RAF-independent MAPK1/3 activation

Pathway network for the RAF-independent MAPK1/3 activation SuperPath

Sources:
  • Reactome

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

Disorders associated with RAF-independent MAPK1/3 activation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK25.93
2Noonan syndrome and noonan-related syndromeEnrichmentMAP2K1, MAP2K2, PTPN115.72
3Noonan syndrome 1EnrichmentMAP2K1, MAP2K2, PTPN115.13
4RasopathyEnrichmentMAP2K1, MAP2K2, PTPN114.97
5Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K24.78
6Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K24.78
7Specific learning disabilityEnrichmentMAPK1, PTPN114.67
8Noonan syndrome 13EnrichmentMAPK13.29
9Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP63.29
10MetachondromatosisEnrichmentPTPN113.18
11Immunodeficiency 35EnrichmentTYK23.18
12Leopard syndrome 1EnrichmentPTPN113.18
13Stuve-wiedemann syndrome 2EnrichmentIL6ST3.18
14Hyper-ige syndrome 4a, autosomal dominant, with recurrent infectionsEnrichmentIL6ST3.18
15Interleukin 6, serum level of, quantitative trait locusEnrichmentIL6R3.18
16Soluble interleukin-6 receptor, serum level of, quantitative trait locusEnrichmentIL6R3.18
17Cardiofaciocutaneous syndrome 4EnrichmentMAP2K23.18
18Hyper-ige syndrome 5, autosomal recessive, with recurrent infectionsEnrichmentIL6R3.18
19Hyper-ige syndrome 4b, autosomal recessive, with recurrent infectionsEnrichmentIL6ST3.18
20Immunodeficiency 94 with autoinflammation and dysmorphic faciesEnrichmentIL6ST3.18
21Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK13.18
22Malignant astrocytomaEnrichmentPTPN113.18
23Melorheostosis, isolatedEnrichmentMAP2K13.13
24Cardiofaciocutaneous syndrome 3EnrichmentMAP2K13.13
25MelorheostosisEnrichmentMAP2K13.13
26Thrombocythemia 3EnrichmentJAK22.88
27Werner syndromeEnrichmentPTPN112.88
28Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.88
29PolycythemiaEnrichmentJAK22.88
30Lymphomatoid papulosisEnrichmentTYK22.88
31Hypereosinophilic syndromeEnrichmentJAK22.88
32Tafro syndromeEnrichmentMAP2K22.88
33Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK22.88
34Polycythemia veraEnrichmentJAK22.70
35Stuve-wiedemann syndrome 1EnrichmentIL6ST2.70
36Tricuspid valve insufficiencyEnrichmentPTPN112.70
37Stüve-wiedemann syndromeEnrichmentIL6ST2.70
38Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.69
39Langerhans cell histiocytosisEnrichmentMAP2K12.66
40Kaposi sarcomaEnrichmentIL62.58
41Erythrocytosis, familial, 1EnrichmentJAK22.58
42Budd-chiari syndromeEnrichmentJAK22.58
43Neurofibromatosis-noonan syndromeEnrichmentMAP2K22.58
44Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.58
45Noonan syndrome with multiple lentiginesEnrichmentPTPN112.58
46Systemic-onset juvenile idiopathic arthritisEnrichmentIL62.58
47Autism spectrum disorderEnrichmentMAP2K1, PTPN112.56
48MicrocephalyEnrichmentMAPK1, PTPN112.55
49Rheumatoid arthritis, systemic juvenileEnrichmentIL62.48
50LymphomaEnrichmentPTPN112.48
51Myeloproliferative neoplasmEnrichmentJAK22.48
52Type 1 diabetes mellitusEnrichmentIL62.40
53Patent ductus arteriosusEnrichmentPTPN112.40
54MyelofibrosisEnrichmentJAK22.33
55Noonan syndrome 3EnrichmentPTPN112.33
56Essential thrombocythemiaEnrichmentJAK22.33
57Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K12.29
58Inflammatory bowel disease 1EnrichmentIL62.22
59Leukemia, acute lymphoblastic 3EnrichmentJAK22.22
60Arteriovenous malformationEnrichmentMAP2K12.18
61Pectus excavatumEnrichmentPTPN112.14
62Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K12.13
63EpicanthusEnrichmentPTPN112.10
64Juvenile myelomonocytic leukemiaEnrichmentPTPN112.10
65Congenital long qt syndromeEnrichmentPTPN112.10
66Lung non-small cell carcinomaEnrichmentMAP2K12.09
67Heart, malformation ofEnrichmentMAPK12.03
68Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP62.03
69Kallmann syndromeEnrichmentDUSP61.93
70Patent foramen ovaleEnrichmentPTPN111.93
71Arteriovenous malformations of the brainEnrichmentIL61.90
72ScoliosisEnrichmentPTPN111.80
73Hydrops fetalis, nonimmuneEnrichmentPTPN111.77
74StrabismusEnrichmentPTPN111.75
75Long qt syndrome 1EnrichmentPTPN111.70
76Non-immune hydrops fetalisEnrichmentPTPN111.69
77Leukemia, acute myeloidEnrichmentJAK21.58
78Type 2 diabetes mellitusEnrichmentIL61.56
79Hypertrophic cardiomyopathyEnrichmentPTPN111.55
80ThrombocytopeniaEnrichmentPTPN111.50
81Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.44
82Primary ovarian insufficiencyEnrichmentJAK21.41
83Inherited cancer-predisposing syndromeEnrichmentPTPN111.07

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