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Symbol
Name
ID
Pomgnt1
protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase
MGI:1915523
Phenotype annotations related to craniofacial
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

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