Back to discover

NPIPB11

Gene

nuclear pore complex interacting protein family member B11

HGNCHGNC:37453EnsemblENSG00000254206NCBI Gene728888
Locus: gene with protein productLocation: 16p11.2

Also known as

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

View full nomenclature history (1)
Previous namesnuclear pore complex interacting protein family, member B11

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.

Neuralgia
Neuritis
Alcohol drinking
Alopecia Areata
Cholelithiasis
Urolithiasis
Psychotic disorder
Sinusitis
Mood Disorders

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.