mTOR signaling pathway

No Pathway Network information available for mTOR signaling pathway

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

Disorders associated with mTOR signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Focal cortical dysplasia, type iiEnrichmentMTOR, RHEB, TSC1, TSC29.85
2Isolated focal cortical dysplasia type iiEnrichmentMTOR, RHEB, TSC1, TSC29.85
3LymphangioleiomyomatosisEnrichmentTSC1, TSC24.91
4Tuberous sclerosis 1EnrichmentTSC1, TSC24.44
5HamartomaEnrichmentTSC1, TSC24.44
6Tuberous sclerosisEnrichmentTSC1, TSC24.14
7HemimegalencephalyEnrichmentMTOR, RHEB3.91
8Breast adenocarcinomaEnrichmentAKT1, RB1CC13.74
9Adult hepatocellular carcinomaEnrichmentTSC1, TSC23.36
10Noonan syndrome and noonan-related syndromeEnrichmentMAP2K1, RAF12.90
11Noonan syndrome 1EnrichmentMAP2K1, RAF12.53
12Proteus syndromeEnrichmentAKT12.45
13Noonan syndrome 5EnrichmentRAF12.45
14Melorheostosis, isolatedEnrichmentMAP2K12.45
15Mucoepithelial dysplasia, hereditaryEnrichmentSREBF12.45
16Cardiomyopathy, dilated, 1nnEnrichmentRAF12.45
17Cardiac valvular dysplasia 1EnrichmentPLD12.45
18Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.45
19Immunodeficiency 15bEnrichmentIKBKB2.45
20Immunodeficiency 15aEnrichmentIKBKB2.45
21Autism 19EnrichmentEIF4E2.45
22Ifap syndrome 2EnrichmentSREBF12.45
23Spinocerebellar ataxia 26EnrichmentEEF22.45
24Thrombocytopenia 4EnrichmentCYCS2.45
25MelorheostosisEnrichmentMAP2K12.45
26Leopard syndrome 2EnrichmentRAF12.45
27Cowden syndrome 6EnrichmentAKT12.45
28TrigonitisEnrichmentRAF12.45
29RasopathyEnrichmentMAP2K1, RAF12.42
30Gabriele-de vries syndromeEnrichmentYY12.15
31Cebalid syndromeEnrichmentMTOR2.15
32Developmental and epileptic encephalopathy 78EnrichmentYY12.15
33InsulinomaEnrichmentYY12.15
34Smith-kingsmore syndromeEnrichmentMTOR2.15
35Long-olsen-distelmaier syndromeEnrichmentRRAGC2.15
36Hereditary breast carcinomaEnrichmentAKT1, RB1CC11.98
37Ifap syndrome 1, with or without bresheck syndromeEnrichmentSREBF11.98
38Polycystic kidney disease, infantile severe, with tuberous sclerosisEnrichmentTSC21.98
39Langerhans cell histiocytosisEnrichmentMAP2K11.98
40Tuberous sclerosis 2EnrichmentTSC21.98
41Xanthinuria, type iiEnrichmentTSC21.98
42Cardiofaciocutaneous syndrome 1EnrichmentMAP2K11.85
43Cardiofaciocutaneous syndromeEnrichmentMAP2K11.85
44Noonan syndrome with multiple lentiginesEnrichmentRAF11.85
45Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.76
46KeratoconusEnrichmentTSC11.68
47Polycystic kidney disease 1 with or without polycystic liver diseaseEnrichmentTSC21.61
48Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.61
49Renal cell carcinoma, papillary, 1EnrichmentMTOR1.61
50Noonan syndrome 3EnrichmentRAF11.61
51Polycystic kidney disease 1EnrichmentTSC21.61
52Pilomyxoid astrocytomaEnrichmentRAF11.61
53Overgrowth syndromeEnrichmentMTOR1.61
54Melanocytic nevus syndrome, congenitalEnrichmentRAF11.55
55Breast cancerEnrichmentAKT1, RB1CC11.54
56Arteriovenous malformationEnrichmentMAP2K11.50
57Cowden syndromeEnrichmentAKT11.50
58Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.46
59Lung non-small cell carcinomaEnrichmentMAP2K11.42
60MeningiomaEnrichmentAKT11.38
61Acute promyelocytic leukemiaEnrichmentPML1.35
62Ovarian cancerEnrichmentAKT1, TSC21.30
63Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.29
64Autosomal dominant polycystic kidney diseaseEnrichmentTSC21.29
65Kidney diseaseEnrichmentTSC11.29
66Rare genetic intellectual disabilityEnrichmentMTOR1.29
67Autism spectrum disorderEnrichmentMAP2K1, TSC21.25
68Inherited cancer-predisposing syndromeEnrichmentTSC1, TSC21.10
69Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.09
70Bladder cancerEnrichmentTSC11.01
71Hirschsprung disease 1EnrichmentSREBF11.01
72Familial hypertrophic cardiomyopathyEnrichmentRAF10.96
73Severe combined immunodeficiencyEnrichmentIKBKB0.96
74Left ventricular noncompactionEnrichmentRAF10.93
75Type 2 diabetes mellitusEnrichmentIRS10.86
76West syndromeEnrichmentTSC20.84
77ThrombocytopeniaEnrichmentCYCS0.80
78Familial isolated dilated cardiomyopathyEnrichmentRAF10.77
79Myeloma, multipleEnrichmentSGK10.74
80Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentPPARGC1A0.73
81Autosomal recessive non-syndromic intellectual disabilityEnrichmentCLIP10.73
82Primary ovarian insufficiencyEnrichmentRICTOR0.72
83Dilated cardiomyopathyEnrichmentRAF10.61
84Colorectal cancerEnrichmentAKT10.57
85Congenital nervous system abnormalityEnrichmentTSC20.50
86Nervous system diseaseEnrichmentTSC20.50

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