Gene Gene information from NCBI Gene database.
Entrez ID 387758
Gene name Fin bud initiation factor homolog
Gene symbol FIBIN
Synonyms (NCBI Gene)
-
Chromosome 11
Chromosome location 11p14.2
miRNA miRNA information provided by mirtarbase database.
270
miRTarBase ID miRNA Experiments Reference
MIRT446853 hsa-miR-3606-3p PAR-CLIP 22100165
MIRT446852 hsa-miR-513a-3p PAR-CLIP 22100165
MIRT446851 hsa-miR-513c-3p PAR-CLIP 22100165
MIRT446850 hsa-miR-3188 PAR-CLIP 22100165
MIRT446849 hsa-miR-3119 PAR-CLIP 22100165
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:0003674 Function Molecular_function ND
GO:0005575 Component Cellular_component ND
GO:0005576 Component Extracellular region IEA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005794 Component Golgi apparatus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617085 33747 ENSG00000176971
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TAL6
Protein name Fin bud initiation factor homolog
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15819 Fibin 15 210 Fin bud initiation factor homologue Family
Sequence
Sequence length 211
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
DENTAL CARIES GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEART FAILURE, DIASTOLIC CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OTOSCLEROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations