Toll-Like receptor Signaling Pathways

Pathway network for the Toll-Like receptor Signaling Pathways SuperPath

Sources:
  • R&D Systems
  • QIAGEN
  • WikiPathways

Pathways in the Toll-Like receptor Signaling Pathways SuperPath

#NameSourceGenes
1Toll-Like receptor Signaling PathwaysR&D Systems
2NOD-like Receptor Signaling PathwaysR&D Systems
3Toll-Like Receptors PathwayQIAGEN
4Inflammasome Activation PathwaysR&D Systems
5TLR4 signaling and toleranceWikiPathways
6Nanomaterial-induced inflammasome activationWikiPathways

Gene overlap in member pathways for Toll-Like receptor Signaling Pathways SuperPath

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

Disorders associated with Toll-Like receptor Signaling Pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Multisystem inflammatory syndrome in childrenEnrichmentIFNA21, IFNA4, IFNB1, IRF3, TLR3, TLR6, TRAF310.26
2Herpes simplex virus encephalitisEnrichmentTBK1, TICAM1, TLR3, TRAF38.23
3Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK4, MYD885.88
4MalariaEnrichmentCD36, IKBKG, TIRAP, TNF5.02
5Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.84
6Autoinflammatory diseaseEnrichmentNLRC4, NLRP12, NLRP3, NOD24.80
7Immunodeficiency 33EnrichmentIKBKG, IRAK44.57
8Histiocytoid hemangiomaEnrichmentFOS, FOSB3.84
9Cerebral malariaEnrichmentCD36, TNF3.68
10Macular degeneration, age-related, 10EnrichmentTLR43.66
11Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.52
12Immunodeficiency 68EnrichmentMYD882.93
13Macroglobulinemia, waldenstrom 1EnrichmentMYD882.93
14Immunodeficiency 39 viral infectionsEnrichmentIRF72.93
15Bacteremia 1EnrichmentTIRAP2.93
16Encephalopathy, acute, infection-induced 7EnrichmentIRF32.93
17Immunodeficiency 132aEnrichmentTRAF32.93
18Immunodeficiency 132bEnrichmentTRAF32.93
19Immunodeficiency 39EnrichmentIRF72.93
20Immunodeficiency 67EnrichmentIRAK42.93
21Autoinflammation with arthritis and vasculitisEnrichmentTBK12.93
22Corticobasal syndromeEnrichmentTBK12.93
23Encephalopathy, acute, infection-induced 8EnrichmentTBK12.93
24Waldenstram macroglobulinemiaEnrichmentMYD882.93
25Polyvalvular heart disease syndromeEnrichmentTAB22.93
26Inflammatory bowel disease 1EnrichmentIL6, NOD22.84
27Systemic lupus erythematosusEnrichmentIRAK1, TLR7, TNF2.79
28Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.63
29Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.63
30Congenital dyserythropoietic anemiaEnrichmentIRAK42.63
31Congenital heart defects, multiple types, 2EnrichmentTAB22.63
32Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.63
33Common variable immunodeficiency 12EnrichmentNFKB12.63
34Pelvic organ prolapseEnrichmentTAB22.45
35Leprosy 3EnrichmentTLR22.42
36Incontinentia pigmentiEnrichmentIKBKG2.42
37Legionnaire diseaseEnrichmentTLR52.42
38Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.42
39Cinca syndromeEnrichmentNLRP32.42
40Keratoendotheliitis fugax hereditariaEnrichmentNLRP32.42
41Immunodeficiency 83 viral infectionsEnrichmentTLR32.42
42Familial cold autoinflammatory syndrome 1EnrichmentNLRP32.42
43Leprosy 5EnrichmentTLR12.42
44Fetal encasement syndromeEnrichmentCHUK2.42
45Muckle-wells syndromeEnrichmentNLRP32.42
46Encephalopathy, acute, infection-induced 6EnrichmentTICAM12.42
47Immunodeficiency 15bEnrichmentIKBKB2.42
48Deafness, autosomal dominant 34, with or without inflammationEnrichmentNLRP32.42
49Immunodeficiency 15aEnrichmentIKBKB2.42
50Immunodeficiency 92EnrichmentREL2.42
51Immunodeficiency 74, covid19-related, x-linkedEnrichmentTLR72.42
52Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.42
53Systemic lupus erythematosus 1EnrichmentTLR52.42
54X-linked immunodeficiency 74EnrichmentTLR72.42
55Systemic lupus erythematosus 17EnrichmentTLR72.42
56Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.42
57MelioidosisEnrichmentTLR52.42
58Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.42
59Immunodeficiency 53EnrichmentRELB2.42
60Bartsocas-papas syndrome 2EnrichmentCHUK2.42
61Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.42
62Cryopyrin associated periodic syndromeEnrichmentNLRP32.42
63Familial amyloid nephropathy with urticaria and deafnessEnrichmentNLRP32.42
64Behcet syndromeEnrichmentTLR42.38
65Diffuse large b-cell lymphomaEnrichmentBTK, MYD882.36
66Kaposi sarcomaEnrichmentIL62.33
67Pediatric systemic lupus erythematosusEnrichmentIRAK12.33
68Systemic-onset juvenile idiopathic arthritisEnrichmentIL62.33
69Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.28
70Frontometaphyseal dysplasia 2EnrichmentMAP3K72.28
71Ataxia-oculomotor apraxia 3EnrichmentPIK3R52.28
72Immunodeficiency 32aEnrichmentIRF82.28
73Short syndromeEnrichmentPIK3R12.28
74Isolated growth hormone deficiency type iiiEnrichmentBTK2.28
75Asthma-related traits 5EnrichmentIRAK32.28
76Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.28
77Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.28
78Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.28
79Cerebral cavernous malformations 5EnrichmentMAP3K32.28
80Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.28
81Verrucous hemangiomaEnrichmentMAP3K32.28
82Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.23
83Rheumatoid arthritis, systemic juvenileEnrichmentIL62.23
84Coronary heart disease 7EnrichmentCD362.22
85Platelet glycoprotein iv deficiencyEnrichmentCD362.22
86Immunodeficiency 103 fungal infectionsEnrichmentCARD92.19
87Vitiligo-associated multiple autoimmune disease susceptibility 1EnrichmentNLRP12.19
88Blau syndromeEnrichmentNOD22.19
89Noonan syndrome 13EnrichmentMAPK12.19
90Respiratory papillomatosis, juvenile recurrent, congenitalEnrichmentNLRP12.19
91Familial cold autoinflammatory syndrome 4EnrichmentNLRC42.19
92Familial cold autoinflammatory syndrome 2EnrichmentNLRP122.19
93Autoinflammation with infantile enterocolitisEnrichmentNLRC42.19
94Palmoplantar carcinoma, multiple self-healingEnrichmentNLRP12.19
95Autoinflammation with arthritis and dyskeratosisEnrichmentNLRP12.19
96Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.19
97Periodic fever-infantile enterocolitis-autoinflammatory syndromeEnrichmentNLRC42.19
98Recurrent hydatidiform moleEnrichmentNLRP72.19
99Arteriovenous malformations of the brainEnrichmentIL6, NLRP32.18
100Type 1 diabetes mellitusEnrichmentIL62.15
101Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.12
102Immunodeficiency, common variable, 10EnrichmentNFKB22.12
103Oocyte/zygote/embryo maturation arrest 7EnrichmentPANX12.12
104Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.12
105Rela fusion-positive ependymomaEnrichmentRELA2.12
106Leprosy 1EnrichmentTLR62.12
107Pericardial effusionEnrichmentNLRP32.12
108Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.12
109Motor neuron diseaseEnrichmentTBK12.08
110Gastric cancerEnrichmentIL1B2.02
111Gordon holmes syndromeEnrichmentRNF2161.98
112Immunodeficiency 32bEnrichmentIRF81.98
113Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2EnrichmentPIK3R51.98
114Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK1.98
115Histiocytoma, angiomatoid fibrousEnrichmentCREB11.98
116Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC11.98
117Agammaglobulinemia, x-linkedEnrichmentBTK1.98
118Immunodeficiency 57 with autoinflammationEnrichmentRIPK11.98
119Progressive non-fluent aphasiaEnrichmentTBK11.98
120Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentTLR81.94
121Nasopharyngeal carcinomaEnrichmentNFKBIA1.94
122Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.93
123Ciliary dyskinesia, primary, 3EnrichmentNFKB11.93
124Immunodeficiency 127EnrichmentTNF1.92
125Migraine with or without aura 1EnrichmentTAB21.89
126Yao syndromeEnrichmentNOD21.89
127Crohn's diseaseEnrichmentNOD21.89
128Partial hydatidiform moleEnrichmentNLRP71.89
129Aortic valve disease 1EnrichmentTAB21.82
130Anemia, autoimmune hemolyticEnrichmentTLR81.82
131Immunodeficiency, common variable, 1EnrichmentNFKB21.82
132Congenital generalized lipodystrophyEnrichmentFOS1.82
133Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.82
134Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK1.81
135Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3R11.81
136Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R11.81
137Agammaglobulinemia 1EnrichmentBTK1.81
138Frontometaphyseal dysplasiaEnrichmentMAP3K71.81
139Immunodeficiency 14EnrichmentPIK3R11.81
140Melanoma of soft tissueEnrichmentCREB11.81
141Psoriatic arthritisEnrichmentTNF1.75
142Hepatitis c virusEnrichmentIFNL31.75
143Migraine without auraEnrichmentTNF1.75
144Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.72
145Female infertility due to oocyte meiotic arrestEnrichmentPANX11.72
146Spinal muscular atrophy, type iiiEnrichmentNAIP1.71
147Spinal muscular atrophy, type iEnrichmentNAIP1.71
148Spinal muscular atrophy, type iiEnrichmentNAIP1.71
149Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3R21.68
150Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.68
151Patent foramen ovaleEnrichmentTAB21.68
152Blood platelet diseaseEnrichmentCD361.63
153Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.59
154Vascular dementiaEnrichmentTNF1.53
155Lennox-gastaut syndromeEnrichmentMAPK101.52
156Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.51
157Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.51
158Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.49
159Hydatidiform mole, recurrent, 1EnrichmentNLRP71.49
160Rheumatoid arthritisEnrichmentTLR11.47
161Coronary heart disease 5EnrichmentIKBKG1.47
162Overgrowth syndromeEnrichmentPIK3R11.44
163Leukemia, chronic lymphocyticEnrichmentP2RX71.42
164Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.34
165Type 2 diabetes mellitusEnrichmentIL61.31
166Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.29
167Immune deficiency diseaseEnrichmentRIPK11.25
168GliosarcomaEnrichmentNFKBIA1.22
169Giant cell glioblastomaEnrichmentNFKBIA1.20
170AsthmaEnrichmentTNF1.20
171Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK11.18
172Human immunodeficiency virus type 1EnrichmentTLR31.17
173Specific learning disabilityEnrichmentMAPK11.16
174Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentRNF2161.15
175Alzheimer's diseaseEnrichmentTNF1.13
176Colorectal cancerEnrichmentPIK3R1, TLR21.12
177Dilated cardiomyopathyEnrichmentTAB21.04
178Esophageal atresia/tracheoesophageal fistulaEnrichmentIRF81.02
179LeukodystrophyEnrichmentRNF2161.00
180Heart, malformation ofEnrichmentMAPK10.96
181Severe combined immunodeficiencyEnrichmentIKBKB0.92
182Breast cancerEnrichmentJUN0.60
183Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.60
184Myeloma, multipleEnrichmentPIK3R20.59
185MicrocephalyEnrichmentMAPK10.26

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