Egln2 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 10/29/2024 MGI 6.24