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Symbol
Name
ID
B4gat1
beta-1,4-glucuronyltransferase 1
MGI:1919680
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Spasticity
Hypotonia
Severe muscular hypotonia
Muscular dystrophy
Disease(s) Associated with B4GAT1
congenital muscular dystrophy-dystroglycanopathy type A13

Mouse Phenotypes
skeletal muscle atrophy
dystrophic muscle
Availability Mouse Genotype
B4gat1m1Ddg/B4gat1m1Ddg
B4gat1m1Ddg/B4gat1tm1(KOMP)Vlcg

Contributing Projects:
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
The Jackson Laboratory