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Details of MOGS gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| MOGS | GCS1 | Q13724 | MOGS_HUMAN | 7841
| ENSG00000115275
| Mannosyl-oligosaccharide glucosidase | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Type IIb congenital disorder of glycosylation (CDGIIb) [MIM:606056]: Characterized by marked generalized hypotonia and hypomotility of the neonate, dysmorphic features, including a prominent occiput, short palpebral fissures, retrognathia, high arched palate, generalized edema, and hypoplastic genitalia. Symptoms of the infant included hepatomegaly, hypoventilation, feeding problems and seizures. The clinical course was progressive and the infant did not survive more than a few months. Note=The disease is caused by mutations affecting the gene represented in this entry. |
606056 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
| Mogs | CG1597 | F13H10.4 | |
