WormBase Tree Display for Gene: MGI:109522
expand all nodes | collapse all nodes | view schema
| MGI:109522 | Identity | Name | CGC_name | Ugt8a | Inferred_automatically | AGR_import |
|---|---|---|---|---|---|---|
| Other_name | MGD_old:MGD-MRK-36113 | |||||
| MGD_old:MGD-MRK-39521 | ||||||
| MGI:2139820 | ||||||
| MGI:2139983 | ||||||
| Public_name | Ugt8a | |||||
| DB_info | Database | MGI | id | 109522 | ||
| AGR | cURI | MGI:109522 | ||||
| EnsEMBL | ENSEMBL_geneID | ENSMUSG00000032854 | ||||
| UniProt | UniProt_AC | Q64676 | ||||
| Species | Mus musculus | |||||
| Status | Live | |||||
| Gene_info | Biotype | SO:0001217 | ||||
| Ortholog (45) | ||||||
| Structured_description | Automated_description | PHENOTYPE: Mutants fail to make galactolipid galactocerebroside and its sulfated derivative that are normal myelin constituents. Mutants have tremors, ataxia, progressive hindlimb paralysis and vacuole formation in ventral spinal cord due to abnormal myelin sheath. [provided by MGI curators] | Inferred_automatically | AGR_import |
