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Symbol
Name
ID
Pomt1
protein-O-mannosyltransferase 1
MGI:2138994
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Prolonged QT interval
Abnormal left ventricular function
Left ventricular systolic dysfunction
Left ventricular hypertrophy
Cardiomyopathy
Disease(s) Associated with POMT1
autosomal recessive limb-girdle muscular dystrophy type 2K
muscular dystrophy-dystroglycanopathy

Mouse Phenotypes
increased vasodilation
Availability Mouse Genotype
Pomt1Gt(OST194127)Lex/Pomt1+

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
02/23/2021
MGI 6.16
The Jackson Laboratory