|
Symbol Name ID |
Mgat2
mannoside acetylglucosaminyltransferase 2 MGI:2384966 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Progressive microcephaly |
Cerebellar hypoplasia |
Brain atrophy |
Hypsarrhythmia |
Aggressive behavior |
Motor stereotypy |
Stereotypical hand wringing |
Self-mutilation |
Intellectual disability, severe |
Unsteady gait |
Global developmental delay |
Severe global developmental delay |
Peripheral neuropathy |
Seizure |
Infantile spasms |
| Disease(s) Associated with MGAT2 | ||||||||||||||||
| congenital disorder of glycosylation type IIa |
| Mouse Phenotypes | nervous system phenotype |
abnormal PNS synaptic transmission |
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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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