MTOR signalling

Pathway network for the MTOR signalling SuperPath

Sources:
  • Reactome
  • WikiPathways

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

Disorders associated with MTOR signalling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Focal cortical dysplasia, type iiEnrichmentMTOR, RHEB, TSC1, TSC210.55
2Isolated focal cortical dysplasia type iiEnrichmentMTOR, RHEB, TSC1, TSC210.55
3LymphangioleiomyomatosisEnrichmentTSC1, TSC27.49
4Tuberous sclerosis 1EnrichmentTSC1, TSC27.01
5HamartomaEnrichmentTSC1, TSC27.01
6Tuberous sclerosisEnrichmentTSC1, TSC26.71
7Adult hepatocellular carcinomaEnrichmentTSC1, TSC25.93
8HemimegalencephalyEnrichmentMTOR, RHEB4.52
9Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT23.66
10Akt2-related familial partial lipodystrophyEnrichmentAKT23.66
11Inherited cancer-predisposing syndromeEnrichmentTSC1, TSC23.55
12Polycystic kidney disease, infantile severe, with tuberous sclerosisEnrichmentTSC23.18
13Tuberous sclerosis 2EnrichmentTSC23.18
14Xanthinuria, type iiEnrichmentTSC23.18
15KeratoconusEnrichmentTSC12.88
16Polycystic kidney disease 1 with or without polycystic liver diseaseEnrichmentTSC22.81
17Polycystic kidney disease 1EnrichmentTSC22.81
18Immunodeficiency due to defect in mapbp-interacting proteinEnrichmentLAMTOR22.75
19Parkinson disease 18, autosomal dominantEnrichmentEIF4G12.75
20Autism 19EnrichmentEIF4E2.75
21Primary immunodeficiency syndrome due to p14 deficiencyEnrichmentLAMTOR22.75
22Tubular renal disease-cardiomyopathy syndromeEnrichmentRRAGD2.75
23Cardiomyopathy, familial hypertrophic, 6EnrichmentPRKAG22.67
24Glycogen storage disease of heart, lethal congenitalEnrichmentPRKAG22.67
25Skeletal muscle glycogen content and metabolism quantitative trait locusEnrichmentPRKAG32.67
26Intestinal polyposis syndromeEnrichmentSTK112.67
27Proteus syndromeEnrichmentAKT12.58
28Cowden syndrome 6EnrichmentAKT12.58
29Takenouchi-kosaki syndromeEnrichmentCDC422.58
30Low density lipoprotein cholesterol level quantitative trait locus 3EnrichmentHMGCR2.58
31Muscular dystrophy, limb-girdle, autosomal recessive 28EnrichmentHMGCR2.58
32Nocarh syndromeEnrichmentCDC422.58
33Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.58
34Autosomal dominant polycystic kidney diseaseEnrichmentTSC22.48
35Kidney diseaseEnrichmentTSC12.48
36Hypomagnesemia 7, renal, with or without dilated cardiomyopathyEnrichmentRRAGD2.45
37Cebalid syndromeEnrichmentMTOR2.45
38Smith-kingsmore syndromeEnrichmentMTOR2.45
39Long-olsen-distelmaier syndromeEnrichmentRRAGC2.45
40Peutz-jeghers syndromeEnrichmentSTK112.37
41Polyhydramnios, megalencephaly, and symptomatic epilepsyEnrichmentSTRADA2.37
42Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.28
43Immune system diseaseEnrichmentCDC422.28
44Testicular germ cell cancerEnrichmentSTK112.19
45Testicular cancerEnrichmentSTK112.19
46Apc-associated polyposis conditionsEnrichmentSTK112.19
47Bladder cancerEnrichmentTSC12.19
48Type 2 diabetes mellitusEnrichmentAKT22.03
49West syndromeEnrichmentTSC22.01
50Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC421.98
51Familial adenomatous polyposis 1EnrichmentSTK111.97
52Generalized juvenile polyposis/juvenile polyposis coliEnrichmentSTK111.97
53Renal cell carcinoma, papillary, 1EnrichmentMTOR1.91
54Overgrowth syndromeEnrichmentMTOR1.91
55Testicular germ cell tumorEnrichmentSTK111.89
56Breast adenocarcinomaEnrichmentAKT11.80
57MelanomaEnrichmentSTK111.67
58Ovarian cancerEnrichmentTSC21.65
59Congenital nervous system abnormalityEnrichmentTSC21.63
60Nervous system diseaseEnrichmentTSC21.63
61Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.63
62Limb-girdle muscular dystrophyEnrichmentHMGCR1.63
63Cowden syndromeEnrichmentAKT11.63
64Autism spectrum disorderEnrichmentTSC21.62
65Lip and oral cavity carcinomaEnrichmentSTK111.60
66Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.58
67Rare genetic intellectual disabilityEnrichmentMTOR1.58
68MeningiomaEnrichmentAKT11.50
69Wolff-parkinson-white syndromeEnrichmentPRKAG21.47
70Melanoma, cutaneous malignant 1EnrichmentSTK111.45
71Parkinson disease, late-onsetEnrichmentEIF4G11.38
72Pancreatic cancerEnrichmentSTK111.28
73Familial hypertrophic cardiomyopathyEnrichmentPRKAG21.17
74Benign epilepsy with centrotemporal spikesEnrichmentSTRADA1.08
75Centralopathic epilepsyEnrichmentSTRADA1.06
76Gastric cancerEnrichmentSTK111.06
77Hypertrophic cardiomyopathyEnrichmentPRKAG21.06
78Hereditary breast carcinomaEnrichmentAKT10.96
79Primary ovarian insufficiencyEnrichmentRICTOR0.84
80Breast cancerEnrichmentAKT10.74
81Colorectal cancerEnrichmentAKT10.68

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