|
Symbol Name ID |
Ifng
interferon gamma MGI:107656 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retinal arteritis |
Conjunctival telangiectasia |
Retinal hamartoma |
Optic atrophy |
Achromatic retinal patches |
Proptosis |
Strabismus |
Nystagmus |
Ophthalmoparesis |
Diplopia |
Amaurosis fugax |
Visual impairment |
Blindness |
Visual field defect |
Visual loss |
Inflammatory abnormality of the eye |
Decreased lacrimation |
Ptosis |
| Disease(s) Associated with IFNG | ||||||||||||||||||
| ataxia telangiectasia | ||||||||||||||||||
| chronic granulomatous disease | ||||||||||||||||||
| graft-versus-host disease | ||||||||||||||||||
| Graves' disease | ||||||||||||||||||
| temporal arteritis | ||||||||||||||||||
| tuberous sclerosis 2 |
| Mouse Phenotypes | cornea vascularization |
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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 05/14/2024 MGI 6.23 |
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