|
Symbol Name ID |
Ifna1
interferon alpha 1 MGI:107668 |
| Darker colors indicate more annotations |
| Human Phenotypes | Facial palsy |
Increased CSF protein concentration |
Abnormal cerebrospinal fluid morphology |
Peripheral neuropathy |
| Disease(s) Associated with IFNA17 | ||||
| sarcoidosis |
| Mouse Phenotypes | seizures |
abnormal brain vasculature morphology |
CNS inflammation |
meningoencephalitis |
abnormal brain ependyma morphology |
abnormal choroid plexus morphology |
abnormal basal ganglion morphology |
abnormal cerebellum morphology |
abnormal cerebellar granule layer morphology |
calcified brain |
astrocytosis |
neurodegeneration |
axon degeneration |
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| Availability | Mouse Genotype | |||||||||||||
| Tg(Gfap-Ifna1)12Ilc/0 | ||||||||||||||
| Tg(Gfap-Ifna1)39Ilc/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 05/07/2024 MGI 6.23 |
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