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Symbol
Name
ID
Mgat2
mannoside acetylglucosaminyltransferase 2
MGI:2384966
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Myopathy
Muscular hypotonia
Generalized hypotonia
Muscular hypotonia of the trunk
Muscle weakness
Disease(s) Associated with MGAT2
congenital disorder of glycosylation type II

Mouse Phenotypes
abnormal muscle development
Availability Mouse Genotype
Mgat2tm1.1Jxm/Mgat2tm1.1Jxm

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/12/2018
MGI 6.12
The Jackson Laboratory