Symbol Name ID |
Ifng
interferon gamma MGI:107656 |
Darker colors indicate more annotations |
Human Phenotypes | Muscle hemorrhage |
Dupuytren contracture |
Cardiac rhabdomyoma |
Myositis |
Muscle weakness |
Skeletal muscle atrophy |
Calcinosis |
Intramuscular hematoma |
Disease(s) Associated with IFNG | ||||||||
factor VIII deficiency | ||||||||
graft-versus-host disease | ||||||||
Graves' disease | ||||||||
systemic scleroderma | ||||||||
temporal arteritis | ||||||||
tuberous sclerosis 2 |
Mouse Phenotypes | abnormal myocardial fiber morphology |
cardiac muscle atrophy |
cardiac muscle degeneration |
dilated cardiomyopathy |
decreased cardiac muscle contractility |
skeletal muscle fibrosis |
impaired skeletal muscle regeneration |
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Availability | Mouse Genotype | |||||||
Ifngtm1Ts/Ifngtm1Ts | ||||||||
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 05/14/2024 MGI 6.23 |
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