ARHGAP31

Gene

Rho GTPase activating protein 31

HGNCHGNC:29216 EnsemblENSG00000031081 NCBI Gene57514

Locus: gene with protein productLocation: 3q13.32-q13.33

Also known as

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

Also known asCDGAP

View full nomenclature history (1)

Alias symbolsCDGAP

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.

Hypertension

Cerebral Palsy

Genetic Diseases, Inborn

Celiac Disease

Lupus Erythematosus, Systemic

Autoimmune 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.

Rho GTPase activating proteins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.