GOLGA6L7

Gene

golgin A6 family like 7

HGNCHGNC:37442 EnsemblENSG00000261649 NCBI Gene728310

Locus: gene with protein productLocation: 15q13.1

Also known as

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

Also known asGOLGA6L7P

View full nomenclature history (3)

Previous symbolsGOLGA6L7P

Previous namesgolgi autoantigen, golgin subfamily a, 6-like 7 (pseudogene), golgin A6 family-like 7, pseudogene

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.

Hair color

Uveitis

Iron Metabolism 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.

Gene family

HGNC gene-group membership.

Golgin related

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.