WormBase Tree Display for Gene: HGNC:17282
expand all nodes | collapse all nodes | view schema
| HGNC:17282 | Identity | Name | CGC_name | Rims1 | Inferred_automatically | AGR_import |
|---|---|---|---|---|---|---|
| Other_name (15) | ||||||
| Public_name | Rims1 | |||||
| DB_info | Database | HGNC | id | 17282 | ||
| AGR | cURI | HGNC:17282 | ||||
| EnsEMBL | ENSEMBL_geneID | ENSG00000079841 | ||||
| UniProt | UniProt_AC | Q86UR5 | ||||
| Species | Homo sapiens | |||||
| Status | Live | |||||
| Gene_info | Biotype | SO:0001217 | ||||
| Ortholog | WBGene00006750 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | ||
| Hieranoid | ||||||
| Inparanoid | ||||||
| OMA | ||||||
| OrthoFinder | ||||||
| OrthoInspector | ||||||
| Panther | ||||||
| SonicParanoid | ||||||
| Structured_description | Automated_description | The protein encoded by this gene is a RAS gene superfamily member that regulates synaptic vesicle exocytosis. This gene also plays a role in the regulation of voltage-gated calcium channels during neurotransmitter and insulin release. Mutations have suggested a role cognition and have been identified as the cause of cone-rod dystrophy type 7. Multiple transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Mar 2012] | Inferred_automatically | AGR_import |
