RASA2

Gene

RAS p21 protein activator 2

HGNCHGNC:9872 EnsemblENSG00000155903 NCBI Gene5922

Locus: gene with protein productLocation: 3q23

Also known as

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

Also known asGAP1M

View full nomenclature history (2)

Alias symbolsGAP1M

Alias namesRas GTPase-activating protein 2

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.

Noonan syndrome

Obesity disorder

Osteoarthritis, Knee

Neurodegenerative Diseases

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.

Pleckstrin homology domain containingC2 and RasGAP 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.