About   Help   FAQ
Symbol
Name
ID
Cpt1c
carnitine palmitoyltransferase 1c
MGI:2446526
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Urinary incontinence
Disease(s) Associated with CPT1C
hereditary spastic paraplegia 73

Mouse Phenotypes
abnormal spatial learning
decreased food intake
Availability Mouse Genotype
Cpt1ctm1Fghe/Cpt1ctm1Fghe
Cpt1ctm1Mdln/Cpt1ctm1Mdln

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