Overview of interferons-mediated signaling pathway

Pathway network for the Overview of interferons-mediated signaling pathway SuperPath

Sources:
  • WikiPathways
  • Reactome
  • R&D Systems
  • QIAGEN
  • GeneGo (Thomson Reuters)

Pathways in the Overview of interferons-mediated signaling pathway SuperPath

#NameSourceGenes
1Overview of interferons-mediated signaling pathwayWikiPathways
2Interferon alpha/beta signalingReactome
3Jak/STAT Signaling PathwayR&D Systems
4all-trans-Retinoic Acid Mediated ApoptosisQIAGEN
5Cytokine NetworkQIAGEN
6Immune response IFN alpha/beta signaling pathwayGeneGo (Thomson Reuters)
7Regulation of IFNA/IFNB signalingReactome
8Type III interferon signalingWikiPathways

Gene overlap in member pathways for Overview of interferons-mediated signaling pathway SuperPath

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

Disorders associated with Overview of interferons-mediated signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Multisystem inflammatory syndrome in childrenEnrichmentIFNA21, IFNA4, IFNA6, IFNAR2, IFNB19.34
2Hepatitis bEnrichmentIFNAR2, IFNGR1, IL10RB7.13
3Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT37.06
4Behcet syndromeEnrichmentIFNGR1, IL10, IL12A, STAT45.87
5Il10-related early-onset inflammatory bowel diseaseEnrichmentIL10, IL10RA, IL10RB5.77
6Oligoarticular juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB, STAT45.52
7Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB, STAT45.52
8Immunodeficiency 44EnrichmentIFNAR2, STAT24.98
9Psoriatic arthritisEnrichmentLTA, TNF4.74
10Hepatitis c virusEnrichmentIFNG, IFNL34.66
11Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.66
12Severe cutaneous adverse reactionEnrichmentHLA-A, HLA-B4.51
13Human immunodeficiency virus type 1EnrichmentCXCL12, IFNG, IL104.17
14Erythrocytosis, familial, 1EnrichmentEPOR, JAK23.93
15AsthmaEnrichmentIL13, TNF3.48
16MyelofibrosisEnrichmentJAK2, SRC3.39
17Primary biliary cholangitisEnrichmentIL12A, IL12RB13.15
18Immunodeficiency 35EnrichmentTYK23.13
19Pseudo-torch syndrome 3EnrichmentSTAT23.13
20Immunodeficiency 31aEnrichmentSTAT13.13
21Immunodeficiency 31bEnrichmentSTAT13.13
22Immunodeficiency 65 viral infectionsEnrichmentIRF93.13
23Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK13.13
24Aicardi-goutiares syndromeEnrichmentADAR, SAMHD12.96
25Aicardi-goutieres syndromeEnrichmentADAR, SAMHD12.87
26Immunodeficiency 31cEnrichmentSTAT12.83
27Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.83
28Lymphomatoid papulosisEnrichmentTYK22.83
29Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK22.83
30Acute promyelocytic leukemiaEnrichmentSTAT3, STAT5B2.82
31MetachondromatosisEnrichmentPTPN112.72
32Dermatitis, atopic, 4EnrichmentSOCS32.72
33Leopard syndrome 1EnrichmentPTPN112.72
34Immunodeficiency 106 viral infectionsEnrichmentIFNAR12.72
35Pseudo-torch syndrome 2EnrichmentUSP182.72
36Vegetative pyoderma gangrenosumEnrichmentPTPN62.72
37Bullous pyoderma gangrenosumEnrichmentPTPN62.72
38Pustular pyoderma gangrenosumEnrichmentPTPN62.72
39Classic pyoderma gangrenosumEnrichmentPTPN62.72
40Malignant astrocytomaEnrichmentPTPN112.72
41Inflammatory bowel disease 25EnrichmentIL10RB2.66
42Immunodeficiency 38 with basal ganglia calcificationEnrichmentISG152.61
43Leprosy 4EnrichmentLTA2.60
44Immunodeficiency 69EnrichmentIFNG2.60
45Graft-versus-host diseaseEnrichmentIL102.60
46Allergic rhinitisEnrichmentIL132.60
47Immunodeficiency 29EnrichmentIL12B2.60
48MacrodactylyEnrichmentPIK3CA2.56
49Helicobacter pylori infectionEnrichmentIFNGR12.56
50Megalencephaly, autosomal dominantEnrichmentPIK3CA2.56
51Cowden syndrome 5EnrichmentPIK3CA2.56
52Immunodeficiency 27aEnrichmentIFNGR12.56
53Cerebral cavernous malformations 4EnrichmentPIK3CA2.56
54Short syndromeEnrichmentPIK3R12.56
55Immunodeficiency 27bEnrichmentIFNGR12.56
56Hemifacial myohyperplasiaEnrichmentPIK3CA2.56
57Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.56
58Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.56
59Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.56
60Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.56
61HypospadiasEnrichmentPIK3CA2.56
62Rare venous malformationEnrichmentPIK3CA2.56
63Diaphragmatic eventrationEnrichmentPIK3CA2.56
64Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.56
65Rare combined vascular malformationEnrichmentPIK3CA2.56
66Cavernous lymphangiomaEnrichmentPIK3CA2.56
67Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.56
68Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial ifngammar2 deficiencyEnrichmentIFNGR22.56
69Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.56
70Eccrine angiomatous hamartomaEnrichmentPIK3CA2.56
71Macrodactyly of toeEnrichmentPIK3CA2.56
72Arteriovenous malformations of the brainEnrichmentEGFR, IL62.49
73Caspase 8 deficiencyEnrichmentCASP82.47
74Thrombocytopenia 4EnrichmentCYCS2.47
75Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.47
76Microphthalmia, syndromic 12EnrichmentRARB2.47
77Perrault syndrome 7EnrichmentDAP32.47
78Immunodeficiency 45EnrichmentIFNAR22.42
79Werner syndromeEnrichmentPTPN112.42
80Systemic lupus erythematosusEnrichmentIL10, TNF2.37
81Inflammatory bowel disease 25, autosomal recessiveEnrichmentIL10RB2.35
82Chronic mucocutaneous candidiasisEnrichmentSTAT12.35
83Type 1 diabetes mellitus 10EnrichmentIL2RA2.35
84Hypomagnesemia 4, renalEnrichmentEGF2.35
85Immunodeficiency 30EnrichmentIL12RB12.35
86Microvascular complications of diabetes 2EnrichmentEPO2.35
87Whim syndrome 1EnrichmentCXCR42.35
88Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.35
89Stuve-wiedemann syndrome 2EnrichmentIL6ST2.35
90Hyper-ige syndrome 4a, autosomal dominant, with recurrent infectionsEnrichmentIL6ST2.35
91Spondylometaphyseal dysplasia with corneal dystrophyEnrichmentPLCB32.35
92Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B2.35
93Hyper-ige syndrome 6, autosomal dominant, with recurrent infectionsEnrichmentSTAT62.35
94Immunodeficiency 63 with lymphoproliferation and autoimmunityEnrichmentIL2RB2.35
95Disabling pansclerotic morphea of childhoodEnrichmentSTAT42.35
96Auriculocondylar syndrome 2aEnrichmentPLCB42.35
97T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.35
98Systemic lupus erythematosus 11EnrichmentSTAT42.35
99Interleukin 6, serum level of, quantitative trait locusEnrichmentIL6R2.35
100Surfactant metabolism dysfunction, pulmonary, 5EnrichmentCSF2RB2.35
101Soluble interleukin-6 receptor, serum level of, quantitative trait locusEnrichmentIL6R2.35
102Hyper-ige syndrome 5, autosomal recessive, with recurrent infectionsEnrichmentIL6R2.35
103Erythrocytosis, familial, 5EnrichmentEPO2.35
104Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.35
105Thrombocytopenia 6EnrichmentSRC2.35
106Hyper-ige syndrome 4b, autosomal recessive, with recurrent infectionsEnrichmentIL6ST2.35
107Immunodeficiency 94 with autoinflammation and dysmorphic faciesEnrichmentIL6ST2.35
108Auriculocondylar syndrome 2bEnrichmentPLCB42.35
109T-b+ severe combined immunodeficiency due to jak3 deficiencyEnrichmentJAK32.35
110Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.35
111Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.35
112Egf-related primary hypomagnesemia with intellectual disabilityEnrichmentEGF2.35
113Immunodeficiency 117EnrichmentIRF12.31
114Immunodeficiency 127EnrichmentTNF2.30
115Keratosis, seborrheicEnrichmentPIK3CA2.26
116Noonan syndrome 8EnrichmentPIK3CA2.26
117Thrombocythemia 3EnrichmentJAK22.26
118Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.26
119PolycythemiaEnrichmentJAK22.26
120Hypereosinophilic syndromeEnrichmentJAK22.26
121Spondyloarthropathy 1EnrichmentHLA-B2.25
122Prostate cancer, hereditary, 1EnrichmentRNASEL2.25
123Skin/hair/eye pigmentation, variation in, 8EnrichmentIRF42.25
124Orofacial cleft 6EnrichmentIRF62.25
125Psoriasis 1EnrichmentHLA-C2.25
126Popliteal pterygium syndromeEnrichmentIRF62.25
127Chilblain lupus 2EnrichmentSAMHD12.25
128Immunodeficiency 39 viral infectionsEnrichmentIRF72.25
129Encephalopathy, acute, infection-induced 7EnrichmentIRF32.25
130Immunodeficiency 32aEnrichmentIRF82.25
131Immunodeficiency 131EnrichmentIRF42.25
132Leukoencephalopathy, developmental delay, and episodic neurologic regression syndromeEnrichmentEIF2AK22.25
133Aicardi-goutieres syndrome 5EnrichmentSAMHD12.25
134Immunodeficiency 39EnrichmentIRF72.25
135Ankylosing spondylitis 1EnrichmentHLA-B2.25
136Systemic lupus erythematosus 10EnrichmentIRF52.25
137Birdshot chorioretinopathyEnrichmentHLA-A2.25
138Influenza, severeEnrichmentIFITM32.25
139Inflammatory bowel disease 14EnrichmentIRF52.25
140Immunodeficiency 100 with pulmonary alveolar proteinosis and hypogammaglobulinemiaEnrichmentOAS12.25
141Reactive arthritisEnrichmentHLA-B2.25
142Irf6-related disordersEnrichmentIRF62.25
143Autosomal dominant popliteal pterygium syndromeEnrichmentIRF62.25
144Dystonia 33EnrichmentEIF2AK22.25
145Pulmonary arterial hypertension associated with connective tissue diseaseEnrichmentHLA-B2.25
146Whipple diseaseEnrichmentIRF42.25
147Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemiaEnrichmentOAS12.25
148Adar-related hereditary spastic paraplegiaEnrichmentADAR2.25
149Immune thrombocytopeniaEnrichmentSOCS12.24
150Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.24
151Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS12.24
152Tricuspid valve insufficiencyEnrichmentPTPN112.24
153Grange syndromeEnrichmentDAP32.17
154Intellectual developmental disorder, autosomal dominant 48EnrichmentRARB2.17
155Oculootodental syndromeEnrichmentFADD2.17
156Severe covid-19EnrichmentIL10RB, JAK32.13
157Takayasu arteritisEnrichmentIL12B2.12
158Tuberous sclerosis 1EnrichmentIFNG2.12
159Tuberous sclerosis 2EnrichmentIFNG2.12
160Migraine without auraEnrichmentTNF2.12
161Anemia, autoimmune hemolyticEnrichmentSOCS12.12
162Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.12
163Noonan syndrome with multiple lentiginesEnrichmentPTPN112.12
164Polycythemia veraEnrichmentJAK22.09
165Pompe disease, infantile-onsetEnrichmentPIK3CA2.09
166Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.09
167Immunodeficiency 28EnrichmentIFNGR22.09
168Immunodeficiency 14EnrichmentPIK3R12.09
169KeratoacanthomaEnrichmentPIK3CA2.09
170Hemangiopericytoma, malignantEnrichmentSTAT62.05
171Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.05
172Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA2.05
173Inflammatory bowel disease 28, autosomal recessiveEnrichmentIL10RA2.05
174Diamond-blackfan anemia-likeEnrichmentEPO2.05
175Inflammatory bowel disease 28EnrichmentIL10RA2.05
176Ocular melanomaEnrichmentPLCB42.05
177Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.05
178LymphomaEnrichmentPTPN112.02
179Kaposi sarcomaEnrichmentIL62.00
180Cerebral malariaEnrichmentTNF2.00
181Systemic-onset juvenile idiopathic arthritisEnrichmentIL62.00
182Laryngeal squamous cell carcinomaEnrichmentTNFRSF10B1.99
183Budd-chiari syndromeEnrichmentJAK21.96
184Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA1.96
185Cerebrovascular diseaseEnrichmentPIK3CA1.96
186Familial cerebral cavernous malformationsEnrichmentPIK3CA1.96
187Immunodeficiency 32bEnrichmentIRF81.95
188Dyschromatosis symmetrica hereditariaEnrichmentADAR1.95
189Aicardi-goutieres syndrome 6EnrichmentADAR1.95
190Stevens-johnson syndromeEnrichmentHLA-B1.95
191Van der woude syndromeEnrichmentIRF61.95
192Symmetrical dyschromatosis of extremitiesEnrichmentADAR1.95
193Submucosal cleft palateEnrichmentUBB1.95
194Cleft hard palateEnrichmentUBB1.95
195Patent ductus arteriosusEnrichmentPTPN111.94
196Rheumatoid arthritis, systemic juvenileEnrichmentIL61.90
197Vascular dementiaEnrichmentTNF1.90
198Idiopathic aplastic anemiaEnrichmentIFNG1.90
199Noonan syndrome 3EnrichmentPTPN111.87
200Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentJAK31.87
201Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT31.87
202Stuve-wiedemann syndrome 1EnrichmentIL6ST1.87
203Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR1.87
204Primary polycythemiaEnrichmentEPOR1.87
205Hyper ige syndromeEnrichmentSTAT31.87
206Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR1.87
207Stüve-wiedemann syndromeEnrichmentIL6ST1.87
208Capillary malformations, congenitalEnrichmentPIK3CA1.87
209Myeloproliferative neoplasmEnrichmentJAK21.87
210HemimegalencephalyEnrichmentPIK3CA1.87
211Type 1 diabetes mellitusEnrichmentIL61.83
212Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.79
213Cowden syndrome 1EnrichmentPIK3CA1.79
214Hemihyperplasia, isolatedEnrichmentPIK3CA1.79
215Breast adenocarcinomaEnrichmentPIK3CA1.79
216Lung squamous cell carcinomaEnrichmentPIK3CA1.79
217Van der woude syndrome 1EnrichmentIRF61.78
218Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB81.78
219Uvula, bifidEnrichmentUBB1.78
220Cleft soft palateEnrichmentUBB1.78
221Torsion dystonia 1EnrichmentEIF2AK21.78
222Proteosome-associated autoinflammatory syndromeEnrichmentPSMB81.78
223Familial chilblain lupusEnrichmentSAMHD11.78
224Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.77
225Auriculocondylar syndrome 1EnrichmentPLCB41.75
226Developmental and epileptic encephalopathy 12EnrichmentPLCB11.75
227Adenosine deaminase deficiencyEnrichmentJAK31.75
228Pediatric systemic lupus erythematosusEnrichmentSTAT41.75
229Nevus, epidermalEnrichmentPIK3CA1.72
230Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.72
231Essential thrombocythemiaEnrichmentJAK21.72
232Gallbladder cancerEnrichmentPIK3CA1.72
233Overgrowth syndromeEnrichmentPIK3R11.72
234ThrombocytopeniaEnrichmentPTPN11, SRC1.71
235Pectus excavatumEnrichmentPTPN111.68
236Specific learning disabilityEnrichmentPTPN111.68
237Temporal arteritisEnrichmentHLA-B1.65
238Cleft lip and alveolusEnrichmentIRF61.65
239Familial infantile bilateral striatal necrosisEnrichmentADAR1.65
240Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentJAK31.65
241Hereditary pulmonary alveolar proteinosisEnrichmentCSF2RB1.65
242Rheumatoid arthritisEnrichmentIL101.65
243Inflammatory bowel disease 1EnrichmentIL61.65
244EpicanthusEnrichmentPTPN111.64
245Juvenile myelomonocytic leukemiaEnrichmentPTPN111.64
246Congenital long qt syndromeEnrichmentPTPN111.64
247Colorectal cancerEnrichmentPIK3CA, PIK3R11.63
248Squamous cell carcinoma, head and neckEnrichmentTNFRSF10B1.63
249Leukemia, acute lymphoblastic 3EnrichmentJAK21.61
250Arteriovenous malformationEnrichmentPIK3CA1.61
251Adult hepatocellular carcinomaEnrichmentPIK3CA1.61
252Cowden syndromeEnrichmentPIK3CA1.61
253Aplastic anemiaEnrichmentIFNG1.61
254Lung non-small cell carcinomaEnrichmentIRF11.58
255Melanoma, uvealEnrichmentPLCB41.57
256Renal tubular dysgenesisEnrichmentAGTR11.57
257Autosomal dominant secondary polycythemiaEnrichmentEPO1.57
258Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.57
259Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.57
260Cleft upper lipEnrichmentIRF61.56
261Diffuse cutaneous systemic sclerosisEnrichmentIRF51.56
262Noonan syndrome and noonan-related syndromeEnrichmentPTPN111.55
263Alzheimer's diseaseEnrichmentTNF1.49
264MeningiomaEnrichmentPIK3CA1.49
265Lip and oral cavity carcinomaEnrichmentPIK3CA1.49
266Limited sclerodermaEnrichmentIRF51.48
267Patent foramen ovaleEnrichmentPTPN111.47
268Permanent neonatal diabetes mellitusEnrichmentSTAT31.45
269Diffuse large b-cell lymphomaEnrichmentSOCS11.45
270B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentHLA-C1.41
271Developmental and epileptic encephalopathy 14EnrichmentPLCB11.40
272Lynch syndromeEnrichmentPIK3CA1.40
273Noonan syndrome 1EnrichmentPTPN111.36
274Microphthalmia/coloboma 12EnrichmentRARB1.36
275ScoliosisEnrichmentPTPN111.35
276IchthyosisEnrichmentIL2RB1.32
277Hydrops fetalis, nonimmuneEnrichmentPTPN111.31
278RasopathyEnrichmentPTPN111.31
279Coloboma of maculaEnrichmentRARB1.30
280StrabismusEnrichmentPTPN111.30
281Perrault syndrome 1EnrichmentDAP31.28
282Myocardial infarctionEnrichmentLTA1.27
283Endometrial cancerEnrichmentPIK3CA1.25
284Long qt syndrome 1EnrichmentPTPN111.25
285MalariaEnrichmentTNF1.25
286Nk-cell enteropathyEnrichmentJAK31.24
287Non-immune hydrops fetalisEnrichmentPTPN111.24
288Hepatocellular carcinomaEnrichmentPIK3CA1.23
289OsteoporosisEnrichmentSRC1.21
290Lung cancer susceptibility 3EnrichmentEGFR1.21
291GliosarcomaEnrichmentEGFR1.16
292MicrophthalmiaEnrichmentRARB1.14
293Hypertension, essentialEnrichmentAGTR11.13
294Giant cell glioblastomaEnrichmentEGFR1.13
295Lung cancerEnrichmentIRF11.12
296Cleft lip/palateEnrichmentIRF61.12
297Bladder cancerEnrichmentPIK3CA1.12
298Prostate cancerEnrichmentPIK3CA1.12
299Type 2 diabetes mellitusEnrichmentPTPN11.11
300Hypertrophic cardiomyopathyEnrichmentPTPN111.10
301Cleft palate, isolatedEnrichmentIRF61.04
302Gastric cancerEnrichmentIRF11.00
303Esophageal atresia/tracheoesophageal fistulaEnrichmentIRF80.99
304Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.99
305Leukemia, acute myeloidEnrichmentJAK20.98
306Hereditary breast carcinomaEnrichmentPIK3CA0.95
307Tooth agenesisEnrichmentIRF60.93
308Inherited cancer-predisposing syndromeEnrichmentEGFR, PTPN110.93
309Autoinflammatory diseaseEnrichmentPSMB80.90
310HypertelorismEnrichmentPIK3CA0.88
311Severe combined immunodeficiencyEnrichmentJAK30.86
312Primary ovarian insufficiencyEnrichmentJAK20.83
313Benign epilepsy with centrotemporal spikesEnrichmentPLCB10.77
314Breast cancerEnrichmentIL20.76
315Centralopathic epilepsyEnrichmentPLCB10.75
316West syndromeEnrichmentPLCB10.74
317Autism spectrum disorderEnrichmentPTPN110.72
318Cerebral palsyEnrichmentSAMHD10.71
319MicrocephalyEnrichmentPTPN110.68
320Ovarian cancerEnrichmentPIK3CA0.62
321Myeloma, multipleEnrichmentSAMHD10.57

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