Signaling by Overexpressed Wild-Type EGFR in Cancer

Pathway network for the Signaling by Overexpressed Wild-Type EGFR in Cancer SuperPath

Sources:
  • Reactome

Gene overlap in member pathways for Signaling by Overexpressed Wild-Type EGFR in Cancer SuperPath

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

Disorders associated with Signaling by Overexpressed Wild-Type EGFR in Cancer SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hypomagnesemia 4, renalEnrichmentEGF3.23
2Egf-related primary hypomagnesemia with intellectual disabilityEnrichmentEGF3.23
3Ovarian cancerEnrichmentAKT1, CDKN1B, EGFR3.14
4Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR2.75
5Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR2.75
6Proteus syndromeEnrichmentAKT12.75
7Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.75
8Noonan syndrome 13EnrichmentMAPK12.75
9Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.75
10Neuroendocrine tumorEnrichmentCDKN1B2.75
11Cowden syndrome 6EnrichmentAKT12.75
12Capillary hemangiomaEnrichmentAKT32.75
13Akt2-related familial partial lipodystrophyEnrichmentAKT22.75
14Cowden syndrome 1EnrichmentEGFR2.45
15Lung squamous cell carcinomaEnrichmentEGFR2.45
16Histiocytoma, angiomatoid fibrousEnrichmentCREB12.45
17Multiple endocrine neoplasia, type ivEnrichmentCDKN1B2.45
18Intravascular large b-cell lymphomaEnrichmentBCL22.45
19Senior-loken syndrome 7EnrichmentAKT32.45
20Bardet-biedl syndrome 16EnrichmentAKT32.45
21Primary mediastinal large b-cell lymphomaEnrichmentXPO12.45
22Squamous cell carcinoma, head and neckEnrichmentEGFR2.38
23Adult hepatocellular carcinomaEnrichmentEGF2.28
24High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL22.28
25Melanoma of soft tissueEnrichmentCREB12.28
26Lung non-small cell carcinomaEnrichmentEGFR2.19
27Lip and oral cavity carcinomaEnrichmentEGFR2.15
28Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT32.15
29Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.15
30Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT32.15
31Congenital generalized lipodystrophyEnrichmentFOS2.15
32Mantle cell lymphomaEnrichmentCCND12.15
33Primary hyperparathyroidismEnrichmentCDKN1B2.15
34Lung cancer susceptibility 3EnrichmentEGFR2.08
35Von hippel-lindau syndromeEnrichmentCCND12.05
36Follicular lymphomaEnrichmentBCL22.05
37Histiocytoid hemangiomaEnrichmentFOS2.05
38HemimegalencephalyEnrichmentAKT32.05
39GliosarcomaEnrichmentEGFR2.03
40Giant cell glioblastomaEnrichmentEGFR2.00
41Colorectal cancerEnrichmentAKT1, CCND11.99
42Breast adenocarcinomaEnrichmentAKT11.98
43Arteriovenous malformations of the brainEnrichmentEGFR1.95
44Multiple endocrine neoplasia, type iEnrichmentCDKN1B1.91
45MegacolonEnrichmentAKT31.91
46Tooth agenesisEnrichmentTGFA1.89
47Cowden syndromeEnrichmentAKT11.80
48Bladder cancerEnrichmentEGFR1.77
49Leukemia, chronic lymphocyticEnrichmentCCND11.76
50PolymicrogyriaEnrichmentAKT31.76
51Lung cancerEnrichmentEGFR1.73
52Specific learning disabilityEnrichmentMAPK11.71
53MeningiomaEnrichmentAKT11.68
54Inherited cancer-predisposing syndromeEnrichmentCDKN1B, EGFR1.65
55Heart, malformation ofEnrichmentMAPK11.50
56Type 2 diabetes mellitusEnrichmentAKT21.14
57Hereditary breast carcinomaEnrichmentAKT11.12
58Myeloma, multipleEnrichmentCCND11.02
59Breast cancerEnrichmentAKT10.90
60MicrocephalyEnrichmentMAPK10.71

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