ARHGAP19 (Rho GTPase activating protein 19)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 84986 |
| Gene name | Rho GTPase activating protein 19 |
| Gene symbol | ARHGAP19 |
| Synonyms (NCBI Gene) |
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| Chromosome | 10 |
| Chromosome location | 10q24.1 |
| Summary | Members of the ARHGAP family, such as ARHGAP19, encode negative regulators of Rho GTPases (see RHOA; MIM 165390), which are involved in cell migration, proliferation, and differentiation, actin remodeling, and G1 cell cycle progression (Lv et al., 2007 [P |
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miRNA
miRNA information provided by mirtarbase database.
161
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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Q14CB8 | ||||||||||
| Protein name | Rho GTPase-activating protein 19 (Rho-type GTPase-activating protein 19) | ||||||||||
| Protein function | GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Strong expression in fetal heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Weak expression in adult pancreas, spleen, thymus, and ovary. {ECO:0000269|PubMed:17454002}. | ||||||||||
| Sequence |
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| Sequence length | 494 | ||||||||||
| 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.).
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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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