PMID: 21131649

Puechal X, Bienvenu T, Genin E, Berthelot JM, Sibilia J, Gaudin P, Marcelli C, Lasbleiz S, Michou L, Cornelis F, Kahan A, Dusser DJ
Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis.
Ann Rheum Dis. 2011 Apr;70(4):653-9. Epub 2010 Dec 3., [PubMed]
Sentences
No. Mutations Sentence Comment
61 ABCC7 p.Arg75Gln
X
ABCC7 p.Arg75Gln 21131649:61:232
status: NEW
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ABCC7 p.Arg75Gln
X
ABCC7 p.Arg75Gln 21131649:61:532
status: NEW
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ABCC7 p.Arg75Gln
X
ABCC7 p.Arg75Gln 21131649:61:654
status: NEW
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ABCC7 p.Ser1235Arg
X
ABCC7 p.Ser1235Arg 21131649:61:706
status: NEW
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ABCC7 p.Phe1052Val
X
ABCC7 p.Phe1052Val 21131649:61:389
status: NEW
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ABCC7 p.Ser977Phe
X
ABCC7 p.Ser977Phe 21131649:61:496
status: NEW
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ABCC7 p.Gly424Ser
X
ABCC7 p.Gly424Ser 21131649:61:216
status: NEW
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Table 1 CFTR genotypes of the family population Family (N=24) CFTR genotypes RA-DB (N=30) DB only (N=8) RA only (N=24) Unaffected individuals (N=76) 1 c.1584G>A (p.Glu528Glu ):- 1 -:- 1 2 p.Gly424Ser+p.Gly576Ala 1 p.Gly424Ser:- 1 p.Arg75Gln:- 1 1 3 p.Phe508del (c.1521_1523delCTT)+5T (c.1210-12[5]) 1 p.Phe508del:- 1 2 2 5T (c.1210-12[5]):- 1 -:- 1 4 5T (c.1210-12[5]):- 1 1 2 -:- 1 2 1 p.Phe1052Val:- 1 5 5T (c.1210-12[5]):- 1 6 p.Phe508del+p.Ser977Phe-5T (c.1210-12[5]) 1 1 1 p.Phe508del:- 1 p.Ser977Phe-5T (c.1210-12[5]):- 3 7 p.Arg75Gln:- 2 8 p.Asp1152His+c.262_263delTT 1 1 p.Asp1152His+c.-7G>C 1 c.262_263delTT:- 1 9 c.1584G>A (p.Glu528Glu ):- 1 p.Arg75Gln:- 1 -:- 1 5 10 10 c.-7G>C:- 1 -:- 1 8 11 p.Ser1235Arg:- 1 1 -:- 1 12 p.Ala923Ala:- 1 1 13 c.1584G>A (p.Glu528Glu ):- 1 1 1 p.Ala923Ala:- 1 14 c.1584G>A (p.Glu528Glu ):- 2 1 -:- 1 3 15 -:- 1 1 5 16 -:- 1 1 7 17 -:- 2 1 3 18 -:- 1 1 19 -:- 1 1 2 20 -:- 1 1 21 -:- 1 1 3 22 -:- 1 1 6 23 -:- 1 1 3 24 -:- 1 1 7 Total no. Login to comment
82 ABCC7 p.Asp1152His
X
ABCC7 p.Asp1152His 21131649:82:27
status: NEW
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Both sisters carried the p.Asp1152His mutation, which has previously been identified as a Group A or Group B mutation, and the Group A c.262 263delTT mutation.13 Thus, 18 of the 30 patients with RA-DB (60%) carried at least one mutant CFTR allele and 3 of these 30 patients (10%) were compound heterozygous (table 1). Login to comment