Signaling downstream of RAS mutants

Pathway network for the Signaling downstream of RAS mutants SuperPath

Sources:
  • Reactome

Pathways in the Signaling downstream of RAS mutants SuperPath

#NameSourceGenes
1Signaling downstream of RAS mutantsReactome
2Signaling by RAS mutantsReactome
3Signaling by moderate kinase activity BRAF mutantsReactome
4Paradoxical activation of RAF signaling by kinase inactive BRAFReactome
5Signaling by RAF1 mutantsReactome
6Negative regulation of MAPK pathwayReactome
7MAP2K and MAPK activationReactome
8RAF activationReactome
9Signaling by high-kinase activity BRAF mutantsReactome

Gene overlap in member pathways for Signaling downstream of RAS mutants SuperPath

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

Disorders associated with Signaling downstream of RAS mutants SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome 1Direct
2Costello syndromeDirect
3Noonan syndrome with multiple lentiginesDirect
4Hypertrophic cardiomyopathyDirect
5RasopathyEnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, RAF116.00
6Noonan syndrome and noonan-related syndromeEnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, RAF111.21
7Lung non-small cell carcinomaEnrichmentBRAF, HRAS, KRAS, MAP2K1, NRAS10.25
8Cardiofaciocutaneous syndrome 1EnrichmentBRAF, KRAS, MAP2K1, MAP2K210.13
9Cardiofaciocutaneous syndromeEnrichmentBRAF, KRAS, MAP2K1, MAP2K210.13
10Melanocytic nevus syndrome, congenitalEnrichmentBRAF, HRAS, NRAS, RAF18.53
11Langerhans cell histiocytosisEnrichmentBRAF, MAP2K1, NRAS7.77
12Dysfibrinogenemia, congenitalEnrichmentFGA, FGB, FGG7.77
13Familial dysfibrinogenemiaEnrichmentFGA, FGB, FGG7.77
14Familial hypofibrinogenemiaEnrichmentFGA, FGB, FGG7.77
15Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS7.16
16Afibrinogenemia, congenitalEnrichmentFGA, FGB, FGG7.16
17ThrombocytopeniaEnrichmentFGG, ITGA2B, ITGB3, SRC, VWF6.81
18Nevus, epidermalEnrichmentHRAS, KRAS, NRAS6.22
19Thyroid cancer, nonmedullary, 2EnrichmentBRAF, HRAS, NRAS6.22
20Noonan syndrome 3EnrichmentHRAS, KRAS, RAF16.22
21Pilomyxoid astrocytomaEnrichmentBRAF, KRAS, RAF16.22
22Follicular thyroid carcinomaEnrichmentBRAF, HRAS, NRAS6.22
23Differentiated thyroid carcinomaEnrichmentBRAF, HRAS, KRAS, NRAS6.02
24Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM1, CALM2, CALM36.02
25Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS5.16
26Noonan syndrome-like disorder with loose anagen hairEnrichmentPPP1CB, SHOC25.16
27Baraitser-winter cerebrofrontofacial syndromeEnrichmentACTB, ACTG15.16
28Large congenital melanocytic nevusEnrichmentHRAS, NRAS4.69
29Bleeding disorder, platelet-type, 16EnrichmentITGA2B, ITGB34.69
30Arteriovenous malformations of the brainEnrichmentBRAF, IL17RD, KRAS4.65
31Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS4.39
32Long qt syndrome 1EnrichmentCALM1, CALM2, CALM34.18
33Lung cancerEnrichmentBRAF, KRAS, PPP2R1B4.09
34Fetomaternal alloimmune thrombocytopenia 1EnrichmentITGA2B, ITGB33.99
35MyelofibrosisEnrichmentJAK2, SRC3.85
36Capillary malformation-arteriovenous malformation 1EnrichmentKRAS, MAP2K13.85
37Leukemia, chronic myeloidEnrichmentKRAS, NRAS3.85
38Gallbladder cancerEnrichmentBRAF, KRAS3.85
39Glanzmann thrombasthenia 1EnrichmentITGA2B, ITGB33.85
40Leukemia, acute myeloidEnrichmentJAK2, KRAS, NRAS3.80
41Arteriovenous malformationEnrichmentHRAS, MAP2K13.61
42Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K13.52
43Autosomal dominant macrothrombocytopeniaEnrichmentITGA2B, ITGB33.52
44Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS3.35
45Lip and oral cavity carcinomaEnrichmentBRAF, HRAS3.35
46Lung cancer susceptibility 3EnrichmentBRAF, KRAS3.21
47MicrocephalyEnrichmentACTB, ACTG1, CAMK2B, MAPK13.07
48Dandy-walker syndromeEnrichmentBRAF, PPP1CB3.04
49Dilated cardiomyopathyEnrichmentBRAF, RAF1, VCL2.91
50Colorectal cancerEnrichmentBRAF, NRAS, SRC2.81
51Oculoectodermal syndromeEnrichmentKRAS2.58
52Pallister-killian syndromeEnrichmentARAF2.58
53Noonan syndrome 5EnrichmentRAF12.58
54Melorheostosis, isolatedEnrichmentMAP2K12.58
55Noonan syndrome 7EnrichmentBRAF2.58
56Leopard syndrome 3EnrichmentBRAF2.58
57Cardiomyopathy, dilated, 1nnEnrichmentRAF12.58
58Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.58
59Melanosis, neurocutaneousEnrichmentNRAS2.58
60Noonan syndrome 6EnrichmentNRAS2.58
61Noonan syndrome 11EnrichmentMRAS2.58
62Intellectual developmental disorder, autosomal recessive 63EnrichmentCAMK2A2.58
63Intellectual developmental disorder, autosomal dominant 54EnrichmentCAMK2B2.58
64Houge-janssens syndrome 4EnrichmentPPP2R5C2.58
65Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.58
66Houge-janssens syndrome 2EnrichmentPPP2R1A2.58
67LymphangiomaEnrichmentBRAF2.58
68Noonan syndrome-like disorder with loose anagen hair 1EnrichmentSHOC22.58
69Phace associationEnrichmentBRAF2.58
70MelorheostosisEnrichmentMAP2K12.58
71Leopard syndrome 2EnrichmentRAF12.58
72Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.58
73Long qt syndrome 16EnrichmentCALM32.58
74Visual impairment and progressive phthisis bulbiEnrichmentMARK32.58
75Thrombocytopenia 6EnrichmentSRC2.58
76Noonan syndrome-like disorder with loose anagen hair 2EnrichmentPPP1CB2.58
77Intellectual developmental disorder, autosomal dominant 53EnrichmentCAMK2A2.58
78TrigonitisEnrichmentRAF12.58
79Intellectual developmental disorder, autosomal dominant 59EnrichmentCAMK2G2.58
80Long qt syndrome 15EnrichmentCALM22.58
81Congenital pulmonary airway malformationEnrichmentKRAS2.58
82Syringocystadenoma papilliferumEnrichmentBRAF2.58
83GangliogliomaEnrichmentBRAF2.58
84Nongerminomatous germ cell tumorEnrichmentBRAF2.58
85Phace syndromeEnrichmentBRAF2.58
86Phakomatosis pigmentokeratoticaEnrichmentHRAS2.58
87Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A2.58
88Classic hairy cell leukemiaEnrichmentBRAF2.58
89Neurocutaneous melanocytosisEnrichmentNRAS2.58
90Von willebrand disease, type 1EnrichmentVWF2.58
91Baraitser-winter syndrome 1EnrichmentACTB2.58
92Von willebrand disease, type 2EnrichmentVWF2.58
93Noonan syndrome 13EnrichmentMAPK12.58
94Intellectual developmental disorder, x-linked, syndromic, houge typeEnrichmentCNKSR22.58
95Von willebrand disease, type 3EnrichmentVWF2.58
96Fetomaternal alloimmune thrombocytopenia 2EnrichmentITGA2B2.58
97Congenital smooth muscle hamartoma, with or without hemihypertrophyEnrichmentACTB2.58
98Cardiomyopathy, dilated, 1wEnrichmentVCL2.58
99Becker nevus syndromeEnrichmentACTB2.58
100Dystonia-deafness syndrome 1EnrichmentACTB2.58
101Cardiomyopathy, familial hypertrophic, 15EnrichmentVCL2.58
102Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic faciesEnrichmentRAP1B2.58
103Von willebrand's diseaseEnrichmentVWF2.58
104Thrombocytopenia 8, with dysmorphic features and developmental delayEnrichmentACTB2.58
105Baraitser-winter syndromeEnrichmentACTB2.58
106Congenital fibrinogen deficiencyEnrichmentFGG2.58
107Congenital smooth muscle hamartomaEnrichmentACTB2.58
108Capillary leak syndromeEnrichmentTLN12.58
109Developmental malformations-deafness-dystonia syndromeEnrichmentACTB2.58
110Bladder cancerEnrichmentHRAS, KRAS2.58
111Immunodeficiency due to defect in mapbp-interacting proteinEnrichmentLAMTOR22.53
112Hypogonadotropic hypogonadism 18 with or without anosmiaEnrichmentIL17RD2.53
113Primary immunodeficiency syndrome due to p14 deficiencyEnrichmentLAMTOR22.53
114Long qt syndromeEnrichmentCALM1, CALM22.52
115Non-immune hydrops fetalisEnrichmentHRAS, KRAS2.52
116Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP62.50
117Pulmonic stenosisEnrichmentBRAF2.28
118Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM12.28
119Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.28
120Thrombocythemia 3EnrichmentJAK22.28
121Long qt syndrome 14EnrichmentCALM12.28
122Houge-janssens syndrome 1EnrichmentPPP2R5D2.28
123PolycythemiaEnrichmentJAK22.28
124Houge-janssens syndrome 3EnrichmentPPP2CA2.28
125Hypereosinophilic syndromeEnrichmentJAK22.28
126Tafro syndromeEnrichmentMAP2K22.28
127Wooly hair nevusEnrichmentHRAS2.28
128Spondyloepimetaphyseal dysplasia, strudwick typeEnrichmentFN12.28
129Spondylometaphyseal dysplasia, corner fracture typeEnrichmentFN12.28
130Deafness, autosomal dominant 20EnrichmentACTG12.28
131Baraitser-winter syndrome 2EnrichmentACTG12.28
132Neurodevelopmental disorder with variable familial hypercholanemiaEnrichmentWDR832.23
133Submucosal cleft palateEnrichmentUBB2.20
134Cleft hard palateEnrichmentUBB2.20
135Autosomal dominant non-syndromic intellectual disabilityEnrichmentCAMK2A, CAMK2B2.11
136Ataxia-telangiectasiaEnrichmentBRAF2.10
137Polycythemia veraEnrichmentJAK22.10
138Tethered spinal cord syndromeEnrichmentBRAF2.10
139Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK22.10
140Polycystic kidney disease 4EnrichmentSHOC22.10
141SpermatocytomaEnrichmentHRAS2.10
142Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentITGB32.10
143Periventricular nodular heterotopia 1EnrichmentVWF2.10
144Glomerulopathy with fibronectin deposits 2EnrichmentFN12.10
145Bleeding disorder, platelet-type, 24EnrichmentITGB32.10
146Familial isolated dilated cardiomyopathyEnrichmentRAF1, VCL2.06
147Uvula, bifidEnrichmentUBB2.02
148Cleft soft palateEnrichmentUBB2.02
149Myeloma, multipleEnrichmentBRAF, KRAS2.02
150Erythrocytosis, familial, 1EnrichmentJAK21.98
151Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS1.98
152Thyroid cancer, nonmedullary, 1EnrichmentBRAF1.98
153Budd-chiari syndromeEnrichmentJAK21.98
154Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.98
155Lung sarcomatoid carcinomaEnrichmentKRAS1.98
156CraniopharyngiomaEnrichmentBRAF1.98
157Pilocytic astrocytomaEnrichmentKRAS1.98
158Newborn respiratory distress syndromeEnrichmentBRAF1.98
159Epidermolytic nevusEnrichmentHRAS1.98
160Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.98
161Aminoacylase 1 deficiencyEnrichmentACTB1.98
162Pseudomyogenic hemangioendotheliomaEnrichmentACTB1.98
163CholangiocarcinomaEnrichmentPTPN31.90
164Polycystic kidney disease 3 with or without polycystic liver diseaseEnrichmentSHOC21.88
165Myeloproliferative neoplasmEnrichmentJAK21.88
166Amyloidosis, hereditary systemic 2EnrichmentFGA1.88
167Glanzmann thrombasthenia 2EnrichmentITGB31.88
168Coloboma of choroid and retinaEnrichmentACTG11.88
169Wilms tumor 5EnrichmentBRAF1.80
170Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.80
171Breast adenocarcinomaEnrichmentKRAS1.80
172Lung squamous cell carcinomaEnrichmentKRAS1.80
173Breast cancerEnrichmentKRAS, PHB11.77
174Familial hypercholanemiaEnrichmentWDR831.76
175Essential thrombocythemiaEnrichmentJAK21.73
176Thrombophilia due to thrombin defectEnrichmentFGA1.73
177Polycystic kidney disease 4 with or without polycystic liver diseaseEnrichmentSHOC21.68
178Lymphoma, non-hodgkin, familialEnrichmentBRAF1.68
179Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.68
180Spastic paraplegia 4, autosomal dominantEnrichmentFGG1.68
181Cardiomyopathy, familial hypertrophic, 4EnrichmentBRAF1.63
182Leukemia, acute lymphoblastic 3EnrichmentJAK21.63
183Primary hyperaldosteronismEnrichmentBRAF1.63
184Ventricular septal defectEnrichmentBRAF1.63
185MelanomaEnrichmentBRAF1.58
186Cat eye syndromeEnrichmentACTG11.58
187Pectus excavatumEnrichmentSHOC21.54
188Specific learning disabilityEnrichmentMAPK11.54
189Protein-deficiency anemiaEnrichmentNRAS1.47
190OsteoporosisEnrichmentSRC1.44
191Wilms tumor 1EnrichmentBRAF1.41
192Lynch syndromeEnrichmentKRAS1.41
193RhabdomyosarcomaEnrichmentHRAS1.38
194Melanoma, cutaneous malignant 1EnrichmentBRAF1.35
195Sudden infant death syndromeEnrichmentCALM21.35
196Heart, malformation ofEnrichmentMAPK11.33
197Diffuse large b-cell lymphomaEnrichmentBRAF1.31
198LissencephalyEnrichmentACTG11.27
199Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP61.26
200Myocardial infarctionEnrichmentITGB31.25
201Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.21
202Pancreatic cancerEnrichmentKRAS1.19
203Kallmann syndromeEnrichmentIL17RD1.18
204Hydrops fetalis, nonimmuneEnrichmentHRAS1.18
205Familial hypertrophic cardiomyopathyEnrichmentRAF11.08
206CakutEnrichmentACTG11.06
207Left ventricular noncompactionEnrichmentRAF11.05
208DystoniaEnrichmentCAMK2B1.05
209Non-syndromic x-linked intellectual disabilityEnrichmentCNKSR21.04
210Non-syndromic genetic deafnessEnrichmentACTG11.04
211Nonsyndromic hearing lossEnrichmentACTG10.98
212Gastric cancerEnrichmentKRAS0.97
213Nephrotic syndromeEnrichmentFN10.97
214Hereditary breast carcinomaEnrichmentKRAS0.96
215Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentACTG10.89
216Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.87
217Undetermined early-onset epileptic encephalopathyEnrichmentCNKSR20.86
218Primary ovarian insufficiencyEnrichmentJAK20.84
219AutismEnrichmentCAMK2G0.76
220Rare genetic deafnessEnrichmentACTG10.72
221Ovarian cancerEnrichmentKRAS0.63
222Congenital nervous system abnormalityEnrichmentCAMK2B0.61
223Nervous system diseaseEnrichmentCAMK2B0.61
224Autism spectrum disorderEnrichmentMAP2K10.60
225Complex neurodevelopmental disorderEnrichmentPPP2CA0.55

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