BPIFB1

Gene

BPI fold containing family B member 1

HGNCHGNC:16108 EnsemblENSG00000125999 NCBI Gene92747

Locus: gene with protein productLocation: 20q11.21

Also known as

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

Also known asC20orf114 · dJ1187J4.1 · MGC14597 · bA49G10.6 · LPLUNC1 · VEMSGP

View full nomenclature history (8)

Previous symbolsC20orf114

Alias symbolsdJ1187J4.1, MGC14597, bA49G10.6, LPLUNC1, VEMSGP

Previous nameschromosome 20 open reading frame 114

Alias namesvon Ebner minor salivary gland protein

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.

Poisoning

Carcinoma, Squamous Cell

Liver Diseases

Nasopharyngeal Carcinoma

Retinitis Pigmentosa

Neoplasms

Pulmonary Disease, Chronic Obstructive

Early-onset non-syndromic cataract

Posterior polar cataract

Cystic Fibrosis

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.

BPI fold containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.