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Symbol
Name
ID
Pomk
protein-O-mannose kinase
MGI:1921903
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Disease(s) Associated with POMK
congenital muscular dystrophy-dystroglycanopathy type A12

Mouse Phenotypes
impaired cued conditioning behavior
tremors
decreased grip strength
increased chemical nociceptive threshold
Availability Mouse Genotype
PomkGt(OST243203)Lex/PomkGt(OST243203)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
04/16/2024
MGI 6.23
The Jackson Laboratory