Symbol Name ID |
Elovl5
ELOVL fatty acid elongase 5 MGI:1916051 |
Darker colors indicate more annotations |
Human Phenotypes | Nystagmus |
Slow saccadic eye movements |
Disease(s) Associated with ELOVL5 | ||
spinocerebellar ataxia type 38 |
Mouse Phenotypes | impaired pupillary reflex |
abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
abnormal iris morphology |
abnormal lens morphology |
cataract |
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Availability | Mouse Genotype | ||||||
Elovl5em1(IMPC)Tcp/Elovl5em1(IMPC)Tcp |
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 05/28/2024 MGI 6.13 |
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