Egln2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Egln2
egl-9 family hypoxia-inducible factor 2
MGI:1932287

7 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Egln2^tm1Fong/Egln2^tm1Fong involves: 129S6/SvEvTac * C57BL/6	normal cardiovascular system phenotype	J:133568
	normal hematopoietic system phenotype	J:132720
Egln2^tm1Fong/Egln2^tm1Fong involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N	normal cardiovascular system phenotype	J:114669
	normal embryo phenotype	J:114669
Egln2^tm1Pec/Egln2^tm1Pec involves: 129S/SvEv * Swiss	abnormal mitochondrial physiology	J:132630
	abnormal muscle physiology	J:132630
	decreased oxygen consumption	J:132630
	skeletal muscle necrosis	J:132630

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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