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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Sgms2
sphingomyelin synthase 2
MGI:1921692
18 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Sgms2tm1Jia/Sgms2tm1Jia
involves: 129 * C57BL/6
abnormal cell physiology J:162192
abnormal circulating protein level J:162192
abnormal hepatocyte physiology J:162192
abnormal lipid level J:162192, J:162226
abnormal macrophage morphology J:162226
abnormal macrophage physiology J:162192, J:162226
abnormal sphingomyelin level J:162192
hemolysis J:162192
Sgms2tm1Jia/Sgms2tm1Jia
Not Specified
abnormal ceramide level J:220024, J:228568
abnormal sphingomyelin level J:228568
normal homeostasis/metabolism phenotype J:228568
Sgms2tm1Kenw/Sgms2tm1Kenw
B6.129S2-Sgms2tm1Kenw
abnormal cell physiology J:175924
abnormal circulating glucose level J:175924
decreased circulating triglyceride level J:175924
decreased epididymal fat pad weight J:175924
decreased susceptibility to diet-induced hepatic steatosis J:175924
decreased susceptibility to diet-induced obesity J:175924
improved glucose tolerance J:175924
increased circulating free fatty acids level J:175924
increased insulin sensitivity J:175924

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
04/16/2024
MGI 6.23
The Jackson Laboratory