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Symbol Name ID |
Mogs
mannosyl-oligosaccharide glucosidase MGI:1929872 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Abnormality of visual evoked potentials |
| Disease(s) Associated with MOGS | ||
| congenital disorder of glycosylation type IIb |
| Mouse Phenotypes | anophthalmia |
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| Availability | Mouse Genotype | |
| Mogstm1(KOMP)Vlcg/Mogs+ | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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