Symbol Name ID |
Pomgnt1
protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase MGI:1915523 |
Darker colors indicate more annotations |
Human Phenotypes | Micrognathia |
Malar flattening |
Microcephaly |
Midface retrusion |
Everted lower lip vermilion |
Short nasal bridge |
Disease(s) Associated with POMGNT1 | ||||||
congenital muscular dystrophy-dystroglycanopathy type A3 | ||||||
muscular dystrophy-dystroglycanopathy type B3 |
Mouse Phenotypes | abnormal tongue muscle morphology |
|
Availability | Mouse Genotype | |
Pomgnt1Gt(OST179231)Lex/Pomgnt1Gt(OST179231)Lex |
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 04/23/2024 MGI 6.23 |
|
|