Symbol Name ID |
Rnaseh2c
ribonuclease H2, subunit C MGI:1915459 |
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 RNASEH2C | |||||||||||||||
Aicardi-Goutieres syndrome |
Mouse Phenotypes | abnormal pelvic girdle bone morphology |
|
Availability | Mouse Genotype | |
Rnaseh2ctm1(KOMP)Wtsi/Rnaseh2c+ |
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 08/02/2024 MGI 6.24 |
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