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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nkx6-2
NK6 homeobox 2
MGI:1352738
7 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nkx6-2tm1(cre/ERT2)Fsh/Nkx6-2tm1(cre/ERT2)Fsh
involves: 129S6/SvEvTac * C57BL/6 * Swiss Webster
normal mortality/aging J:155164
Nkx6-2tm1Ercs/Nkx6-2tm1Ercs
involves: 129P2/OlaHsd * C57BL/6
no abnormal phenotype detected J:71607
Nkx6-2tm1Gow/Nkx6-2tm1Gow
involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac
abnormal myelination J:94807
abnormal nerve conduction J:94807
abnormal optic nerve morphology J:94807
axon degeneration J:94807
impaired coordination J:94807
Nkx6-2tm1Qiu/Nkx6-2tm1Qiu
Not Specified
no abnormal phenotype detected J:69975

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