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Symbol Name ID |
Alg11
ALG11 alpha-1,2-mannosyltransferase MGI:2142632 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased corneal reflex |
Strabismus |
Abnormality of vision |
| Disease(s) Associated with ALG11 | |||
| congenital disorder of glycosylation Ip |
| Mouse Phenotypes | persistence of hyaloid vascular system |
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| Availability | Mouse Genotype | |
| Alg11tm1.1(KOMP)Vlcg/Alg11+ | ||
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 05/28/2024 MGI 6.13 |
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