CFTR Chromosome 7

CF transmembrane conductance regulator
1397 variants 18 Drug Response 1379 Health Risk

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What This Gene Does
This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome. [provided by RefSeq, Aug 2017]
Gene Info
Gene Group
"Chloride channels, ATP-gated CFTR|ATP binding cassette subfamily C"
Locus Type
gene with protein product
Location
7q31.2
Ensembl
ENSG00000001626
Associated Conditions (64)
Cystic fibrosis
ivacaftor response - Efficacy
Hereditary pancreatitis
CFTR-related disorder
Bronchiectasis with or without elevated sweat chloride 1
Congenital bilateral aplasia of vas deferens from CFTR mutation
Congenital bilateral absence of vas deferens
Male infertility
Obstructive azoospermia
Melanoma-pancreatic cancer syndrome
Cystic fibrosis diagnostic test
Fetal cystic hygroma
Respiratory ciliopathies including non-CF bronchiectasis
Nephronophthisis 14
Uterine carcinosarcoma
See cases
Spermatogenic failure
Y-linked
2
Lung disease
+44 more conditions
Key Variants
RS115545701
drug response
Cystic fibrosis, ivacaftor response - Efficacy, Hereditary pancreatitis
Drug Response
RS11971167
drug response
Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis, Hereditary pancreatitis
Drug Response
RS141033578
drug response
Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
Drug Response
RS150212784
drug response
Cystic fibrosis, ivacaftor response - Efficacy, Hereditary pancreatitis
Drug Response
RS186045772
drug response
Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
Drug Response
RS202179988
drug response
Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis, ivacaftor response - Efficacy
Drug Response
RS397508288
drug response
Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, CFTR-related disorder
Drug Response
RS397508513
drug response
Cystic fibrosis, ivacaftor response - Efficacy, Cystic fibrosis
Drug Response
RS75541969
drug response
Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
Drug Response
RS121908753
Pathogenic; drug response
Cystic fibrosis, ivacaftor response - Efficacy, Bronchiectasis with or without elevated sweat chloride 1
Drug Response
RS121908757
Pathogenic; drug response
Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
Drug Response
RS121909013
Pathogenic; drug response
Cystic fibrosis, ivacaftor response - Efficacy, CFTR-related disorder
Drug Response
All Variants (1397)
RSID Category Clinical Significance Conditions
RS115545701 Drug Response drug response Cystic fibrosis, ivacaftor response - Efficacy, Hereditary pancreatitis
RS11971167 Drug Response drug response Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis, Hereditary pancreatitis
RS141033578 Drug Response drug response Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS150212784 Drug Response drug response Cystic fibrosis, ivacaftor response - Efficacy, Hereditary pancreatitis
RS186045772 Drug Response drug response Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS202179988 Drug Response drug response Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis, ivacaftor response - Efficacy
RS397508288 Drug Response drug response Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, CFTR-related disorder
RS397508513 Drug Response drug response Cystic fibrosis, ivacaftor response - Efficacy, Cystic fibrosis
RS75541969 Drug Response drug response Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS121908753 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, Bronchiectasis with or without elevated sweat chloride 1
RS121908757 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS121909013 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, CFTR-related disorder
RS121909041 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, Hereditary pancreatitis
RS193922525 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, CFTR-related disorder
RS267606723 Drug Response Pathogenic; drug response Cystic fibrosis, Cystic fibrosis, ivacaftor response - Efficacy
RS368505753 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS397508442 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS74503330 Drug Response Pathogenic; drug response Cystic fibrosis, ivacaftor response - Efficacy, CFTR-related disorder
RS1039221071 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS1048183757 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1057516216 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Fetal cystic hygroma, CFTR-related disorder
RS113857788 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS1160986735 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1162745955 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1163866901 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS117400534 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS1177201180 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Hereditary pancreatitis
RS1185896776 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, CFTR-related disorder
RS1189108407 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1195721615 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS121908759 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS121908790 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS121908805 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Obstructive azoospermia
RS121909040 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS121909046 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Nephronophthisis 14
RS121909047 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS1234696445 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1322987429 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, CFTR-related disorder
RS1336644939 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1338239866 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1367201083 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS1375786834 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Bronchiectasis with or without elevated sweat chloride 1, Cystic fibrosis
RS137975784 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS138025486 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, CFTR-related disorder
RS138634146 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS138642693 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, CFTR-related disorder
RS139322772 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, CFTR-related disorder
RS139379077 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Hereditary pancreatitis
RS139688774 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, Cystic fibrosis
RS139729994 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
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