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Symbol Name ID |
Elovl4
ELOVL fatty acid elongase 4 MGI:1933331 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Supranuclear gaze palsy |
Nystagmus |
Impaired smooth pursuit |
| Disease(s) Associated with ELOVL4 | |||
| spinocerebellar ataxia type 34 |
| Mouse Phenotypes | vision/eye phenotype |
abnormal photoreceptor outer segment morphology |
short retina rod cell outer segment |
retina cone cell degeneration |
abnormal retina rod cell morphology |
retina rod cell degeneration |
retina photoreceptor degeneration |
abnormal retina pigment epithelium morphology |
abnormal eye morphology |
abnormal retina morphology |
thin retina outer nuclear layer |
abnormal retina outer plexiform layer morphology |
abnormal retina photoreceptor layer morphology |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
abnormal vision |
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| Availability | Mouse Genotype | |||||||||||||||||
| Elovl4tm1Kzh/Elovl4+ | ||||||||||||||||||
| Elovl4tm1Rayy/Elovl4+ | ||||||||||||||||||
| Elovl4tm1Sie/Elovl4+ | ||||||||||||||||||
| Elovl4tm1Wked/Elovl4+ | ||||||||||||||||||
| Elovl4tm3Kzh/Elovl4tm3Kzh Tg(Rho-cre)#Yzl/? (conditional) |
* | |||||||||||||||||
| Elovl4tm3Kzh/Elovl4tm3Kzh Tg(Rho-icre)1Ck/? (conditional) |
* | |||||||||||||||||
| Elovl4tm3Kzh/Elovl4tm3Kzh Tg(OPN1LW-cre)4Yzl/? (conditional) |
* | |||||||||||||||||
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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