Gastrin-CREB signalling pathway via PKC and MAPK

No Pathway Network information available for Gastrin-CREB signalling pathway via PKC and MAPK

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

Disorders associated with Gastrin-CREB signalling pathway via PKC and MAPK SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Lung non-small cell carcinomaEnrichmentEGFR, HRAS, KRAS, NRAS10.30
2Noonan syndrome and noonan-related syndromeEnrichmentHRAS, KRAS, NRAS, SOS19.89
3Noonan syndrome 1EnrichmentHRAS, KRAS, NRAS, SOS19.09
4Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS9.08
5RasopathyEnrichmentHRAS, KRAS, NRAS, SOS18.88
6Nevus, epidermalEnrichmentHRAS, KRAS, NRAS8.15
7Noonan syndrome 3EnrichmentHRAS, KRAS, SOS18.15
8Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS6.41
9Bladder cancerEnrichmentEGFR, HRAS, KRAS6.14
10Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS6.14
11Large congenital melanocytic nevusEnrichmentHRAS, NRAS5.93
12Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS5.63
13Lung squamous cell carcinomaEnrichmentEGFR, KRAS5.23
14Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS5.09
15Leukemia, chronic myeloidEnrichmentKRAS, NRAS5.09
16Follicular thyroid carcinomaEnrichmentHRAS, NRAS5.09
17Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS4.96
18Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS4.59
19Lip and oral cavity carcinomaEnrichmentEGFR, HRAS4.59
20Lung cancer susceptibility 3EnrichmentEGFR, KRAS4.45
21Arteriovenous malformations of the brainEnrichmentEGFR, KRAS4.18
22Specific learning disabilityEnrichmentMAPK1, RPS6KA34.04
23Non-immune hydrops fetalisEnrichmentHRAS, KRAS3.74
24Lung cancerEnrichmentEGFR, KRAS3.72
25Leukemia, acute myeloidEnrichmentKRAS, NRAS3.52
26Oculoectodermal syndromeEnrichmentKRAS3.18
27Noonan syndrome 4EnrichmentSOS13.18
28Melanosis, neurocutaneousEnrichmentNRAS3.18
29Noonan syndrome 6EnrichmentNRAS3.18
30Cardiofaciocutaneous syndrome 2EnrichmentKRAS3.18
31Coronary heart disease 6EnrichmentMMP33.18
32Congenital pulmonary airway malformationEnrichmentKRAS3.18
33Phakomatosis pigmentokeratoticaEnrichmentHRAS3.18
34Neurocutaneous melanocytosisEnrichmentNRAS3.18
35Fibromatosis, gingival, 1EnrichmentSOS12.88
36Costello syndromeEnrichmentHRAS2.88
37Pulmonic stenosisEnrichmentSOS12.88
38Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.88
39Wooly hair nevusEnrichmentHRAS2.88
40Coffin-lowry syndromeEnrichmentRPS6KA32.88
41Noonan syndrome 13EnrichmentMAPK12.88
42Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.88
43Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.88
44Ovarian cancerEnrichmentEGFR, KRAS2.72
45Nuchal bleb, familialEnrichmentSOS12.70
46Langerhans cell histiocytosisEnrichmentNRAS2.70
47Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR2.70
48SpermatocytomaEnrichmentHRAS2.70
49Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR2.70
50Cardiofaciocutaneous syndrome 1EnrichmentKRAS2.58
51Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS2.58
52Cardiofaciocutaneous syndromeEnrichmentKRAS2.58
53Lung sarcomatoid carcinomaEnrichmentKRAS2.58
54Pilocytic astrocytomaEnrichmentKRAS2.58
55Epidermolytic nevusEnrichmentHRAS2.58
56Gingival fibromatosisEnrichmentSOS12.58
57Scoliosis, isolated 1EnrichmentMAPK72.58
58Histiocytoma, angiomatoid fibrousEnrichmentCREB12.58
59Cowden syndrome 1EnrichmentEGFR2.40
60Breast adenocarcinomaEnrichmentKRAS2.40
61Melanoma of soft tissueEnrichmentCREB12.40
62Squamous cell carcinoma, head and neckEnrichmentEGFR2.33
63Capillary malformation-arteriovenous malformation 1EnrichmentKRAS2.33
64Gallbladder cancerEnrichmentKRAS2.33
65Pilomyxoid astrocytomaEnrichmentKRAS2.33
66Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.28
67Arteriovenous malformationEnrichmentHRAS2.22
68Myopathy, x-linked, with excessive autophagyEnrichmentHRAS2.18
69Aortic valve disease 1EnrichmentSOS12.07
70Protein-deficiency anemiaEnrichmentNRAS2.07
7146,xy partial gonadal dysgenesisEnrichmentSOS12.03
72Lynch syndromeEnrichmentKRAS2.00
73RhabdomyosarcomaEnrichmentHRAS1.98
74GliosarcomaEnrichmentEGFR1.98
75Gastroesophageal refluxEnrichmentRPS6KA31.98
76Orthostatic intoleranceEnrichmentRPS6KA31.98
77Giant cell glioblastomaEnrichmentEGFR1.95
78Ventricular septal defectEnrichmentRPS6KA31.93
79Pancreatic cancerEnrichmentKRAS1.78
80Hydrops fetalis, nonimmuneEnrichmentHRAS1.77
81Heart, malformation ofEnrichmentMAPK11.63
82Gastric cancerEnrichmentKRAS1.55
83Hereditary breast carcinomaEnrichmentKRAS1.54
84Hereditary breast ovarian cancer syndromeEnrichmentKRAS1.44
85Myeloma, multipleEnrichmentKRAS1.44
86Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA31.33
87Breast cancerEnrichmentKRAS1.31
88Colorectal cancerEnrichmentNRAS1.25
89HypertelorismEnrichmentRPS6KA31.17
90Inherited cancer-predisposing syndromeEnrichmentEGFR1.07
91MicrocephalyEnrichmentMAPK10.82

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