Symbol Name ID |
Pmm2
phosphomannomutase 2 MGI:1859214 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased circulating IgA level |
Decreased circulating IgG level |
Hypocholesterolemia |
Hypoalbuminemia |
Reduced thyroxin-binding globulin |
Elevated circulating hepatic transaminase concentration |
Hyperinsulinemia |
Insulin resistance |
Edema |
Anasarca |
Nonimmune hydrops fetalis |
Lymphedema |
Fever |
Type I transferrin isoform profile |
Hepatic steatosis |
Proteinuria |
Elevated circulating growth hormone concentration |
Elevated circulating thyroid-stimulating hormone concentration |
Disease(s) Associated with PMM2 | ||||||||||||||||||
congenital disorder of glycosylation Ia |
Mouse Phenotypes | abnormal blood homeostasis |
increased blood urea nitrogen level |
decreased circulating insulin-like growth factor I level |
decreased circulating antithrombin level |
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Availability | Mouse Genotype | ||||
Pmm2tm1.1Jins/Pmm2tm2.1Jins | |||||
Pmm2tm1b(EUCOMM)Hmgu/Pmm2+ |
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 04/30/2024 MGI 6.23 |
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