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Symbol
Name
ID
Elovl5
ELOVL fatty acid elongase 5
MGI:1916051
Phenotype annotations related to vision/eye
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
Availability Mouse Genotype
Elovl5em1(IMPC)Tcp/Elovl5em1(IMPC)Tcp

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
05/28/2024
MGI 6.13
The Jackson Laboratory