FAM8A1

Gene

family with sequence similarity 8 member A1

HGNCHGNC:16372 EnsemblENSG00000137414 NCBI Gene51439

Locus: gene with protein productLocation: 6p22.3

Also known as

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

Also known asAHCP

View full nomenclature history (2)

Alias symbolsAHCP

Previous namesfamily with sequence similarity 8, member A1

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.

Psoriasis

Skin Diseases

Arthritis, Psoriatic

Dermatitis, Seborrheic

Erythematosquamous dermatosis

Macular Degeneration

Psoriasis vulgaris

Cholelithiasis

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 2023-07-10.

Open TargetsGene–disease associations from the Open Targets Platform.