About   Help   FAQ
Symbol
Name
ID
Chat
choline acetyltransferase
MGI:88392
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Poor suck
Weak cry
Disease(s) Associated with CHAT
congenital myasthenic syndrome 6

Mouse Phenotypes
behavior/neurological phenotype
abnormal habituation to a new environment
tremors
weakness
tail dragging
abnormal gait
decreased vertical activity
increased vertical activity
decreased locomotor activity
hyperactivity
carpoptosis
Availability Mouse Genotype
Chat/Slc18a3tm1.2Vpra/Chat/Slc18a3tm1.2Vpra *
Chat/Slc18a3tm1Vpra/Chat/Slc18a3tm1Vpra *
Chattm1.1Jrs/Chattm1.1Jrs
Chattm1Fhg/Chattm1Fhg
Chat/Slc18a3tm1.1Vpra/Chat+ *
Chat/Slc18a3tm1Vpra/Chat/Slc18a3tm1.1Vpra *
Chattm1Jrs/Chattm1Jrs
Tg(CAG-cre/Esr1*)1Lbe/0  (conditional)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory