Gene Gene information from NCBI Gene database.
Entrez ID 149428
Gene name BCL2 interacting protein like
Gene symbol BNIPL
Synonyms (NCBI Gene)
BNIP-SBNIP-SalphaBNIP-SbetaBNIPL-1BNIPL-2BNIPL1BNIPL2BNIPSPP753
Chromosome 1
Chromosome location 1q21.3
Summary The protein encoded by this gene interacts with several other proteins, such as BCL2, ARHGAP1, MIF and GFER. It may function as a bridge molecule between BCL2 and ARHGAP1/CDC42 in promoting cell death. Alternatively spliced transcript variants encoding di
miRNA miRNA information provided by mirtarbase database.
106
miRTarBase ID miRNA Experiments Reference
MIRT823521 hsa-miR-3122 CLIP-seq
MIRT823522 hsa-miR-335 CLIP-seq
MIRT823523 hsa-miR-3689a-3p CLIP-seq
MIRT823524 hsa-miR-3689c CLIP-seq
MIRT823525 hsa-miR-3913-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 12681488, 12901880
GO:0005634 Component Nucleus IDA 11741952
GO:0005737 Component Cytoplasm IBA
GO:0005829 Component Cytosol IDA 11741952
GO:0006915 Process Apoptotic process IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611275 16976 ENSG00000163141
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7Z465
Protein name Bcl-2/adenovirus E1B 19 kDa-interacting protein 2-like protein
Protein function May be a bridge molecule between BCL2 and ARHGAP1/CDC42 in promoting cell death.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12496 BNIP2 83 211 Bcl2-/adenovirus E1B nineteen kDa-interacting protein 2 Family
PF13716 CRAL_TRIO_2 212 350 Divergent CRAL/TRIO domain Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 2 is expressed in placenta and lung. {ECO:0000269|PubMed:12681488}.
Sequence
Sequence length 357
Interactions View interactions
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 Evidence Score
TYPE 2 DIABETES MELLITUS 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
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 15112343 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 28901451 Associate
★☆☆☆☆
Found in Text Mining only
Colorectal Carcinoma Colorectal Cancer BEFREE 31485655
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 31485655 Associate
★☆☆☆☆
Found in Text Mining only
Laryngeal Neoplasms Laryngeal neoplasm Pubtator 38302910 Associate
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 15112343, 16143817
★☆☆☆☆
Found in Text Mining only
Mitochondrial Diseases Mitochondrial disease Pubtator 38286121 Associate
★☆☆☆☆
Found in Text Mining only