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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Egln2tm1Fong/Egln2tm1Fong
involves: 129S6/SvEvTac * C57BL/6 		normal cardiovascular system phenotype J:133568
normal hematopoietic system phenotype J:132720
Egln2tm1Fong/Egln2tm1Fong
involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N 		normal cardiovascular system phenotype J:114669
normal embryo phenotype J:114669
Egln2tm1Pec/Egln2tm1Pec
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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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory