|
Symbol Name ID |
Ifih1
interferon induced with helicase C domain 1 MGI:1918836 |
| Darker colors indicate more annotations |
| Human Phenotypes | Plagiocephaly |
Microcephaly |
Primary microcephaly |
Progressive microcephaly |
Calcification of the aorta |
Flexion contracture |
Multiple joint contractures |
Scoliosis |
Arthritis |
Arthropathy |
Enchondroma |
Cerebellar calcifications |
Cerebral calcification |
Basal ganglia calcification |
Intracerebral periventricular calcifications |
| Disease(s) Associated with IFIH1 | |||||||||||||||
| Aicardi-Goutieres syndrome |
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 04/16/2024 MGI 6.23 |
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