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 09/17/2024 MGI 6.24 |
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