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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 |
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| 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 04/23/2024 MGI 6.23 |
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