Human Disease and Mouse Model Detail
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Human Disease
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Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation
OMIM ID: 611291
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Synonyms
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Scid, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive, with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Nhej1
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NHEJ1*
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1:1 Homology
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Analysis Tools