAi Products for Gene knock-down (TP53 )
               OriGene 29mer shRNA kit in GFP-retroviral vectors (see all 7 ): NM_001126112 Applied Biosystems Silencer ® siRNAs for TP53 Sigma-Aldrich siRNA for TP53 Sigma-Aldrich shRNA Panels and shRNA for TP53 Explore Sigma-Aldrich super-pooled esiRNAs                OriGene GFP tagged cDNA clones in CMV expression vector (see all 7 ): NM_000546                                  Myc/DDK tagged cDNA clones in CMV expression vector (see all 7 ): NM_000546                                  untagged cDNA clones in CMV expression vector (see all 7 ): NM_000546  Primers: Browse
Quantitative PCR Central at Invitrogen for Q-PCR LUX™ Primers               OriGene genome-wide validated SYBR primer pairs: NM_000546 UniProtKB/Swiss-Prot: P53_HUMAN, P04637 Function : Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosisdepending on the physiological circumstances and cell type. Involved in cell cycle regulation as atrans-activator that acts to negatively regulate cell division by controlling a set of genesrequired 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 orinduction of apoptosis,also regulating a G2 checkpoint through cyclin B1,transcriptional activatorthrough acetylation of transactivation site by CREBBP binding MDM2 resulting in transcriptionalsilencing 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 modulatorof TFIIH (GTF2H),associated in nucleotide excision repair,activated by ATM in association with14.3.3 proteins (YWHA*),tumor suppressor gene (see TSG17A),mutated in cancers such as pancreas andendometrial carcinomas,in Barrett's adenocarcinoma (and esophageal squamous cell carcinoma),inhepatocellular carcinoma with poor prognosis
15/29 MGI mutant phenotypes (inferred from 44 alleles ) (MGI details for Trp53) (see all 29
):5/12 Gene Ontology (GO) molecular function terms (links to tree view) (see all 12
):
About this table
Pathways & Interactions for TP53
(Pathways according to Invitrogen
(maps by GeneGo ),
Millipore ,
Cell Signaling Technology ,
Sigma-Aldrich ,
KEGG
and/or UniProtKB ,
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 Apr 2009 via
Entrez Gene .)
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5/31 Sigma-Aldrich "Your Favorite Gene" Pathways for TP53 (Your Favorite Gene powered by Ingenuity) (see all 31
) Gene Network CentralTM Interacting Genes and Proteins Network for TP53 5/824 Interacting proteins for TP53 (ENSP00000269305 3 P04637 1 , 2 ) via UniProtKB, MINT, and/or STRING (see all 824
)Interactant Interaction Details GeneCard External ID(s) UBC P62988 1 , 2 STRING (score=.999 ) EBI-366083, EBI-413034 MINT-4051326 MINT-4304004 MINT-4054804 MINT-4304143 MINT-6801380 MINT-6615153 MINT-6541035 MINT-6799774 MINT-7013815 MINT-4052207 MINT-5114741 - - (xeno) Q9PST7 1 EBI-366083, EBI-617698 MINT-69740 MINT-6628483 MINT-6733190 MINT-69730 MINT-73318 MINT-6628495 MINT-6628706 MINT-6733198 MINT-73205 MINT-73319 MINT-6627917 MINT-6628699 MINT-5162111 MINT-6628692 EBI-366083, EBI-1782562 RPS27AP11 P62988 1 , 2 EBI-366083, EBI-413034 MINT-4051326 MINT-4304004 MINT-4054804 MINT-4304143 MINT-6801380 MINT-6615153 MINT-6541035 MINT-6799774 MINT-7013815 MINT-4052207 MINT-5114741 RPS27AP12 P62988 1 , 2 EBI-366083, EBI-413034 MINT-4051326 MINT-4304004 MINT-4054804 MINT-4304143 MINT-6801380 MINT-6615153 MINT-6541035 MINT-6799774 MINT-7013815 MINT-4052207 MINT-5114741 RPS27AP16 P62988 1 , 2 EBI-366083, EBI-413034 MINT-4051326 MINT-4304004 MINT-4054804 MINT-4304143 MINT-6801380 MINT-6615153 MINT-6541035 MINT-6799774 MINT-7013815 MINT-4052207 MINT-5114741 UBA52 P62988 1 , 2 EBI-366083, EBI-413034 MINT-4051326 MINT-4304004 MINT-4054804 MINT-4304143 MINT-6801380 MINT-6615153 MINT-6541035 MINT-6799774 MINT-7013815 MINT-4052207 MINT-5114741 UBB P62988 1 , 2 EBI-366083, EBI-413034 MINT-4051326 MINT-4304004 MINT-4054804 MINT-4304143 MINT-6801380 MINT-6615153 MINT-6541035 MINT-6799774 MINT-7013815 MINT-4052207 MINT-5114741
About this table 5/48 Gene Ontology (GO) biological process terms (links to tree view) (see all 48
):
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:0001836 release of cytochrome c from mitochondria
IEA -- GO:0002309 T cell proliferation during immune response
IEA --
About this table
Drugs & Compounds for TP53 (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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Compounds for TP53 available from Tocris Bioscience About this table 10/18 Novoseek chemical compound relationships for TP53 gene (see all 18
)
Compound
Score
Articles
PubMed IDs for Articles with Shared Sentences (# sentences)
hpvs
70.81
69
11002226 (2), 8726818 (2), 9714244 (1), 10029413 (1) (see all 48 )
noxa
70.34
71
17216584 (4), 17653088 (3), 15598651 (3), 15878356 (2) (see all 41 )
progesterone
68.44
658
12416559 (6), 14595509 (5), 9635673 (5), 9744308 (5) (see all 99 )
aflatoxin b1
63.74
200
16280384 (6), 8921985 (5), 1310637 (5), 10446974 (5) (see all 88 )
advexin
57.44
9
19086841 (2), 16856803 (2), 12749760 (2), 17483435 (1)
crcs
56.64
37
10533474 (4), 16084947 (3), 11037343 (2), 19147861 (2) (see all 18 )
bpde
55.33
104
7586197 (6), 17630511 (6), 10786695 (5), 17942461 (4) (see all 32 )
dutp
51.24
18
11920781 (1), 14761612 (1), 11867201 (1), 14739302 (1) (see all 15 )
proline
51.05
271
14612423 (7), 11053443 (6), 8986812 (4), 16054204 (4) (see all 99 )
o6-methylguanine
48.25
18
14724564 (2), 19107440 (1), 19047896 (1), 10945617 (1) (see all 13 )
About this table 2 PharmGKB drug compound relationships for TP53 gene About this table
Transcripts for TP53(GenBank/EMBL/DDBJ Accessions according to
Unigene
(Build 219 Homo sapiens; Jun 2 2009) 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 Invitrogen ,
Millipore , and/or
Abnova ,
siRNAs from Applied Biosystems ,
Sigma-Aldrich ,
shRNA from
Sigma-Aldrich ,
OriGene ,
Tagged/untagged cDNA clones from
OriGene , Expression Assays from Applied Biosystems )About This Section
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Inhib. RNA: Invitrogen RNAi Products for gene knock-down (TP53 ) Millipore RNAi Products for the Analysis of TP53 Gene knock-down Abnova Chimera RNAi Products for Gene knock-down (TP53 )
               OriGene 29mer shRNA kit in GFP-retroviral vectors (see all 7 ): NM_001126112 Sigma-Aldrich siRNA for TP53 Sigma-Aldrich shRNA Panels and shRNA for TP53 Explore Sigma-Aldrich super-pooled esiRNAs
Applied Biosystems Silencer ® siRNAs: NM_000546 NM_001126112 NM_001126113 NM_001126114 NM_001126115 NM_001126116 NM_001126117
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
Applied Biosystems TaqMan ® Gene Expression Assays: NM_000546 NM_001126112 NM_001126113 NM_001126114 NM_001126115 NM_001126116 NM_001126117
               OriGene GFP tagged cDNA clones in CMV expression vector (see all 7 ): NM_000546                                  Myc/DDK tagged cDNA clones in CMV expression vector (see all 7 ): NM_000546                                  untagged cDNA clones in CMV expression vector (see all 7 ): NM_000546  
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
):AW865736 X02469 AA379547 AA291539 AY627884 S66666 X60018 BE886147 AI539544 CK904490 CR608294 BU174921 AA358870 X60016 BQ057682 BQ066009 BX952582 CA432254 AA662570 BU673953 X60012 CR624912 BQ923115 AB082923
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 3 Ensembl transcripts including schematic representations : ENST00000396473
ENST00000359597
ENST00000269305
Expression for TP53
(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 219 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
)
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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 Data from
(Publications) and GNF BioGPS About these images About these images CGAP SAGE TAG: TTTTGTAGAGSOURCE GeneReport for Unigene cluster: Hs.654481 Expression variation in blood from EXPOLDB for TP53
Orthologs for TP53
(Orthologs according to
1,2 HomoloGene (2 older version, for species not in 1 newer version),
3 euGenes ,
4 SGD
and/or
5 MGI Jun 06 2009,
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 (Paralogs according to 1 HomoloGene and 2 Ensembl , Pseudogenes according to 3 Pseudogene.org )About This Section
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Paralogs for TP53 gene TP73 2 TP63 2
SNPs/Variants for TP53 (According to the
1 NCBI SNP Database ,
2 Ensembl ,
3 PupaSUITE , and
UniProtKB ,
Linkage Disequilibrium by HapMap ,
Genotyping Reagents from
Applied Biosystems )
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HapMap Linkage Disequilibrium images for TP53 (up to first 250kb)
Disorders & Mutations for TP53
(in which this Gene is Involved, According to
OMIM, UniProtKB ,
Novoseek , PharmGKB ,
Genatlas , GeneTests ,
Blood group antigen gene mutations by BGMUT ,
HGMD, GAD ,
HuGE Navigator ,
BCGD ,
and/or TGDB .)
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OMIM: 191170 disorders : 114500 151623 114550 259500 260500 161550 260350 202300 114480 151623 UniProtKB/Swiss-Prot: P53_HUMAN, P04637
TP53 is found in increased amounts in a wide variety of transformed cells. TP53 isfrequently 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 anautosomal dominant familial cancer syndrome that in its classic form is defined by the existenceof a proband affected by a sarcoma before 45 years with a first degree relative affected by anytumor before 45 years and another first degree relative with any tumor before 45 years or asarcoma at any age. Other clinical definitions for LFS have been proposed (PubMed:8118819 andPubMed:8718514) and called Li-Fraumeni like syndrome (LFL). In these families affected relativesdevelop a diverse set of malignancies at unusually early ages. Four types of cancers account for80% of tumors occurring in TP53 germline mutation carriers: breast cancers, soft tissue and bonesarcomas, brain tumors (astrocytomas) and adrenocortical carcinomas. Less frequent tumors includechoroid 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 knownas nasopharyngeal cancer Defects in TP53 are found in Barrett metaplasia; also known as Barrett esophagus. It is acondition in which the normally stratified squamous epithelium of the lower esophagus is replacedby a metaplastic columnar epithelium. The condition develops as a complication in approximately10% of patients with chronic gastroesophageal reflux disease and predisposes to the development ofesophageal adenocarcinoma Defects in TP53 are involved in head and neck squamous cell carcinomas (HNSCC)[MIM:275355] Defects in TP53 are involved in oral squamous cell carcinoma (OSCC). Cigarette smoke is aprime 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 plexuspapilloma is a slow-growing benign tumor of the choroid plexus that often invades theleptomeninges. In children it is usually in a lateral ventricle but in adults it is more often inthe fourth ventricle. Hydrocephalus is common, either from obstruction or from tumor secretion ofcerebrospinal fluid. If it undergoes malignant transformation it is called a choroid plexuscarcinoma. 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 ahigh incidence of associated tumors. ADCC occurs with increased frequency in patients with theBeckwith-Wiedemann syndrome [MIM:130650] and is a component tumor in Li-Fraumeni syndrome[MIM:151623]
10/97 Novoseek disease relationships for TP53 gene (see all 97
)
Disease
Score
Articles
PubMed IDs for Articles with Shared Sentences (# sentences)
tumors
93.74
22625
8777377 (10), 7901994 (9), 8007011 (9), 8324748 (8) (see all 99 )
li-fraumeni syndrome
90.46
320
1373881 (5), 17483435 (3), 10980596 (3), 10484981 (3) (see all 99 )
cancer
89.81
6346
17598983 (10), 18223686 (8), 15055300 (7), 12561442 (7) (see all 99 )
carcinoma
87.49
3225
9110348 (10), 8062281 (9), 16033093 (8), 7927312 (8) (see all 99 )
carcinoma squamous cell
86.80
1827
9127380 (8), 8826924 (7), 10445528 (6), 11255264 (6) (see all 99 )
retinoblastoma
85.08
679
10792093 (8), 9337350 (6), 11306502 (5), 8224613 (5) (see all 99 )
microsatellite instability
84.49
335
9731891 (6), 9716224 (5), 11290569 (5), 12612901 (5) (see all 99 )
allelic loss
83.88
399
16293976 (5), 7909153 (5), 8467510 (4), 11520271 (4) (see all 99 )
adenocarcinoma
82.64
1486
12823203 (7), 17982662 (7), 9379505 (6), 10674608 (6) (see all 99 )
breast cancer
81.53
2563
7917542 (8), 8679460 (8), 12170762 (7), 15566648 (6) (see all 99 )
About this table 5 PharmGKB disease relationships for TP53 gene About this table GeneTests: TP53 Li-Fraumeni Syndrome Human Gene Mutation Database : TP53 Genetic Association Database: TP53 Human Genome Epidemiology Navigator: TP53 (724 documents) Tumor Gene Database : TP53 Breast Cancer Gene Database : TP53
Medical News for TP53 (Possibly Related Articles in
Doctor's Guide )
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Publications for TP53 (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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10/11043 PubMed articles for TP53 gene (see all 11043
): 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) Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family. (PubMed id 10484981) 1, 3, 4 Gueran S.... Imirzalioglu N. (1999) Spectrum of p53 tumor suppressor gene mutations and breast cancer survival. (PubMed id 14997055) 1, 3, 6 Lai H....Lai S. (2004) Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain. (PubMed id 8875929) 1, 3, 4 Kussie P.H.... Pavletich N.P. (1996) Joint effects of single nucleotide polymorphisms in P53BP1 and p53 on breast cancer risk in a Chinese population. (PubMed id 16314399) 1, 3, 6 Ma H....Shen H. (2006) 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) Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk. (PubMed id 12802680) 1, 3, 6 Hwang S.J....Strong L.C. (2003) [p53 gene polymorphism with susceptibility to esophageal cancer and lung cancer in Chinese population] (PubMed id 12921568) 1, 3, 6 Zhang J.H....He M. (2003) Genetic polymorphisms in cell cycle regulatory genes MDM2 and TP53 are associated with susceptibility to lung cancer. (PubMed id 16287156) 1, 3, 6 Zhang X....Lin D. (2006) Association of genetic polymorphisms of MK, IL-4, p16, p21, p53 genes and human gastric cancer in Taiwan. (PubMed id 16289646) 1, 3, 6 Lai K.C....Tsai F.J. (2005)
Search for TP53
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Genome Databases showing TP53
(According to
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AceView ,
euGenes ,
Ensembl ,
miRBase ,
ECgene ,
and/or
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Other Databases showing TP53
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--
Specialized Databases showing TP53 (According to ATLAS , HORDE , IMGT , MTDB, LEIDEN , UniProtKB/Swiss-Prot , and/or UniProtKB/TrEMBL ,Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot )About This Section
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Name Description
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.genetests.org/query?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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Licensable Technologies for TP53 gene: Services for TP53 (Reagents available from Applied Biosystems , Antibodies and assays by Cell
Signaling Technology , Abcam , Novus Biologicals ,Sigma-Aldrich , R&D Systems , Millipore , Abnova , and/or Invitrogen , Clones available from OriGene ,and/or Invitrogen , Drugs and/or compounds by Sigma-Aldrich , Enzo Life Sciences , and/or Tocris Bioscience )About This Section
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Products for TP53:
Antibodies & Assays for TP53   (p53)
Tocris compounds for TP53
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GeneCards Homepage - Last full update: 2 Jul 2009
Incremental update: 13 Oct 2009