Signal transduction_JNK pathway

No Pathway Network information available for Signal transduction_JNK pathway

Pathways in the Signal transduction_JNK pathway SuperPath

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

Disorders associated with Signal transduction_JNK pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome 1EnrichmentHRAS, RAF1, SOS1, SOS26.09
2Noonan syndrome 3EnrichmentHRAS, RAF1, SOS15.96
3RasopathyEnrichmentHRAS, RAF1, SOS1, SOS25.86
4Noonan syndrome and noonan-related syndromeEnrichmentHRAS, RAF1, SOS14.85
5Autoimmune lymphoproliferative syndromeEnrichmentFAS, FASLG4.21
6Lung cancerEnrichmentFAS, FASLG, MAP3K83.83
7Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.55
8Lip and oral cavity carcinomaEnrichmentHRAS, TP533.18
946,xy partial gonadal dysgenesisEnrichmentMAP3K1, SOS13.04
10RhabdomyosarcomaEnrichmentHRAS, TP532.92
11Behcet syndromeEnrichmentFAS, TNFRSF1A2.77
12Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.49
13Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.49
14Noonan syndrome 5EnrichmentRAF12.49
15Noonan syndrome 4EnrichmentSOS12.49
16Cardiomyopathy, dilated, 1nnEnrichmentRAF12.49
17Noonan syndrome 9EnrichmentSOS22.49
1846,xy sex reversal 6EnrichmentMAP3K12.49
19Frontometaphyseal dysplasia 2EnrichmentMAP3K72.49
20Bone marrow failure syndrome 5EnrichmentTP532.49
21Papilloma of choroid plexusEnrichmentTP532.49
22Basal cell carcinoma 7EnrichmentTP532.49
23Anaplastic thyroid carcinomaEnrichmentTP532.49
24Leopard syndrome 2EnrichmentRAF12.49
25Multiple sclerosis 5EnrichmentTNFRSF1A2.49
26Ductal carcinoma in situEnrichmentTP532.49
27Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.49
28Takenouchi-kosaki syndromeEnrichmentCDC422.49
29TrigonitisEnrichmentRAF12.49
30Thyroid gland undifferentiated carcinomaEnrichmentTP532.49
31Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.49
32Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.49
33Cerebral cavernous malformations 5EnrichmentMAP3K32.49
34Choroid plexus cancerEnrichmentTP532.49
35Nocarh syndromeEnrichmentCDC422.49
36Pleomorphic xanthoastrocytomaEnrichmentTP532.49
37Phakomatosis pigmentokeratoticaEnrichmentHRAS2.49
38Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.49
39Verrucous hemangiomaEnrichmentMAP3K32.49
40Bladder cancerEnrichmentHRAS, TP532.40
41Fibromatosis, gingival, 1EnrichmentSOS12.19
42Adrenocortical carcinoma, hereditaryEnrichmentTP532.19
43Costello syndromeEnrichmentHRAS2.19
44Cervical cancerEnrichmentTP532.19
45Pulmonic stenosisEnrichmentSOS12.19
46Lymphoma, hodgkin, classicEnrichmentTP532.19
47Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.19
48Immunodeficiency 127EnrichmentTNF2.19
49Congenital fibrosarcomaEnrichmentTP532.19
50Li-fraumeni syndrome 1EnrichmentTP532.19
51SarcomaEnrichmentTP532.19
52Cervix carcinomaEnrichmentTP532.19
53Immune system diseaseEnrichmentCDC422.19
54Hodgkin's lymphomaEnrichmentTP532.19
55Intermittent hydrarthrosisEnrichmentTNFRSF1A2.19
56Pleomorphic rhabdomyosarcomaEnrichmentTP532.19
57Wooly hair nevusEnrichmentHRAS2.19
58Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.01
59Nuchal bleb, familialEnrichmentSOS12.01
60Osteogenic sarcomaEnrichmentTP532.01
61Psoriatic arthritisEnrichmentTNF2.01
62Nasopharyngeal carcinomaEnrichmentTP532.01
63Anus, imperforateEnrichmentMAP4K42.01
64Large congenital melanocytic nevusEnrichmentHRAS2.01
65Atypical teratoid rhabdoid tumorEnrichmentTP532.01
66Anaplastic astrocytomaEnrichmentTP532.01
67Frontometaphyseal dysplasiaEnrichmentMAP3K72.01
68Squamous cell carcinomaEnrichmentTP532.01
69AdenocarcinomaEnrichmentTP532.01
70Migraine without auraEnrichmentTNF2.01
71Bone osteosarcomaEnrichmentTP532.01
72SpermatocytomaEnrichmentHRAS2.01
73Vogt-koyanagi-harada diseaseEnrichmentFAS2.01
74Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.89
75Small cell cancer of the lungEnrichmentTP531.89
76Thyroid cancer, nonmedullary, 1EnrichmentTP531.89
77Lung sarcomatoid carcinomaEnrichmentTP531.89
78Embryonal rhabdomyosarcomaEnrichmentTP531.89
79Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC421.89
80Noonan syndrome with multiple lentiginesEnrichmentRAF11.89
81Epidermolytic nevusEnrichmentHRAS1.89
82Cerebral malariaEnrichmentTNF1.89
83Gingival fibromatosisEnrichmentSOS11.89
84Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.89
85Rhabdomyosarcoma 2EnrichmentTP531.79
86LymphomaEnrichmentTP531.79
87Vascular dementiaEnrichmentTNF1.79
88Acute megakaryocytic leukemiaEnrichmentTP531.79
89Li-fraumeni syndromeEnrichmentTP531.71
90Adrenocortical carcinomaEnrichmentTP531.71
91Breast adenocarcinomaEnrichmentTP531.71
92Esophageal cancerEnrichmentTP531.65
93Nevus, epidermalEnrichmentHRAS1.65
94Multiple endocrine neoplasia, type iEnrichmentMAP4K21.65
95Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.65
96Squamous cell carcinoma, head and neckEnrichmentTP531.65
97Essential thrombocythemiaEnrichmentTP531.65
98Gallbladder cancerEnrichmentTP531.65
99Pilomyxoid astrocytomaEnrichmentRAF11.65
100Follicular thyroid carcinomaEnrichmentHRAS1.65
101B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.65
102Breast cancerEnrichmentJUN, TP531.61
103Glioma susceptibility 1EnrichmentTP531.59
104Renal hypodysplasia/aplasia 1EnrichmentMAP4K41.59
105Lymphoma, non-hodgkin, familialEnrichmentTP531.59
106Lennox-gastaut syndromeEnrichmentMAPK101.59
107Charge syndromeEnrichmentTNFRSF1A1.54
108Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.54
109Arteriovenous malformationEnrichmentHRAS1.54
110Adult hepatocellular carcinomaEnrichmentTP531.54
111Primary hyperaldosteronismEnrichmentTP531.54
112Leukemia, chronic lymphocyticEnrichmentTP531.50
113Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.50
114Familial colorectal cancerEnrichmentTP531.50
115AsthmaEnrichmentTNF1.45
116Myelodysplastic syndromeEnrichmentTP531.45
11746,xy complete gonadal dysgenesisEnrichmentMAP3K11.45
118Lung non-small cell carcinomaEnrichmentHRAS1.45
119Aortic valve disease 1EnrichmentSOS11.38
120Alzheimer's diseaseEnrichmentTNF1.38
121Ovarian cancerEnrichmentMAP3K1, TP531.37
122Multiple sclerosisEnrichmentTNFRSF1A1.35
123Lung cancer susceptibility 3EnrichmentTP531.35
124GliosarcomaEnrichmentTP531.30
125Giant cell glioblastomaEnrichmentTP531.27
126Arteriovenous malformations of the brainEnrichmentMAP4K41.22
127Diffuse large b-cell lymphomaEnrichmentTP531.22
128HepatoblastomaEnrichmentTP531.18
129Inherited cancer-predisposing syndromeEnrichmentMAP4K2, TP531.17
130Hepatocellular carcinomaEnrichmentTP531.16
131Diamond-blackfan anemia 1EnrichmentTP531.14
132MalariaEnrichmentTNF1.14
133Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.12
134Autoinflammatory diseaseEnrichmentTNFRSF1A1.12
135Pancreatic cancerEnrichmentTP531.11
136Hydrops fetalis, nonimmuneEnrichmentHRAS1.09
137Prostate cancerEnrichmentTP531.05
138Differentiated thyroid carcinomaEnrichmentHRAS1.05
139Non-immune hydrops fetalisEnrichmentHRAS1.02
140Familial hypertrophic cardiomyopathyEnrichmentRAF10.99
141Left ventricular noncompactionEnrichmentRAF10.97
142Diamond-blackfan anemiaEnrichmentTP530.96
143Systemic lupus erythematosusEnrichmentTNF0.92
144Leukemia, acute myeloidEnrichmentTP530.91
145Gastric cancerEnrichmentTP530.88
146Hereditary breast carcinomaEnrichmentTP530.87
147Familial isolated dilated cardiomyopathyEnrichmentRAF10.80
148Hereditary breast ovarian cancer syndromeEnrichmentTP530.79
149Myeloma, multipleEnrichmentTP530.78
150Dilated cardiomyopathyEnrichmentRAF10.64
151Colorectal cancerEnrichmentTP530.61

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