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Symbol
Name
ID
Chat
choline acetyltransferase
MGI:88392
Phenotype annotations related to digestive/alimentary system
Darker colors indicate more annotations
Human Phenotypes
Dysphagia
Disease(s) Associated with CHAT
congenital myasthenic syndrome 6

Mouse Phenotypes
rectal prolapse
Availability Mouse Genotype
Chattm1Mlt/Chattm1Mlt
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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory