|
Symbol Name ID |
Cyp4v3
cytochrome P450, family 4, subfamily v, polypeptide 3 MGI:2142763 |
| Darker colors indicate more annotations |
| Human Phenotypes | Corneal crystals |
Marginal corneal dystrophy |
Chorioretinal atrophy |
Retinal degeneration |
High myopia |
Progressive night blindness |
Reduced visual acuity |
Constriction of peripheral visual field |
Paracentral scotoma |
Progressive visual loss |
| Disease(s) Associated with CYP4V2 | ||||||||||
| Bietti crystalline corneoretinal dystrophy |
| Mouse Phenotypes | abnormal photoreceptor inner segment morphology |
abnormal photoreceptor outer segment morphology |
short retina rod cell outer segment |
abnormal retina cone cell outer segment morphology |
retina photoreceptor degeneration |
abnormal retina pigment epithelium morphology |
abnormal eye morphology |
abnormal retina morphology |
abnormal retina inner nuclear layer morphology |
abnormal retina inner plexiform layer morphology |
thin retina outer nuclear layer |
increased susceptibility to age-related retinal degeneration |
decreased total retina thickness |
retina deposits |
abnormal sclera morphology |
abnormal optic choroid morphology |
abnormal eye physiology |
abnormal electroretinogram waveform feature |
decreased a-wave amplitude |
decreased b-wave amplitude |
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| Availability | Mouse Genotype | ||||||||||||||||||||
| Cyp4v3em1(IMPC)Mbp/Cyp4v3em1(IMPC)Mbp | |||||||||||||||||||||
| Cyp4v3em1Xsu/Cyp4v3em1Xsu | |||||||||||||||||||||
| Cyp4v3tm1(KOMP)Vlcg/Cyp4v3tm1(KOMP)Vlcg | |||||||||||||||||||||
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 |
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