Symbol Name ID |
Cpt1c
carnitine palmitoyltransferase 1c MGI:2446526 |
Darker colors indicate more annotations |
Human Phenotypes | Distal lower limb muscle weakness |
Lower limb spasticity |
Progressive spastic paraparesis |
Spastic paraplegia |
Progressive spastic paraplegia |
Spastic gait |
EMG abnormality |
Difficulty walking |
Proximal muscle weakness |
Skeletal muscle atrophy |
Distal lower limb amyotrophy |
Disease(s) Associated with CPT1C | |||||||||||
hereditary spastic paraplegia 73 |
Mouse Phenotypes | decreased skeletal muscle cell glucose uptake |
|
Availability | Mouse Genotype | |
Cpt1ctm1Dhwu/Cpt1ctm1Dhwu |
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 08/02/2024 MGI 6.24 |
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