MAP Kinase Signaling

No Pathway Network information available for MAP Kinase Signaling

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

Disorders associated with MAP Kinase Signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RasopathyEnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, MRAS, NF1, NRAS, PTPN11, RAF1, SHOC2, SOS110.92
2Noonan syndrome and noonan-related syndromeEnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, PTPN11, RAF1, SHOC2, SOS110.67
3Noonan syndrome 1EnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, MRAS, NRAS, PTPN11, RAF1, RRAS, SHOC2, SOS110.50
4Noonan syndrome 3EnrichmentHRAS, KRAS, PTPN11, RAF1, SOS19.11
5Cardiofaciocutaneous syndrome 1EnrichmentBRAF, KRAS, MAP2K1, MAP2K28.34
6Cardiofaciocutaneous syndromeEnrichmentBRAF, KRAS, MAP2K1, MAP2K28.34
7Lung non-small cell carcinomaEnrichmentBRAF, HRAS, KRAS, MAP2K1, NRAS7.79
8Juvenile myelomonocytic leukemiaEnrichmentKRAS, NF1, NRAS, PTPN11, RRAS7.56
9Melanocytic nevus syndrome, congenitalEnrichmentBRAF, HRAS, NRAS, RAF16.51
10Langerhans cell histiocytosisEnrichmentBRAF, MAP2K1, NRAS6.25
11Specific learning disabilityEnrichmentMAPK1, PTPN11, RPS6KA3, YWHAG5.84
12Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS5.65
13Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC42, PTPN11, YWHAZ5.65
14Noonan syndrome with multiple lentiginesEnrichmentBRAF, PTPN11, RAF15.65
15Nevus, epidermalEnrichmentHRAS, KRAS, NRAS4.72
16Thyroid cancer, nonmedullary, 2EnrichmentBRAF, HRAS, NRAS4.72
17Pilomyxoid astrocytomaEnrichmentBRAF, KRAS, RAF14.72
18Follicular thyroid carcinomaEnrichmentBRAF, HRAS, NRAS4.72
19Pulmonic stenosisEnrichmentBRAF, SOS14.16
20Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS4.16
21Differentiated thyroid carcinomaEnrichmentBRAF, HRAS, KRAS, NRAS4.03
22Large congenital melanocytic nevusEnrichmentHRAS, NRAS3.69
23Neurofibromatosis-noonan syndromeEnrichmentMAP2K2, NF13.39
24Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS3.39
25Pilocytic astrocytomaEnrichmentKRAS, NF13.39
26Arteriovenous malformations of the brainEnrichmentBRAF, KRAS, MAP4K43.31
27Histiocytoid hemangiomaEnrichmentFOS, FOSB3.17
28Capillary malformation-arteriovenous malformation 1EnrichmentKRAS, MAP2K12.85
29Leukemia, chronic myeloidEnrichmentKRAS, NRAS2.85
30Gallbladder cancerEnrichmentBRAF, KRAS2.85
31Bladder cancerEnrichmentHRAS, KRAS, NF12.76
32Non-immune hydrops fetalisEnrichmentHRAS, KRAS, PTPN112.67
33Lung cancerEnrichmentBRAF, KRAS, MAP3K82.63
34Arteriovenous malformationEnrichmentHRAS, MAP2K12.62
35Ventricular septal defectEnrichmentBRAF, RPS6KA32.62
36Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K12.53
37Pectus excavatumEnrichmentPTPN11, SHOC22.44
38Lip and oral cavity carcinomaEnrichmentBRAF, HRAS2.37
39Aortic valve disease 1EnrichmentSOS1, TAB22.30
40Lung cancer susceptibility 3EnrichmentBRAF, KRAS2.23
41RhabdomyosarcomaEnrichmentHRAS, NF12.12
42MetachondromatosisEnrichmentPTPN112.08
43Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.08
44Coffin-lowry syndromeEnrichmentRPS6KA32.08
45Oculoectodermal syndromeEnrichmentKRAS2.08
46Pallister-killian syndromeEnrichmentARAF2.08
47Noonan syndrome 5EnrichmentRAF12.08
48Noonan syndrome 4EnrichmentSOS12.08
49Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosisEnrichmentRAC22.08
50Melorheostosis, isolatedEnrichmentMAP2K12.08
51Noonan syndrome 7EnrichmentBRAF2.08
52Leopard syndrome 3EnrichmentBRAF2.08
53Leopard syndrome 1EnrichmentPTPN112.08
54Cardiomyopathy, dilated, 1nnEnrichmentRAF12.08
55Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.08
56Melanosis, neurocutaneousEnrichmentNRAS2.08
57Iga nephropathy 3EnrichmentSPRY22.08
58Noonan syndrome 6EnrichmentNRAS2.08
59Frontometaphyseal dysplasia 2EnrichmentMAP3K72.08
60Sturge-weber syndromeEnrichmentGNAQ2.08
61Noonan syndrome 11EnrichmentMRAS2.08
62Noonan syndrome 13EnrichmentMAPK12.08
63Neurodevelopmental disorder with structural brain anomalies and dysmorphic faciesEnrichmentRAC32.08
64Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.08
65Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemiaEnrichmentRAC22.08
66Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.08
67Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.08
68Houge-janssens syndrome 2EnrichmentPPP2R1A2.08
69LymphangiomaEnrichmentBRAF2.08
70Noonan syndrome-like disorder with loose anagen hair 1EnrichmentSHOC22.08
71Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.08
72Phace associationEnrichmentBRAF2.08
73Charcot-marie-tooth disease, axonal, type 2fEnrichmentHSPB12.08
74MelorheostosisEnrichmentMAP2K12.08
75Leopard syndrome 2EnrichmentRAF12.08
76Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.08
77Spermatogenic failure 93EnrichmentSTK332.08
78Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP62.08
79Neurocardiofaciodigital syndromeEnrichmentMAPKAPK52.08
80Macular dystrophy, patterned, 3EnrichmentMAPKAPK32.08
81Developmental and epileptic encephalopathy 56EnrichmentYWHAG2.08
82Immunodeficiency 22EnrichmentLCK2.08
83Thrombocytopenia 6EnrichmentSRC2.08
84Takenouchi-kosaki syndromeEnrichmentCDC422.08
85Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.08
86Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopeniaEnrichmentRAC22.08
87TrigonitisEnrichmentRAF12.08
88Plexiform neurofibromaEnrichmentNF12.08
89NeurofibromaEnrichmentNF12.08
90Autoinflammation with pulmonary and cutaneous vasculitisEnrichmentHCK2.08
91Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.08
92NeurofibromatosisEnrichmentNF12.08
935q14.3 microdeletion syndromeEnrichmentMEF2C2.08
94Chromosome 17q11.2 deletion syndromeEnrichmentNF12.08
95Congenital pulmonary airway malformationEnrichmentKRAS2.08
96Cerebral cavernous malformations 5EnrichmentMAP3K32.08
97Optic nerve gliomaEnrichmentNF12.08
98Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.08
99Infantile lad-like disease due to rac2 deficiencyEnrichmentRAC22.08
100Reticular dysgenesis-like severe combined immunodeficiencyEnrichmentRAC22.08
101Nocarh syndromeEnrichmentCDC422.08
102Syringocystadenoma papilliferumEnrichmentBRAF2.08
103Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.08
104GangliogliomaEnrichmentBRAF2.08
105Nongerminomatous germ cell tumorEnrichmentBRAF2.08
106Phace syndromeEnrichmentBRAF2.08
107Phakomatosis pigmentokeratoticaEnrichmentHRAS2.08
108Mef2c-related disorderEnrichmentMEF2C2.08
109Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A2.08
110Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.08
111Classic hairy cell leukemiaEnrichmentBRAF2.08
112Verrucous hemangiomaEnrichmentMAP3K32.08
113Rac2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndromeEnrichmentRAC22.08
114Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.08
115Neurocutaneous melanocytosisEnrichmentNRAS2.08
116Polyvalvular heart disease syndromeEnrichmentTAB22.08
117Malignant astrocytomaEnrichmentPTPN112.08
118Patent foramen ovaleEnrichmentPTPN11, TAB22.02
119Myeloma, multipleEnrichmentBRAF, KRAS, NF11.95
120Autism spectrum disorderEnrichmentMAP2K1, MEF2C, NF1, PTPN111.89
121Cafe-au-lait spots, multipleEnrichmentNF11.78
122Fibromatosis, gingival, 1EnrichmentSOS11.78
123Scoliosis, isolated 1EnrichmentMAPK71.78
124Costello syndromeEnrichmentHRAS1.78
125Encephalocraniocutaneous lipomatosisEnrichmentKRAS1.78
126Neuronopathy, distal hereditary motor, autosomal dominant 3EnrichmentHSPB11.78
127Developmental and epileptic encephalopathy 50EnrichmentCAD1.78
128Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC11.78
129Werner syndromeEnrichmentPTPN111.78
130Chromosome 17q11.2 duplication syndrome, 1.4-mbEnrichmentNF11.78
131Noonan syndrome-like disorder with loose anagen hairEnrichmentSHOC21.78
132Kala-azar 2EnrichmentGSTP11.78
133Congenital heart defects, multiple types, 2EnrichmentTAB21.78
134Bardet-biedl syndrome 9EnrichmentNF11.78
135Immune system diseaseEnrichmentCDC421.78
136Houge-janssens syndrome 3EnrichmentPPP2CA1.78
137Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB21.78
138Pleomorphic rhabdomyosarcomaEnrichmentNF11.78
139Tafro syndromeEnrichmentMAP2K21.78
140Phakomatosis cesioflammeaEnrichmentGNAQ1.78
141Wooly hair nevusEnrichmentHRAS1.78
142Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN111.71
143Pelvic organ prolapseEnrichmentTAB21.61
144Ataxia-telangiectasiaEnrichmentBRAF1.61
145Watson syndromeEnrichmentNF11.61
146Nuchal bleb, familialEnrichmentSOS11.61
147Neurofibromatosis, familial spinalEnrichmentNF11.61
148Chromosome 17q11.2 deletion syndrome, 1.4-mbEnrichmentNF11.61
149Miller-dieker lissencephaly syndromeEnrichmentYWHAE1.61
150Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE1.61
151Anus, imperforateEnrichmentMAP4K41.61
152Tethered spinal cord syndromeEnrichmentBRAF1.61
153Bacteremia 2EnrichmentMAPKAPK31.61
154Polycystic kidney disease 4EnrichmentSHOC21.61
155Frontometaphyseal dysplasiaEnrichmentMAP3K71.61
156Brain cancerEnrichmentNF11.61
157SpermatocytomaEnrichmentHRAS1.61
158Tricuspid valve insufficiencyEnrichmentPTPN111.61
159Anastomosing haemangiomaEnrichmentGNAQ1.61
160Dilated cardiomyopathyEnrichmentBRAF, RAF1, TAB21.54
161Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS1.48
162Thyroid cancer, nonmedullary, 1EnrichmentBRAF1.48
163Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.48
164Congenital generalized lipodystrophyEnrichmentFOS1.48
165Lung sarcomatoid carcinomaEnrichmentKRAS1.48
166Embryonal rhabdomyosarcomaEnrichmentNF11.48
167CraniopharyngiomaEnrichmentBRAF1.48
168TuberculosisEnrichmentMAPKAPK31.48
169Newborn respiratory distress syndromeEnrichmentBRAF1.48
170Epidermolytic nevusEnrichmentHRAS1.48
171Middle aortic syndromeEnrichmentNF11.48
172Gingival fibromatosisEnrichmentSOS11.48
173Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.48
174Colorectal cancerEnrichmentBRAF, NRAS, SRC1.44
175Capillary malformations, congenitalEnrichmentGNAQ1.39
176Neuronopathy, distal hereditary motor, autosomal dominant 2EnrichmentHSPB11.39
177Polycystic kidney disease 3 with or without polycystic liver diseaseEnrichmentSHOC21.39
178Rhabdomyosarcoma 2EnrichmentNF11.39
179LymphomaEnrichmentPTPN111.39
180Endometrial stromal sarcomaEnrichmentYWHAE1.39
181Leukemia, acute myeloidEnrichmentKRAS, NRAS1.36
182Klippel-trenaunay-weber syndromeEnrichmentGNAQ1.31
183Melanoma, uvealEnrichmentGNAQ1.31
184Wilms tumor 5EnrichmentBRAF1.31
185Patent ductus arteriosusEnrichmentPTPN111.31
186Breast adenocarcinomaEnrichmentKRAS1.31
187Lung squamous cell carcinomaEnrichmentKRAS1.31
188Kidney clear cell sarcomaEnrichmentYWHAE1.31
189Gastric cancerEnrichmentKRAS, NF11.30
190Multiple endocrine neoplasia, type iEnrichmentMAP4K21.24
191MyelofibrosisEnrichmentSRC1.24
192ThrombocytopeniaEnrichmentPTPN11, SRC1.22
193Gastroesophageal refluxEnrichmentRPS6KA31.19
194Renal hypodysplasia/aplasia 1EnrichmentMAP4K41.19
195Polycystic kidney disease 4 with or without polycystic liver diseaseEnrichmentSHOC21.19
196Lymphoma, non-hodgkin, familialEnrichmentBRAF1.19
197Orthostatic intoleranceEnrichmentRPS6KA31.19
198Ewing sarcomaEnrichmentNF11.19
199Lennox-gastaut syndromeEnrichmentMAPK101.19
200Neurofibromatosis, type iEnrichmentNF11.14
201Cardiomyopathy, familial hypertrophic, 4EnrichmentBRAF1.14
202Leukemia, acute lymphoblastic 3EnrichmentNF11.14
203Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.14
204Primary hyperaldosteronismEnrichmentBRAF1.14
205Hereditary breast ovarian cancer syndromeEnrichmentKRAS, NF11.11
206MelanomaEnrichmentBRAF1.10
207MicrocephalyEnrichmentMAPK1, PTPN11, YWHAG1.08
208Migraine with or without aura 1EnrichmentTAB21.06
209EpicanthusEnrichmentPTPN111.02
210Congenital long qt syndromeEnrichmentPTPN111.02
211Inherited cancer-predisposing syndromeEnrichmentMAP4K2, NF1, PTPN111.01
212Protein-deficiency anemiaEnrichmentNRAS0.99
213OsteoporosisEnrichmentSRC0.96
214PheochromocytomaEnrichmentNF10.96
21546,xy partial gonadal dysgenesisEnrichmentSOS10.96
216Wilms tumor 1EnrichmentBRAF0.93
217Lynch syndromeEnrichmentKRAS0.93
218Breast cancerEnrichmentJUN, KRAS0.89
219Melanoma, cutaneous malignant 1EnrichmentBRAF0.88
220Dandy-walker syndromeEnrichmentBRAF0.88
221Heart, malformation ofEnrichmentMAPK10.85
222Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP60.85
223Diffuse large b-cell lymphomaEnrichmentBRAF0.83
224Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentNF10.79
225Skin diseaseEnrichmentNF10.77
226MalariaEnrichmentMAPKAPK30.76
227Kallmann syndromeEnrichmentDUSP60.76
228Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF10.74
229ScoliosisEnrichmentPTPN110.74
230Pancreatic cancerEnrichmentKRAS0.72
231Developmental and epileptic encephalopathy 1EnrichmentCAD0.72
232StrabismusEnrichmentPTPN110.69
233Long qt syndrome 1EnrichmentPTPN110.65
234Familial hypertrophic cardiomyopathyEnrichmentRAF10.62
235Severe combined immunodeficiencyEnrichmentLCK0.62
236Left ventricular noncompactionEnrichmentRAF10.60
237Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA30.58
238Complex neurodevelopmental disorderEnrichmentPPP2CA, RAC30.56
239Charcot-marie-tooth diseaseEnrichmentHSPB10.54
240Hypertrophic cardiomyopathyEnrichmentPTPN110.52
241Hereditary breast carcinomaEnrichmentKRAS0.51
242Autosomal dominant non-syndromic intellectual disabilityEnrichmentYWHAZ0.47
243HypertelorismEnrichmentRPS6KA30.45
244Familial isolated dilated cardiomyopathyEnrichmentRAF10.45
245Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.43
246Undetermined early-onset epileptic encephalopathyEnrichmentYWHAG0.43
247Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.41
248Ovarian cancerEnrichmentKRAS0.24

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