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Symbol
Name
ID
Cpt1c
carnitine palmitoyltransferase 1c
MGI:2446526
Phenotype annotations related to muscle
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 muscle cell glucose uptake
Availability Mouse Genotype
Cpt1ctm1Dhwu/Cpt1ctm1Dhwu

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
04/09/2024
MGI 6.23
The Jackson Laboratory