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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Egln2
egl-9 family hypoxia-inducible factor 2
MGI:1932287
13 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Egln1tm2Fong/Egln1tm2Fong
Egln2tm2Fong/Egln2tm2Fong
Egln3tm2Fong/Egln3tm2Fong
Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
involves: 129S6/SvEvTac * C57BL/6NCr * CD-1 		increased hematocrit J:186085
Egln2tm1Fong/Egln2tm1Fong
Egln3tm1Fong/Egln3tm1Fong
involves: 129S6/SvEvTac * C57BL/6 		abnormal autopod morphology J:132720
abnormal definitive hematopoiesis J:132720
abnormal snout morphology J:132720
abnormal splenic cell ratio J:132720
decreased litter size J:132720
enlarged liver J:132720
enlarged spleen J:132720
extramedullary hematopoiesis J:132720
increased hematocrit J:132720
increased hemoglobin content J:132720
polycythemia J:132720
reddish skin J:132720
Egln2tm1Pec/Egln2tm1Pec
Epas1tm1Pec/Epas1+
involves: 129S/SvEv * Swiss 		normal muscle phenotype J:132630
Egln2tm1Pec/Egln2tm1Pec
Hif1atm1Pec/Hif1a+
involves: 129S/SvEv * Swiss 		normal muscle phenotype 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
12/17/2024
MGI 6.24 		The Jackson Laboratory