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Symbol Name ID |
Rag1
recombination activating 1 MGI:97848 |
| Darker colors indicate more annotations |
| Human Phenotypes | Erythroderma |
Skin rash |
Alopecia |
Pallor |
Thickened skin |
| Disease(s) Associated with RAG1 | |||||
| Omenn syndrome | |||||
| severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive |
| Mouse Phenotypes | dermatitis |
abnormal coat/hair pigmentation |
mixed cellular infiltration to dermis |
epidermal hyperplasia |
scaly skin |
abnormal skin pigmentation |
thick skin |
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| Availability | Mouse Genotype | |||||||
| Rag1tm1Mom/Rag1tm1Mom | ||||||||
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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