ARHGAP22 (Rho GTPase activating protein 22)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 58504 |
| Gene name | Rho GTPase activating protein 22 |
| Gene symbol | ARHGAP22 |
| Synonyms (NCBI Gene) |
RhoGAP2RhoGap22
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| Chromosome | 10 |
| Chromosome location | 10q11.22-q11.23 |
| Summary | This gene encodes a member of the GTPase activating protein family which activates a GTPase belonging to the RAS superfamily of small GTP-binding proteins. The encoded protein is insulin-responsive, is dependent on the kinase Akt and requires the Akt-depe |
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miRNA
miRNA information provided by mirtarbase database.
107
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q7Z5H3 | |||||||||||||||
| Protein name | Rho GTPase-activating protein 22 (Rho-type GTPase-activating protein 22) | |||||||||||||||
| Protein function | Rho GTPase-activating protein involved in the signal transduction pathway that regulates endothelial cell capillary tube formation during angiogenesis. Acts as a GTPase activator for the RAC1 by converting it to an inactive GDP-bound state. Inhi | |||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 698 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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