IGF1 pathway

No Pathway Network information available for IGF1 pathway

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

Disorders associated with IGF1 pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome 3EnrichmentHRAS, PTPN11, RAF1, SOS19.22
2Noonan syndrome and noonan-related syndromeEnrichmentHRAS, PTPN11, RAF1, SOS17.65
3Noonan syndrome 1EnrichmentHRAS, PTPN11, RAF1, SOS16.84
4RasopathyEnrichmentHRAS, PTPN11, RAF1, SOS16.61
5Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.88
6Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN11, YWHAZ4.58
7Noonan syndrome with multiple lentiginesEnrichmentPTPN11, RAF14.58
8Breast adenocarcinomaEnrichmentAKT1, PIK3CA4.18
9Nevus, epidermalEnrichmentHRAS, PIK3CA4.04
10Type 2 diabetes mellitusEnrichmentIRS1, IRS2, PTPN14.02
11Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.91
12Arteriovenous malformationEnrichmentHRAS, PIK3CA3.80
13Cowden syndromeEnrichmentAKT1, PIK3CA3.80
14Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, PIK3CA3.71
15Lung non-small cell carcinomaEnrichmentHRAS, PIK3CA3.62
16MeningiomaEnrichmentAKT1, PIK3CA3.54
17Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA3.54
18Breast cancerEnrichmentAKT1, PIK3CA, SHC13.27
19Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R13.08
20Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.86
21Bladder cancerEnrichmentHRAS, PIK3CA2.76
22Non-immune hydrops fetalisEnrichmentHRAS, PTPN112.70
23MacrodactylyEnrichmentPIK3CA2.67
24Proteus syndromeEnrichmentAKT12.67
25MetachondromatosisEnrichmentPTPN112.67
26Noonan syndrome 5EnrichmentRAF12.67
27Noonan syndrome 4EnrichmentSOS12.67
28Megalencephaly, autosomal dominantEnrichmentPIK3CA2.67
29Leopard syndrome 1EnrichmentPTPN112.67
30Cardiomyopathy, dilated, 1nnEnrichmentRAF12.67
31Cowden syndrome 5EnrichmentPIK3CA2.67
32Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.67
33Cerebral cavernous malformations 4EnrichmentPIK3CA2.67
34Short syndromeEnrichmentPIK3R12.67
35Hemifacial myohyperplasiaEnrichmentPIK3CA2.67
36Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.67
37Leopard syndrome 2EnrichmentRAF12.67
38Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.67
39Cowden syndrome 6EnrichmentAKT12.67
40Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.67
41Congenital heart defects and ectodermal dysplasiaEnrichmentPRKD12.67
42TrigonitisEnrichmentRAF12.67
43Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.67
44HypospadiasEnrichmentPIK3CA2.67
45Rare venous malformationEnrichmentPIK3CA2.67
46Diaphragmatic eventrationEnrichmentPIK3CA2.67
47Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.67
48Rare combined vascular malformationEnrichmentPIK3CA2.67
49Cavernous lymphangiomaEnrichmentPIK3CA2.67
50Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.67
51Phakomatosis pigmentokeratoticaEnrichmentHRAS2.67
52Silver-russell syndrome due to maternal uniparental disomy of chromosome 7EnrichmentGRB102.67
53Malignant epithelial tumor of salivary glandsEnrichmentPRKD12.67
54Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.67
55Eccrine angiomatous hamartomaEnrichmentPIK3CA2.67
56Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.67
57Macrodactyly of toeEnrichmentPIK3CA2.67
58Malignant astrocytomaEnrichmentPTPN112.67
59Hereditary breast carcinomaEnrichmentAKT1, PIK3CA2.40
60Fibromatosis, gingival, 1EnrichmentSOS12.37
61Costello syndromeEnrichmentHRAS2.37
62Pulmonic stenosisEnrichmentSOS12.37
63Keratosis, seborrheicEnrichmentPIK3CA2.37
64Noonan syndrome 8EnrichmentPIK3CA2.37
65Werner syndromeEnrichmentPTPN112.37
66Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.37
67Wooly hair nevusEnrichmentHRAS2.37
68Pompe disease, infantile-onsetEnrichmentPIK3CA2.19
69Nuchal bleb, familialEnrichmentSOS12.19
70Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.19
71Miller-dieker lissencephaly syndromeEnrichmentYWHAE2.19
72Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE2.19
73Large congenital melanocytic nevusEnrichmentHRAS2.19
74Immunodeficiency 14EnrichmentPIK3R12.19
75SpermatocytomaEnrichmentHRAS2.19
76Growth delay due to insulin-like growth factor i resistanceEnrichmentIGF1R2.19
77Tricuspid valve insufficiencyEnrichmentPTPN112.19
78KeratoacanthomaEnrichmentPIK3CA2.19
79Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS2.07
80Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.07
81Chromosome 22q11.2 deletion syndrome, distalEnrichmentCRKL2.07
82Cerebrovascular diseaseEnrichmentPIK3CA2.07
83Epidermolytic nevusEnrichmentHRAS2.07
84Familial cerebral cavernous malformationsEnrichmentPIK3CA2.07
85Gingival fibromatosisEnrichmentSOS12.07
86Capillary malformations, congenitalEnrichmentPIK3CA1.97
87Insulin-like growth factor iEnrichmentIGF1R1.97
88LymphomaEnrichmentPTPN111.97
89HemimegalencephalyEnrichmentPIK3CA1.97
90Endometrial stromal sarcomaEnrichmentYWHAE1.97
91Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.89
92Cowden syndrome 1EnrichmentPIK3CA1.89
93Hemihyperplasia, isolatedEnrichmentPIK3CA1.89
94Patent ductus arteriosusEnrichmentPTPN111.89
95Lung squamous cell carcinomaEnrichmentPIK3CA1.89
96Kidney clear cell sarcomaEnrichmentYWHAE1.89
97Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.83
98Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.83
99Gallbladder cancerEnrichmentPIK3CA1.83
100Pilomyxoid astrocytomaEnrichmentRAF11.83
101Follicular thyroid carcinomaEnrichmentHRAS1.83
102Overgrowth syndromeEnrichmentPIK3R11.83
103Adult hepatocellular carcinomaEnrichmentPIK3CA1.72
104Ovarian cancerEnrichmentAKT1, PIK3CA1.71
105Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.67
106Pectus excavatumEnrichmentPTPN111.63
107Specific learning disabilityEnrichmentPTPN111.63
108EpicanthusEnrichmentPTPN111.60
109Juvenile myelomonocytic leukemiaEnrichmentPTPN111.60
110Congenital long qt syndromeEnrichmentPTPN111.60
111Aortic valve disease 1EnrichmentSOS11.56
112Chromosome 1p36 deletion syndromeEnrichmentPRKCZ1.56
113Nk-cell enteropathyEnrichmentIGF1R1.56
114MicrocephalyEnrichmentIGF1R, PTPN111.55
11546,xy partial gonadal dysgenesisEnrichmentSOS11.53
116Lynch syndromeEnrichmentPIK3CA1.50
117RhabdomyosarcomaEnrichmentHRAS1.47
118Patent foramen ovaleEnrichmentPTPN111.42
119Endometrial cancerEnrichmentPIK3CA1.36
120Hepatocellular carcinomaEnrichmentPIK3CA1.34
121Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.30
122ScoliosisEnrichmentPTPN111.30
123StrabismusEnrichmentPTPN111.25
124Prostate cancerEnrichmentPIK3CA1.22
125Differentiated thyroid carcinomaEnrichmentHRAS1.22
126Long qt syndrome 1EnrichmentPTPN111.21
127Lung cancerEnrichmentPIK3CA1.18
128Familial hypertrophic cardiomyopathyEnrichmentRAF11.17
129Left ventricular noncompactionEnrichmentRAF11.14
130Gastric cancerEnrichmentPIK3CA1.06
131Hypertrophic cardiomyopathyEnrichmentPTPN111.06
132ThrombocytopeniaEnrichmentPTPN111.01
133Autosomal dominant non-syndromic intellectual disabilityEnrichmentYWHAZ0.99
134HypertelorismEnrichmentPIK3CA0.98
135Familial isolated dilated cardiomyopathyEnrichmentRAF10.97
136Hereditary breast ovarian cancer syndromeEnrichmentBCAR10.95
137Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.95
138Dilated cardiomyopathyEnrichmentRAF10.80
139Autism spectrum disorderEnrichmentPTPN110.68
140Inherited cancer-predisposing syndromeEnrichmentPTPN110.61

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