Symbol Name ID |
Ifng
interferon gamma MGI:107656 |
Darker colors indicate more annotations |
Human Phenotypes | Wolff-Parkinson-White syndrome |
Cardiac rhabdomyoma |
Pulmonary lymphangiomyomatosis |
Hepatosplenomegaly |
Splenomegaly |
Disease(s) Associated with IFNG | |||||
immunodeficiency 69 | |||||
tuberous sclerosis 2 |
Mouse Phenotypes | liver vascular congestion |
abnormal myocardial fiber morphology |
cardiac muscle atrophy |
cardiac muscle degeneration |
abnormal heart morphology |
enlarged heart |
dilated heart left ventricle |
cardiac interstitial fibrosis |
dilated cardiomyopathy |
decreased cardiac muscle contractility |
abnormal heart echocardiography feature |
corneal vascularization |
myocarditis |
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Availability | Mouse Genotype | |||||||||||||
Ifngtm1Ts/Ifngtm1Ts | ||||||||||||||
Ifngtm1.1(KOMP)Vlcg/Ifng+ | ||||||||||||||
Tg(APCS-Ifng)5Imeg/0 |
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 02/23/2021 MGI 6.16 |
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