|
Symbol Name ID |
Mgat2
mannoside acetylglucosaminyltransferase 2 MGI:2384966 |
| Darker colors indicate more annotations |
| Human Phenotypes | Brachycephaly |
Dolichocephaly |
Mandibular prognathia |
Retrognathia |
Microcephaly |
Progressive microcephaly |
Macrocephaly |
Short neck |
Proximal placement of thumb |
Brachydactyly |
Coxa valga |
Slender long bone |
Abnormal rib cage morphology |
Pectus excavatum |
Thoracolumbar kyphoscoliosis |
Kyphosis |
Scoliosis |
Osteopenia |
| Disease(s) Associated with MGAT2 | ||||||||||||||||||
| congenital disorder of glycosylation type IIa |
| Mouse Phenotypes | kyphoscoliosis |
decreased bone mineral density |
delayed bone ossification |
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| Availability | Mouse Genotype | |||
| Mgat2tm1.1Jxm/Mgat2tm1.1Jxm | ||||
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 04/23/2024 MGI 6.23 |
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