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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 integument
Darker colors indicate more annotations
Human Phenotypes
Abnormality of the skin
Hyperkeratosis
Disease(s) Associated with ELOVL4
spinocerebellar ataxia type 34

Mouse Phenotypes
impaired skin barrier function
abnormal epidermal layer morphology
abnormal epidermis stratum corneum morphology
abnormal skin appearance
reddish skin
shiny skin
abnormal skin condition
thin skin
Availability Mouse Genotype
Elovl4tm1Kzh/Elovl4tm1Kzh
Elovl4tm1Wked/Elovl4tm1Wked
Elovl4tm2Kzh/Elovl4tm2Kzh

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