RASD2 (RASD family member 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 23551 |
| Gene name | RASD family member 2 |
| Gene symbol | RASD2 |
| Synonyms (NCBI Gene) |
RhesTEM2
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| Chromosome | 22 |
| Chromosome location | 22q12.3 |
| Summary | This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the prote |
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miRNA
miRNA information provided by mirtarbase database.
78
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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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Q96D21 | ||||||||||
| Protein name | GTP-binding protein Rhes (Ras homolog enriched in striatum) (Tumor endothelial marker 2) | ||||||||||
| Protein function | GTPase signaling protein that binds to and hydrolyzes GTP. Regulates signaling pathways involving G-proteins-coupled receptor and heterotrimeric proteins such as GNB1, GNB2 and GNB3. May be involved in selected striatal competencies, mainly loco | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Pancreatic endocrine cells (islets of Langerhans). {ECO:0000269|PubMed:11976265}. | ||||||||||
| Sequence |
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| Sequence length | 266 | ||||||||||
| Interactions | View interactions | ||||||||||
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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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