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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	Abdominal pain	Feeding difficulties in infancy	Autistic behavior
Disease(s) Associated with POMT1	Abdominal pain	Feeding difficulties in infancy	Autistic behavior
autosomal recessive limb-girdle muscular dystrophy type 2K
congenital muscular dystrophy-dystroglycanopathy type A1

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)
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