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Symbol
Name
ID
Cpt1c
carnitine palmitoyltransferase 1c
MGI:2446526
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Claw toe deformity
Disease(s) Associated with CPT1C
hereditary spastic paraplegia 73

Mouse Phenotypes
decreased bone mineral content
Availability Mouse Genotype
Cpt1ctm1b(EUCOMM)Wtsi/Cpt1ctm1b(EUCOMM)Wtsi

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
04/23/2024
MGI 6.23
The Jackson Laboratory