TNF signaling

Pathway network for the TNF signaling SuperPath

Sources:
  • Reactome

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

Disorders associated with TNF signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Motor neuron diseaseEnrichmentOPTN, TBK14.75
2Caspase 8 deficiencyEnrichmentCASP83.02
3Polyglucosan body myopathy 1 with or without immunodeficiencyEnrichmentRBCK13.02
4Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD3.02
5Autoinflammation with arthritis and vasculitisEnrichmentTBK13.02
6Corticobasal syndromeEnrichmentTBK13.02
7Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK13.02
8Encephalopathy, acute, infection-induced 8EnrichmentTBK13.02
9Familial behcet-like autoinflammatory syndromeEnrichmentTNFAIP33.02
10Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentOPTN, TBK12.87
11Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.81
12Incontinentia pigmentiEnrichmentIKBKG2.81
13Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.81
14Fetal encasement syndromeEnrichmentCHUK2.81
15Frontometaphyseal dysplasia 2EnrichmentMAP3K72.81
16Immunodeficiency 15bEnrichmentIKBKB2.81
17Immunodeficiency 15aEnrichmentIKBKB2.81
18Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.81
19Bartsocas-papas syndrome 2EnrichmentCHUK2.81
20Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.81
21Polyvalvular heart disease syndromeEnrichmentTAB22.81
22Cylindromatosis, familialEnrichmentCYLD2.72
23Trichoepithelioma, multiple familial, 1EnrichmentCYLD2.72
24Autoinflammatory syndrome, familial, behcet-like 1EnrichmentTNFAIP32.72
25Frontotemporal dementia and/or amyotrophic lateral sclerosis 8EnrichmentCYLD2.72
26Brooke-spiegler syndromeEnrichmentCYLD2.72
27Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.72
28Amyotrophic lateral sclerosis 12 with or without frontotemporal dementiaEnrichmentOPTN2.72
29Amyotrophic lateral sclerosis type 12EnrichmentOPTN2.72
30Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.72
31Oculootodental syndromeEnrichmentFADD2.72
32Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosisEnrichmentRBCK12.72
33Immunodeficiency 107 invasive staphylococcus aureus infectionEnrichmentOTULIN2.59
34Deeah syndromeEnrichmentMADD2.59
35Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessiveEnrichmentOTULIN2.59
36Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotoniaEnrichmentMADD2.59
37Immunodeficiency 86EnrichmentSPPL2A2.59
38Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominantEnrichmentOTULIN2.59
39Glycogen storage disease ivEnrichmentRBCK12.54
40Glaucoma, normal tensionEnrichmentOPTN2.54
41Immunodeficiency 33EnrichmentIKBKG2.51
42Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG2.51
43Congenital heart defects, multiple types, 2EnrichmentTAB22.51
44Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.51
45Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.51
46Submucosal cleft palateEnrichmentUBB2.51
47Cleft hard palateEnrichmentUBB2.51
48Systemic lupus erythematosusEnrichmentTNFAIP3, UBE2L32.35
49Pelvic organ prolapseEnrichmentTAB22.33
50Uvula, bifidEnrichmentUBB2.33
51Cleft soft palateEnrichmentUBB2.33
52Frontometaphyseal dysplasiaEnrichmentMAP3K72.33
53Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC32.32
54Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentOPTN2.32
55Herpes simplex virus encephalitisEnrichmentTBK12.32
56Spinocerebellar ataxia 48EnrichmentSTUB12.29
57Glaucoma, primary open angleEnrichmentOPTN2.24
58Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK12.24
59Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK12.24
60Inflammatory skin and bowel disease, neonatal, 1EnrichmentADAM172.20
61Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.11
62Craniometaphyseal dysplasia, autosomal dominantEnrichmentOTULIN2.11
63Adult hepatocellular carcinomaEnrichmentCASP82.07
64Progressive non-fluent aphasiaEnrichmentTBK12.07
65Neonatal inflammatory skin and bowel diseaseEnrichmentADAM172.02
66Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK12.02
67Chondrocalcinosis 2EnrichmentOTULIN1.99
68Immune deficiency diseaseEnrichmentRIPK11.98
69Multiple acyl-coa dehydrogenase deficiency, severe neonatal typeEnrichmentMADD1.89
70Coronary heart disease 5EnrichmentIKBKG1.86
71Spinocerebellar ataxia, autosomal recessive 16EnrichmentSTUB11.81
72Migraine with or without aura 1EnrichmentTAB21.77
73Aortic valve disease 1EnrichmentTAB21.70
74Hepatocellular carcinomaEnrichmentCASP81.68
75Severe covid-19EnrichmentRBCK11.56
76Patent foramen ovaleEnrichmentTAB21.56
77Lung cancerEnrichmentCASP81.52
78Left ventricular noncompactionEnrichmentMIB21.48
79MalariaEnrichmentIKBKG1.46
80Severe combined immunodeficiencyEnrichmentIKBKB1.30
81Hereditary breast ovarian cancer syndromeEnrichmentRIPK11.29
82Myeloma, multipleEnrichmentCYLD1.28
83Breast cancerEnrichmentCASP81.16
84Dilated cardiomyopathyEnrichmentTAB20.93
85Inherited cancer-predisposing syndromeEnrichmentCYLD0.92
86Complex neurodevelopmental disorderEnrichmentMADD0.56

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