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Gene Gene information from NCBI Gene database.
Entrez ID 8717
Gene name TNFRSF1A associated via death domain
Gene symbol TRADD
Synonyms (NCBI Gene)
Hs.89862
Chromosome 16
Chromosome location 16q22.1
Summary The protein encoded by this gene is a death domain containing adaptor molecule that interacts with TNFRSF1A/TNFR1 and mediates programmed cell death signaling and NF-kappaB activation. This protein binds adaptor protein TRAF2, reduces the recruitment of i
miRNA miRNA information provided by mirtarbase database.
99 Show/Hide all (99)
miRTarBase ID miRNA Experiments Reference
MIRT495119 hsa-miR-4717-5p PAR-CLIP 23708386
MIRT495118 hsa-miR-15a-3p PAR-CLIP 23708386
MIRT495116 hsa-miR-1295b-3p PAR-CLIP 23708386
MIRT495117 hsa-miR-922 PAR-CLIP 23708386
MIRT495115 hsa-miR-4530 PAR-CLIP 23708386
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
51 Show/Hide all (51)
GO ID Ontology Definition Evidence Reference
GO:0002947 Component Tumor necrosis factor receptor superfamily complex IBA
GO:0002947 Component Tumor necrosis factor receptor superfamily complex IDA 23429285
GO:0005068 Function Transmembrane receptor protein tyrosine kinase adaptor activity IBA
GO:0005068 Function Transmembrane receptor protein tyrosine kinase adaptor activity IPI 8612133
GO:0005515 Function Protein binding IPI 1040062, 7758105, 8565075, 8943045, 8985253, 9020361, 10848577, 10892748, 11112409, 11374864, 11684708, 14743216, 16611992, 18198944, 19379743, 19524513, 19641494, 19781631, 20628368, 22510408, 23429285, 23955153, 24025841, 24130170, 30561431, 32296183, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603500 12030 ENSG00000102871
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q15628
Protein name Tumor necrosis factor receptor type 1-associated DEATH domain protein (TNFR1-associated DEATH domain protein) (TNFRSF1A-associated via death domain)
Protein function Adapter molecule for TNFRSF1A/TNFR1 that specifically associates with the cytoplasmic domain of activated TNFRSF1A/TNFR1 mediating its interaction with FADD (PubMed:23955153, PubMed:7758105, PubMed:8612133). Overexpression of TRADD leads to two
PDB 1F2H , 1F3V , 5XME , 6AC0 , 7CSQ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00531 Death 217 → 304 Death domain Domain
PF09034 TRADD_N 51 → 161 TRADD, N-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Found in all examined tissues. {ECO:0000269|PubMed:7758105}.
Sequence
Sequence length 312
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway Reactome Pathway
MAPK signaling pathway Caspase activation via Death Receptors in the presence of ligand
NF-kappa B signaling pathway Regulation by c-FLIP
Sphingolipid signaling pathway RIPK1-mediated regulated necrosis
Apoptosis CASP8 activity is inhibited
Necroptosis TNFR1-induced proapoptotic signaling
RIG-I-like receptor signaling pathway Regulation of TNFR1 signaling
IL-17 signaling pathway TNFR1-induced NFkappaB signaling pathway
TNF signaling pathway Regulation of necroptotic cell death
Adipocytokine signaling pathway Dimerization of procaspase-8
Alcoholic liver disease TNF signaling
Pathogenic Escherichia coli infection  
Shigellosis  
Salmonella infection  
Tuberculosis  
Hepatitis C  
Measles  
Human cytomegalovirus infection  
Influenza A  
Human papillomavirus infection  
Kaposi sarcoma-associated herpesvirus infection  
Herpes simplex virus 1 infection  
Epstein-Barr virus infection  
Human immunodeficiency virus 1 infection  
Viral carcinogenesis  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
TRADD-related disorder Uncertain significance ClinVar —
★★★★★
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Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (30)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alzheimer Disease Alzheimer disease Pubtator 39396083 Associate
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Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 16951485 Stimulate
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Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 37904685 Associate
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Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 25732226
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Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 38214751 Associate
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Found in Text Mining only
Coronary Artery Disease Coronary artery disease Pubtator 32710445 Associate
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Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 11420694, 23908590, 26164206
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Found in Text Mining only
Glioblastoma Glioblastoma Pubtator 23908590 Associate
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Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 11420694, 23908590, 26164206
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Found in Text Mining only
Glioma Glioma BEFREE 11420694, 23908590
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Found in Text Mining only