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Symbol
Name
ID

Elovl4
ELOVL fatty acid elongase 4
MGI:1933331

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Spasticity

Peripheral axonal neuropathy

Cerebral cortical atrophy

Cerebellar atrophy

Ataxia

Dysdiadochokinesis

Gait ataxia

Limb ataxia

Fasciculations

Intention tremor

Abnormal pyramidal sign

Dysarthria

Hyperreflexia

Hyporeflexia

Disease(s) Associated with ELOVL4

spinocerebellar ataxia type 34

Mouse Phenotypes		abnormal synaptic vesicle exocytosis	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 synaptic vesicle number
Availability	Mouse Genotype	abnormal synaptic vesicle exocytosis	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 synaptic vesicle number
	Elovl4^tm1Wked/Elovl4^tm1Wked
	Elovl4^tm1Kzh/Elovl4⁺
	Elovl4^tm1Rayy/Elovl4⁺
	Elovl4^tm1Sie/Elovl4⁺
	Elovl4^tm3Kzh/Elovl4^tm3Kzh Tg(Rho-cre)#Yzl/? (conditional)
	Elovl4^tm3Kzh/Elovl4^tm3Kzh Tg(Rho-icre)1Ck/? (conditional)

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23