Nephrin/Neph1 signaling in the kidney podocyte

No Pathway Network information available for Nephrin/Neph1 signaling in the kidney podocyte

Pathways in the Nephrin/Neph1 signaling in the kidney podocyte SuperPath

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

Disorders associated with Nephrin/Neph1 signaling in the kidney podocyte SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Genetic steroid-resistant nephrotic syndromeEnrichmentCD2AP, NPHS1, NPHS2, TRPC66.55
2Focal segmental glomerulosclerosisEnrichmentNPHS1, NPHS2, TRPC65.32
3Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.08
4Breast adenocarcinomaEnrichmentAKT1, PIK3CA4.39
5Nephrotic syndromeEnrichmentNPHS1, NPHS2, TRPC64.30
6Nephrotic syndrome, type 1EnrichmentNPHS1, NPHS24.01
7Cowden syndromeEnrichmentAKT1, PIK3CA4.01
8MeningiomaEnrichmentAKT1, PIK3CA3.75
9Breast cancerEnrichmentAKT1, JUN, PIK3CA3.58
10Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R13.39
11MacrodactylyEnrichmentPIK3CA2.77
12Proteus syndromeEnrichmentAKT12.77
13Megalencephaly, autosomal dominantEnrichmentPIK3CA2.77
14Cowden syndrome 5EnrichmentPIK3CA2.77
15Focal segmental glomerulosclerosis 2EnrichmentTRPC62.77
16Cerebral cavernous malformations 4EnrichmentPIK3CA2.77
17Short syndromeEnrichmentPIK3R12.77
18Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.77
19Hemifacial myohyperplasiaEnrichmentPIK3CA2.77
20Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.77
21Focal segmental glomerulosclerosis 3EnrichmentCD2AP2.77
22Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.77
23Cowden syndrome 6EnrichmentAKT12.77
24Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.77
25Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.77
26HypospadiasEnrichmentPIK3CA2.77
27Rare venous malformationEnrichmentPIK3CA2.77
28Diaphragmatic eventrationEnrichmentPIK3CA2.77
29Familial nephrotic syndromeEnrichmentNPHS12.77
30Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.77
31Rare combined vascular malformationEnrichmentPIK3CA2.77
32Cavernous lymphangiomaEnrichmentPIK3CA2.77
33Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.77
34Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.77
35Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.77
36Eccrine angiomatous hamartomaEnrichmentPIK3CA2.77
37Macrodactyly of toeEnrichmentPIK3CA2.77
38Hereditary breast carcinomaEnrichmentAKT1, PIK3CA2.60
39Nephrotic syndrome, type 2EnrichmentNPHS22.47
40Keratosis, seborrheicEnrichmentPIK3CA2.47
41Noonan syndrome 8EnrichmentPIK3CA2.47
42Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.47
43Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.47
44Nephrotic syndrome, type 23EnrichmentKIRREL12.47
45Genetic nephrotic syndromeEnrichmentNPHS22.47
46Idiopathic nephrotic syndromeEnrichmentNPHS22.47
47Pompe disease, infantile-onsetEnrichmentPIK3CA2.29
48Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.29
49Nephrotic syndrome, type 24EnrichmentNPHS22.29
50Immunodeficiency 14EnrichmentPIK3R12.29
51KeratoacanthomaEnrichmentPIK3CA2.29
52Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.17
53Cerebrovascular diseaseEnrichmentPIK3CA2.17
54Familial cerebral cavernous malformationsEnrichmentPIK3CA2.17
55Capillary malformations, congenitalEnrichmentPIK3CA2.07
56HemimegalencephalyEnrichmentPIK3CA2.07
57Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.99
58Cowden syndrome 1EnrichmentPIK3CA1.99
59Hemihyperplasia, isolatedEnrichmentPIK3CA1.99
60Lung squamous cell carcinomaEnrichmentPIK3CA1.99
61Nevus, epidermalEnrichmentPIK3CA1.93
62Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.93
63Gallbladder cancerEnrichmentPIK3CA1.93
64Overgrowth syndromeEnrichmentPIK3R11.93
65Ovarian cancerEnrichmentAKT1, PIK3CA1.90
66Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.82
67Arteriovenous malformationEnrichmentPIK3CA1.82
68Adult hepatocellular carcinomaEnrichmentPIK3CA1.82
69Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.77
70Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.77
71Lung non-small cell carcinomaEnrichmentPIK3CA1.73
72Lip and oral cavity carcinomaEnrichmentPIK3CA1.70
73Chronic kidney diseaseEnrichmentNPHS21.66
74Nk-cell enteropathyEnrichmentPIK3CB1.66
75Lynch syndromeEnrichmentPIK3CA1.60
76Kidney diseaseEnrichmentNPHS11.60
77Endometrial cancerEnrichmentPIK3CA1.46
78Hepatocellular carcinomaEnrichmentPIK3CA1.44
79Bladder cancerEnrichmentPIK3CA1.32
80Prostate cancerEnrichmentPIK3CA1.32
81Lung cancerEnrichmentPIK3CA1.28
82Gastric cancerEnrichmentPIK3CA1.15
83HypertelorismEnrichmentPIK3CA1.07

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