Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55909
Gene name Gene Name - the full gene name approved by the HGNC.
Bridging integrator 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BIN3
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p21.3
Summary Summary of gene provided in NCBI Entrez Gene.
The product of this gene is a member of the BAR domain protein family. The encoded protein is comprised solely of a BAR domain which is predicted to form coiled-coil structures and proposed to mediate dimerization, sense and induce membrane curvature, and
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT026045 hsa-miR-196a-5p Sequencing 20371350
MIRT027575 hsa-miR-98-5p Microarray 19088304
MIRT032138 hsa-let-7d-5p Sequencing 20371350
MIRT045640 hsa-miR-149-5p CLASH 23622248
MIRT821509 hsa-let-7a CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 18654987, 32296183, 33961781, 35271311
GO:0005737 Component Cytoplasm IEA
GO:0005856 Component Cytoskeleton IEA
GO:0006897 Process Endocytosis IBA
GO:0006897 Process Endocytosis IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606396 1054 ENSG00000147439
Protein
UniProt ID Q9NQY0
Protein name Bridging integrator 3
Protein function Involved in cytokinesis and septation where it has a role in the localization of F-actin.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03114 BAR 10 225 BAR domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed except in brain. {ECO:0000269|PubMed:11274158}.
Sequence
Sequence length 253
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Breast Cancer Breast cancer N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Otosclerosis Otosclerosis N/A N/A GWAS
Parkinson Disease Parkinson's disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 36068491
Esophageal Neoplasms Associate 36475339
Glioblastoma Associate 35915159
Neoplasms Associate 35915159, 36475339