Gene
ARHGAP31
Rho GTPase activating protein 31
- HGNC 29216↗(opens in a new tab)
- Ensembl gene ENSG00000031081↗(opens in a new tab)
- NCBI Gene 57514↗(opens in a new tab)
Summary
- Cytogenetic location
- 3q13.32-q13.33
- Coordinates
- Chromosome 3: 119,294,383–119,420,714 (GRCh38)
- Exons
- 12 exons across 126.3 kb
- Protein
- 1,444 amino acids
- Also known as
- CDGAP
- MANE Select transcript
- ENST00000264245.9NM_020754.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads ARHGAP31 yet. The test sequences your whole genome, so your data includes it all the same.
How ARHGAP31 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 9.3 kb of the gene's 126.3 kb; 4,335 of those bases code for the protein.
How a genome test reads ARHGAP31
2
positions in ARHGAP31 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 126.3 kb of ARHGAP31, introns included, not only the 9.3 kb of exons.
Traits linked to ARHGAP31
The Human Phenotype Ontology lists these as features of the rare conditions ARHGAP31 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the integument
- Absence of part of skin at birth
- Absent/small skin
- Sparse hair
- Absent fingernail
- Absent/small toenails
- Hair loss
- Small fingernail
- Aplasia cutis congenita on trunk or limbs
Show 2 more traits
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). ARHGAP31 gene: Rho GTPase activating protein 31. Retrieved 17 October 2026, from https://dantelabs.com/genes/arhgap31
Dante Labs. ARHGAP31 gene: Rho GTPase activating protein 31 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/arhgap31
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