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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Irx6
Iroquois homeobox 6
MGI:1927642
10 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Irx6tm1b(KOMP)Mbp/Irx6tm1b(KOMP)Mbp
C57BL/6N-Irx6tm1b(KOMP)Mbp/Kmpc
abnormal coat/hair pigmentation J:211773
abnormal eye morphology J:211773
abnormal liver morphology J:211773
abnormal seminal vesicle morphology J:211773
abnormal skin coloration J:211773
increased circulating phosphate level J:211773
Irx6tm1Chow/Irx6tm1Chow
involves: 129S1/Sv * 129S1/SvImj * 129X1/SvJ
abnormal cone electrophysiology J:189955
abnormal retina bipolar cell morphology J:189955
abnormal retina inner plexiform layer morphology J:189955
abnormal rod electrophysiology J:189955

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