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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cyp4v3
cytochrome P450, family 4, subfamily v, polypeptide 3
MGI:2142763
29 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cyp4v3em1(IMPC)Mbp/Cyp4v3em1(IMPC)Mbp
C57BL/6NCrl-Cyp4v3em1(IMPC)Mbp/Mmucd
abnormal eye morphology J:211773
abnormal liver morphology J:211773
enlarged liver J:211773
hyperactivity J:211773
preweaning lethality, incomplete penetrance J:211773
Cyp4v3em1Xsu/Cyp4v3em1Xsu
C57BL/6J-Cyp4v3em1Xsu
abnormal electroretinogram waveform feature J:321817
abnormal eye physiology J:321817
abnormal glial cell physiology J:321817
abnormal lipid metabolism J:321817
abnormal photoreceptor inner segment morphology J:321817
abnormal photoreceptor outer segment morphology J:321817
abnormal retina cone cell outer segment morphology J:321817
abnormal retina inner nuclear layer morphology J:321817
abnormal retina inner plexiform layer morphology J:321817
abnormal retina morphology J:321817
abnormal retina pigment epithelium morphology J:321817
abnormal sclera morphology J:321817
decreased a-wave amplitude J:321817
decreased b-wave amplitude J:321817
decreased total retina thickness J:321817
increased microglial cell activation J:321817
increased susceptibility to age-related retinal degeneration J:321817
oxidative stress J:321817
retina deposits J:321817
retina photoreceptor degeneration J:321817
short retina rod cell outer segment J:321817
thin retina outer nuclear layer J:321817
Cyp4v3tm1(KOMP)Vlcg/Cyp4v3tm1(KOMP)Vlcg
B6(Cg)-Cyp4v3tm1(KOMP)Vlcg
abnormal fatty acids level J:230232
abnormal optic choroid morphology J:230232
abnormal retina morphology J:230232

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
04/30/2024
MGI 6.23
The Jackson Laboratory