MAPK targets/ Nuclear events mediated by MAP kinases

Pathway network for the MAPK targets/ Nuclear events mediated by MAP kinases SuperPath

Sources:
  • Reactome

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

Disorders associated with MAPK targets/ Nuclear events mediated by MAP kinases SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Melanoma of soft tissueEnrichmentATF1, CREB16.16
2Specific learning disabilityEnrichmentMAPK1, RPS6KA33.86
3Coffin-lowry syndromeEnrichmentRPS6KA33.29
4Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA33.29
5Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA33.29
6Noonan syndrome 13EnrichmentMAPK13.02
7Houge-janssens syndrome 2EnrichmentPPP2R1A3.02
8Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP63.02
9Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A3.02
10Histiocytoma, angiomatoid fibrousEnrichmentCREB12.99
11Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.79
12Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.79
135q14.3 microdeletion syndromeEnrichmentMEF2C2.79
14Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.79
15Mef2c-related disorderEnrichmentMEF2C2.79
16Scoliosis, isolated 1EnrichmentMAPK72.72
17Houge-janssens syndrome 1EnrichmentPPP2R5D2.72
18Houge-janssens syndrome 3EnrichmentPPP2CA2.72
19Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.42
20Gastroesophageal refluxEnrichmentRPS6KA32.38
21Orthostatic intoleranceEnrichmentRPS6KA32.38
22Ventricular septal defectEnrichmentRPS6KA32.33
23Congenital generalized lipodystrophyEnrichmentFOS2.04
24Histiocytoid hemangiomaEnrichmentFOS1.94
25Heart, malformation ofEnrichmentMAPK11.77
26Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP61.77
27Lennox-gastaut syndromeEnrichmentMAPK101.74
28Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA31.73
29Kallmann syndromeEnrichmentDUSP61.66
30HypertelorismEnrichmentRPS6KA31.58
31Lung cancerEnrichmentPPP2R1B1.52
32Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C1.05
33MicrocephalyEnrichmentMAPK10.95
34Complex neurodevelopmental disorderEnrichmentPPP2CA0.95
35Breast cancerEnrichmentJUN0.80
36Autism spectrum disorderEnrichmentMEF2C0.79

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