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Symbol
Name
ID

Pomt1
protein-O-mannosyltransferase 1
MGI:2138994

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Abdominal pain	Feeding difficulties	Excessive daytime somnolence	Autistic behavior
Disease(s) Associated with POMT1	Decreased fetal movement	Abdominal pain	Feeding difficulties	Excessive daytime somnolence	Autistic behavior
autosomal recessive limb-girdle muscular dystrophy type 2K
congenital muscular dystrophy-dystroglycanopathy type A1
muscular dystrophy-dystroglycanopathy

Mouse Phenotypes		abnormal optokinetic reflex
Availability	Mouse Genotype	abnormal optokinetic reflex
	Pomt1^{tm1c(EUCOMM)Hmgu}/Pomt1^{tm1c(EUCOMM)Hmgu} Tg(Crx-cre)1Tfur/0 (conditional)

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)
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support.	last database update 02/23/2021 MGI 6.16