IL-2R Gamma Polyclonal Antibody, 100ul[BT-AP04492] Transporters Shprintzen-Goldberg syndrome and neonatal progeroid

Shprintzen-Goldberg syndrome and neonatal progeroid syndrome

This gene encodes a protein that is a member of the integrin superfamily

This gene is found in a cluster with other desmoglein family members on chromosome 18

which associates with the promoter region of the glucocorticoid receptor gene (hGR gene)

while the 10

IL-2R Gamma Polyclonal Antibody, 100ul[BT-AP04492] Transporters Shprintzen-Goldberg syndrome and neonatal progeroidCytokine receptor common subunit gamma encoded by IL2RG is an important signaling component of many interleukin receptors, including those of interleukin 2, 4, 7 and 21, and is thus referred to as the common gamma chain. Mutations in this gene cause X linked severe combined immunodeficiency (XSCID), as well as X linked combined immunodeficiency (XCID), a less severe immunodeficiency disorder.