Symbol Name ID |
Ifng
interferon gamma MGI:107656 |
Darker colors indicate more annotations |
Human Phenotypes | Epistaxis |
Gingival bleeding |
Oral cavity bleeding |
Retinal arteritis |
Trismus |
Sinusitis |
Microcephaly |
Adenoma sebaceum |
Gingival fibromatosis |
Gingivitis |
Oral ulcer |
Stomatitis |
Glossitis |
Impaired mastication |
Recurrent pharyngitis |
Conjunctival telangiectasia |
Retinal hamartoma |
Disease(s) Associated with IFNG | |||||||||||||||||
ataxia telangiectasia | |||||||||||||||||
chronic granulomatous disease | |||||||||||||||||
factor VIII deficiency | |||||||||||||||||
graft-versus-host disease | |||||||||||||||||
temporal arteritis | |||||||||||||||||
tuberous sclerosis 2 |
Mouse Phenotypes | alveolar process atrophy |
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Availability | Mouse Genotype | |
Ifngtm1Ts/Ifngtm1Ts |
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 04/23/2024 MGI 6.23 |
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