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Symbol Name ID |
Dclre1c
DNA cross-link repair 1C MGI:2441769 |
| Darker colors indicate more annotations |
| Human Phenotypes | Purpura |
Vasculitis |
Lymph node hypoplasia |
Lymphadenopathy |
Generalized lymphadenopathy |
Aplasia of the thymus |
Hypoplasia of the thymus |
Splenomegaly |
Absent tonsils |
| Disease(s) Associated with DCLRE1C | |||||||||
| common variable immunodeficiency | |||||||||
| Omenn syndrome | |||||||||
| severe combined immunodeficiency with sensitivity to ionizing radiation |
| Mouse Phenotypes | decreased systemic arterial systolic blood pressure |
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| Availability | Mouse Genotype | |
| Dclre1cm3Btlr/Dclre1cm3Btlr | ||
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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