Gene Gene information from NCBI Gene database.
Entrez ID 84231
Gene name TNF receptor associated factor 7
Gene symbol TRAF7
Synonyms (NCBI Gene)
CAFDADDRFWD1RNF119
Chromosome 16
Chromosome location 16p13.3
Summary Tumor necrosis factor (TNF; see MIM 191160) receptor-associated factors, such as TRAF7, are signal transducers for members of the TNF receptor superfamily (see MIM 191190). TRAFs are composed of an N-terminal cysteine/histidine-rich region containing zinc
SNPs SNP information provided by dbSNP.
4
SNP ID Visualize variation Clinical significance Consequence
rs1331463984 G>A Pathogenic-likely-pathogenic Coding sequence variant, missense variant, non coding transcript variant
rs1567252467 A>G,T Pathogenic Missense variant, stop gained, non coding transcript variant, coding sequence variant
rs1567252659 C>G,T Pathogenic Missense variant, non coding transcript variant, coding sequence variant
rs1567254067 A>G Pathogenic Missense variant, non coding transcript variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
198
miRTarBase ID miRNA Experiments Reference
MIRT052480 hsa-let-7a-5p CLASH 23622248
MIRT042237 hsa-miR-484 CLASH 23622248
MIRT714201 hsa-miR-3127-3p HITS-CLIP 19536157
MIRT714200 hsa-miR-6756-3p HITS-CLIP 19536157
MIRT714199 hsa-miR-370-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
GO ID Ontology Definition Evidence Reference
GO:0000151 Component Ubiquitin ligase complex IBA
GO:0000151 Component Ubiquitin ligase complex IDA 14743216
GO:0004842 Function Ubiquitin-protein transferase activity IDA 14743216
GO:0005515 Function Protein binding IPI 14743216, 15001576, 21903422, 32707033, 33961781
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606692 20456 ENSG00000131653
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6Q0C0
Protein name E3 ubiquitin-protein ligase TRAF7 (EC 2.3.2.-) (EC 2.3.2.27) (RING finger and WD repeat-containing protein 1) (RING finger protein 119) (RING-type E3 ubiquitin transferase TRAF7) (TNF receptor-associated factor 7)
Protein function E3 ubiquitin and SUMO-protein ligase that plays a role in different biological processes such as innate immunity, inflammation or apoptosis (PubMed:15001576, PubMed:37086853). Potentiates MAP3K3-mediated activation of JUN/AP1 and DDIT3 transcrip
PDB 8IMS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13445 zf-RING_UBOX 131 167 RING-type zinc-finger Domain
PF00400 WD40 386 424 WD domain, G-beta repeat Repeat
PF00400 WD40 429 465 WD domain, G-beta repeat Repeat
PF00400 WD40 589 629 WD domain, G-beta repeat Repeat
PF00400 WD40 633 669 WD domain, G-beta repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed with high levels in skeletal muscle, heart, colon, spleen, kidney, liver and placenta. {ECO:0000269|PubMed:15001576}.
Sequence
MSSGKSARYNRFSGGPSNLPTPDVTTGTRMETTFGPAFSAVTTITKADGTSTYKQHCRTP
SSSSTLAYSPRDEEDSMPPISTPRRSDSAISVRSLHSESSMSLRSTFSLPEEEEEPEPLV
FAEQPSVKLCCQLCCSVFKDPVITTCGHTFCRRCALKSEKCPVDNVKLTVVVNNIAVAEQ
IGELFIHCRHGCRVAGSGKPPIFEVDPRGCPFTIKLSARKDHEGSCDYRPVRCPNNPSCP
PLLRMNLEAHLKECEHIKCPHSKYGCTFIGNQDTYETHLETCRFEGLKEFLQQTDDRFHE
MHVALAQKDQEIAFLRSMLGKLSEKIDQLEKSLELKFDVLDENQSKLSEDLMEFRRDASM
LNDELSHINARLNMGILGSYDPQQIFKCKGTFVGHQGPVWCLCVYSMGDLLFSGSSDKTI
KVWD
TCTTYKCQKTLEGHDGIVLALCIQGCKLYSGSADCTIIVWDIQNLQKVNTIRAHDN
PVCTLVSSHNVLFSGSLKAIKVWDIVGTELKLKKELTGLNHWVRALVAAQSYLYSGSYQT
IKIWDIRTLDCIHVLQTSGGSVYSIAVTNHHIVCGTYENLIHVWDIESKEQVRTLTGHVG
TVYALAVISTPDQTKVFSASYDRSLRVWS
MDNMICTQTLLRHQGSVTALAVSRGRLFSGA
VDSTVKVWT
C
Sequence length 670
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Antigen processing: Ubiquitination & Proteasome degradation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
86
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cardiac, facial, and digital anomalies with developmental delay Pathogenic; Likely pathogenic rs2141297268, rs2141291233, rs2141298490, rs2545012659, rs1331463984, rs1567254067, rs1567252467, rs1567252659, rs2093132159, rs2093135960 RCV003336419
RCV004996009
RCV002272641
RCV003444192
RCV000714967
RCV000714968
RCV000714969
RCV000714970
RCV001796982
RCV001269306
See cases Likely pathogenic; Pathogenic rs2141298772 RCV001420198
TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Likely pathogenic; Pathogenic rs1331463984 RCV002274096
TRAF7-related disorder Likely pathogenic; Pathogenic rs2093132159 RCV001249423
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Adrenocortical carcinoma, hereditary Benign rs187643207 RCV005908186
Cervical cancer Benign rs187643207 RCV005908187
Clear cell carcinoma of kidney Benign rs187643207 RCV005908188
Colon adenocarcinoma Benign rs187643207 RCV005908182
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
3 methylcrotonyl CoA carboxylase 1 deficiency Associate 26655088
Adenomatoid Tumor Associate 29148537, 30171198, 31371807
Blepharophimosis Associate 32376980
Carcinoma Papillary Associate 30171198, 31371807
Congenital Abnormalities Associate 29961569
Daneman Davy Mancer syndrome Associate 29961569
Developmental Disabilities Associate 29961569, 32376980, 34088006
Drug Related Side Effects and Adverse Reactions Associate 22219201
Ductus Arteriosus Patent Associate 32376980
Familial cylindromatosis Inhibit 16230348