Elovl4 Phenotype Annotations - Multigenic Genotypes

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Elovl4^tm1Wked/Elovl4^tm1Wked 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
Elovl4^tm2Kzh/Elovl4^tm2Kzh 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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