ARHGAP5 Rho GTPase activating protein 5
Gene ID: 394, updated on 5-Mar-2024Gene type: protein coding
Also known as: GFI2; p190-B; RhoGAP5; p190BRhoGAP
- See all available tests in GTR for this gene
- Go to complete Gene record for ARHGAP5
- Go to Variation Viewer for ARHGAP5 variants
Summary
Rho GTPase activating protein 5 negatively regulates RHO GTPases, a family which may mediate cytoskeleton changes by stimulating the hydrolysis of bound GTP. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Genomic context
- Location:
- 14q12
- Sequence:
- Chromosome: 14; NC_000014.9 (32077304..32159728)
- Total number of exons:
- 7
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for ARHGAP5 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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