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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Elovl4
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4
MGI:1933331
38 phenotypes from 6 alleles in 8 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Elovl4tm1Kzh/Elovl4+
involves: C57BL/6
abnormal cone electrophysiology J:124499
abnormal photoreceptor outer segment morphology J:124499
abnormal rod electrophysiology J:124499
Elovl4tm1Kzh/Elovl4tm1Kzh
involves: C57BL/6
abnormal epidermis stratum corneum morphology J:161118
abnormal erythrocyte morphology J:124499
abnormal forelimb morphology J:124499
abnormal skin appearance J:161118
abnormal skin condition J:161118
decreased fetal size J:124499
decreased fetal weight J:124499
impaired skin barrier function J:161118
perinatal lethality J:161118
shiny skin J:161118
thin skin J:161118
weight loss J:161118
Elovl4tm1Rayy/Elovl4+
involves: 129 * C57BL/6J
abnormal cone electrophysiology J:114752
abnormal eye electrophysiology J:114752
abnormal eye morphology J:114752
abnormal fatty acid level J:114752
abnormal photoreceptor outer segment morphology J:114752
abnormal retina morphology J:114752
abnormal retinal outer plexiform layer morphology J:114752
abnormal retinal pigment epithelium morphology J:114752
abnormal retinal rod cell outer segment morphology J:114752
retinal cone cell degeneration J:114752
retinal photoreceptor degeneration J:114752
retinal rod cell degeneration J:114752
thin retinal outer nuclear layer J:114752
Elovl4tm1Sie/Elovl4+
involves: 129P2/OlaHsd * C57BL/6
abnormal fertility/fecundity J:112264
abnormal retina morphology J:112264
abnormal retinal photoreceptor layer morphology J:112264
abnormal retinal rod cell outer segment morphology J:112264
Elovl4tm1Sie/Elovl4tm1Sie
involves: 129P2/OlaHsd * C57BL/6
prenatal lethality, complete penetrance J:112264
Elovl4tm1Wked/Elovl4+
involves: 129S/SvEv * 129S1/Sv
abnormal retinal pigment epithelium morphology J:121481
abnormal rod electrophysiology J:121481
abnormal vision J:121481
Elovl4tm1Wked/Elovl4tm1Wked
involves: 129S/SvEv * 129S1/Sv
abnormal epidermal layer morphology J:121481
abnormal epidermis stratum corneum morphology J:121481
impaired skin barrier function J:121481
lethargy J:121481
neonatal lethality, complete penetrance J:121481
reddish skin J:121481
Elovl4tm2Kzh/Elovl4tm2Kzh
involves: 129X1/SvJ * C57BL/6
abnormal epidermis stratum corneum morphology J:161118
abnormal skin appearance J:161118
abnormal skin condition J:161118
impaired skin barrier function J:161118
perinatal lethality J:161118
shiny skin J:161118
thin skin J:161118
weight loss J:161118
Elovl4tm3Kzh/Elovl4tm3Kzh
Tg(OPN1LW-cre)4Yzl/?
involves: FVB/N
normal homeostasis/metabolism phenotype J:194246
normal vision/eye phenotype J:194246
Elovl4tm3Kzh/Elovl4tm3Kzh
Tg(Rho-cre)#Yzl/?
Not Specified
abnormal retinal rod cell morphology J:194246
decreased unsaturated fatty acid level J:194246
normal vision/eye phenotype J:194246
Elovl4tm3Kzh/Elovl4tm3Kzh
Tg(Rho-icre)1Ck/?
involves: C57BL/6 * SJL
abnormal retinal rod cell morphology J:194246
decreased unsaturated fatty acid level J:194246
normal vision/eye phenotype J:194246

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last database update
05/14/2019
MGI 6.14
The Jackson Laboratory