MAP kinase activation

Pathway network for the MAP kinase activation SuperPath

Sources:
  • Reactome

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

Disorders associated with MAP kinase activation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chronic mucocutaneous candidiasisEnrichmentIL17F, IL17RA, IL17RC5.57
2Melanoma of soft tissueEnrichmentATF1, CREB14.20
3Specific learning disabilityEnrichmentMAPK1, RPS6KA32.94
4Incontinentia pigmentiEnrichmentIKBKG2.93
5Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.93
6Melorheostosis, isolatedEnrichmentMAP2K12.93
7Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.93
8Fetal encasement syndromeEnrichmentCHUK2.93
9Immunodeficiency 15bEnrichmentIKBKB2.93
10Immunodeficiency 15aEnrichmentIKBKB2.93
11Neurodevelopmental, jaw, eye, and digital syndromeEnrichmentFBXW112.93
12Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.93
13MelorheostosisEnrichmentMAP2K12.93
14Bartsocas-papas syndrome 2EnrichmentCHUK2.93
15Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.93
16Immunodeficiency 33EnrichmentIKBKG2.63
17Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.63
18Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG2.63
19Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.63
20Common variable immunodeficiency 12EnrichmentNFKB12.63
21Submucosal cleft palateEnrichmentUBB2.63
22Cleft hard palateEnrichmentUBB2.63
23Uvula, bifidEnrichmentUBB2.45
24Langerhans cell histiocytosisEnrichmentMAP2K12.45
25Cleft soft palateEnrichmentUBB2.45
26Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.33
27Coffin-lowry syndromeEnrichmentRPS6KA32.33
28Blau syndromeEnrichmentNOD22.33
29Frontometaphyseal dysplasia 2EnrichmentMAP3K72.33
30Noonan syndrome 13EnrichmentMAPK12.33
31Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.33
32Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.33
33Houge-janssens syndrome 2EnrichmentPPP2R1A2.33
34Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.33
35Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP62.33
36Macular dystrophy, patterned, 3EnrichmentMAPKAPK32.33
37Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.33
385q14.3 microdeletion syndromeEnrichmentMEF2C2.33
39Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.33
40Mef2c-related disorderEnrichmentMEF2C2.33
41Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A2.33
42Polyvalvular heart disease syndromeEnrichmentTAB22.33
43Cardiofaciocutaneous syndrome 1EnrichmentMAP2K12.33
44Cardiofaciocutaneous syndromeEnrichmentMAP2K12.33
45MalariaEnrichmentIKBKG, MAPKAPK32.30
46Candidiasis, familial, 6EnrichmentIL17F2.28
47Candidiasis, familial, 9EnrichmentIL17RC2.28
48PsoriasisEnrichmentIL17RA2.28
49Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.23
50Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K12.08
51Common variable immunodeficiencyEnrichmentNFKB12.08
52Scoliosis, isolated 1EnrichmentMAPK72.03
53Histiocytoma, angiomatoid fibrousEnrichmentCREB12.03
54Yao syndromeEnrichmentNOD22.03
55Houge-janssens syndrome 1EnrichmentPPP2R5D2.03
56Congenital heart defects, multiple types, 2EnrichmentTAB22.03
57Houge-janssens syndrome 3EnrichmentPPP2CA2.03
58Crohn's diseaseEnrichmentNOD22.03
59Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.03
60Isolated split hand-split foot malformationEnrichmentBTRC2.03
61Lung cancerEnrichmentMAP3K8, PPP2R1B2.02
62Immunodeficiency 51EnrichmentIL17RA1.98
63Coronary heart disease 5EnrichmentIKBKG1.98
64Arteriovenous malformationEnrichmentMAP2K11.98
65Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.93
66Ciliary dyskinesia, primary, 3EnrichmentNFKB11.93
67Lung non-small cell carcinomaEnrichmentMAP2K11.89
68Pelvic organ prolapseEnrichmentTAB21.86
69Bacteremia 2EnrichmentMAPKAPK31.86
70Frontometaphyseal dysplasiaEnrichmentMAP3K71.86
71Noonan syndrome and noonan-related syndromeEnrichmentMAP2K11.76
72Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.73
73Congenital generalized lipodystrophyEnrichmentFOS1.73
74TuberculosisEnrichmentMAPKAPK31.73
75Pediatric systemic lupus erythematosusEnrichmentIRAK11.73
76Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.64
77Histiocytoid hemangiomaEnrichmentFOS1.64
78Noonan syndrome 1EnrichmentMAP2K11.57
79RasopathyEnrichmentMAP2K11.52
80Gastroesophageal refluxEnrichmentRPS6KA31.44
81Orthostatic intoleranceEnrichmentRPS6KA31.44
82Lennox-gastaut syndromeEnrichmentMAPK101.44
83Severe combined immunodeficiencyEnrichmentIKBKB1.42
84Inflammatory bowel disease 1EnrichmentNOD21.39
85Ventricular septal defectEnrichmentRPS6KA31.39
86Migraine with or without aura 1EnrichmentTAB21.30
87Aortic valve disease 1EnrichmentTAB21.23
88Heart, malformation ofEnrichmentMAPK11.09
89Patent foramen ovaleEnrichmentTAB21.09
90Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP61.09
91Behcet syndromeEnrichmentNOD21.07
92Autism spectrum disorderEnrichmentMAP2K1, MEF2C1.04
93Kallmann syndromeEnrichmentDUSP60.99
94Autoinflammatory diseaseEnrichmentNOD20.98
95Complex neurodevelopmental disorderEnrichmentFBXW11, PPP2CA0.95
96Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA30.81
97Systemic lupus erythematosusEnrichmentIRAK10.78
98HypertelorismEnrichmentRPS6KA30.67
99Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.63
100Breast cancerEnrichmentJUN0.53
101Dilated cardiomyopathyEnrichmentTAB20.51
102MicrocephalyEnrichmentMAPK10.36

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