Plasma membrane estrogen receptor signaling

No Pathway Network information available for Plasma membrane estrogen receptor signaling

Pathways in the Plasma membrane estrogen receptor signaling SuperPath

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

Disorders associated with Plasma membrane estrogen receptor signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Breast cancerEnrichmentAKT1, ESR1, PIK3CA, SHC15.07
2Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.05
3Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R1, SRC4.82
4Hemihyperplasia, isolatedEnrichmentPIK3CA, RHOA4.35
5Breast adenocarcinomaEnrichmentAKT1, PIK3CA4.35
6Hereditary breast carcinomaEnrichmentAKT1, ESR1, PIK3CA4.21
7Cowden syndromeEnrichmentAKT1, PIK3CA3.97
8MeningiomaEnrichmentAKT1, PIK3CA3.71
9MacrodactylyEnrichmentPIK3CA2.75
10Proteus syndromeEnrichmentAKT12.75
11Immunodeficiency 50EnrichmentMSN2.75
12Noonan syndrome 4EnrichmentSOS12.75
13Megalencephaly, autosomal dominantEnrichmentPIK3CA2.75
14Cowden syndrome 5EnrichmentPIK3CA2.75
15Cerebral cavernous malformations 4EnrichmentPIK3CA2.75
16Short syndromeEnrichmentPIK3R12.75
17Hemifacial myohyperplasiaEnrichmentPIK3CA2.75
18Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.75
19Ovarian dysgenesis 8EnrichmentESR22.75
20Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.75
21Cowden syndrome 6EnrichmentAKT12.75
22Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.75
23Thrombocytopenia 6EnrichmentSRC2.75
24Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.75
25Intellectual developmental disorder, autosomal dominant 42EnrichmentGNB12.75
26Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.75
27Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.75
28HypospadiasEnrichmentPIK3CA2.75
29Rare venous malformationEnrichmentPIK3CA2.75
30Diaphragmatic eventrationEnrichmentPIK3CA2.75
31Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.75
32Rare combined vascular malformationEnrichmentPIK3CA2.75
33Cavernous lymphangiomaEnrichmentPIK3CA2.75
34Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.75
35Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.75
36Eccrine angiomatous hamartomaEnrichmentPIK3CA2.75
37Macrodactyly of toeEnrichmentPIK3CA2.75
38Fibromatosis, gingival, 1EnrichmentSOS12.45
39Pulmonic stenosisEnrichmentSOS12.45
40Keratosis, seborrheicEnrichmentPIK3CA2.45
41Noonan syndrome 8EnrichmentPIK3CA2.45
42Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.45
43Metaphyseal anadysplasia 2EnrichmentMMP92.45
44Metaphyseal anadysplasiaEnrichmentMMP92.45
45Cerebral visual impairmentEnrichmentGNB12.45
46Thyroid carcinoma, familial medullaryEnrichmentESR22.28
47Pompe disease, infantile-onsetEnrichmentPIK3CA2.28
48Nuchal bleb, familialEnrichmentSOS12.28
49Multicentric osteolysis, nodulosis, and arthropathyEnrichmentMMP22.28
50Estrogen resistanceEnrichmentESR12.28
51Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.28
52Immunodeficiency 14EnrichmentPIK3R12.28
53Migraine without auraEnrichmentESR12.28
54Growth delay due to insulin-like growth factor i resistanceEnrichmentIGF1R2.28
55KeratoacanthomaEnrichmentPIK3CA2.28
56Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.15
57Arthrogryposis multiplex congenita 3, myogenic typeEnrichmentESR12.15
58Cerebrovascular diseaseEnrichmentPIK3CA2.15
59Familial cerebral cavernous malformationsEnrichmentPIK3CA2.15
60Gingival fibromatosisEnrichmentSOS12.15
61Capillary malformations, congenitalEnrichmentPIK3CA2.05
62Alzheimer disease 2EnrichmentNOS32.05
63Insulin-like growth factor iEnrichmentIGF1R2.05
64Pre-eclampsiaEnrichmentNOS32.05
65HemimegalencephalyEnrichmentPIK3CA2.05
66Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.98
67Cowden syndrome 1EnrichmentPIK3CA1.98
68Lung squamous cell carcinomaEnrichmentPIK3CA1.98
69Nevus, epidermalEnrichmentPIK3CA1.91
70MyelofibrosisEnrichmentSRC1.91
71Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.91
72Noonan syndrome 3EnrichmentSOS11.91
73Gallbladder cancerEnrichmentPIK3CA1.91
74Overgrowth syndromeEnrichmentPIK3R11.91
75Ovarian cancerEnrichmentAKT1, PIK3CA1.87
76HypothyroidismEnrichmentGNB11.85
77Arteriovenous malformationEnrichmentPIK3CA1.80
78Adult hepatocellular carcinomaEnrichmentPIK3CA1.80
79Stroke, ischemicEnrichmentNOS31.76
80Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.76
81Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.76
82Migraine with or without aura 1EnrichmentESR11.71
83Leukemia, acute lymphoblasticEnrichmentGNB11.71
84Myelodysplastic syndromeEnrichmentGNB11.71
85Lung non-small cell carcinomaEnrichmentPIK3CA1.71
86MicrocephalyEnrichmentGNB1, IGF1R1.70
87Lip and oral cavity carcinomaEnrichmentPIK3CA1.68
88Aortic valve disease 1EnrichmentSOS11.64
89Nk-cell enteropathyEnrichmentIGF1R1.64
90OsteoporosisEnrichmentSRC1.61
9146,xy partial gonadal dysgenesisEnrichmentSOS11.61
92Lynch syndromeEnrichmentPIK3CA1.58
93Noonan syndrome and noonan-related syndromeEnrichmentSOS11.58
94Alzheimer disease, familial, 1EnrichmentNOS31.53
95Hypertension, essentialEnrichmentNOS31.53
96Cleft palate, isolatedEnrichmentGNB11.53
97Endometrial cancerEnrichmentPIK3CA1.44
98Hepatocellular carcinomaEnrichmentPIK3CA1.42
99Myocardial infarctionEnrichmentESR11.42
100Noonan syndrome 1EnrichmentSOS11.40
101RasopathyEnrichmentSOS11.35
102StrabismusEnrichmentGNB11.33
103Bladder cancerEnrichmentPIK3CA1.30
104Prostate cancerEnrichmentPIK3CA1.30
105Lung cancerEnrichmentPIK3CA1.26
106DystoniaEnrichmentGNB11.22
107Cerebral palsyEnrichmentGNB11.18
108Gastric cancerEnrichmentPIK3CA1.13
109ThrombocytopeniaEnrichmentSRC1.09
110Autosomal dominant non-syndromic intellectual disabilityEnrichmentGNB11.07
111HypertelorismEnrichmentPIK3CA1.05
112Hereditary breast ovarian cancer syndromeEnrichmentBCAR11.03
113Primary ovarian insufficiencyEnrichmentNOS31.00
114Autism spectrum disorderEnrichmentGNB10.75

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