Efficient detection of thirty-seven new IL2RG mutations in human X-linked severe combined immunodeficiency

X-linked severe combined immunodeficiency (XSCID) is a rare and potentially fatal disease caused by mutations of IL2RG, the gene encoding the interleukin-2 receptor gamma chain, a component of multiple cytokine receptors that are essential for lymphocyte development and function. To date, over 100 d...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 95(2000), 1 Pt 1 vom: 25. Apr., Seite 33-8
1. Verfasser: Niemela, J E (VerfasserIn)
Weitere Verfasser: Puck, J M, Fischer, R E, Fleisher, T A, Hsu, A P
Format: Aufsatz
Sprache:English
Veröffentlicht: 2000
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Receptors, Interleukin-2
LEADER 01000naa a22002652 4500
001 NLM107205084
003 DE-627
005 20231222142531.0
007 tu
008 231222s2000 xx ||||| 00| ||eng c
028 5 2 |a pubmed24n0358.xml 
035 |a (DE-627)NLM107205084 
035 |a (NLM)10794430 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Niemela, J E  |e verfasserin  |4 aut 
245 1 0 |a Efficient detection of thirty-seven new IL2RG mutations in human X-linked severe combined immunodeficiency 
264 1 |c 2000 
336 |a Text  |b txt  |2 rdacontent 
337 |a ohne Hilfsmittel zu benutzen  |b n  |2 rdamedia 
338 |a Band  |b nc  |2 rdacarrier 
500 |a Date Completed 12.05.2000 
500 |a Date Revised 08.04.2022 
500 |a published: Print 
500 |a GENBANK: L19546 
500 |a Citation Status MEDLINE 
520 |a X-linked severe combined immunodeficiency (XSCID) is a rare and potentially fatal disease caused by mutations of IL2RG, the gene encoding the interleukin-2 receptor gamma chain, a component of multiple cytokine receptors that are essential for lymphocyte development and function. To date, over 100 different mutations of IL2RG resulting in XSCID have been published. Using nonradioactive, direct DNA sequencing of a single PCR amplicon containing the whole IL2RG gene, we found IL2RG mutations in 78 previously unpublished unrelated cases of XSCID. We report 37 newly identified mutations of IL2RG, including 23 point mutations, 10 small deletions, 3 instances of the same single nucleotide insertion, 1 large deletion, and 2 complex mutations. More than half of the mutations (22 of 37) were predicted to result in unstable IL2RG mRNA. The remaining 14 mutations disrupted conserved functional motifs common to all cytokine receptor family members; changed protein conformation, charge, or hydrophobicity; or altered the intracellular portion of the protein, which is critical for proper interaction with signal-transducing molecules including Janus family tyrosine kinase 3 
650 4 |a Journal Article 
650 7 |a Receptors, Interleukin-2  |2 NLM 
700 1 |a Puck, J M  |e verfasserin  |4 aut 
700 1 |a Fischer, R E  |e verfasserin  |4 aut 
700 1 |a Fleisher, T A  |e verfasserin  |4 aut 
700 1 |a Hsu, A P  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Clinical immunology (Orlando, Fla.)  |d 1999  |g 95(2000), 1 Pt 1 vom: 25. Apr., Seite 33-8  |w (DE-627)NLM098196855  |x 1521-7035  |7 nnns 
773 1 8 |g volume:95  |g year:2000  |g number:1 Pt 1  |g day:25  |g month:04  |g pages:33-8 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_11 
912 |a GBV_ILN_24 
912 |a GBV_ILN_350 
951 |a AR 
952 |d 95  |j 2000  |e 1 Pt 1  |b 25  |c 04  |h 33-8