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
RS199672530 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS199791061 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
RS200321110 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Hereditary pancreatitis
RS200520623 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS200901072 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS201295415 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Bronchiectasis with or without elevated sweat chloride 1, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS201381687 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS201386642 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, CFTR-related disorder
RS201410793 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS201434579 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, Hereditary pancreatitis
RS201591901 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS201864483 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Breast neoplasm, CFTR-related disorder
RS201880593 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, CFTR-related disorder
RS201888075 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, CFTR-related disorder
RS201958172 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Infertility disorder, Bronchiectasis with or without elevated sweat chloride 1
RS202074317 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2115902212 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2115902247 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS2115902456 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2116030305 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis
RS2116226142 Health Risk Conflicting classifications of pathogenicity Bronchiectasis with or without elevated sweat chloride 1, Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis
RS2116670348 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS2116684480 Health Risk Conflicting classifications of pathogenicity Hereditary pancreatitis, Hereditary pancreatitis
RS2484928867 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2485009084 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS2485009619 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2485014993 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2485017153 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2485065411 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS2485065974 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, CFTR-related disorder
RS2485146738 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS2896226 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS34911792 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Obstructive azoospermia
RS35516286 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS368393738 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
RS368516826 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS368543375 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS369294289 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, Cystic fibrosis
RS369521395 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Bronchiectasis with or without elevated sweat chloride 1
RS370586917 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS371315549 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Hereditary pancreatitis
RS371315682 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Congenital bilateral aplasia of vas deferens from CFTR mutation, CFTR-related disorder
RS371475225 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS372610364 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Cystic fibrosis
RS373016758 Health Risk Conflicting classifications of pathogenicity CFTR-related disorder, CFTR-related disorder
RS373885282 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, Hereditary pancreatitis, Congenital bilateral aplasia of vas deferens from CFTR mutation
RS374013084 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS374453187 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
RS375552160 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
RS375845215 Health Risk Conflicting classifications of pathogenicity Cystic fibrosis, CFTR-related disorder, Cystic fibrosis
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