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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cpt1c
carnitine palmitoyltransferase 1c
MGI:2446526
20 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cpt1ctm1b(EUCOMM)Wtsi/Cpt1ctm1b(EUCOMM)Wtsi
C57BL/6N-Cpt1ctm1b(EUCOMM)Wtsi/Ucd
abnormal uterus morphology J:211773
decreased bone mineral content J:211773
decreased brain weight J:211773
increased total body fat amount J:211773
Cpt1ctm1Dhwu/Cpt1ctm1Dhwu
involves: 129 * C57BL/6J
decreased skeletal muscle cell glucose uptake J:148205
enhanced gluconeogenesis J:148205
normal growth/size/body region phenotype J:148205
increased circulating glucose level J:148205
increased circulating insulin level J:148205
increased liver triglyceride level J:148205
insulin resistance J:148205
Cpt1ctm1Fghe/Cpt1ctm1Fghe
B6.129S-Cpt1ctm1Fghe
abnormal dendritic spine morphology J:186508
abnormal lipid level J:186508
abnormal spatial learning J:186508
Cpt1ctm1Mdln/Cpt1ctm1Mdln
involves: C57BL/6
decreased body weight J:109455
decreased food intake J:109455
hepatic steatosis J:109455
hyperlipidemia J:109455
increased circulating triglyceride level J:109455
increased susceptibility to weight gain J:109455
insulin resistance J:109455

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
12/10/2024
MGI 6.24
The Jackson Laboratory