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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Foxk2
forkhead box K2
MGI:1916087
12 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Foxk2em1(IMPC)J/Foxk2em1(IMPC)J
C57BL/6NJ-Foxk2em1(IMPC)J/J
abnormal bone structure J:211773
abnormal retina blood vessel morphology J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased grip strength J:211773
Foxk2tm1.1Sven/Foxk2tm1.1Sven
B6.129P2-Foxk2tm1.1Sven
decreased adipocyte glucose uptake J:273343
Foxk2tm1.2Sven/Foxk2tm1.2Sven
B6.Cg-Foxk2tm1.2Sven
decreased body weight J:273343
decreased cellular glucose uptake J:273343
decreased circulating lactate level J:273343
decreased skeletal muscle cell glucose uptake J:273343
impaired glucose tolerance J:273343
increased circulating insulin level J:273343

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
12/17/2024
MGI 6.24
The Jackson Laboratory