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STOML1

Gene

stomatin like 1

HGNCHGNC:14560EnsemblENSG00000067221NCBI Gene9399
Locus: gene with protein productLocation: 15q24.1

Also known as

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

Also known ashUNC-24 · SLP-1 · STORP · FLJ36370
View full nomenclature history (8)
Alias symbolshUNC-24, SLP-1, STORP, FLJ36370
Previous namesstomatin (EPB72)-like 1
Alias namesstomatin-like 1, stomatin (EBP72)-like 1, EPB72-like 1

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.

Coronary Artery Disease
Cardiovascular Diseases
Myocardial Infarction
Juvenile myoclonic epilepsy
Lennox-Gastaut syndrome

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.

Stomatin familySCP2 domain 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.