BNIPL

Gene

BCL2 interacting protein like

HGNCHGNC:16976 EnsemblENSG00000163141 NCBI Gene149428

Locus: gene with protein productLocation: 1q21.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asBNIPl-1 · BNIPL-2 · PP753 · BNIP-S · BNIP-Salpha · BNIP-Sbeta

View full nomenclature history (7)

Alias symbolsBNIPl-1, BNIPL-2, PP753, BNIP-S, BNIP-Salpha, BNIP-Sbeta

Previous namesBCL2/adenovirus E1B 19kD interacting protein like

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Spontaneous coronary artery dissection

Wolff-Parkinson's-White syndrome

Arrhythmogenic Right Ventricular Dysplasia

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

BCH domain containingCRAL-TRIO lipid binding domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.

Open TargetsGene–disease associations from the Open Targets Platform.