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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Elovl4
ELOVL fatty acid elongase 4
MGI:1933331
18 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Elovl4tm1Wked/Elovl4tm1Wked
Tg(IVL-Elovl4)#Wked/0
Tg(KRT14-Elovl4)#Mpag/0
involves: 129 * C57BL/6
abnormal CNS synaptic transmission J:277065
abnormal energy homeostasis J:277065
abnormal excitatory postsynaptic potential J:277065
abnormal nervous system electrophysiology J:277065
decreased body weight J:277065
delayed eyelid opening J:277065
increased cellular glucose import J:277065
postnatal growth retardation J:277065
postnatal lethality, complete penetrance J:277065
seizures J:277065
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

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
11/12/2024
MGI 6.24
The Jackson Laboratory