Table 3.

Fourteen Different Insertions and Deletions in SCID Patients With IL2RG Defects

IL2RG ExoncDNA MutationNucleotide Sequence ContextCodonProtein AlterationmRNA Detected3-150γc on Cell Surface3-151Reference3-152
67delTG Follows 10-bp inverted repeat L18 Frame shift, signal NA − 
    Peptide 
140delG Follows 9-bp polypyrimidine L42 Frame shift Trace − 
373insA Within 7-bp poly-A K120 Frame shift − − 
 398delT, 406delAGCT Complex deletion F128 Frame shift − − 
 447delA Follows 2-bp repeat M145 Frame shift − − 
534delTGGAAC Imperfect double inverted repeat; deletion motif WN174-5 Delete 2 amino acids − 
 542delCA Same as above N176 Frame shift − − 
707delTG Slippage in 2-bp repeat C231 Frame shift − − 
 725duplication9bp Flanking inverted repeat QHW235-7 Repeat 3 amino acids 
833delT Inverted repeat; del. motif I273 Frame shift NA NA 
 835insAT Same as above I274 Frame shift 
 851delGT Slippage in 2-bp repeat V279 Frame shift 
922insTA Del. motif Y303 Frame shift NA NA 
 924delC Same as above H304 Frame shift 
IL2RG ExoncDNA MutationNucleotide Sequence ContextCodonProtein AlterationmRNA Detected3-150γc on Cell Surface3-151Reference3-152
67delTG Follows 10-bp inverted repeat L18 Frame shift, signal NA − 
    Peptide 
140delG Follows 9-bp polypyrimidine L42 Frame shift Trace − 
373insA Within 7-bp poly-A K120 Frame shift − − 
 398delT, 406delAGCT Complex deletion F128 Frame shift − − 
 447delA Follows 2-bp repeat M145 Frame shift − − 
534delTGGAAC Imperfect double inverted repeat; deletion motif WN174-5 Delete 2 amino acids − 
 542delCA Same as above N176 Frame shift − − 
707delTG Slippage in 2-bp repeat C231 Frame shift − − 
 725duplication9bp Flanking inverted repeat QHW235-7 Repeat 3 amino acids 
833delT Inverted repeat; del. motif I273 Frame shift NA NA 
 835insAT Same as above I274 Frame shift 
 851delGT Slippage in 2-bp repeat V279 Frame shift 
922insTA Del. motif Y303 Frame shift NA NA 
 924delC Same as above H304 Frame shift 

Abbreviation: NA, not available.

F3-150

By Northern blot.

F3-151

By cell surface IF staining with TUGh4 antibody.

F3-152

Previous publications, including those by our group, clinical reports, and identical mutations found by others.

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