WormBase Tree Display for Gene: HGNC:19358
expand all nodes | collapse all nodes | view schema
| HGNC:19358 | Identity | Name | CGC_name | Alg12 | Inferred_automatically | AGR_import |
|---|---|---|---|---|---|---|
| Other_name (19) | ||||||
| Public_name | Alg12 | |||||
| DB_info | Database | HGNC | id | 19358 | ||
| AGR | cURI | HGNC:19358 | ||||
| EnsEMBL | ENSEMBL_geneID | ENSG00000182858 | ||||
| UniProt | UniProt_AC | Q9BV10 | ||||
| OMIM | gene | 607144 | ||||
| DO | id | DOID:0080559 | ||||
| Species | Homo sapiens | |||||
| Status | Live | |||||
| Gene_info | Biotype | SO:0001217 | ||||
| Ortholog | WBGene00022629 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | ||
| Hieranoid | ||||||
| Inparanoid | ||||||
| OMA | ||||||
| OrthoFinder | ||||||
| OrthoInspector | ||||||
| Panther | ||||||
| PhylomeDB | ||||||
| SonicParanoid | ||||||
| Structured_description | Automated_description | This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. [provided by RefSeq, Jul 2008] | Inferred_automatically | AGR_import |
