Recombinase Activating Gene 1 Deficiency is related to severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative and omenn syndrome. An important gene associated with Recombinase Activating Gene 1 Deficiency is RAG1 (Recombination Activating 1), and among its related pathways/superpathways is Interleukin-7 signaling.