Symbol Name ID |
Ifng
interferon gamma MGI:107656 |
Darker colors indicate more annotations |
Human Phenotypes | Hypothyroidism |
Precocious puberty |
Disease(s) Associated with IFNG | ||
tuberous sclerosis 2 |
Mouse Phenotypes | abnormal uterine NK cell morphology |
increased uterine NK cell number |
thymus atrophy |
abnormal seminal vesicle morphology |
increased T cell derived lymphoma incidence |
abnormal pancreatic beta cell physiology |
pancreas inflammation |
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Availability | Mouse Genotype | |||||||
Ifngtm1.1Hayg/Ifngtm1.1Hayg | ||||||||
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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