Gene Gene information from NCBI Gene database.
Entrez ID 497189
Gene name TIFA inhibitor
Gene symbol TIFAB
Synonyms (NCBI Gene)
-
Chromosome 5
Chromosome location 5q31.1
Summary TIFAB associates with TIFA (MIM 609028) and inhibits TIFA-mediated activation of NF-kappa-B (NFKB1; MIM 164011) (Matsumura et al., 2004 [PubMed 15047173]).[supplied by OMIM, Mar 2009]
miRNA miRNA information provided by mirtarbase database.
13
miRTarBase ID miRNA Experiments Reference
MIRT1424741 hsa-miR-1231 CLIP-seq
MIRT1424742 hsa-miR-3120-5p CLIP-seq
MIRT1424743 hsa-miR-4667-5p CLIP-seq
MIRT1424744 hsa-miR-4700-5p CLIP-seq
MIRT1424745 hsa-miR-516b CLIP-seq
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:0002224 Process Toll-like receptor signaling pathway IEA
GO:0002244 Process Hematopoietic progenitor cell differentiation IEA
GO:0005515 Function Protein binding IPI 15047173, 32101751
GO:0007356 Process Thorax and anterior abdomen determination IGI 23419067
GO:0010468 Process Regulation of gene expression IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612663 34024 ENSG00000255833
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZNK6
Protein name TRAF-interacting protein with FHA domain-containing protein B (TIFA-like protein)
Protein function Inhibits TIFA-mediated TRAF6 activation possibly by inducing a conformational change in TIFA.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00498 FHA 36 108 FHA domain Family
Sequence
MEKPLTVLRVSLYHPTLGPSAFANVPPRLQHDTSPLLLGRGQDAHLQLQLPRLSRRHLSL
EPYLEKGSALLAFCLKALSRKGCVWVNGLTLRYLEQVPLSTVNRVSFS
GIQMLVRVEEGT
SLEAFVCYFHVSPSPLIYRPEAEETDEWEGISQGQPPPGSG
Sequence length 161
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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 Evidence Score
CORONARY ANEURYSM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
AURAL ATRESIA, CONGENITAL Aural Atresia, Congenital BEFREE 30267110
★☆☆☆☆
Found in Text Mining only
Coronary Aneurysm Coronary Aneurysm BEFREE 30267110
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Mucocutaneous Lymph Node Syndrome Kawasaki disease BEFREE 30267110
★☆☆☆☆
Found in Text Mining only
MYELODYSPLASTIC SYNDROME Myelodysplastic Syndrome BEFREE 28386122
★☆☆☆☆
Found in Text Mining only