Gene Gene information from NCBI Gene database.
Entrez ID 10906
Gene name TRAF-type zinc finger domain containing 1
Gene symbol TRAFD1
Synonyms (NCBI Gene)
FLN29
Chromosome 12
Chromosome location 12q24.13
Summary The innate immune system confers host defense against viral and microbial infection, and TRAFD1 is a negative feedback regulator that controls excessive immune responses (Sanada et al., 2008 [PubMed 18849341]).[supplied by OMIM, Dec 2009]
miRNA miRNA information provided by mirtarbase database.
272
miRTarBase ID miRNA Experiments Reference
MIRT018198 hsa-miR-335-5p Microarray 18185580
MIRT029570 hsa-miR-26b-5p Microarray 19088304
MIRT043867 hsa-miR-378a-3p CLASH 23622248
MIRT043116 hsa-miR-324-5p CLASH 23622248
MIRT040555 hsa-miR-92b-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 17500595, 23275563, 25416956, 26618866, 31515488, 32296183, 35156780, 36012204
GO:0005739 Component Mitochondrion IBA
GO:0008270 Function Zinc ion binding IEA
GO:0045824 Process Negative regulation of innate immune response IBA
GO:0045824 Process Negative regulation of innate immune response IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613197 24808 ENSG00000135148
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O14545
Protein name TRAF-type zinc finger domain-containing protein 1 (Protein FLN29)
Protein function Negative feedback regulator that controls excessive innate immune responses. Regulates both Toll-like receptor 4 (TLR4) and DDX58/RIG1-like helicases (RLH) pathways. May inhibit the LTR pathway by direct interaction with TRAF6 and attenuation of
PDB 2D9K
Family and domains
Sequence
MAEFLDDQETRLCDNCKKEIPVFNFTIHEIHCQRNIGMCPTCKEPFPKSDMETHMAAEHC
QVTCKCNKKLEKRLLKKHEETECPLRLAVCQHCDLELSILKLKEHEDYCGARTELCGNCG
RNVLVKDLKTHPEVCGREGEEKRNEVAIPPNAYDESWGQDGIWIASQLLRQIEALDPPMR
LPRRPLRAFESDVFHNRTTNQRNITAQVSIQNNLFEEQERQERNRGQQPPKEGGEESANL
DFMLALSLQNEGQASSVAEQDFWRAVCEADQSHGGPRSLSDIKGAADEIMLPCEFCEELY
PEELLIDHQTSCNPSRALPSLNTGSSSPRGVEEPDVIFQNFLQQAASNQLDSLMGLSNSH
PVEESIIIPCEFCGVQLEEEVLFHHQDQCDQRPATATNHVTEGIPRLDSQPQETSPELPR
RRVRHQGDLSSGYLDDTKQETANGPTSCLPPSRPINNMTATYNQLSRSTSGPRPGCQPSS
PCVPKLSNSDSQDIQGRNRDSQNGAIAPGHVSVIRPPQNLYPENIVPSFSPGPSGRYGAS
GRSEGGRNSRVTPAAANYRSRTAKAKPSKQQGAGDAEEEEEE
Sequence length 582
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial cancer of breast Benign rs61740854 RCV005908710
Hepatocellular carcinoma Benign rs61740854 RCV005908711