Symbol Name ID |
Cpt1c
carnitine palmitoyltransferase 1c MGI:2446526 |
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 |
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 08/02/2024 MGI 6.24 |
![]() |
|