Mechanisms of CFTR activation by S-nitrosoglutathione (normal and CF)

No Pathway Network information available for Mechanisms of CFTR activation by S-nitrosoglutathione (normal and CF)

Pathways in the Mechanisms of CFTR activation by S-nitrosoglutathione (normal and CF) SuperPath

#NameSourceGenes
1Mechanisms of CFTR activation by S-nitrosoglutathione (normal and CF)GeneGo (Thomson Reuters)
2CFTR folding and maturation (norm and CF)GeneGo (Thomson Reuters)

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

Disorders associated with Mechanisms of CFTR activation by S-nitrosoglutathione (normal and CF) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Muscular dystrophy, limb-girdle, autosomal dominant 1EnrichmentDNAJB62.67
2Congenital disorder of glycosylation, type iw, autosomal recessiveEnrichmentSTT3A2.67
3Even-plus syndromeEnrichmentHSPA92.67
4Anemia, sideroblastic, 4EnrichmentHSPA92.67
5Congenital disorder of glycosylation, type irEnrichmentDDOST2.67
6Congenital disorder of glycosylation, type iiccEnrichmentUGGT12.67
7Congenital disorder of glycosylation iwEnrichmentSTT3A2.67
8Aquagenic palmoplantar keratodermaEnrichmentCFTR2.67
9Man1b1-congenital disorder of glycosylationEnrichmentMAN1B12.67
10Pyloric stenosis, infantile hypertrophic, 1EnrichmentNOS12.66
11Ceroid lipofuscinosis, neuronal, 4EnrichmentDNAJC52.66
12AceruloplasminemiaEnrichmentCP2.66
13Glucocorticoid deficiency 5EnrichmentTXNRD22.66
14Spermatogenic failure, y-linked, 2EnrichmentCFTR2.37
15Rafiq syndromeEnrichmentMAN1B12.37
16Congenital disorder of glycosylation, type ixEnrichmentSTT3B2.37
17Fibrolamellar carcinomaEnrichmentDNAJB12.37
18Congenital disorder of glycosylation, type iw, autosomal dominantEnrichmentSTT3A2.37
19Autosomal recessive sideroblastic anemiaEnrichmentHSPA92.37
20Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)EnrichmentRPN12.37
21Hermansky-pudlak syndrome 3EnrichmentCP2.35
22Amed syndrome, digenicEnrichmentADH52.35
23Spastic tetraplegia and axial hypotonia, progressiveEnrichmentSOD12.35
24Nuchal bleb, familialEnrichmentCFTR2.19
25Idiopathic bronchiectasisEnrichmentCFTR2.07
26Idiopathic achalasiaEnrichmentNOS12.05
27Alzheimer disease 2EnrichmentNOS31.96
28Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentSOD11.96
29Pre-eclampsiaEnrichmentNOS31.96
30Familial glucocorticoid deficiencyEnrichmentTXNRD21.96
31Congenital anomalies of kidney and urinary tract 1EnrichmentTRAP11.88
32Motor neuron diseaseEnrichmentSOD11.81
33Bronchiectasis with or without elevated sweat chloride 1EnrichmentCFTR1.72
34Vas deferens, congenital bilateral aplasia ofEnrichmentCFTR1.72
35Amyotrophic lateral sclerosis 1EnrichmentSOD11.66
36Stroke, ischemicEnrichmentNOS31.66
37Neurodegeneration with brain iron accumulationEnrichmentCP1.66
38Hereditary chronic pancreatitisEnrichmentCFTR1.53
39Lynch syndromeEnrichmentCFTR1.50
40Neuronal ceroid lipofuscinosisEnrichmentDNAJC51.49
41Hermansky-pudlak syndromeEnrichmentCP1.49
42Hermansky-pudlak syndrome 1EnrichmentCP1.46
43Pancreatitis, hereditaryEnrichmentCFTR1.45
44Alzheimer disease, familial, 1EnrichmentNOS31.43
45Hypertension, essentialEnrichmentNOS31.43
46Parkinson's diseaseEnrichmentDNAJB61.40
47MalariaEnrichmentNOS21.30
48Parkinson disease, late-onsetEnrichmentDNAJB61.30
49Cystic fibrosisEnrichmentCFTR1.18
50Male infertilityEnrichmentCFTR1.15
51CakutEnrichmentTRAP11.14
52Familial isolated dilated cardiomyopathyEnrichmentTXNRD20.95
53Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentCFTR0.95
54Autosomal recessive non-syndromic intellectual disabilityEnrichmentMAN1B10.93
55Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSOD10.92
56Primary ovarian insufficiencyEnrichmentNOS30.91

Loading...
Loading...
Loading...