PMID: 18243066

Ratbi I, Genin E, Legendre M, Le Floch A, Costa C, Cherkaoui-Deqqaqi S, Goossens M, Sefiani A, Girodon E
Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco.
J Cyst Fibros. 2008 Sep;7(5):440-3. Epub 2008 Feb 1., [PubMed]
Sentences
No. Mutations Sentence Comment
27 ABCC7 p.Gly551Asp
X
ABCC7 p.Gly551Asp 18243066:27:164
status: NEW
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ABCC7 p.Arg117His
X
ABCC7 p.Arg117His 18243066:27:56
status: NEW
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ABCC7 p.Ala455Glu
X
ABCC7 p.Ala455Glu 18243066:27:114
status: NEW
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ABCC7 p.Trp1282*
X
ABCC7 p.Trp1282* 18243066:27:295
status: NEW
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ABCC7 p.Arg553*
X
ABCC7 p.Arg553* 18243066:27:171
status: NEW
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ABCC7 p.Arg334Trp
X
ABCC7 p.Arg334Trp 18243066:27:83
status: NEW
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ABCC7 p.Arg347Pro
X
ABCC7 p.Arg347Pro 18243066:27:90
status: NEW
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ABCC7 p.Arg347His
X
ABCC7 p.Arg347His 18243066:27:97
status: NEW
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ABCC7 p.Asn1303Lys
X
ABCC7 p.Asn1303Lys 18243066:27:323
status: NEW
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ABCC7 p.Gly542*
X
ABCC7 p.Gly542* 18243066:27:157
status: NEW
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ABCC7 p.Arg1162*
X
ABCC7 p.Arg1162* 18243066:27:260
status: NEW
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ABCC7 p.Val520Phe
X
ABCC7 p.Val520Phe 18243066:27:139
status: NEW
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ABCC7 p.Gly85Glu
X
ABCC7 p.Gly85Glu 18243066:27:40
status: NEW
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ABCC7 p.Ser549Asn
X
ABCC7 p.Ser549Asn 18243066:27:197
status: NEW
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ABCC7 p.Arg560Thr
X
ABCC7 p.Arg560Thr 18243066:27:178
status: NEW
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We screened for 32 CFTR gene mutations (G85E, 394delTT, R117H, 621+1GNT, 711+1GNT, R334W, R347P, R347H, 1078delT, A455E, I507del, F508del, V520F, 1717-1GNA, G542X, G551D, R553X, R560T, S549R(TNG), S549N, 1898+1GNA, 2183AANG, 2184delA, 2789+5GNA, 3120 + 1G NA, R1162X, 3659delC, 3849 + 10kbC NT, W1282X, 3905insT, 3876delA, N1303K) and the (T)5 splicing variant of intron 8, using a commercial kit (CF v3 Genotyping Assay, Abbott, Rungis, France). Login to comment
64 ABCC7 p.Trp1282*
X
ABCC7 p.Trp1282* 18243066:64:109
status: NEW
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ABCC7 p.Asn1303Lys
X
ABCC7 p.Asn1303Lys 18243066:64:117
status: NEW
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ABCC7 p.Gly542*
X
ABCC7 p.Gly542* 18243066:64:125
status: NEW
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ABCC7 p.Arg1162*
X
ABCC7 p.Arg1162* 18243066:64:135
status: NEW
view ABCC7 p.Arg1162* details
Beside F508del, other frequent mutations were found among North African populations, in particular 711+1GNT, W1282X, N1303K, G542X and R1162X [1,4,6]. Login to comment