Signaling mediated by p38-alpha and p38-beta

No Pathway Network information available for Signaling mediated by p38-alpha and p38-beta

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

Disorders associated with Signaling mediated by p38-alpha and p38-beta SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Melanoma of soft tissueEnrichmentATF1, CREB14.76
2Breast cancerEnrichmentESR1, JUN, TP533.10
3MalariaEnrichmentMAPKAPK3, NOS22.85
4Hyperlipidemia, familial combined, 1EnrichmentUSF12.61
5Heterochromia iridisEnrichmentMITF2.61
6Tietz albinism-deafness syndromeEnrichmentMITF2.61
7Lichtenstein-knorr syndromeEnrichmentSLC9A12.61
8Bone marrow failure syndrome 5EnrichmentTP532.61
9Intellectual developmental disorder, x-linked 41EnrichmentGDI12.61
10Papilloma of choroid plexusEnrichmentTP532.61
11Basal cell carcinoma 7EnrichmentTP532.61
12Autism 19EnrichmentEIF4E2.61
13Anaplastic thyroid carcinomaEnrichmentTP532.61
14Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.61
15Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafnessEnrichmentMITF2.61
16Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.61
17Charcot-marie-tooth disease, axonal, type 2fEnrichmentHSPB12.61
18Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorderEnrichmentPLA2G4A2.61
19Achromatopsia 7EnrichmentATF62.61
20Neurocardiofaciodigital syndromeEnrichmentMAPKAPK52.61
21Macular dystrophy, patterned, 3EnrichmentMAPKAPK32.61
22Ductal carcinoma in situEnrichmentTP532.61
23Gastrointestinal ulceration, recurrent, with dysfunctional plateletsEnrichmentPLA2G4A2.61
24Thyroid gland undifferentiated carcinomaEnrichmentTP532.61
25Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.61
26Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.61
275q14.3 microdeletion syndromeEnrichmentMEF2C2.61
28Choroid plexus cancerEnrichmentTP532.61
29Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.61
30Pleomorphic xanthoastrocytomaEnrichmentTP532.61
31Cryptogenic multifocal ulcerous stenosing enteritisEnrichmentPLA2G4A2.61
32Mef2c-related disorderEnrichmentMEF2C2.61
33Adrenocortical carcinoma, hereditaryEnrichmentTP532.31
34Cervical cancerEnrichmentTP532.31
35Histiocytoma, angiomatoid fibrousEnrichmentCREB12.31
36Neuronopathy, distal hereditary motor, autosomal dominant 3EnrichmentHSPB12.31
37Lymphoma, hodgkin, classicEnrichmentTP532.31
38Melanoma, cutaneous malignant 8EnrichmentMITF2.31
39Papillary renal cell carcinomaEnrichmentMITF2.31
40Congenital fibrosarcomaEnrichmentTP532.31
41Li-fraumeni syndrome 1EnrichmentTP532.31
42SarcomaEnrichmentTP532.31
43Cervix carcinomaEnrichmentTP532.31
44Hodgkin's lymphomaEnrichmentTP532.31
45Pleomorphic rhabdomyosarcomaEnrichmentTP532.31
46Hereditary breast carcinomaEnrichmentESR1, TP532.29
47Waardenburg syndrome, type 2aEnrichmentMITF2.14
48Osteogenic sarcomaEnrichmentTP532.14
49Nasopharyngeal carcinomaEnrichmentTP532.14
50Estrogen resistanceEnrichmentESR12.14
51Bacteremia 2EnrichmentMAPKAPK32.14
52Atypical teratoid rhabdoid tumorEnrichmentTP532.14
53Anaplastic astrocytomaEnrichmentTP532.14
54Myxoid liposarcomaEnrichmentDDIT32.14
55Squamous cell carcinomaEnrichmentTP532.14
56AdenocarcinomaEnrichmentTP532.14
57Migraine without auraEnrichmentESR12.14
58Bone osteosarcomaEnrichmentTP532.14
59Cryptogenic cirrhosisEnrichmentKRT82.14
60Hereditary breast ovarian cancer syndromeEnrichmentMITF, TP532.10
61Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C, PPARGC1A2.06
62Small cell cancer of the lungEnrichmentTP532.01
63Thyroid cancer, nonmedullary, 1EnrichmentTP532.01
64Arthrogryposis multiplex congenita 3, myogenic typeEnrichmentESR12.01
65Lung sarcomatoid carcinomaEnrichmentTP532.01
66Embryonal rhabdomyosarcomaEnrichmentTP532.01
67TuberculosisEnrichmentMAPKAPK32.01
68Clear cell papillary renal cell carcinomaEnrichmentMITF2.01
69Hyperlipidemia, familial combined, 3EnrichmentUSF11.92
70Neuronopathy, distal hereditary motor, autosomal dominant 2EnrichmentHSPB11.92
71Rhabdomyosarcoma 2EnrichmentTP531.92
72LymphomaEnrichmentTP531.92
73Acute megakaryocytic leukemiaEnrichmentTP531.92
74Li-fraumeni syndromeEnrichmentTP531.84
75Waardenburg syndrome, type 4aEnrichmentMITF1.84
76Adrenocortical carcinomaEnrichmentTP531.84
77Breast adenocarcinomaEnrichmentTP531.84
78Waardenburg syndromeEnrichmentMITF1.84
79Esophageal cancerEnrichmentTP531.77
80Waardenburg syndrome, type 1EnrichmentMITF1.77
81Squamous cell carcinoma, head and neckEnrichmentTP531.77
82Waardenburg syndrome, type 2eEnrichmentMITF1.77
83Essential thrombocythemiaEnrichmentTP531.77
84Gallbladder cancerEnrichmentTP531.77
85B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.77
86Glioma susceptibility 1EnrichmentTP531.71
87Lymphoma, non-hodgkin, familialEnrichmentTP531.71
88Adult hepatocellular carcinomaEnrichmentTP531.66
89Primary hyperaldosteronismEnrichmentTP531.66
90Leukemia, chronic lymphocyticEnrichmentTP531.62
91MelanomaEnrichmentMITF1.62
92AchromatopsiaEnrichmentATF61.62
93Familial colorectal cancerEnrichmentTP531.62
94Migraine with or without aura 1EnrichmentESR11.58
95Myelodysplastic syndromeEnrichmentTP531.58
96Lip and oral cavity carcinomaEnrichmentTP531.54
97Lung cancer susceptibility 3EnrichmentTP531.47
98RhabdomyosarcomaEnrichmentTP531.42
99GliosarcomaEnrichmentTP531.42
100Melanoma, cutaneous malignant 1EnrichmentMITF1.39
101Giant cell glioblastomaEnrichmentTP531.39
102Inherited cancer-predisposing syndromeEnrichmentMITF, TP531.39
103Diffuse large b-cell lymphomaEnrichmentTP531.34
104HepatoblastomaEnrichmentTP531.30
105Hepatocellular carcinomaEnrichmentTP531.28
106Myocardial infarctionEnrichmentESR11.28
107Diamond-blackfan anemia 1EnrichmentTP531.26
108Ear malformationEnrichmentMITF1.25
109Pancreatic cancerEnrichmentTP531.23
110Bladder cancerEnrichmentTP531.17
111Prostate cancerEnrichmentTP531.17
112Non-syndromic x-linked intellectual disabilityEnrichmentGDI11.08
113Diamond-blackfan anemiaEnrichmentTP531.08
114Non-syndromic genetic deafnessEnrichmentMITF1.08
115Leukemia, acute myeloidEnrichmentTP531.03
116Charcot-marie-tooth diseaseEnrichmentHSPB11.02
117Nonsyndromic hearing lossEnrichmentMITF1.01
118Gastric cancerEnrichmentTP531.00
119Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentMITF0.92
120Myeloma, multipleEnrichmentTP530.89
121Cone-rod dystrophy 2EnrichmentATF60.82
122Rare genetic deafnessEnrichmentMITF0.76
123Colorectal cancerEnrichmentTP530.72
124Ovarian cancerEnrichmentTP530.66
125Autism spectrum disorderEnrichmentMEF2C0.63
126Hereditary retinal dystrophyEnrichmentATF60.29
127Fundus dystrophyEnrichmentATF60.29

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