Cytosolic sensors of pathogen-associated DNA

Pathway network for the Cytosolic sensors of pathogen-associated DNA SuperPath

Sources:
  • Reactome
  • WikiPathways

Pathways in the Cytosolic sensors of pathogen-associated DNA SuperPath

#NameSourceGenes
1Cytosolic sensors of pathogen-associated DNAReactome
2Cytosolic DNA-sensing pathwayWikiPathways
3ZBP1(DAI) mediated induction of type I IFNsReactome
4RIP-mediated NFkB activation via ZBP1Reactome
5STING mediated induction of host immune responsesReactome
6Regulation of innate immune responses to cytosolic DNAReactome
7IRF3-mediated induction of type I IFNReactome
8IkBA variant leads to EDA-IDReactome
9DEx/H-box helicases activate type I IFN and inflammatory cytokines productionReactome
10IRF3 mediated activation of type 1 IFNReactome
11LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN productionReactome
12CLEC7A/inflammasome pathwayReactome
13STAT6-mediated induction of chemokinesReactome
14Selenium micronutrient networkWikiPathways
15Regulation by TREX1Reactome

Gene overlap in member pathways for Cytosolic sensors of pathogen-associated DNA SuperPath

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

Disorders associated with Cytosolic sensors of pathogen-associated DNA SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Immune deficiency diseaseDirect
2Herpes simplex virus encephalitisEnrichmentTBK1, TICAM1, TLR37.50
3Multisystem inflammatory syndrome in childrenEnrichmentIFNA21, IFNA4, IFNA6, IFNB1, IRF37.02
4Common variable immunodeficiencyEnrichmentNFKB1, NFKB26.16
5Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadismEnrichmentPOLR1C, POLR3A, POLR3B6.00
6Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.83
7Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3005.79
8Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3005.79
9Familial chilblain lupusEnrichmentSTING1, TREX15.59
10Rare genetic intellectual disabilityEnrichmentCREBBP, EP3004.94
11Polr3-related leukodystrophyEnrichmentPOLR3A, POLR3B4.18
12Hypomyelinating leukodystrophy 7EnrichmentPOLR3A, POLR3B3.88
13Sting-associated vasculopathy, infantile-onsetEnrichmentSTING13.66
14Hyper-ige syndrome 6, autosomal dominant, with recurrent infectionsEnrichmentSTAT63.66
15Sting-associated vasculopathy with onset in infancyEnrichmentSTING13.66
16Autoinflammation with arthritis and vasculitisEnrichmentTBK13.66
17Corticobasal syndromeEnrichmentTBK13.66
18Encephalopathy, acute, infection-induced 8EnrichmentTBK13.66
19Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB23.66
20Vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestationsEnrichmentTREX13.66
21Chilblain lupus 1EnrichmentTREX13.66
22Chilblain lupusEnrichmentTREX13.66
23Aicardi-goutieres syndrome 1EnrichmentTREX13.53
24Thrombotic microangiopathyEnrichmentTREX13.53
25Encephalopathy, acute, infection-induced 7EnrichmentIRF33.43
26Menke-hennekam syndrome 1EnrichmentCREBBP3.43
27Adenoid ameloblastomaEnrichmentCTNNB13.43
28Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP3.43
29Menke-hennekam syndromeEnrichmentCREBBP3.43
30Microcystic stromal tumorEnrichmentCTNNB13.43
31Caspase 8 deficiencyEnrichmentCASP83.43
32Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1EnrichmentTREX13.43
33Vascular dementiaEnrichmentTREX13.43
34Colorectal cancerEnrichmentCTNNB1, EP3003.40
35Hemangiopericytoma, malignantEnrichmentSTAT63.35
36Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK13.35
37Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB13.35
38Immunodeficiency, common variable, 10EnrichmentNFKB23.35
39Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA3.35
40Rela fusion-positive ependymomaEnrichmentRELA3.35
41Common variable immunodeficiency 12EnrichmentNFKB13.35
42Treacher collins syndrome 1EnrichmentPOLR1C, POLR1D3.34
43Immunodeficiency 68EnrichmentMYD883.29
44Macroglobulinemia, waldenstrom 1EnrichmentMYD883.29
45Immunodeficiency 39 viral infectionsEnrichmentIRF73.29
46Immunodeficiency 39EnrichmentIRF73.29
47Intellectual developmental disorder, autosomal dominant 75EnrichmentDHX93.29
48Waldenstram macroglobulinemiaEnrichmentMYD883.29
49Congenital nervous system abnormalityEnrichmentCREBBP, CTNNB13.22
50Nervous system diseaseEnrichmentCREBBP, CTNNB13.22
51Aicardi-goutiares syndromeEnrichmentTREX13.18
52Thumb deformityEnrichmentCREBBP3.13
53Osteopathia striata with cranial sclerosisEnrichmentCTNNB13.13
54Menke-hennekam syndrome 2EnrichmentEP3003.13
55Childhood hepatocellular carcinomaEnrichmentCTNNB13.13
56Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP3.13
57Juvenile nasopharyngeal angiofibromaEnrichmentCTNNB13.13
58TeratomaEnrichmentCTNNB13.13
59Aicardi-goutieres syndromeEnrichmentTREX13.13
60MicrocephalyEnrichmentCTNNB1, EP3003.10
61Immunodeficiency, common variable, 1EnrichmentNFKB23.05
62Ataxia-telangiectasia-like disorder 1EnrichmentMRE113.02
63Immunodeficiency 26 with or without neurologic abnormalitiesEnrichmentPRKDC3.02
64Myeloproliferative/lymphoproliferative neoplasms, familialEnrichmentDDX413.02
65Ddx41-related hematologic malignancy predisposition syndromeEnrichmentDDX413.02
66Transient predisposition to invasive pyogenic bacterial infectionEnrichmentMYD882.99
67Desmoid disease, hereditaryEnrichmentCTNNB12.96
68Neurodevelopmental disorder with spastic diplegia and visual defectsEnrichmentCTNNB12.96
69Anus, imperforateEnrichmentCTNNB12.96
70Exudative vitreoretinopathy 7EnrichmentCTNNB12.96
71Tethered spinal cord syndromeEnrichmentCREBBP2.96
72Desmoid tumorEnrichmentCTNNB12.96
73Intraocular pressure quantitative trait locusEnrichmentCREBBP2.96
74Incontinentia pigmentiEnrichmentIKBKG2.90
75Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.90
76Immunodeficiency 83 viral infectionsEnrichmentTLR32.90
77Fetal encasement syndromeEnrichmentCHUK2.90
78Encephalopathy, acute, infection-induced 6EnrichmentTICAM12.90
79Immunodeficiency 15bEnrichmentIKBKB2.90
80Immunodeficiency 15aEnrichmentIKBKB2.90
81Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.90
82Bartsocas-papas syndrome 2EnrichmentCHUK2.90
83Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.90
84Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.90
85PilomatrixomaEnrichmentCTNNB12.83
86Alazami syndromeEnrichmentCTNNB12.83
87CraniopharyngiomaEnrichmentCTNNB12.83
88Motor neuron diseaseEnrichmentTBK12.81
89Exudative vitreoretinopathy 1EnrichmentCTNNB12.73
90Rubinstein-taybi syndrome 2EnrichmentEP3002.73
91Progressive non-fluent aphasiaEnrichmentTBK12.70
92Weyers acrofacial dysostosisEnrichmentCTNNB12.66
93Adrenocortical carcinomaEnrichmentCTNNB12.66
94HypertrichosisEnrichmentCREBBP2.66
95Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK12.66
96Ciliary dyskinesia, primary, 3EnrichmentNFKB12.66
97Muscular dystrophy, limb-girdle, autosomal recessive 8EnrichmentTRIM322.66
98Bardet-biedl syndrome 11EnrichmentTRIM322.66
99Autosomal recessive limb-girdle muscular dystrophy type 2hEnrichmentTRIM322.66
100Submucosal cleft palateEnrichmentUBB2.66
101Cleft hard palateEnrichmentUBB2.66
102Immunodeficiency 33EnrichmentIKBKG2.60
103Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.60
104Diamond-blackfan anemia 12EnrichmentNKIRAS12.60
105Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.60
106Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.60
107Gallbladder cancerEnrichmentCTNNB12.59
108Systemic lupus erythematosusEnrichmentTREX12.54
109Exudative vitreoretinopathyEnrichmentCTNNB12.53
110Charge syndromeEnrichmentEP3002.48
111Adult hepatocellular carcinomaEnrichmentCTNNB12.48
112Uvula, bifidEnrichmentUBB2.48
113Cleft soft palateEnrichmentUBB2.48
114Diffuse large b-cell lymphomaEnrichmentCREBBP, MYD882.45
115Nasopharyngeal carcinomaEnrichmentNFKBIA2.43
116Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemiaEnrichmentMRE112.42
117Nijmegen breakage syndrome-like disorderEnrichmentMRE112.42
118LeukodystrophyEnrichmentPOLR3A, POLR3B2.40
119Immunodeficiency 101EnrichmentPOLR3F2.33
120Leukodystrophy, hypomyelinating, 21EnrichmentPOLR3K2.33
121Treacher collins syndrome 2EnrichmentPOLR1D2.33
122OdontoleukodystrophyEnrichmentPOLR3A2.33
123Inherited acute myeloid leukemiaEnrichmentDDX412.32
124MedulloblastomaEnrichmentCTNNB12.29
125Heart diseaseEnrichmentCREBBP2.29
126Tenorio syndromeEnrichmentRNF1252.27
127Immunodeficiency 38 with basal ganglia calcificationEnrichmentISG152.27
128Spinocerebellar ataxia, autosomal recessive 25EnrichmentATG52.27
129Autoimmune lymphoproliferative syndrome, type iiaEnrichmentCASP102.27
130Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.27
131Singleton-merten syndrome 2EnrichmentRIGI2.27
132Adar-related hereditary spastic paraplegiaEnrichmentADAR2.27
133Polydactyly, postaxial, type a1EnrichmentEP3002.26
134Corpus callosum, agenesis ofEnrichmentCREBBP2.26
135Isolated corpus callosum agenesisEnrichmentCREBBP2.26
136Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP2.26
137Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.20
138Polycystic liver diseaseEnrichmentCTNNB12.20
139Autosomal dominant polycystic liver diseaseEnrichmentCTNNB12.20
140Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK12.13
141Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK12.13
142HepatoblastomaEnrichmentCTNNB12.11
143Hepatocellular carcinomaEnrichmentCTNNB12.09
144Colonic benign neoplasmEnrichmentMRE112.07
145ScoliosisEnrichmentCREBBP2.05
146Treacher collins syndrome 3EnrichmentPOLR1C2.03
147Leukodystrophy, hypomyelinating, 4EnrichmentPOLR3A2.03
148Waardenburg syndrome, type 4cEnrichmentPOLR2F2.03
149Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadismEnrichmentPOLR3B2.03
150Leukoencephalopathy, progressive, with ovarian failureEnrichmentPOLR1C2.03
151Charcot-marie-tooth disease, demyelinating, type 1iEnrichmentPOLR3B2.03
152Short stature, oligodontia, dysmorphic facies, and motor delayEnrichmentPOLR3GL2.03
153Leukodystrophy, hypomyelinating, 11EnrichmentPOLR1C2.03
154Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung diseaseEnrichmentPOLR2F2.03
155HyperostosisEnrichmentPOLR3GL2.03
156Limb-girdle muscular dystrophyEnrichmentTRIM322.00
157Myelodysplastic syndromeEnrichmentDDX411.98
158Bladder cancerEnrichmentCTNNB11.97
159Cylindromatosis, familialEnrichmentCYLD1.97
160Trichoepithelioma, multiple familial, 1EnrichmentCYLD1.97
161Dyschromatosis symmetrica hereditariaEnrichmentADAR1.97
162Aicardi-goutieres syndrome 6EnrichmentADAR1.97
163Frontotemporal dementia and/or amyotrophic lateral sclerosis 8EnrichmentCYLD1.97
164Brooke-spiegler syndromeEnrichmentCYLD1.97
165Singleton-merten syndromeEnrichmentRIGI1.97
166Symmetrical dyschromatosis of extremitiesEnrichmentADAR1.97
167Oculootodental syndromeEnrichmentFADD1.97
168Coronary heart disease 5EnrichmentIKBKG1.95
169Lung cancerEnrichmentCASP81.93
170Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK11.89
171Waardenburg syndrome, type 2aEnrichmentPOLR2F1.85
172Wiedemann-rautenstrauch syndromeEnrichmentPOLR3A1.85
173Infantile cerebellar-retinal degenerationEnrichmentPOLR3H1.85
174Optic atrophy 9EnrichmentPOLR3H1.85
175Viss syndromeEnrichmentPOLR3B1.85
176Neonatal pseudo-hydrocephalic progeroid syndromeEnrichmentPOLR3A1.85
177Gastric cancerEnrichmentIL1B1.80
178Creatine phosphokinase, elevated serumEnrichmentTRIM321.76
179Isolated elevated serum creatine phosphokinase levelsEnrichmentTRIM321.76
180GliosarcomaEnrichmentNFKBIA1.70
181Myeloma, multipleEnrichmentCREBBP1.69
182Autosomal recessive limb-girdle muscular dystrophyEnrichmentTRIM321.68
183Charcot-marie-tooth diseaseEnrichmentDHX91.68
184Giant cell glioblastomaEnrichmentNFKBIA1.68
185Kaposi sarcomaEnrichmentIL61.67
186Autoimmune lymphoproliferative syndromeEnrichmentCASP101.67
187Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.67
188Familial infantile bilateral striatal necrosisEnrichmentADAR1.67
189Hereditary retinal dystrophyEnrichmentTREX11.67
190Fundus dystrophyEnrichmentTREX11.67
191Human immunodeficiency virus type 1EnrichmentTLR31.65
192Hypogonadotropic hypogonadism 1 with or without anosmiaEnrichmentPOLR2F1.63
193AutismEnrichmentCREBBP1.58
194Rheumatoid arthritis, systemic juvenileEnrichmentIL61.57
195Breast cancerEnrichmentCASP81.56
196Hereditary breast ovarian cancer syndromeEnrichmentMRE11, RIPK11.56
197Waardenburg syndrome, type 4aEnrichmentPOLR2F1.55
198Waardenburg syndromeEnrichmentPOLR2F1.55
199MalariaEnrichmentIKBKG1.55
200Type 1 diabetes mellitusEnrichmentIL61.50
201Waardenburg syndrome, type 1EnrichmentPOLR2F1.49
202Waardenburg syndrome, type 2eEnrichmentPOLR2F1.49
203Ovarian cancerEnrichmentCTNNB11.44
204Leukemia, acute myeloidEnrichmentDDX411.42
205Severe combined immunodeficiencyEnrichmentIKBKB1.39
206Lymphoma, non-hodgkin, familialEnrichmentCASP101.37
207MyopathyEnrichmentTRIM321.36
208Bardet-biedl syndromeEnrichmentTRIM321.34
209Inflammatory bowel disease 1EnrichmentIL61.32
210Movement diseaseEnrichmentPOLR3A1.29
21146 xx gonadal dysgenesisEnrichmentPOLR3H1.26
212Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentPOLR3B1.19
213Arteriovenous malformations of the brainEnrichmentIL61.01
214Tooth agenesisEnrichmentPOLR3GL1.00
215Kallmann syndromeEnrichmentPOLR2F0.99
216Inherited cancer-predisposing syndromeEnrichmentMRE110.92
217Hirschsprung disease 1EnrichmentPOLR2F0.89
218Severe covid-19EnrichmentCASP100.84
219Optic atrophy plus syndromeEnrichmentPOLR3H0.73
220Type 2 diabetes mellitusEnrichmentIL60.69
221Spastic ataxiaEnrichmentPOLR3A0.65
222Rare genetic deafnessEnrichmentPOLR2F0.51

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