|
Symbol Name ID |
Pmm2
phosphomannomutase 2 MGI:1859214 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cataract |
Rod-cone dystrophy |
Photoreceptor layer loss on macular OCT |
Hypertelorism |
Strabismus |
Esodeviation |
Esotropia |
Nystagmus |
Myopia |
| Disease(s) Associated with PMM2 | |||||||||
| congenital disorder of glycosylation Ia |
| Mouse Phenotypes | abnormal eye morphology |
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| Availability | Mouse Genotype | |
| Pmm2tm1.1Jins/Pmm2tm2.1Jins | ||
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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