Symbol Name ID |
Egln1
egl-9 family hypoxia-inducible factor 1 MGI:1932286 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | muscle phenotype |
abnormal myocardium layer morphology |
increased myocardial fiber size |
myocardial fiber degeneration |
abnormal trabecula carnea morphology |
thin ventricle myocardium compact layer |
dilated cardiomyopathy |
decreased ventricle muscle contractility |
decreased cardiomyocyte apoptosis |
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Availability | Mouse Genotype | |||||||||
Egln1tm1Fong/Egln1tm1Fong | ||||||||||
Egln1tm1Fong/Egln1+ | * | |||||||||
Egln1tm1.1Brei/Egln1tm1.1Brei Myl2tm1(cre)Krc/Myl2+ (conditional) |
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Egln1tm1Kael/Egln1tm1Kael Tg(CAG-cre/Esr1*)5Amc/0 (conditional) |
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Egln1tm1Kael/Egln1tm1Kael Tg(Myh6-cre)2182Mds/0 (conditional) |
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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last database update 04/30/2024 MGI 6.23 |
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