Symbol Name ID |
B4gat1
beta-1,4-glucuronyltransferase 1 MGI:1919680 |
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 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 08/21/2024 MGI 6.24 |
![]() |
|