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Symbol
Name
ID
Elovl4
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4
MGI:1933331
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Spasticity
Peripheral axonal neuropathy
Cerebellar atrophy
Ataxia
Dysdiadochokinesis
Gait ataxia
Limb ataxia
Abnormal pyramidal sign
Dysarthria
Hyperreflexia
Hyporeflexia
Fasciculations
Intention tremor
Disease(s) Associated with ELOVL4
spinocerebellar ataxia type 34

Mouse Phenotypes
abnormal photoreceptor outer segment morphology
abnormal retinal rod cell outer segment morphology
retinal cone cell degeneration
abnormal retinal rod cell morphology
retinal rod cell degeneration
retinal photoreceptor degeneration
Availability Mouse Genotype
Elovl4tm1Kzh/Elovl4+
Elovl4tm1Rayy/Elovl4+
Elovl4tm1Sie/Elovl4+
Elovl4tm3Kzh/Elovl4tm3Kzh
Tg(Rho-cre)#Yzl/?  (conditional)
Elovl4tm3Kzh/Elovl4tm3Kzh
Tg(Rho-icre)1Ck/?  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO)
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Funding Information
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last database update
05/14/2019
MGI 6.14
The Jackson Laboratory