Eloa Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Eloa
elongin A
MGI:1351315

23 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Eloa^em1(IMPC)Mbp/Eloa⁺ C57BL/6N-Eloa^em1(IMPC)Mbp/MbpMmucd	abnormal eye morphology	J:211773
	abnormal heart morphology	J:211773
	abnormal liver morphology	J:211773
	anophthalmia	J:211773
	decreased body length	J:211773
	enlarged heart	J:211773
	small liver	J:211773
Eloa^em1(IMPC)Mbp/Eloa^em1(IMPC)Mbp C57BL/6N-Eloa^em1(IMPC)Mbp/MbpMmucd	abnormal embryo turning	J:211773
	abnormal heart morphology	J:211773
	embryonic growth retardation	J:211773
	preweaning lethality, complete penetrance	J:211773
Eloa^tm1Aso/Eloa^tm1Aso involves: 129S/SvEv * C57BL/6	abnormal embryonic neuroepithelium morphology	J:119126
	decreased cell proliferation	J:119126
	decreased embryo size	J:119126
	decreased embryonic neuroepithelium thickness	J:119126
	delayed brain development	J:119126
	delayed hepatic development	J:119126
	early cellular replicative senescence	J:119126
	embryonic growth retardation	J:119126
	embryonic lethality during organogenesis, complete penetrance	J:119126
	heart hypoplasia	J:119126
	increased embryonic tissue cell apoptosis	J:119126
	increased fibroblast apoptosis	J:119126
	pallor	J:119126
	thin ventricular wall	J:119126

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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