Cholesterol and Sphingolipids transport / Recycling to plasma membrane in lung (normal and CF)

No Pathway Network information available for Cholesterol and Sphingolipids transport / Recycling to plasma membrane in lung (normal and CF)

Pathways in the Cholesterol and Sphingolipids transport / Recycling to plasma membrane in lung (normal and CF) SuperPath

#NameSourceGenes
1Cholesterol and Sphingolipids transport / Recycling to plasma membrane in lung (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 Cholesterol and Sphingolipids transport / Recycling to plasma membrane in lung (normal and CF) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hypoalphalipoproteinemia, primary, 2EnrichmentABCA1, APOA15.25
2Hypoalphalipoproteinemia, primary, 1EnrichmentABCA1, APOA14.95
3Lipodystrophy, congenital generalized, type 3EnrichmentCAV12.85
4Focal segmental glomerulosclerosis 4EnrichmentAPOL12.85
5Pulmonary hypertension, primary, 3EnrichmentCAV12.85
6Tubulointerstitial kidney disease, autosomal dominant 6EnrichmentAPOA42.85
7Lipodystrophy, familial partial, type 7EnrichmentCAV12.85
8Leukoencephalopathy with dystonia and motor neuropathyEnrichmentSCP22.85
9Aquagenic palmoplantar keratodermaEnrichmentCFTR2.85
10Aapoaii amyloidosisEnrichmentAPOA22.85
11HypoalphalipoproteinemiaEnrichmentABCA12.85
12Tangier diseaseEnrichmentABCA12.55
13Spermatogenic failure, y-linked, 2EnrichmentCFTR2.55
14Alzheimer disease 9EnrichmentABCA72.55
15GlomerulonephritisEnrichmentAPOL12.55
16Hypoalphalipoproteinemia, primary, 2, intermediateEnrichmentAPOA12.55
17Amyloidosis, hereditary systemic 3EnrichmentAPOA12.55
18SchizophreniaEnrichmentAPOL2, APOL42.52
19Nuchal bleb, familialEnrichmentCFTR2.38
20Spastic paraplegia 50, autosomal recessiveEnrichmentAPOA12.38
21Idiopathic bronchiectasisEnrichmentCFTR2.25
22Amyloidosis, hereditary systemic 2EnrichmentAPOA12.16
23Diffuse cutaneous systemic sclerosisEnrichmentCAV12.16
24Limited sclerodermaEnrichmentCAV12.08
25Early-onset autosomal dominant alzheimer diseaseEnrichmentABCA72.01
26Bronchiectasis with or without elevated sweat chloride 1EnrichmentCFTR1.90
27Vas deferens, congenital bilateral aplasia ofEnrichmentCFTR1.90
28Coronary heart disease 5EnrichmentABCA11.90
29Heritable pulmonary arterial hypertensionEnrichmentCAV11.82
30Hypercholesterolemia, familial, 1EnrichmentAPOA21.74
31Hereditary chronic pancreatitisEnrichmentCFTR1.71
32Familial hypercholesterolemiaEnrichmentAPOA21.68
33Lynch syndromeEnrichmentCFTR1.68
34Isolated congenital microcephalyEnrichmentRAB11A1.65
35Pancreatitis, hereditaryEnrichmentCFTR1.63
36Focal segmental glomerulosclerosisEnrichmentAPOL11.56
37Cystic fibrosisEnrichmentCFTR1.36
38Male infertilityEnrichmentCFTR1.33
39Genetic steroid-resistant nephrotic syndromeEnrichmentAPOL11.33
40Autosomal dominant non-syndromic intellectual disabilityEnrichmentRAB11A1.17
41Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentCFTR1.12
42Breast cancerEnrichmentABCA11.00

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