ARHGAP5

Gene

Rho GTPase activating protein 5

HGNCHGNC:675 EnsemblENSG00000100852 NCBI Gene394

Locus: gene with protein productLocation: 14q12

Also known as

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

Also known asGFI2 · RhoGAP5 · p190-B · p190BRhoGAP

View full nomenclature history (5)

Previous symbolsGFI2

Alias symbolsRhoGAP5, p190-B, p190BRhoGAP

Previous namesgrowth factor independent 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.

Neurodegenerative Diseases

Iron Metabolism Disorders

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.