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Symbol
Name
ID

Crppa
CDP-L-ribitol pyrophosphorylase A
MGI:1923097

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Myalgia
Disease(s) Associated with CRPPA	Decreased fetal movement	Myalgia
autosomal recessive limb-girdle muscular dystrophy type 2U
congenital muscular dystrophy-dystroglycanopathy A7

Mouse Phenotypes		decreased grip strength
Availability	Mouse Genotype	decreased grip strength
	Crppa^em2Mbp/Crppa^em2Mbp Myf5^tm3(cre)Sor/Myf5⁺ (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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