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Symbol
Name
ID

Chst3
carbohydrate sulfotransferase 3
MGI:1858224

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Intellectual disability	Waddling gait	Delayed gross motor development
Disease(s) Associated with CHST3
spondyloepiphyseal dysplasia with congenital joint dislocations

Mouse Phenotypes		nervous system phenotype	decreased prepulse inhibition
Availability	Mouse Genotype	nervous system phenotype	decreased prepulse inhibition
	Chst3^tm1Dgen/Chst3^tm1Dgen
	Chst3^tm1Tmu/Chst3^tm1Tmu	*

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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