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PROM1

Gene

prominin 1

HGNCHGNC:9454EnsemblENSG00000007062NCBI Gene8842
Locus: gene with protein productLocation: 4p15.32

Also known as

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

Also known asPROML1 · MCDR2 · STGD4 · AC133 · CD133 · RP41 · CORD12
View full nomenclature history (12)
Previous symbolsPROML1, MCDR2, STGD4
Alias symbolsAC133, CD133, RP41, CORD12
Previous namesprominin (mouse)-like 1, macular dystrophy, retinal 2, Stargardt disease 4 (autosomal dominant)
Alias namesAC133 antigen, Retinitis pigmentosa 41, Cone-rod dystrophy 12

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.

Retinitis Pigmentosa
Cone rod dystrophy
Cone-rod dystrophy

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.

CD moleculesProminin family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-06-06.
Open TargetsGene–disease associations from the Open Targets Platform.