IL-26 signaling pathways

No Pathway Network information available for IL-26 signaling pathways

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

Disorders associated with IL-26 signaling pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Il10-related early-onset inflammatory bowel diseaseEnrichmentIL10, IL10RB, TGFB16.50
2Cerebral malariaEnrichmentICAM1, TNF4.41
3Inflammatory bowel disease 25, autosomal recessiveEnrichmentIL10RB, TGFB14.02
4Alzheimer's diseaseEnrichmentMPO, TNF3.30
5MalariaEnrichmentICAM1, TNF2.80
6PycnodysostosisEnrichmentCTSK2.59
7Dermatitis, atopic, 4EnrichmentSOCS32.59
8Graft-versus-host diseaseEnrichmentIL102.59
9T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.59
10Immunodeficiency 42EnrichmentRORC2.59
11Immunodeficiency 31aEnrichmentSTAT12.59
12Loeys-dietz syndrome 6EnrichmentSMAD22.59
13Immunodeficiency 31bEnrichmentSTAT12.59
14Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.59
15Congenital heart defects, multiple types, 8, with or without heterotaxyEnrichmentSMAD22.59
16Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.59
17Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.59
18Systemic lupus erythematosusEnrichmentIL10, TNF2.35
19Camurati-engelmann disease 1EnrichmentTGFB12.29
20Aortic aneurysm, familial thoracic 2EnrichmentACTA22.29
21Smooth muscle dysfunction syndromeEnrichmentACTA22.29
22Aortic aneurysm, familial thoracic 6EnrichmentACTA22.29
23Moyamoya disease 5EnrichmentACTA22.29
24Osteopetrosis, autosomal recessive 2EnrichmentTNFSF112.29
25Immunodeficiency 31cEnrichmentSTAT12.29
26Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.29
27Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.29
28Immunodeficiency 127EnrichmentTNF2.29
29Rela fusion-positive ependymomaEnrichmentRELA2.29
30Recessive dystrophic epidermolysis bullosaEnrichmentMMP12.29
31Camurati-engelmann diseaseEnrichmentTGFB12.29
32Metaphyseal anadysplasia 2EnrichmentMMP92.29
33Metaphyseal anadysplasiaEnrichmentMMP92.29
34Familial thoracic aortic aneurysm and aortic dissectionEnrichmentACTA2, SMAD22.24
35Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.11
36Psoriatic arthritisEnrichmentTNF2.11
37Nail disorder, nonsyndromic congenital, 9EnrichmentCTSK2.11
38Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT32.11
39Hyper ige syndromeEnrichmentSTAT32.11
40Loeys-dietz syndrome 1EnrichmentSMAD22.11
41Inflammatory bowel disease 25EnrichmentIL10RB2.11
42Myxoid liposarcomaEnrichmentDDIT32.11
43T-cell acute lymphoblastic leukemiaEnrichmentBAX2.11
44Migraine without auraEnrichmentTNF2.11
45Kaposi sarcomaEnrichmentIL61.99
46Myeloperoxidase deficiencyEnrichmentMPO1.99
47Autoimmune lymphoproliferative syndromeEnrichmentACTA21.99
48Hepatitis bEnrichmentIL10RB1.99
49Autosomal recessive osteopetrosisEnrichmentTNFSF111.99
50Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.99
51Rheumatoid arthritis, systemic juvenileEnrichmentIL61.89
52Vascular dementiaEnrichmentTNF1.89
53Moyamoya disease 1EnrichmentACTA21.81
54Type 1 diabetes mellitusEnrichmentIL61.81
55Chronic mucocutaneous candidiasisEnrichmentSTAT11.81
56Alzheimer's disease 1EnrichmentMPO1.75
57Permanent neonatal diabetes mellitusEnrichmentSTAT31.69
58Rheumatoid arthritisEnrichmentIL101.64
59Inflammatory bowel disease 1EnrichmentIL61.64
60Mitochondrial myopathy, infantile, transientEnrichmentMT-CO21.64
61Loeys-dietz syndromeEnrichmentSMAD21.64
62Familial colorectal cancerEnrichmentMT-CO21.59
63Mitochondrial myopathy with reversible cytochrome c oxidase deficiencyEnrichmentMT-CO21.59
64Primary bone dysplasiaEnrichmentCTSK1.59
65AsthmaEnrichmentTNF1.55
66OsteochondrodysplasiaEnrichmentCTSK1.55
67Acute promyelocytic leukemiaEnrichmentSTAT31.48
68Lung cancer susceptibility 3EnrichmentACTA21.45
69Cox deficiency, benign infantile mitochondrial myopathyEnrichmentMT-CO21.45
70Alzheimer disease, familial, 1EnrichmentMPO1.37
71Human immunodeficiency virus type 1EnrichmentIL101.34
72Arteriovenous malformations of the brainEnrichmentIL61.32
73Behcet syndromeEnrichmentIL101.32
74Diffuse large b-cell lymphomaEnrichmentSTAT31.32
75Mitochondrial complex iv deficiency, nuclear type 1EnrichmentMT-CO21.26
76ScoliosisEnrichmentCTSK1.22
77Tetralogy of fallotEnrichmentMT-CO21.19
78Mitochondrial complex v deficiency, mitochondrial type 1EnrichmentMT-CO21.19
79Neuropathy, ataxia, and retinitis pigmentosaEnrichmentMT-CO21.19
80Striatonigral degeneration, infantile, mitochondrialEnrichmentMT-CO21.19
81Camptodactyly of fingersEnrichmentMT-CO21.19
82Severe covid-19EnrichmentIL10RB1.14
83Lung cancerEnrichmentACTA21.10
84Cystic fibrosisEnrichmentTGFB11.10
85Connective tissue diseaseEnrichmentACTA21.10
86Leber hereditary optic neuropathy, modifier ofEnrichmentMT-CO21.04
87Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodesEnrichmentMT-CO21.03
88Type 2 diabetes mellitusEnrichmentIL60.99
89Gastric cancerEnrichmentIL1B0.98
90HypertelorismEnrichmentMT-CO20.90
91Leigh syndrome, nuclearEnrichmentMT-CO20.79
92Leigh diseaseEnrichmentMT-CO20.75
93Colorectal cancerEnrichmentBAX0.69
94Mitochondrial diseaseEnrichmentMT-CO20.69
95Leber plus diseaseEnrichmentMT-CO20.66
96Retinitis pigmentosaEnrichmentMT-CO20.37

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