Class I PI3K signaling events

No Pathway Network information available for Class I PI3K signaling events

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

Disorders associated with Class I PI3K signaling events SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Cowden syndromeEnrichmentAKT1, PIK3CA, PTEN6.14
2MeningiomaEnrichmentAKT1, PIK3CA, PTEN5.72
3Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.88
4Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R1, SRC4.48
5HemimegalencephalyEnrichmentPIK3CA, PTEN4.36
6Cowden syndrome 1EnrichmentPIK3CA, PTEN4.18
7Hemihyperplasia, isolatedEnrichmentPIK3CA, RHOA4.18
8Breast adenocarcinomaEnrichmentAKT1, PIK3CA4.18
9Hereditary breast carcinomaEnrichmentAKT1, PIK3CA, PTEN3.96
10Autosomal non-syndromic agammaglobulinemiaEnrichmentBLNK, PIK3R13.71
11Breast cancerEnrichmentAKT1, PIK3CA, PTEN3.27
12Diffuse large b-cell lymphomaEnrichmentBTK, PTEN3.13
13Endometrial cancerEnrichmentPIK3CA, PTEN3.04
14Ovarian cancerEnrichmentAKT1, PIK3CA, PTEN2.90
15Bladder cancerEnrichmentPIK3CA, PTEN2.76
16Prostate cancerEnrichmentPIK3CA, PTEN2.76
17MacrodactylyEnrichmentPIK3CA2.67
18Proteus syndromeEnrichmentAKT12.67
19Vacterl association with hydrocephalusEnrichmentPTEN2.67
20Megalencephaly, autosomal dominantEnrichmentPIK3CA2.67
21Cowden syndrome 5EnrichmentPIK3CA2.67
22Cerebral cavernous malformations 4EnrichmentPIK3CA2.67
23Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.67
24Short syndromeEnrichmentPIK3R12.67
25Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.67
26Isolated growth hormone deficiency type iiiEnrichmentBTK2.67
27Papillary tumor of the pineal regionEnrichmentPTEN2.67
28Hemifacial myohyperplasiaEnrichmentPIK3CA2.67
29Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.67
30Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.67
31Cowden syndrome 6EnrichmentAKT12.67
32Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.67
33Immunodeficiency 97 with autoinflammationEnrichmentPIK3CG2.67
34Glioma susceptibility 2EnrichmentPTEN2.67
35Immunodeficiency 22EnrichmentLCK2.67
36Thrombocytopenia 6EnrichmentSRC2.67
37Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.67
38Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.67
39Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.67
40HypospadiasEnrichmentPIK3CA2.67
41ColitisEnrichmentSYK2.67
42Rare venous malformationEnrichmentPIK3CA2.67
43Diaphragmatic eventrationEnrichmentPIK3CA2.67
44Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.67
45Rare combined vascular malformationEnrichmentPIK3CA2.67
46Cavernous lymphangiomaEnrichmentPIK3CA2.67
47Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.67
48Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeEnrichmentPTEN2.67
49Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.67
50Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.67
51Eccrine angiomatous hamartomaEnrichmentPIK3CA2.67
52Macrodactyly of toeEnrichmentPIK3CA2.67
53Gastric cancerEnrichmentPIK3CA, PTEN2.42
54Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK2.37
55Agammaglobulinemia 4, autosomal recessiveEnrichmentBLNK2.37
56Keratosis, seborrheicEnrichmentPIK3CA2.37
57Noonan syndrome 8EnrichmentPIK3CA2.37
58Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.37
59Agammaglobulinemia, x-linkedEnrichmentBTK2.37
60Periventricular nodular heterotopia 8EnrichmentARF12.37
61Agammaglobulinemia 4EnrichmentBLNK2.37
62Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.37
63Vacterl with hydrocephalusEnrichmentPTEN2.37
64ArthritisEnrichmentSYK2.37
65Juvenile polyposis of infancyEnrichmentPTEN2.37
66Pompe disease, infantile-onsetEnrichmentPIK3CA2.19
67Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK2.19
68Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.19
69Agammaglobulinemia 1EnrichmentBTK2.19
70Immunodeficiency 14EnrichmentPIK3R12.19
71Laryngeal squamous cell carcinomaEnrichmentPTEN2.19
72KeratoacanthomaEnrichmentPIK3CA2.19
73Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.07
74Cerebrovascular diseaseEnrichmentPIK3CA2.07
75Familial cerebral cavernous malformationsEnrichmentPIK3CA2.07
76GliomaEnrichmentPTEN2.07
77Capillary malformations, congenitalEnrichmentPIK3CA1.97
78Macrocephaly/autism syndromeEnrichmentPTEN1.97
79HemangiomaEnrichmentPTEN1.97
80Acute megakaryocytic leukemiaEnrichmentPTEN1.97
81Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.89
82Lung squamous cell carcinomaEnrichmentPIK3CA1.89
83Nevus, epidermalEnrichmentPIK3CA1.83
84Thyroid cancer, nonmedullary, 2EnrichmentPTEN1.83
85MyelofibrosisEnrichmentSRC1.83
86Squamous cell carcinoma, head and neckEnrichmentPTEN1.83
87Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.83
88Gallbladder cancerEnrichmentPIK3CA1.83
89Follicular thyroid carcinomaEnrichmentPTEN1.83
90Overgrowth syndromeEnrichmentPIK3R11.83
91Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.72
92Arteriovenous malformationEnrichmentPIK3CA1.72
93Adult hepatocellular carcinomaEnrichmentPIK3CA1.72
94Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.67
95MelanomaEnrichmentPTEN1.67
96Immune deficiency diseaseEnrichmentSYK1.63
97Meningioma, familialEnrichmentPTEN1.63
98Lung non-small cell carcinomaEnrichmentPIK3CA1.63
99Uterine corpus cancerEnrichmentPTEN1.63
100Lip and oral cavity carcinomaEnrichmentPIK3CA1.60
101Nk-cell enteropathyEnrichmentPIK3CB1.56
102OsteoporosisEnrichmentSRC1.53
103Periventricular nodular heterotopiaEnrichmentARF11.53
104Lynch syndromeEnrichmentPIK3CA1.50
105RhabdomyosarcomaEnrichmentPTEN1.47
106Hepatocellular carcinomaEnrichmentPIK3CA1.34
107Lung cancerEnrichmentPIK3CA1.18
108Severe combined immunodeficiencyEnrichmentLCK1.17
109ThrombocytopeniaEnrichmentSRC1.01
110HypertelorismEnrichmentPIK3CA0.98
111Hereditary breast ovarian cancer syndromeEnrichmentPTEN0.95
112Myeloma, multipleEnrichmentSGK10.95
113Congenital nervous system abnormalityEnrichmentPTEN0.69
114Nervous system diseaseEnrichmentPTEN0.69
115Autism spectrum disorderEnrichmentPTEN0.68
116Inherited cancer-predisposing syndromeEnrichmentPTEN0.61

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