ARHGAP20 Rho GTPase activating protein 20
Gene ID: 57569, updated on 17-Jun-2024Gene type: protein coding
Also known as: RARHOGAP
- See all available tests in GTR for this gene
- Go to complete Gene record for ARHGAP20
- Go to Variation Viewer for ARHGAP20 variants
Summary
The protein encoded by this gene is an activator of RHO-type GTPases, transducing a signal from RAP1 to RHO and impacting neurite outgrowth. [provided by RefSeq, Sep 2016]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. GeneReviews: Not available | |
| Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. GeneReviews: Not available | |
| Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study. GeneReviews: Not available |
Genomic context
- Location:
- 11q22.3-q23.1
- Sequence:
- Chromosome: 11; NC_000011.10 (110577043..110713189, complement)
- Total number of exons:
- 20
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for ARHGAP20 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
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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