Interleukin-1 family signaling

Pathway network for the Interleukin-1 family signaling SuperPath

Sources:
  • Reactome

Pathways in the Interleukin-1 family signaling SuperPath

#NameSourceGenes
1Interleukin-1 family signalingReactome
2Interleukin-1 signalingReactome
3Interleukin-18 signalingReactome
4Interleukin-38 signalingReactome

Gene overlap in member pathways for Interleukin-1 family signaling SuperPath

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

Disorders associated with Interleukin-1 family signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1AsthmaEnrichmentALOX5, IL134.78
2Immunodeficiency 33EnrichmentIKBKG, IRAK44.26
3Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.26
4Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK4, MYD884.26
5Nasopharyngeal carcinomaEnrichmentNFKBIA, TP533.79
6Intellectual developmental disorder, x-linked 21EnrichmentIL1RAPL13.53
7Allergic rhinitisEnrichmentIL133.23
8Hepatitis, fulminant viralEnrichmentIL18BP3.23
9Inflammatory bowel disease 31, autosomal recessiveEnrichmentIL373.23
10AtherosclerosisEnrichmentALOX53.23
11Inflammatory bowel diseaseEnrichmentIL373.23
12Patent foramen ovaleEnrichmentPSMC3, PTPN11, TAB23.11
13Diffuse large b-cell lymphomaEnrichmentMYD88, STAT3, TP533.04
14LymphomaEnrichmentPTPN11, TP532.99
15Common variable immunodeficiencyEnrichmentNFKB1, NFKB22.95
16Isolated split hand-split foot malformationEnrichmentBTRC, SEM12.83
17Patent ductus arteriosusEnrichmentPSMC3, PTPN112.82
18Autoinflammatory diseaseEnrichmentIL1RN, IL36RN, NOD22.74
19Adult hepatocellular carcinomaEnrichmentCASP8, TP532.72
20Gastric cancerEnrichmentIL1B, IL1RN, TP532.40
21Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentSQSTM1, TBK12.35
22GliosarcomaEnrichmentNFKBIA, TP532.21
23Giant cell glioblastomaEnrichmentNFKBIA, TP532.16
24Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.13
25Paget disease of bone 3EnrichmentSQSTM12.13
26Incontinentia pigmentiEnrichmentIKBKG2.13
27Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.13
28Immunodeficiency 68EnrichmentMYD882.13
29Caspase 8 deficiencyEnrichmentCASP82.13
30Brachyphalangy, polydactyly, and tibial aplasia/hypoplasiaEnrichmentHMGB12.13
31Macroglobulinemia, waldenstrom 1EnrichmentMYD882.13
32Melorheostosis, isolatedEnrichmentMAP2K12.13
33Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.13
34Fetal encasement syndromeEnrichmentCHUK2.13
35Blau syndromeEnrichmentNOD22.13
36Chronic recurrent multifocal osteomyelitis 2, with periostitis and pustulosisEnrichmentIL1RN2.13
37Frontometaphyseal dysplasia 2EnrichmentMAP3K72.13
38Immunodeficiency 15bEnrichmentIKBKB2.13
39Myopathy, distal, with rimmed vacuolesEnrichmentSQSTM12.13
40Neurodevelopmental disorder with microcephaly, hypotonia, and absent languageEnrichmentPSMB12.13
41Frontotemporal dementia and/or amyotrophic lateral sclerosis 3EnrichmentSQSTM12.13
42Immunodeficiency 15aEnrichmentIKBKB2.13
43Neurodevelopmental, jaw, eye, and digital syndromeEnrichmentFBXW112.13
44Bone marrow failure syndrome 5EnrichmentTP532.13
45Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.13
46Stankiewicz-isidor syndromeEnrichmentPSMD122.13
47Papilloma of choroid plexusEnrichmentTP532.13
48Basal cell carcinoma 7EnrichmentTP532.13
49Anaplastic thyroid carcinomaEnrichmentTP532.13
50Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.13
51Asthma-related traits 5EnrichmentIRAK32.13
52Deafness, cataract, impaired intellectual development, and polyneuropathyEnrichmentPSMC32.13
53Microvascular complications of diabetes 4EnrichmentIL1RN2.13
54Cerebral amyloid angiopathy, app-relatedEnrichmentAPP2.13
55MelorheostosisEnrichmentMAP2K12.13
56Immunodeficiency 67EnrichmentIRAK42.13
57Retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndromeEnrichmentALPK12.13
58Ductal carcinoma in situEnrichmentTP532.13
59Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.13
60Bartsocas-papas syndrome 2EnrichmentCHUK2.13
61Pseudo-torch syndrome 2EnrichmentUSP182.13
62Serum amyloid a amyloidosisEnrichmentSAA12.13
63Thyroid gland undifferentiated carcinomaEnrichmentTP532.13
64Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.13
65Alpk1-related autoinflammatory diseaseEnrichmentALPK12.13
66Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.13
67Cerebral cavernous malformations 5EnrichmentMAP3K32.13
68Choroid plexus cancerEnrichmentTP532.13
69Waldenstram macroglobulinemiaEnrichmentMYD882.13
70Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.13
71Pleomorphic xanthoastrocytomaEnrichmentTP532.13
72Verrucous hemangiomaEnrichmentMAP3K32.13
73Polyvalvular heart disease syndromeEnrichmentTAB22.13
74Noonan syndrome and noonan-related syndromeEnrichmentMAP2K1, PTPN112.00
75MetachondromatosisEnrichmentPTPN111.99
76Leopard syndrome 1EnrichmentPTPN111.99
77Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticityEnrichmentPTPN231.99
78T-cell large granular lymphocyte leukemiaEnrichmentSTAT31.99
79Autoinflammation with arthritis and vasculitisEnrichmentTBK11.99
80Choanal atresia and lymphedemaEnrichmentPTPN141.99
81Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT31.99
82Corticobasal syndromeEnrichmentTBK11.99
83Encephalopathy, acute, infection-induced 8EnrichmentTBK11.99
84Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT31.99
85Vegetative pyoderma gangrenosumEnrichmentPTPN61.99
86Bullous pyoderma gangrenosumEnrichmentPTPN61.99
87Pustular pyoderma gangrenosumEnrichmentPTPN61.99
88Lymphedema-posterior choanal atresia syndromeEnrichmentPTPN141.99
89Classic pyoderma gangrenosumEnrichmentPTPN61.99
90Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT31.99
91Malignant astrocytomaEnrichmentPTPN111.99
92Non-syndromic x-linked intellectual disabilityEnrichmentIL1RAPL11.98
93Hepatocellular carcinomaEnrichmentCASP8, TP531.94
94Cerebral amyloid angiopathy, cst3-relatedEnrichmentAPP1.83
95Adrenocortical carcinoma, hereditaryEnrichmentTP531.83
96Cervical cancerEnrichmentTP531.83
97Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA1.83
98Welander distal myopathyEnrichmentSQSTM11.83
99Yao syndromeEnrichmentNOD21.83
100Lymphoma, hodgkin, classicEnrichmentTP531.83
101Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB11.83
102Immunodeficiency, common variable, 10EnrichmentNFKB21.83
103Diamond-blackfan anemia 12EnrichmentNKIRAS11.83
104Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onsetEnrichmentSQSTM11.83
105Birk-aharoni syndromeEnrichmentPSMC11.83
106Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA1.83
107Proteasome-associated autoinflammatory syndrome 3EnrichmentPSMB41.83
108Rela fusion-positive ependymomaEnrichmentRELA1.83
109Congenital fibrosarcomaEnrichmentTP531.83
110Li-fraumeni syndrome 1EnrichmentTP531.83
111SarcomaEnrichmentTP531.83
112Congenital dyserythropoietic anemiaEnrichmentIRAK41.83
113Congenital heart defects, multiple types, 2EnrichmentTAB21.83
114Cervix carcinomaEnrichmentTP531.83
115Hodgkin's lymphomaEnrichmentTP531.83
116Paget's disease of boneEnrichmentSQSTM11.83
117Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG1.83
11817q24.2 microdeletion syndromeEnrichmentPSMD121.83
119Crohn's diseaseEnrichmentNOD21.83
120Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB21.83
121Common variable immunodeficiency 12EnrichmentNFKB11.83
122Pleomorphic rhabdomyosarcomaEnrichmentTP531.83
123Submucosal cleft palateEnrichmentUBB1.83
124Cleft hard palateEnrichmentUBB1.83
125Spastic paraplegia-paget disease of bone syndromeEnrichmentSQSTM11.83
126Loeys-dietz syndrome 3EnrichmentSMAD31.69
127Psoriasis 14, pustularEnrichmentIL36RN1.69
128Werner syndromeEnrichmentPTPN111.69
129Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK11.69
130Pelvic organ prolapseEnrichmentTAB21.65
131Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB41.65
132Uvula, bifidEnrichmentUBB1.65
133Langerhans cell histiocytosisEnrichmentMAP2K11.65
134Osteogenic sarcomaEnrichmentTP531.65
135Cleft soft palateEnrichmentUBB1.65
136Proteosome-associated autoinflammatory syndromeEnrichmentPSMB41.65
137Atypical teratoid rhabdoid tumorEnrichmentTP531.65
138Anaplastic astrocytomaEnrichmentTP531.65
139Frontometaphyseal dysplasiaEnrichmentMAP3K71.65
140Squamous cell carcinomaEnrichmentTP531.65
141AdenocarcinomaEnrichmentTP531.65
142Bone osteosarcomaEnrichmentTP531.65
143Thyroid hemiagenesisEnrichmentPSMD31.65
144Noonan syndrome 1EnrichmentMAP2K1, PTPN111.64
145Lung cancerEnrichmentCASP8, MAP3K81.63
146RasopathyEnrichmentMAP2K1, PTPN111.54
147Cardiofaciocutaneous syndrome 1EnrichmentMAP2K11.53
148Small cell cancer of the lungEnrichmentTP531.53
149Thyroid cancer, nonmedullary, 1EnrichmentTP531.53
150Paget disease of bone 2, early-onsetEnrichmentSQSTM11.53
151Immunodeficiency, common variable, 1EnrichmentNFKB21.53
152Cardiofaciocutaneous syndromeEnrichmentMAP2K11.53
153Lung sarcomatoid carcinomaEnrichmentTP531.53
154Embryonal rhabdomyosarcomaEnrichmentTP531.53
155Paget's disease of bone 2EnrichmentSQSTM11.53
156Pediatric systemic lupus erythematosusEnrichmentIRAK11.53
157Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT31.52
158Neutrophilic dermatosis, acute febrileEnrichmentPTPN61.52
159Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT31.52
160Hyper ige syndromeEnrichmentSTAT31.52
161Tricuspid valve insufficiencyEnrichmentPTPN111.52
162Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.44
163Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.44
164Rhabdomyosarcoma 2EnrichmentTP531.44
165Acute megakaryocytic leukemiaEnrichmentTP531.44
166Aortic aneurysmEnrichmentSMAD31.39
167Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN111.39
168Noonan syndrome with multiple lentiginesEnrichmentPTPN111.39
169Developmental dysplasia of the hip 1EnrichmentPSMC31.36
170Li-fraumeni syndromeEnrichmentTP531.36
171Adrenocortical carcinomaEnrichmentTP531.36
172Breast adenocarcinomaEnrichmentTP531.36
173Herpes simplex virus encephalitisEnrichmentTBK11.30
174Esophageal cancerEnrichmentTP531.29
175Squamous cell carcinoma, head and neckEnrichmentTP531.29
176Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.29
177Alzheimer's disease 1EnrichmentAPP1.29
178Essential thrombocythemiaEnrichmentTP531.29
179Gallbladder cancerEnrichmentTP531.29
180Early-onset autosomal dominant alzheimer diseaseEnrichmentAPP1.29
181B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.29
182Glioma susceptibility 1EnrichmentTP531.24
183Lymphoma, non-hodgkin, familialEnrichmentTP531.24
184Inflammatory bowel disease 1EnrichmentNOD21.19
185Coronary heart disease 5EnrichmentIKBKG1.19
186Arteriovenous malformationEnrichmentMAP2K11.19
187Primary hyperaldosteronismEnrichmentTP531.19
188Behavioral variant of frontotemporal dementiaEnrichmentSQSTM11.19
189Noonan syndrome 3EnrichmentPTPN111.16
190Motor neuron diseaseEnrichmentTBK11.16
191Oligoarticular juvenile idiopathic arthritisEnrichmentPTPN21.16
192Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentPTPN21.16
193Leukemia, chronic lymphocyticEnrichmentTP531.14
194Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.14
195Ciliary dyskinesia, primary, 3EnrichmentNFKB11.14
196PolymicrogyriaEnrichmentPSMC31.14
197Familial colorectal cancerEnrichmentTP531.14
198Migraine with or without aura 1EnrichmentTAB21.10
199Myelodysplastic syndromeEnrichmentTP531.10
200Lung non-small cell carcinomaEnrichmentMAP2K11.10
201Permanent neonatal diabetes mellitusEnrichmentSTAT31.10
202Lip and oral cavity carcinomaEnrichmentTP531.07
203Loeys-dietz syndromeEnrichmentSMAD31.05
204Progressive non-fluent aphasiaEnrichmentTBK11.05
205Familial thoracic aortic aneurysm and dissectionEnrichmentSMAD31.05
206Aortic valve disease 1EnrichmentTAB21.03
207Alzheimer's diseaseEnrichmentAPP1.03
208Lung cancer susceptibility 3EnrichmentTP531.00
209Pectus excavatumEnrichmentPTPN110.97
210Specific learning disabilityEnrichmentPTPN110.97
211Breast cancerEnrichmentCASP8, TP530.97
212RhabdomyosarcomaEnrichmentTP530.95
213EpicanthusEnrichmentPTPN110.93
214Juvenile myelomonocytic leukemiaEnrichmentPTPN110.93
215Congenital long qt syndromeEnrichmentPTPN110.93
216Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSQSTM1, TBK10.92
217Alzheimer disease, familial, 1EnrichmentAPP0.92
218Acute promyelocytic leukemiaEnrichmentSTAT30.90
219Behcet syndromeEnrichmentNOD20.88
220Aortic aneurysm, familial thoracic 1EnrichmentSMAD30.87
221Complex neurodevelopmental disorderEnrichmentFBXW11, PSMD12, PTPN230.87
222HepatoblastomaEnrichmentTP530.84
223Myocardial infarctionEnrichmentPSMA60.82
224Multisystem inflammatory syndrome in childrenEnrichmentIRAK30.82
225Diamond-blackfan anemia 1EnrichmentTP530.80
226MalariaEnrichmentIKBKG0.80
227Pancreatic cancerEnrichmentTP530.77
228Ehlers-danlos syndromeEnrichmentSMAD30.75
229Bladder cancerEnrichmentTP530.71
230Prostate cancerEnrichmentTP530.71
231Severe combined immunodeficiencyEnrichmentIKBKB0.66
232ScoliosisEnrichmentPTPN110.66
233Colorectal cancerEnrichmentPTPN12, TP530.65
234Hydrops fetalis, nonimmuneEnrichmentPTPN110.63
235Diamond-blackfan anemiaEnrichmentTP530.63
236StrabismusEnrichmentPTPN110.61
237Systemic lupus erythematosusEnrichmentIRAK10.60
238Leukemia, acute myeloidEnrichmentTP530.59
239Long qt syndrome 1EnrichmentPTPN110.58
240Non-immune hydrops fetalisEnrichmentPTPN110.56
241Hereditary breast carcinomaEnrichmentTP530.55
242Connective tissue diseaseEnrichmentSMAD30.55
243Autism spectrum disorderEnrichmentMAP2K1, PTPN110.51
244Hereditary breast ovarian cancer syndromeEnrichmentTP530.47
245Myeloma, multipleEnrichmentTP530.47
246Hereditary spastic paraplegiaEnrichmentPTPN230.45
247Hypertrophic cardiomyopathyEnrichmentPTPN110.45
248MicrocephalyEnrichmentPSMC3, PTPN110.44
249Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD30.44
250ThrombocytopeniaEnrichmentPTPN110.41
251Inherited cancer-predisposing syndromeEnrichmentPTPN11, TP530.41
252Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.36
253Dilated cardiomyopathyEnrichmentTAB20.35
254Ovarian cancerEnrichmentTP530.27

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