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Symbol
Name
ID

Chat
choline acetyltransferase
MGI:88392

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Arthrogryposis multiplex congenita
Disease(s) Associated with CHAT	Arthrogryposis multiplex congenita
congenital myasthenic syndrome 6

Mouse Phenotypes		kyphosis
Availability	Mouse Genotype	kyphosis
	Chat/Slc18a3^tm1.1Vpra/Chat/Slc18a3^tm1.1Vpra
	Chat^tm1.1Jrs/Chat^tm1.1Jrs
	Chat^tm1Fhg/Chat^tm1Fhg
	Chat^tm1Mlt/Chat^tm1Mlt Tg(SLC18A3-cre)KMisa/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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