RASD2

Gene

RASD family member 2

HGNCHGNC:18229 EnsemblENSG00000100302 NCBI Gene23551

Locus: gene with protein productLocation: 22q12.3

Also known as

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

Also known asTEM2 · Rhes · MGC:4834

View full nomenclature history (6)

Alias symbolsTEM2, Rhes, MGC:4834

Previous namesRASD family, member 2

Alias namestumor endothelial marker 2, Ras homolog enriched in striatum

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.

Neurodegenerative Diseases

Intelligence

Heart Arrest

Huntington's Disease

Diabetic Ketoacidosis

Major depressive disorder

Depressive Disorder

Thyroid gland carcinoma

Thyroid Neoplasms

Neoplasms

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.

RAS type GTPase family

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.