TRAF6 mediated IRF7 activation

Pathway network for the TRAF6 mediated IRF7 activation SuperPath

Sources:
  • Reactome
  • GeneGo (Thomson Reuters)

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

Disorders associated with TRAF6 mediated IRF7 activation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Respiratory syncytial virus infectious diseaseDirect
2Multisystem inflammatory syndrome in childrenEnrichmentIFIH1, IFNA21, IFNA4, IFNA6, IFNB1, IRF310.95
3Singleton-merten syndromeEnrichmentIFIH1, RIGI5.33
4Herpes simplex virus encephalitisEnrichmentTICAM1, TLR34.27
5Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3004.15
6Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3004.15
7Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.95
8Rare genetic intellectual disabilityEnrichmentCREBBP, EP3003.31
9MalariaEnrichmentIKBKG, TIRAP2.88
10Immunodeficiency 39 viral infectionsEnrichmentIRF72.66
11Encephalopathy, acute, infection-induced 7EnrichmentIRF32.66
12Singleton-merten syndrome 1EnrichmentIFIH12.66
13Immunodeficiency 95EnrichmentIFIH12.66
14Type 1 diabetes mellitus 19EnrichmentIFIH12.66
15Immunodeficiency 39EnrichmentIRF72.66
16Autoinflammation with arthritis and vasculitisEnrichmentTBK12.66
17Singleton-merten syndrome 2EnrichmentRIGI2.66
18Corticobasal syndromeEnrichmentTBK12.66
19Menke-hennekam syndrome 1EnrichmentCREBBP2.66
20Encephalopathy, acute, infection-induced 8EnrichmentTBK12.66
21Aicardi-goutieres syndrome 7EnrichmentIFIH12.66
22Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.66
23Menke-hennekam syndromeEnrichmentCREBBP2.66
24Incontinentia pigmentiEnrichmentIKBKG2.63
25Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.63
26Immunodeficiency 83 viral infectionsEnrichmentTLR32.63
27Bacteremia 1EnrichmentTIRAP2.63
28Encephalopathy, acute, infection-induced 6EnrichmentTICAM12.63
29Immunodeficiency 92EnrichmentREL2.63
30Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.63
31Macular degeneration, age-related, 10EnrichmentTLR42.63
32Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.63
33Immunodeficiency 53EnrichmentRELB2.63
34Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.63
35Thumb deformityEnrichmentCREBBP2.35
36Menke-hennekam syndrome 2EnrichmentEP3002.35
37Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.35
38Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.35
39Basal ganglia diseaseEnrichmentIFIH12.35
40Immunodeficiency 33EnrichmentIKBKG2.33
41Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.33
42Immunodeficiency, common variable, 10EnrichmentNFKB22.33
43Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.33
44Rela fusion-positive ependymomaEnrichmentRELA2.33
45Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG2.33
46Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.33
47Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.33
48Common variable immunodeficiency 12EnrichmentNFKB12.33
49Chromosome 17q11.2 deletion syndrome, 1.4-mbEnrichmentRNF1352.18
50Tethered spinal cord syndromeEnrichmentCREBBP2.18
51Intraocular pressure quantitative trait locusEnrichmentCREBBP2.18
52Immunodeficiency, common variable, 1EnrichmentNFKB22.03
53Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.96
54Rubinstein-taybi syndrome 2EnrichmentEP3001.96
55Spastic diplegiaEnrichmentIFIH11.96
56Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.93
57HypertrichosisEnrichmentCREBBP1.88
58Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.85
59Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.85
60Motor neuron diseaseEnrichmentTBK11.81
61Charge syndromeEnrichmentEP3001.70
62Progressive non-fluent aphasiaEnrichmentTBK11.70
63Aicardi-goutiares syndromeEnrichmentIFIH11.70
64Coronary heart disease 5EnrichmentIKBKG1.68
65Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.66
66Aicardi-goutieres syndromeEnrichmentIFIH11.66
67Ciliary dyskinesia, primary, 3EnrichmentNFKB11.63
68Immune deficiency diseaseEnrichmentRIPK11.59
69Heart diseaseEnrichmentCREBBP1.52
70Polydactyly, postaxial, type a1EnrichmentEP3001.49
71Corpus callosum, agenesis ofEnrichmentCREBBP1.49
72Isolated corpus callosum agenesisEnrichmentCREBBP1.49
73Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.49
74Diffuse large b-cell lymphomaEnrichmentCREBBP1.38
75Human immunodeficiency virus type 1EnrichmentTLR31.38
76Behcet syndromeEnrichmentTLR41.36
77ScoliosisEnrichmentCREBBP1.29
78Myeloma, multipleEnrichmentCREBBP0.93
79Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK10.92
80Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.91
81AutismEnrichmentCREBBP0.83
82Colorectal cancerEnrichmentEP3000.76
83Congenital nervous system abnormalityEnrichmentCREBBP0.68
84Nervous system diseaseEnrichmentCREBBP0.68
85Autism spectrum disorderEnrichmentRNF1350.67
86MicrocephalyEnrichmentEP3000.62

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