PMID: 15870824

Stuppia L, Antonucci I, Binni F, Brandi A, Grifone N, Colosimo A, De Santo M, Gatta V, Gelli G, Guida V, Majore S, Calabrese G, Palka C, Ravani A, Rinaldi R, Tiboni GM, Ballone E, Venturoli A, Ferlini A, Torrente I, Grammatico P, Calzolari E, Dallapiccola B
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs.
Eur J Hum Genet. 2005 Aug;13(8):959-64., [PubMed]
Sentences
No. Mutations Sentence Comment
64 ABCC7 p.Gly551Asp
X
ABCC7 p.Gly551Asp 15870824:64:144
status: NEW
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ABCC7 p.Arg117His
X
ABCC7 p.Arg117His 15870824:64:299
status: NEW
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ABCC7 p.Ala455Glu
X
ABCC7 p.Ala455Glu 15870824:64:461
status: NEW
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ABCC7 p.Trp1282*
X
ABCC7 p.Trp1282* 15870824:64:184
status: NEW
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ABCC7 p.Arg553*
X
ABCC7 p.Arg553* 15870824:64:154
status: NEW
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ABCC7 p.Arg334Trp
X
ABCC7 p.Arg334Trp 15870824:64:332
status: NEW
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ABCC7 p.Arg347Pro
X
ABCC7 p.Arg347Pro 15870824:64:322
status: NEW
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ABCC7 p.Asn1303Lys
X
ABCC7 p.Asn1303Lys 15870824:64:220
status: NEW
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ABCC7 p.Gly542*
X
ABCC7 p.Gly542* 15870824:64:96
status: NEW
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ABCC7 p.Arg1162*
X
ABCC7 p.Arg1162* 15870824:64:420
status: NEW
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ABCC7 p.Ser1251Asn
X
ABCC7 p.Ser1251Asn 15870824:64:209
status: NEW
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ABCC7 p.Gly85Glu
X
ABCC7 p.Gly85Glu 15870824:64:256
status: NEW
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ABCC7 p.Arg560Thr
X
ABCC7 p.Arg560Thr 15870824:64:164
status: NEW
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ABCC7 p.Gln552*
X
ABCC7 p.Gln552* 15870824:64:174
status: NEW
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ABCC7 p.Glu60*
X
ABCC7 p.Glu60* 15870824:64:277
status: NEW
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of detected carriers Prevalence among detected CFTR mutations DF508 40 (3.34%) 65.58% DI507 0 0 G542X 6 (0.50%) 9.84% 1717-1G-A 1 (0.08%) 1.64% G551D 0 0 R553X 0 0 R560T 0 0 Q552X 0 0 W1282X 7 (0.58 %) 11.48% S1251N 0 0 N1303K 3 (0.20%) 4.91% 394delTT 0 0 G85E 3 (0.25%) 4.91% E60X 0 0 621+1G-T 0 0 R117H 0 0 1078delT 0 0 R347P 0 0 R334W 0 0 2143delT 0 0 2183AA-G 0 0 2184delA 0 0 711+5G-A 0 0 2789+5G-A 1 (0.08%) 1.64% R1162X 0 0 3659del5 0 0 3849+10kbC-T 0 0 A455E 0 0 5T 78 (6.52%) Table 2 Distribution of CFTR mutations and 5T allele according to phenotype for the 1195 individuals Phenotype CF/WT 5T/WT CF/5T WT/WT Infertile males (non-CBAVD), N ¼ 304 20 (6.58%) 30 (9.87%) 0 254 (83.55%) Infertile males (CBAVD), N ¼ 16 0 10 (62.50%) 6 (37.50 %) 0 Infertile females, N ¼ 93 5 (5.37%) 7 (7.53%) 0 81 (87.10%) Unexplained infertility, N ¼ 782 30 (3.84%) 31 (3.96%) 0 721 (92.20%) Total ¼ 1195 55 (4.60%) 78 (5.50%) 6 (0.50%) 1056 (88.40%) CFTR alteration was detected, including a mutation in three cases and the 5T polymorphism in the remaining six. Login to comment
85 ABCC7 p.Trp1282*
X
ABCC7 p.Trp1282* 15870824:85:240
status: NEW
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ABCC7 p.Gly542*
X
ABCC7 p.Gly542* 15870824:85:275
status: NEW
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ABCC7 p.Gly542*
X
ABCC7 p.Gly542* 15870824:85:341
status: NEW
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Altogether, we detected a CFTR mutation or the 5T allele in 139 (11.6%) single partners of our couples, in agreement with the figure Table 3 Couples with both partners carriers of a CFTR mutation or a 5T allele First partner Second partner W1282X/5T 5T/wt 1717-1G4A/5T 5T/wt G542X/5T 5T/wt DF508/wt 5T/wt DF508/wt 5T/wt DF508/wt 5T/wt 5T/wt G542X/wt 5T/wt 1717-1G4A/wt 5T/wt 5T/wt Table 4 Distribution of the different TG-M470V-5T associations in relation to the phenotype for the 67 investigated males Phenotype TG12-V470 TG12-M470 TG11-V470 TG11-M470 Total Fertile men 7 0 9 8 24 CBAVD 11 0 0 2 13 Azoospermia 4 0 0 2 6 Oligozoospermia 8 2 7 7 24 Total 30 2 16 19 67 expected in the general Caucasian population. Login to comment