Toll Comparative Pathway

Pathway network for the Toll Comparative Pathway SuperPath

Sources:
  • QIAGEN
  • GeneGo (Thomson Reuters)

Pathways in the Toll Comparative Pathway SuperPath

Gene overlap in member pathways for Toll Comparative Pathway SuperPath

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

Disorders associated with Toll Comparative Pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM1, CALM2, CALM35.58
2Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK4, MYD885.52
3Immunodeficiency 33EnrichmentIKBKG, IRAK45.39
4Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.39
5Multisystem inflammatory syndrome in childrenEnrichmentIRAK3, IRF3, TLR35.13
6Nasopharyngeal carcinomaEnrichmentNFKBIA, TP534.55
7Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK24.40
8Anastomosing haemangiomaEnrichmentGNA11, GNA144.35
9Systemic-onset juvenile idiopathic arthritisEnrichmentIL6, MIF4.25
10Rheumatoid arthritis, systemic juvenileEnrichmentIL6, MIF4.03
11Histiocytoid hemangiomaEnrichmentFOS, FOSB3.88
12Long qt syndrome 1EnrichmentCALM1, CALM2, CALM33.75
13MalariaEnrichmentIKBKG, TIRAP2.99
14GliosarcomaEnrichmentNFKBIA, TP532.96
15Giant cell glioblastomaEnrichmentNFKBIA, TP532.91
16Diffuse large b-cell lymphomaEnrichmentMYD88, TP532.81
17Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.75
18Immunodeficiency 68EnrichmentMYD882.75
19Macroglobulinemia, waldenstrom 1EnrichmentMYD882.75
20Immunodeficiency 83 viral infectionsEnrichmentTLR32.75
21Bacteremia 1EnrichmentTIRAP2.75
22Encephalopathy, acute, infection-induced 7EnrichmentIRF32.75
23Frontometaphyseal dysplasia 2EnrichmentMAP3K72.75
24Noonan syndrome 13EnrichmentMAPK12.75
25Asthma-related traits 5EnrichmentIRAK32.75
26Immunodeficiency 67EnrichmentIRAK42.75
27Macular degeneration, age-related, 10EnrichmentTLR42.75
28Waldenstram macroglobulinemiaEnrichmentMYD882.75
29Incontinentia pigmentiEnrichmentIKBKG2.69
30Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.69
31Fetal encasement syndromeEnrichmentCHUK2.69
32Immunodeficiency 15bEnrichmentIKBKB2.69
33Immunodeficiency 15aEnrichmentIKBKB2.69
34Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.69
35Bartsocas-papas syndrome 2EnrichmentCHUK2.69
36Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.69
37Polyvalvular heart disease syndromeEnrichmentTAB22.69
38Behcet syndromeEnrichmentIFNGR1, TLR42.66
3946,xy sex reversal 6EnrichmentMAP3K12.51
40Immunodeficiency 69EnrichmentIFNG2.51
41Agammaglobulinemia 10, autosomal dominantEnrichmentSPI12.51
42Bone marrow failure syndrome 5EnrichmentTP532.51
43Papilloma of choroid plexusEnrichmentTP532.51
44Basal cell carcinoma 7EnrichmentTP532.51
45Anaplastic thyroid carcinomaEnrichmentTP532.51
46Ductal carcinoma in situEnrichmentTP532.51
47Thyroid gland undifferentiated carcinomaEnrichmentTP532.51
48Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.51
49Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.51
50AgammaglobulinemiaEnrichmentSPI12.51
51Choroid plexus cancerEnrichmentTP532.51
52Pleomorphic xanthoastrocytomaEnrichmentTP532.51
53Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.45
54Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.45
55Congenital dyserythropoietic anemiaEnrichmentIRAK42.45
56Common variable immunodeficiency 12EnrichmentNFKB12.45
57Helicobacter pylori infectionEnrichmentIFNGR12.43
58Immunodeficiency 27aEnrichmentIFNGR12.43
59Immunodeficiency 27bEnrichmentIFNGR12.43
60Immunodeficiency 31aEnrichmentSTAT12.43
61Long qt syndrome 16EnrichmentCALM32.43
62Achromatopsia 7EnrichmentATF62.43
63Immunodeficiency 31bEnrichmentSTAT12.43
64T-b+ severe combined immunodeficiency due to jak3 deficiencyEnrichmentJAK32.43
65Long qt syndrome 15EnrichmentCALM22.43
66Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.43
67Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial ifngammar2 deficiencyEnrichmentIFNGR22.43
68Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.43
69Hypocalciuric hypercalcemia, familial, type iiEnrichmentGNA112.41
70Pseudohypoparathyroidism, type icEnrichmentGNAS2.41
71Osseous heteroplasia, progressiveEnrichmentGNAS2.41
72Deafness, autosomal recessive 44EnrichmentADCY12.41
73Acth-independent macronodular adrenal hyperplasia 1EnrichmentGNAS2.41
74Neurodevelopmental disorder with hypotonia and dysmorphic faciesEnrichmentGNB22.41
75Pituitary adenoma 3, multiple typesEnrichmentGNAS2.41
76Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.41
77Lodder-merla syndrome, type 2, with developmental delay and with or without cardiac arrhythmiaEnrichmentGNB52.41
78Hypocalcemia, autosomal dominant 2EnrichmentGNA112.41
79Charcot-marie-tooth disease, dominant intermediate fEnrichmentGNB42.41
80Disorders of gnas inactivationEnrichmentGNAS2.41
81Intellectual developmental disorder, autosomal dominant 42EnrichmentGNB12.41
82Sick sinus syndrome 4EnrichmentGNB22.41
83Immunodeficiency 112EnrichmentMAP3K142.41
84Monostotic fibrous dysplasiaEnrichmentGNAS2.41
85Phakomatosis cesiomarmorataEnrichmentGNA112.41
86Kaposiform hemangioendotheliomaEnrichmentGNA142.41
87Mazabraud syndromeEnrichmentGNAS2.41
88Nik deficiencyEnrichmentMAP3K142.41
89Congenital heart defects, multiple types, 2EnrichmentTAB22.38
90Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.38
91Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.38
92Frontometaphyseal dysplasiaEnrichmentMAP3K72.28
93Long qt syndromeEnrichmentCALM1, CALM22.24
94Pelvic organ prolapseEnrichmentTAB22.21
95Adrenocortical carcinoma, hereditaryEnrichmentTP532.21
96Cervical cancerEnrichmentTP532.21
97Lymphoma, hodgkin, classicEnrichmentTP532.21
98Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.21
99Menke-hennekam syndrome 2EnrichmentEP3002.21
100Immunodeficiency 127EnrichmentTNF2.21
101Rela fusion-positive ependymomaEnrichmentRELA2.21
102Congenital fibrosarcomaEnrichmentTP532.21
103Li-fraumeni syndrome 1EnrichmentTP532.21
104SarcomaEnrichmentTP532.21
105Cervix carcinomaEnrichmentTP532.21
106Hodgkin's lymphomaEnrichmentTP532.21
107Pleomorphic rhabdomyosarcomaEnrichmentTP532.21
108Systemic lupus erythematosusEnrichmentIRAK1, TNF2.19
109Severe combined immunodeficiencyEnrichmentIKBKB, JAK32.18
110Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.15
111Pediatric systemic lupus erythematosusEnrichmentIRAK12.15
112Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM12.13
113Thrombocythemia 3EnrichmentJAK22.13
114Long qt syndrome 14EnrichmentCALM12.13
115Immunodeficiency 31cEnrichmentSTAT12.13
116Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.13
117PolycythemiaEnrichmentJAK22.13
118Hypereosinophilic syndromeEnrichmentJAK22.13
119Immunodeficiency 117EnrichmentIRF12.13
120Gastric cancerEnrichmentIL1B, TP532.11
121Pseudohypoparathyroidism, type iaEnrichmentGNAS2.11
122Cutis marmorata telangiectatica congenitaEnrichmentGNA112.11
123Pigmented nodular adrenocortical disease, primary, 1EnrichmentGNAS2.11
124PseudopseudohypoparathyroidismEnrichmentGNAS2.11
125Angioma, tuftedEnrichmentGNA142.11
126Night blindness, congenital stationary, type 1hEnrichmentGNB32.11
127Autosomal dominant hypocalcemiaEnrichmentGNA112.11
128PseudohypoparathyroidismEnrichmentGNAS2.11
129Body mass index quantitative trait locus 19EnrichmentADCY32.11
130Lodder-merla syndrome, type 1, with impaired intellectual development and cardiac arrhythmiaEnrichmentGNB52.11
131Acth-independent macronodular adrenal hyperplasiaEnrichmentGNAS2.11
132Cerebral visual impairmentEnrichmentGNB12.11
133Phakomatosis cesioflammeaEnrichmentGNA112.11
134Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.05
135Herpes simplex virus encephalitisEnrichmentTLR32.05
136Tuberous sclerosis 1EnrichmentIFNG2.03
137Osteogenic sarcomaEnrichmentTP532.03
138Psoriatic arthritisEnrichmentTNF2.03
139Hepatitis c virusEnrichmentIFNG2.03
140Tuberous sclerosis 2EnrichmentIFNG2.03
141Atypical teratoid rhabdoid tumorEnrichmentTP532.03
142Anaplastic astrocytomaEnrichmentTP532.03
143Squamous cell carcinomaEnrichmentTP532.03
144AdenocarcinomaEnrichmentTP532.03
145Migraine without auraEnrichmentTNF2.03
146Bone osteosarcomaEnrichmentTP532.03
147Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.99
148Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentJAK31.96
149Polycythemia veraEnrichmentJAK21.96
150Immunodeficiency 28EnrichmentIFNGR21.96
151Melanoma of soft tissueEnrichmentATF11.96
152Mccune-albright syndromeEnrichmentGNAS1.93
153Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentGNA111.93
154Cushing syndrome due to bilateral macronodular adrenocortical diseaseEnrichmentGNAS1.93
155Common variable immunodeficiencyEnrichmentNFKB11.91
156Kaposi sarcomaEnrichmentIL61.91
157Small cell cancer of the lungEnrichmentTP531.91
158Thyroid cancer, nonmedullary, 1EnrichmentTP531.91
159Lung sarcomatoid carcinomaEnrichmentTP531.91
160Embryonal rhabdomyosarcomaEnrichmentTP531.91
161Cerebral malariaEnrichmentTNF1.91
162Lennox-gastaut syndromeEnrichmentMAPK101.85
163Erythrocytosis, familial, 1EnrichmentJAK21.83
164Budd-chiari syndromeEnrichmentJAK21.83
165Congenital generalized lipodystrophyEnrichmentFOS1.83
166Hepatitis bEnrichmentIFNGR11.83
167Adenosine deaminase deficiencyEnrichmentJAK31.83
168Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.83
169Rhabdomyosarcoma 2EnrichmentTP531.81
170Rubinstein-taybi syndrome 2EnrichmentEP3001.81
171LymphomaEnrichmentTP531.81
172Vascular dementiaEnrichmentTNF1.81
173Acute megakaryocytic leukemiaEnrichmentTP531.81
174Idiopathic aplastic anemiaEnrichmentIFNG1.81
175Spastic paraplegia 17, autosomal dominantEnrichmentGNG31.81
176Pseudohypoparathyroidism, type ibEnrichmentGNAS1.81
177Lipodystrophy, congenital generalized, type 2EnrichmentGNG31.81
178Familial sick sinus syndromeEnrichmentGNB21.81
179Body mass index quantitative trait locus 11EnrichmentADCY3, GNAS1.79
180Ciliary dyskinesia, primary, 3EnrichmentNFKB11.76
181Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentJAK31.74
182Myeloproliferative neoplasmEnrichmentJAK21.74
183Coronary heart disease 5EnrichmentIKBKG1.73
184Li-fraumeni syndromeEnrichmentTP531.73
185Rubinstein-taybi syndrome 1EnrichmentEP3001.73
186Type 1 diabetes mellitusEnrichmentIL61.73
187Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.73
188Adrenocortical carcinomaEnrichmentTP531.73
189Breast adenocarcinomaEnrichmentTP531.73
190Specific learning disabilityEnrichmentMAPK11.71
191Capillary malformations, congenitalEnrichmentGNA111.71
192Esophageal cancerEnrichmentTP531.67
193Squamous cell carcinoma, head and neckEnrichmentTP531.67
194Essential thrombocythemiaEnrichmentTP531.67
195Gallbladder cancerEnrichmentTP531.67
196B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.67
197Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.66
198Chronic mucocutaneous candidiasisEnrichmentSTAT11.66
199Migraine with or without aura 1EnrichmentTAB21.65
200Breast cancerEnrichmentJUN, TP531.65
201Melanoma, uvealEnrichmentGNA111.63
202Glioma susceptibility 1EnrichmentTP531.61
203Lymphoma, non-hodgkin, familialEnrichmentTP531.61
204MyelofibrosisEnrichmentJAK21.59
205Aortic valve disease 1EnrichmentTAB21.58
206BrachydactylyEnrichmentGNAS1.57
207Charge syndromeEnrichmentEP3001.56
208Inflammatory bowel disease 1EnrichmentIL61.56
209Adult hepatocellular carcinomaEnrichmentTP531.56
210Primary hyperaldosteronismEnrichmentTP531.56
211Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.54
212Colorectal cancerEnrichmentEP300, TP531.53
213Leukemia, chronic lymphocyticEnrichmentTP531.52
214Aplastic anemiaEnrichmentIFNG1.52
215Familial colorectal cancerEnrichmentTP531.52
216Autosomal non-syndromic agammaglobulinemiaEnrichmentSPI11.52
217Spastic paraplegia 4, autosomal dominantEnrichmentGNAS1.51
218HypothyroidismEnrichmentGNB11.51
219Heart, malformation ofEnrichmentMAPK11.50
220Human immunodeficiency virus type 1EnrichmentTLR31.50
221Leukemia, acute lymphoblastic 3EnrichmentJAK21.49
222AsthmaEnrichmentTNF1.47
223Myelodysplastic syndromeEnrichmentTP531.47
22446,xy complete gonadal dysgenesisEnrichmentMAP3K11.47
225AchromatopsiaEnrichmentATF61.44
226Patent foramen ovaleEnrichmentTAB21.44
227Lip and oral cavity carcinomaEnrichmentTP531.44
228Ovarian cancerEnrichmentMAP3K1, TP531.41
229Alzheimer's diseaseEnrichmentTNF1.40
230Lung non-small cell carcinomaEnrichmentIRF11.40
231Leukemia, acute lymphoblasticEnrichmentGNB11.38
232Lung cancer susceptibility 3EnrichmentTP531.37
23346,xy partial gonadal dysgenesisEnrichmentMAP3K11.37
234Polydactyly, postaxial, type a1EnrichmentEP3001.34
235Rare genetic intellectual disabilityEnrichmentEP3001.34
236Nk-cell enteropathyEnrichmentJAK31.33
237RhabdomyosarcomaEnrichmentTP531.31
238Arteriovenous malformations of the brainEnrichmentIL61.24
239Sudden infant death syndromeEnrichmentCALM21.22
240HepatoblastomaEnrichmentTP531.20
241Hypertension, essentialEnrichmentGNB31.19
242Cleft palate, isolatedEnrichmentGNB11.19
243Hepatocellular carcinomaEnrichmentTP531.18
244Diamond-blackfan anemia 1EnrichmentTP531.16
245Pancreatic cancerEnrichmentTP531.13
246Attention deficit-hyperactivity disorderEnrichmentGNB51.08
247Bladder cancerEnrichmentTP531.07
248Prostate cancerEnrichmentTP531.07
249Congenital stationary night blindnessEnrichmentGNB31.06
250Cystic fibrosisEnrichmentMIF1.02
251StrabismusEnrichmentGNB11.00
252Severe covid-19EnrichmentJAK30.99
253Diamond-blackfan anemiaEnrichmentTP530.98
254Lung cancerEnrichmentIRF10.95
255Leukemia, acute myeloidEnrichmentTP530.93
256Type 2 diabetes mellitusEnrichmentIL60.91
257Hereditary breast carcinomaEnrichmentTP530.89
258DystoniaEnrichmentGNB10.89
259Cerebral palsyEnrichmentGNB10.85
260Dilated cardiomyopathyEnrichmentTAB20.82
261Hereditary breast ovarian cancer syndromeEnrichmentTP530.80
262Myeloma, multipleEnrichmentTP530.80
263Autosomal dominant non-syndromic intellectual disabilityEnrichmentGNB10.75
264Primary ovarian insufficiencyEnrichmentJAK20.71
265MicrocephalyEnrichmentMAPK10.71
266Cone-rod dystrophy 2EnrichmentATF60.65
267Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentADCY10.53
268Inherited cancer-predisposing syndromeEnrichmentTP530.47
269Congenital nervous system abnormalityEnrichmentGNB50.47
270Nervous system diseaseEnrichmentGNB50.47
271Autism spectrum disorderEnrichmentGNB10.46
272Complex neurodevelopmental disorderEnrichmentGNB20.41
273Hereditary retinal dystrophyEnrichmentATF60.18
274Fundus dystrophyEnrichmentATF60.18

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