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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

TRIM29 Gene

protein-coding   GIFtS: 58
GCID: GC11M120015

Tripartite Motif Containing 29

(Previous name: tripartite motif-containing 29)
  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
Tripartite Motif Containing 291 2     Ataxia Telangiectasia Group D-Associated Protein2 3
Tripartite Motif-Containing 291 2     ATDC2 3
Ataxia-Telangiectasia Group D-Associated Protein1 2     Tripartite Motif-Containing Protein 292
Tripartite Motif Protein TRIM291 2     

External Ids:    HGNC: 172741   Entrez Gene: 236502   Ensembl: ENSG000001376997   OMIM: 6106585   UniProtKB: Q141343   

Export aliases for TRIM29 gene to outside databases

Previous GC identifers: GC11M121981 GC11M121493 GC11M119520 GC11M119521 GC11M119487 GC11M115921


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for TRIM29 Gene:
The protein encoded by this gene belongs to the TRIM protein family. It has multiple zinc finger motifs and a
leucine zipper motif. It has been proposed to form homo- or heterodimers which are involved in nucleic acid
binding. Thus, it may act as a transcriptional regulatory factor involved in carcinogenesis and/or
differentiation. It may also function in the suppression of radiosensitivity since it is associated with ataxia
telangiectasia phenotype. (provided by RefSeq, Jul 2008)

GeneCards Summary for TRIM29 Gene: 
TRIM29 (tripartite motif containing 29) is a protein-coding gene. Diseases associated with TRIM29 include ataxia telangiectasia, and ataxia, and among its related super-pathways are Cell Cycle / Checkpoint Control. GO annotations related to this gene include p53 binding and sequence-specific DNA binding transcription factor activity. An important paralog of this gene is TRIM25.

UniProtKB/Swiss-Prot: TRI29_HUMAN, Q14134
Function: It is able to complement the radiosensitivity defect of an ataxia telangiectasia (AT) fibroblast cell
line

Gene Wiki entry for TRIM29 Gene


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000011.9  NT_033899.8  NC_018922.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the TRIM29 gene promoter:
         Egr-3   HFH-3   Tal-1beta   GATA-2   E47   Egr-2   AREB6   FOXI1   S8   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidTRIM29 promoter sequence
   Search SABiosciences Chromatin IP Primers for TRIM29

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat TRIM29


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 11q23.3   Ensembl cytogenetic band:  11q23.3   HGNC cytogenetic band: 11q23.3

TRIM29 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
TRIM29 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11M120015:  view genomic region     (about GC identifiers)

Start:
119,981,983 bp from pter      End:
120,056,237 bp from pter
Size:
74,255 bases      Orientation:
minus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: TRI29_HUMAN, Q14134 (See protein sequence)
Recommended Name: Tripartite motif-containing protein 29  
Size: 588 amino acids; 65835 Da
Subunit: Interacts with VIM and HINT1
Subcellular location: Cytoplasm. Note=Colocalizes with intermediate filaments
1 PDB 3D structure from and Proteopedia for TRIM29:
2CSV (3D)    
Secondary accessions: Q96AA9 Q9BZY7
Alternative splicing: 2 isoforms:  Q14134-1   Q14134-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for TRIM29: NX_Q14134

Explore proteomics data for TRIM29 at MOPED 

Post-translational modifications:

  • UniProtKB: Constitutively phosphorylated by PKC on serine/threonine in A431 cells
  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q14134

  • TRIM29 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    TRIM29 Protein Expression
    REFSEQ proteins: NP_036233.2  
    ENSEMBL proteins: 
     ENSP00000343129   ENSP00000431869   ENSP00000437078   ENSP00000433122   ENSP00000432285  
     ENSP00000435696   ENSP00000436015   ENSP00000433779   ENSP00000431790   ENSP00000436279  
     ENSP00000435600   ENSP00000433324   ENSP00000436567   ENSP00000433084   ENSP00000445638  

    Human Recombinant Protein Products for TRIM29: 
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    Novus Biologicals TRIM29 Proteins
    Novus Biologicals TRIM29 Lysate
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Browse Proteins at Cloud-Clone Corp. 

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular ----
    GO:0005737cytoplasm IEA--

    TRIM29 for ontologies           About GeneDecksing



    TRIM29 Antibody Products: 
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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    TRIM: Tripartite motif containing / Tripartite motif containing

    1 InterPro protein domain:
     IPR000315 Znf_B-box

    Graphical View of Domain Structure for InterPro Entry Q14134

    ProtoNet protein and cluster: Q14134

    1 Blocks protein domain: IPB000315 B-box zinc finger signature

    UniProtKB/Swiss-Prot: TRI29_HUMAN, Q14134
    Similarity: Contains 1 B box-type zinc finger


    TRIM29 for domains           About GeneDecksing


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: TRI29_HUMAN, Q14134
    Function: It is able to complement the radiosensitivity defect of an ataxia telangiectasia (AT) fibroblast cell
    line

         Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0002039p53 binding IEA--
    GO:0003700sequence-specific DNA binding transcription factor activity TAS8188213
    GO:0005515protein binding IPI16189514
    GO:0008270zinc ion binding IEA--
         
    TRIM29 for ontologies           About GeneDecksing


    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for TRIM29 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for TRIM29

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for TRIM29 
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    miRNA
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    miRTarBase miRNAs that target TRIM29:
    hsa-mir-124 (MIRT002561)

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    SwitchGear 3'UTR luciferase reporter plasmidTRIM29 3' UTR sequence
    Inhib. RNA
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    In Situ Assay
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for TRIM29


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene).
    About This Section

    SuperPaths for TRIM29 About                                                                                                See pathways by source

    SuperPathContained pathways About
    1DNA Damage
    DNA Damage0.32

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways


    1 Cell Signaling Technology (CST) Pathway for TRIM29
        DNA Damage



    TRIM29 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for TRIM29

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/54 Interacting proteins for TRIM29 (Q141341, 2, 3 ENSP000003431294) via UniProtKB, MINT, STRING, and/or I2D (see all 54)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    CEP70Q8NHQ12, 3, ENSP000002649824MINT-67676 I2D: score=5 STRING: ENSP00000264982
    EFCAB4BQ9BSW22, 3, ENSP000004093824MINT-66038 I2D: score=5 STRING: ENSP00000409382
    FXR2P511162, 3, ENSP000002501134MINT-67829 I2D: score=5 STRING: ENSP00000250113
    JAKMIP2Q96AA82, 3, ENSP000002652724MINT-68356 I2D: score=5 STRING: ENSP00000265272
    MAD1L1Q9Y6D92, 3, ENSP000003825624MINT-68034 I2D: score=5 STRING: ENSP00000382562
    About this table

    Gene Ontology (GO): 3 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000122negative regulation of transcription from RNA polymerase II promoter IEA--
    GO:0006366transcription from RNA polymerase II promoter TAS8188213
    GO:1900181negative regulation of protein localization to nucleus IEA--

    TRIM29 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for TRIM29 (TRI29)

    Search CenterWatch for drugs/clinical trials and news about TRIM29 / TRI29

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for TRIM29 gene (2 alternative transcripts): 
    NM_012101.3  NM_058193.1  

    Unigene Cluster for TRIM29:

    Tripartite motif containing 29
    Hs.504115  [show with all ESTs]
    Unigene Representative Sequence: BX648072
    18/21 Ensembl transcripts including schematic representations, and UCSC links where relevant (see all 21):
    ENST00000341846(uc001pwx.3 uc010rzi.2 uc010rzj.2 uc001pwz.3 uc001pxa.3)
    ENST00000524816 ENST00000526161 ENST00000530919 ENST00000524664 ENST00000525887
    ENST00000533302 ENST00000531555 ENST00000525327 ENST00000528870 ENST00000529044
    ENST00000475051 ENST00000524956 ENST00000526881 ENST00000530470 ENST00000532195
    ENST00000529011 ENST00000529495
    miRNA
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    Search QIAGEN for miScript miRNA Assays for microRNAs that regulate TRIM29
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    Inhib. RNA
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    OriGene RNAi products in human, mouse, rat for TRIM29
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    Sirion Biotech Customized lentivirus for stable overexpression of TRIM29 
                         Customized lentivirus expression plasmids for stable overexpression of TRIM29 
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    OriGene qPCR primer pairs and template standards for TRIM29
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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat TRIM29

    Additional mRNA sequence: 

    AF230388.1 AK093404.1 AK122720.1 AK223090.1 AK299459.1 AK299472.1 AK303969.1 AL832678.1 
    BC010644.1 BC017352.2 BX648072.1 L24203.1 

    24/25 DOTS entries (see all 25):

    DT.100840291  DT.215763  DT.92450158  DT.100792033  DT.100792028  DT.95112703  DT.101983193  DT.100792026 
    DT.95169901  DT.91679365  DT.86855491  DT.95169966  DT.100831593  DT.120746901  DT.95169900  DT.92450155 
    DT.95169967  DT.120746950  DT.120746957  DT.91934755  DT.95169899  DT.95169902  DT.100696689  DT.100792036 

    24/263 AceView cDNA sequences (see all 263):

    AI218870 BG994269 CR609266 W61127 BF842505 BG697403 AI961945 AI283390 
    BG679931 AW452441 CB125982 BM766070 BG742909 BI260963 AI961879 BM709993 
    BM836761 BQ025760 BC017352 BU686575 BF594378 AL602740 BG740852 BM838046 

    GeneLoc Exon Structure

    5/15 Alternative Splicing Database (ASD) splice patterns (SP) for TRIM29 (see all 15)    About this scheme

    ExUns: 1 ^ 2a · 2b ^ 3 ^ 4a · 4b · 4c ^ 5a · 5b ^ 6 ^ 7 ^ 8a · 8b ^ 9 ^ 10 ^ 11 ^ 12 ^ 13 ^ 14a · 14b ^ 15 ^ 16a · 16b ^ 17 ^ 18a · 18b ·
    SP1:        -     -                                         -     -                 -     -           -           -     -                                       
    SP2:        -     -                                         -     -                 -     -           -           -     -                       -               
    SP3:                                                              -                 -     -           -           -     -                       -               
    SP4:                                                                                -     -           -           -     -                       -               
    SP5:                                                                                -     -           -           -                             -               

    ExUns: 18c · 18d · 18e · 18f · 18g ^ 19a · 19b
    SP1:                                          
    SP2:                                          
    SP3:                                          
    SP4:                                          
    SP5:                                          


    ECgene alternative splicing isoforms for TRIM29

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    TRIM29 expression in normal human tissues (normalized intensities)      TRIM29 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TTGCATATCA
    TRIM29 Expression
    About this image


    TRIM29 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/21 selected tissues (see all 21) fully expand
     
     Epithelium
             Human Bronchial Epithelial Cells (HBEpiC)   
     
     Lung (Respiratory System)    fully expand to see all 6 entries
             bronchus ; respiratory epithelial cells   
             Trachea   
     
     Oral Cavity (Gastrointestinal Tract)    fully expand to see all 5 entries
             Human Oral Keritinocytes (HOK)   
             mouth   
     
     Tooth (Integumentary System)    fully expand to see all 4 entries
             visceral organ/oral region/upper jaw   
     
     Nose (Sensory Organs)    fully expand to see all 3 entries
             nasopharynx ; respiratory epithelial cells   
             sensory organ/nose/naris   

    See TRIM29 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for TRIM29

    SOURCE GeneReport for Unigene cluster: Hs.504115

    UniProtKB/Swiss-Prot: TRI29_HUMAN, Q14134
    Tissue specificity: Expressed in placenta, prostate and thymus

        SABiosciences Custom PCR Arrays for TRIM29
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    In Situ
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for TRIM29

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for TRIM29 gene from 4/11 species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Trim291 , 5 tripartite motif-containing 291, 5 86.71(n)1
    89.61(a)1
      9 (24.28 cM)5
    721691  NM_023655.21  NP_076144.21 
     433107635 
    chicken
    (Gallus gallus)
    Aves TRIM291 tripartite motif-containing 29 68.88(n)
    66.05(a)
      419754  XM_417892.3  XP_417892.3 
    lizard
    (Anolis carolinensis)
    Reptilia TRIM296
    tripartite motif containing 29
    57(a)
    1 ↔ 1
    LGa(1090405-1146967)
    African clawed frog
    (Xenopus laevis)
    Amphibia MGC534842 similar to tripartite motif protein 29 73.29(n)    BC044714.1 


    ENSEMBL Gene Tree for TRIM29 (if available)
    TreeFam Gene Tree for TRIM29 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for TRIM29 gene
    TRIM252  TRIM16L2  TRIM472  TRIM162  TRIM652  TRIM82  

    TRIM29 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/647 SNPs in TRIM29 are shown (see all 647)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    VAR_0359624
    A breast cancer sample4--see VAR_0359622 S F mis40--------
    rs1148884821,2
    C,F--119981678(+) GGGAAC/TTCTAG 1 -- ds50011Minor allele frequency- T:0.04WA 118
    rs1883293531,2
    --119981690(+) GTGGGC/TCGGCC 1 -- ds50010--------
    rs1401585031,2
    C--119981694(+) GCCGGC/TCAGAA 1 -- ds50010--------
    rs1503556901,2
    C--119981740(+) CAGGCA/CCACAC 1 -- ds50010--------
    rs107365021,2
    C,F,A,H--119981785(+) AAGGCC/GTGCCT 1 -- ds500115Minor allele frequency- G:0.19NS EA NA WA CSA 797
    rs1912463731,2
    --119981871(+) AGCCAC/TGTTTC 1 -- ds50010--------
    rs108925421,2
    C,F,A,H--119981906(+) GTGCCT/CTCATC 1 -- ds500114Minor allele frequency- C:0.05NS EA NA 1706
    rs1842613941,2
    --119982039(+) TGGATA/GTCTCC 1 -- ut310--------
    rs1143750481,2
    C,F--119982089(+) CCCATA/GGGCCT 1 -- ut311Minor allele frequency- G:0.02WA 118

    HapMap Linkage Disequilibrium report for TRIM29 (119981983 - 120056237 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for TRIM29:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2673699CNV Deletion23128226
    esv2745143CNV Deletion23290073

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 610658    OMIM disorders: --

    11 diseases for TRIM29:    About MalaCards
    ataxia telangiectasia    ataxia    esophageal squamous cell carcinoma    esophagitis
    squamous cell carcinoma    pancreatic cancer    gastric cancer    pancreatitis
    lung cancer    prostatitis    breast cancer

    1 disease from the University of Copenhagen DISEASES database for TRIM29:
    Ataxia telangiectasia

    TRIM29 for disorders           About GeneDecksing

    Genetic Association Database (GAD): TRIM29
    Human Genome Epidemiology (HuGE) Navigator: TRIM29 (2 documents)

    Export disorders for TRIM29 gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for TRIM29 gene, integrated from 9 sources (see all 40):
    (articles sorted by number of sources associating them with TRIM29)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. The tripartite motif family identifies cell compartments. (PubMed id 11331580)1, 2, 3 Reymond A.... Ballabio A. (2001)
    2. Expression of the ATDC (ataxia telangiectasia group D-complementing) gene in A431 human squamous carcinoma cells. (PubMed id 8647648)1, 2, 9 Laderoute K.R.... Kapp L.N. (1996)
    3. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)1, 4 Rose J.E....Uhl G.R. (2010)
    4. A probability-based approach for high-throughput protein phosphorylation analysis and site localization. (PubMed id 16964243)1, 2 Beausoleil S.A.... Gygi S.P. (2006)
    5. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    6. The product of the ataxia-telangiectasia group D complementing gene, ATDC, interacts with a protein kinase C substrate and inhibitor. (PubMed id 7644499)1, 2 Brzoska P.M.... Christman M.F. (1995)
    7. Nucleotide sequence analysis of a candidate gene for ataxia- telangiectasia group D (ATDC). (PubMed id 8188213)1, 2 Leonhardt E.A.... Murnane J.P. (1994)
    8. The ATDC (TRIM29) protein binds p53 and antagonizes p 53-mediated functions. (PubMed id 20368352)1, 9 Yuan Z....Seto E. (2010)
    9. Suppression of anchorage-independent growth by expression of the ataxia-telangiectasia group D complementing gene, ATDC. (PubMed id 16890201)1, 9 Hosoi Y....Miyagawa K. (2006)
    10. Oncogenic function of ATDC in pancreatic cancer through Wnt pathway activation and beta-catenin stabilization. (PubMed id 19249679)1, 9 Wang L....Simeone D.M. (2009)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 23650 HGNC: 17274 AceView: TRIM29 Ensembl:ENSG00000137699 euGenes: HUgn23650
    ECgene: TRIM29 H-InvDB: TRIM29

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for TRIM29 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for TRIM29 Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for TRIM29 gene:
    Search GeneIP for patents involving TRIM29

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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    About This Section

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