|
Symbol Name ID |
Ifng
interferon gamma MGI:107656 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cerebral calcification |
Astrocytoma |
Subependymal giant-cell astrocytoma |
Ependymoma |
Optic nerve glioma |
Cortical tubers |
Hemimegalencephaly |
Subependymal nodules |
Intellectual disability |
Autism |
Attention deficit hyperactivity disorder |
Specific learning disability |
Seizure |
Epileptic spasm |
Infantile spasms |
| Disease(s) Associated with IFNG | |||||||||||||||
| tuberous sclerosis 2 |
| Mouse Phenotypes | CNS inflammation |
increased medulloblastoma incidence |
abnormal cerebellum development |
abnormal cerebellum external granule cell layer morphology |
abnormal cerebellum morphology |
enlarged cerebellum |
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| Availability | Mouse Genotype | ||||||
| Tg(GFAP-tTA)67Pop/0 Tg(tetO-Ifng)184Pop/0 |
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| Tg(GFAP-tTA)78Pop/0 Tg(tetO-Ifng)184Pop/0 |
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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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