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
RS397508567 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
RS397508569 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS397508571 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
RS397508606 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis
RS397508607 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508617 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, CFTR-related disorder
RS397508619 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Bronchiectasis with or without elevated sweat chloride 1
RS397508621 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS397508623 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508634 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS397508651 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508670 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, CFTR-related disorder
RS397508674 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508683 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis, CFTR-related disorder
RS397508692 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508700 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508705 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Bronchiectasis with or without elevated sweat chloride 1
RS397508708 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS397508725 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
RS397508727 Health Risk Conflicting classifications of pathogenicity Congenital bilateral aplasia of vas deferens from CFTR mutation, CFTR-related disorder, Cystic fibrosis
RS397508730 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508748 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508751 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS397508753 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis, Bronchiectasis with or without elevated sweat chloride 1
RS397508754 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508755 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508763 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, Bronchiectasis with or without elevated sweat chloride 1
RS397508766 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, CFTR-related disorder
RS397508769 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508773 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS397508792 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS397508804 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Bronchiectasis with or without elevated sweat chloride 1
RS397508818 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
RS4148725 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Hereditary pancreatitis
RS4727853 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS537934752 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS540577876 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS547248892 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS551227135 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis diagnostic test, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS56093012 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS565971160 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS567934887 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS573016418 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS574740041 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, Cystic fibrosis
RS727504712 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS727504811 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS73717525 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS745414764 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS74551128 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, ivacaftor response - Efficacy, Bronchiectasis with or without elevated sweat chloride 1
RS74571530 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Infertility disorder
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