WormBase Tree Display for Gene: RGD:1304996
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| RGD:1304996 | Identity | Name | CGC_name | Kif1a | Inferred_automatically | AGR_import |
|---|---|---|---|---|---|---|
| Public_name | Kif1a | |||||
| DB_info | Database | RGD | id | 1304996 | ||
| AGR | cURI | RGD:1304996 | ||||
| EnsEMBL | ENSEMBL_geneID | ENSRNOG00000023993 | ||||
| UniProt | UniProt_AC | F1M4A4 | ||||
| Species | Rattus norvegicus | |||||
| Status | Live | |||||
| Gene_info | Biotype | SO:0001217 | ||||
| Ortholog | WBGene00006831 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | ||
| Hieranoid | ||||||
| Inparanoid | ||||||
| OMA | ||||||
| OrthoFinder | ||||||
| OrthoInspector | ||||||
| Panther | ||||||
| PhylomeDB | ||||||
| SonicParanoid | ||||||
| Structured_description | Automated_description | Enables identical protein binding activity and microtubule binding activity. Involved in several processes, including interkinetic nuclear migration; regulation of dendritic spine morphogenesis; and transport along microtubule. Located in several cellular components, including microtubule; neuronal cell body; and secretory vesicle. Part of protein-containing complex. Biomarker of synucleinopathy. Human ortholog(s) of this gene implicated in NESCAV syndrome; hereditary sensory neuropathy; hereditary sensory neuropathy type 2C; hereditary spastic paraplegia; and hereditary spastic paraplegia 30. Orthologous to human KIF1A (kinesin family member 1A); INTERACTS WITH 17beta-estradiol; 4,4'-sulfonyldiphenol; aldehydo-D-glucose. | Inferred_automatically | AGR_import |
