BLTP3A

Gene

bridge-like lipid transfer protein family member 3A

HGNCHGNC:21216 EnsemblENSG00000065060 NCBI Gene54887

Locus: gene with protein productLocation: 6p21.31

Also known as

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

Also known asC6orf107 · UHRF1BP1 · FLJ20302 · dJ349A12.1

View full nomenclature history (6)

Previous symbolsC6orf107, UHRF1BP1

Alias symbolsFLJ20302, dJ349A12.1

Previous namesUHRF1 binding protein 1, chromosome 6 open reading frame 107

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.

Hypothyroidism

Obesity disorder

Coronary Artery Disease

Lupus Erythematosus, Systemic

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.

Bridge-like lipid transfer protein family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-11-25.

Open TargetsGene–disease associations from the Open Targets Platform.