NO-dependent CFTR activation (normal and CF)

No Pathway Network information available for NO-dependent CFTR activation (normal and CF)

Pathways in the NO-dependent CFTR activation (normal and CF) SuperPath

#NameSourceGenes
1NO-dependent CFTR activation (normal and CF)GeneGo (Thomson Reuters)

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with NO-dependent CFTR activation (normal and CF) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Idiopathic bronchiectasisEnrichmentCFTR, SCNN1A, SCNN1B, SCNN1G10.37
2Liddle syndrome 1EnrichmentSCNN1A, SCNN1B, SCNN1G9.16
3Pseudohypoaldosteronism, type ib1, autosomal recessiveEnrichmentSCNN1A, SCNN1B, SCNN1G9.16
4Bronchiectasis with or without elevated sweat chloride 1EnrichmentCFTR, SCNN1B4.52
5Pyloric stenosis, infantile hypertrophic, 1EnrichmentNOS13.02
6Bronchiectasis with or without elevated sweat chloride 2EnrichmentSCNN1A3.02
7Bronchiectasis with or without elevated sweat chloride 3EnrichmentSCNN1G3.02
8Spondylometaphyseal dysplasia, pagnamenta typeEnrichmentPRKG23.02
9Pseudohypoaldosteronism, type ib2, autosomal recessiveEnrichmentSCNN1B3.02
10Liddle syndrome 2EnrichmentSCNN1G3.02
11Liddle syndrome 3EnrichmentSCNN1A3.02
12Pseudohypoaldosteronism, type ib3, autosomal recessiveEnrichmentSCNN1G3.02
13Aquagenic palmoplantar keratodermaEnrichmentCFTR3.02
14ArgininemiaEnrichmentARG12.72
15Spermatogenic failure, y-linked, 2EnrichmentCFTR2.72
16Polymyoclonus, infantileEnrichmentSCNN1B2.72
17Acromesomelic dysplasia 4EnrichmentPRKG22.72
18PseudohypoaldosteronismEnrichmentSCNN1A2.72
19Nuchal bleb, familialEnrichmentCFTR2.54
20Idiopathic achalasiaEnrichmentNOS12.42
21Alzheimer disease 2EnrichmentNOS32.32
22Pre-eclampsiaEnrichmentNOS32.32
23Vas deferens, congenital bilateral aplasia ofEnrichmentCFTR2.07
24Stroke, ischemicEnrichmentNOS32.02
25Hereditary chronic pancreatitisEnrichmentCFTR1.87
26Lynch syndromeEnrichmentCFTR1.85
27Alzheimer disease, familial, 1EnrichmentNOS31.79
28Hypertension, essentialEnrichmentNOS31.79
29Pancreatitis, hereditaryEnrichmentCFTR1.79
30MalariaEnrichmentNOS21.66
31Brugada syndromeEnrichmentSCNN1A1.61
32Cystic fibrosisEnrichmentCFTR1.52
33Male infertilityEnrichmentCFTR1.49
34Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentCFTR1.28
35Primary ovarian insufficiencyEnrichmentNOS31.26

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