PMID: 26115565

Mall MA, Galietta LJ
Targeting ion channels in cystic fibrosis.
J Cyst Fibros. 2015 Sep;14(5):561-70. doi: 10.1016/j.jcf.2015.06.002. Epub 2015 Jun 23., [PubMed]
Sentences
No. Mutations Sentence Comment
595 ABCC7 p.Gly551Asp
X
ABCC7 p.Gly551Asp 26115565:595:54
status: NEW
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Class III includes all those missense mutations (e.g. G551D) that severely reduce the time spent by the CFTR channel in the open state (gating defect). Login to comment
604 ABCC7 p.Gly551Asp
X
ABCC7 p.Gly551Asp 26115565:604:248
status: NEW
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ABCC7 p.Gly551Ser
X
ABCC7 p.Gly551Ser 26115565:604:313
status: NEW
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ABCC7 p.Gly1244Glu
X
ABCC7 p.Gly1244Glu 26115565:604:320
status: NEW
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ABCC7 p.Gly1349Asp
X
ABCC7 p.Gly1349Asp 26115565:604:347
status: NEW
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ABCC7 p.Ser1255Pro
X
ABCC7 p.Ser1255Pro 26115565:604:336
status: NEW
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ABCC7 p.Ser1251Asn
X
ABCC7 p.Ser1251Asn 26115565:604:328
status: NEW
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ABCC7 p.Ser549Arg
X
ABCC7 p.Ser549Arg 26115565:604:306
status: NEW
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ABCC7 p.Ser549Asn
X
ABCC7 p.Ser549Asn 26115565:604:299
status: NEW
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ABCC7 p.Gly178Arg
X
ABCC7 p.Gly178Arg 26115565:604:292
status: NEW
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When tested in clinical trials, the potentiator ivacaftor (also known as VX-770) showed a marked clinical benefit, with substantial improvement of lung function, reduction of pulmonary exacerbations, and increase in body weight in CF patients with G551D and 8 additional Class III mutations (G178R, S549N, S549R, G551S, G1244E, S1251N, S1255P and G1349D) [32-35]. Login to comment
607 ABCC7 p.Gly542*
X
ABCC7 p.Gly542* 26115565:607:26
status: NEW
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Class I mutations such as G542X can be targeted with so called read-through agents. Login to comment