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Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis.

Authors: Clark, PA  Lester, T  Genet, S  Jones, AM  Hendriks, R  Levinsky, RJ  Kinnon, C 
Citation: Clark PA, etal., Hum Genet. 1995 Oct;96(4):427-32.
Pubmed: (View Article at PubMed) PMID:7557965

Mutations in the common gamma chain (gamma c or IL2RG) of the interleukin-2, -4, -7, -9 and -15 receptors have been found to cause X-linked severe combined immunodeficiency (SCIDX1). We report here on the mutations identified in a further ten families. Two of the mutations identified have occurred twice in unrelated families, indicating two possible mutational hotspots. Seven of the mutations, which were identified by single-strand conformational polymorphism (SSCP) analysis, are point mutations, and the eighth is a small deletion. We also report on the first use of assays based on these mutations within IL2RG for unambiguous carrier determination. The consequences for the gamma c proteins produced as a result of these mutations are discussed.

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CRRD Object Information
CRRD ID: 1600009
Created: 2007-02-23
Species: All species
Last Modified: 2007-02-23
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.