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Symbol
Name
ID

Cpt1c
carnitine palmitoyltransferase 1c
MGI:2446526

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Lower limb spasticity	Progressive spastic paraparesis	Progressive spastic paraplegia	Spastic gait	Difficulty walking	Degeneration of the lateral corticospinal tracts	Babinski sign	Abnormal lower-limb motor evoked potentials	Hyperreflexia	Impaired vibration sensation in the lower limbs
Disease(s) Associated with CPT1C
hereditary spastic paraplegia 73

Mouse Phenotypes		decreased brain weight	abnormal dendritic spine morphology
Availability	Mouse Genotype	decreased brain weight	abnormal dendritic spine morphology
	Cpt1c^{tm1b(EUCOMM)Wtsi}/Cpt1c^{tm1b(EUCOMM)Wtsi}
	Cpt1c^tm1Fghe/Cpt1c^tm1Fghe

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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