IL-1 Family Signaling Pathways

Pathway network for the IL-1 Family Signaling Pathways SuperPath

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

Pathways in the IL-1 Family Signaling Pathways SuperPath

#NameSourceGenes
1IL-1 Family Signaling PathwaysR&D Systems
2Pathogen or Damage-activated C-Type Lectin Receptor Signaling PathwaysR&D Systems
3IL1 signaling pathwaySino Biological
4Mucin expression in CF via TLRs, EGFR signaling pathwaysGeneGo (Thomson Reuters)
5Immune response IL-1 signaling pathwayGeneGo (Thomson Reuters)
6Interleukin-1 (IL-1) structural pathwayWikiPathways
7Interleukin-36 pathwayReactome
8Interleukin-33 signalingReactome

Gene overlap in member pathways for IL-1 Family Signaling Pathways SuperPath

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

Disorders associated with IL-1 Family Signaling Pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome 1EnrichmentHRAS, MAP2K1, MAP2K2, RAF1, SOS1, SOS29.24
2RasopathyEnrichmentHRAS, MAP2K1, MAP2K2, RAF1, SOS1, SOS28.91
3Noonan syndrome and noonan-related syndromeEnrichmentHRAS, MAP2K1, MAP2K2, RAF1, SOS18.38
4Cardiofaciocutaneous syndrome 1EnrichmentKRAS, MAP2K1, MAP2K26.30
5Cardiofaciocutaneous syndromeEnrichmentKRAS, MAP2K1, MAP2K26.30
6Noonan syndrome 3EnrichmentHRAS, RAF1, SOS15.55
7Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK4, MYD885.03
8Lung non-small cell carcinomaEnrichmentEGFR, HRAS, MAP2K14.88
9Immunodeficiency 33EnrichmentIKBKG, IRAK44.79
10Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.79
11Nuchal bleb, familialEnrichmentCFTR, SOS14.24
12Pseudomyogenic hemangioendotheliomaEnrichmentFOSB, SERPINE14.02
13MalariaEnrichmentIKBKG, NOS2, TNF3.98
14Diffuse large b-cell lymphomaEnrichmentBTK, CREBBP, MYD883.94
15Noonan syndrome with multiple lentiginesEnrichmentPTPN11, RAF13.82
16Histiocytoid hemangiomaEnrichmentFOS, FOSB3.80
17Lymphoma, mucosa-associated lymphoid typeEnrichmentBCL10, MALT13.60
18Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3003.42
19Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3003.42
20Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.40
21Capillary malformation-arteriovenous malformation 1EnrichmentKRAS, MAP2K13.28
22Pilomyxoid astrocytomaEnrichmentKRAS, RAF13.28
23Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.28
24Arteriovenous malformationEnrichmentHRAS, MAP2K13.17
25Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K13.07
26Psoriasis 14, pustularEnrichmentIL36RN2.99
27Lip and oral cavity carcinomaEnrichmentEGFR, HRAS2.91
28Specific learning disabilityEnrichmentMAPK1, PTPN112.87
29Aortic valve disease 1EnrichmentSOS1, TAB22.84
30Juvenile myelomonocytic leukemiaEnrichmentKRAS, PTPN112.79
3146,xy partial gonadal dysgenesisEnrichmentMAP3K1, SOS12.77
32GliosarcomaEnrichmentEGFR, NFKBIA2.65
33Giant cell glioblastomaEnrichmentEGFR, NFKBIA2.60
34Rare genetic intellectual disabilityEnrichmentCREBBP, EP3002.59
35Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.51
36Immunodeficiency 68EnrichmentMYD882.51
37Macroglobulinemia, waldenstrom 1EnrichmentMYD882.51
38Melorheostosis, isolatedEnrichmentMAP2K12.51
39Immunodeficiency 39 viral infectionsEnrichmentIRF72.51
40Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.51
41Fetal encasement syndromeEnrichmentCHUK2.51
4246,xy sex reversal 6EnrichmentMAP3K12.51
43Frontometaphyseal dysplasia 2EnrichmentMAP3K72.51
44Immunodeficiency 15bEnrichmentIKBKB2.51
45Noonan syndrome 13EnrichmentMAPK12.51
46Immunodeficiency 15aEnrichmentIKBKB2.51
47Autism 19EnrichmentEIF4E2.51
48Immunodeficiency 39EnrichmentIRF72.51
49Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.51
50MelorheostosisEnrichmentMAP2K12.51
51Immunodeficiency 67EnrichmentIRAK42.51
52Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.51
53Bartsocas-papas syndrome 2EnrichmentCHUK2.51
54Immunodeficiency 112EnrichmentMAP3K142.51
55Waldenstram macroglobulinemiaEnrichmentMYD882.51
56Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.51
57Nik deficiencyEnrichmentMAP3K142.51
58Polyvalvular heart disease syndromeEnrichmentTAB22.51
59Arteriovenous malformations of the brainEnrichmentEGFR, IL62.50
60Incontinentia pigmentiEnrichmentIKBKG2.39
61Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.39
62AceruloplasminemiaEnrichmentCP2.39
63Auriculocondylar syndrome 3EnrichmentEDN12.39
64Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.39
65Plasminogen activator inhibitor-1 deficiencyEnrichmentSERPINE12.39
66Question mark ears, isolatedEnrichmentEDN12.39
67Immunodeficiency 31aEnrichmentSTAT12.39
68Immunodeficiency 31bEnrichmentSTAT12.39
69Heme oxygenase 1 deficiencyEnrichmentHMOX12.39
70Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.39
71Congenital plasminogen activator inhibitor type 1 deficiencyEnrichmentSERPINE12.39
72Leprosy 3EnrichmentTLR22.35
73Legionnaire diseaseEnrichmentTLR52.35
74Noonan syndrome 5EnrichmentRAF12.35
75Noonan syndrome 4EnrichmentSOS12.35
76Cardiomyopathy, dilated, 1nnEnrichmentRAF12.35
77Bacteremia 1EnrichmentTIRAP2.35
78Noonan syndrome 9EnrichmentSOS22.35
79Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.35
80Immunodeficiency 92EnrichmentREL2.35
81Systemic lupus erythematosus 1EnrichmentTLR52.35
82Leopard syndrome 2EnrichmentRAF12.35
83MelioidosisEnrichmentTLR52.35
84Thrombocytopenia 6EnrichmentSRC2.35
85Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.35
86Immunodeficiency 53EnrichmentRELB2.35
87TrigonitisEnrichmentRAF12.35
88Aquagenic palmoplantar keratodermaEnrichmentCFTR2.35
89Extrinsic allergic alveolitisEnrichmentMUC5B2.35
90Phakomatosis pigmentokeratoticaEnrichmentHRAS2.35
91Chronic recurrent multifocal osteomyelitis 2, with periostitis and pustulosisEnrichmentIL1RN2.35
92Microvascular complications of diabetes 4EnrichmentIL1RN2.35
93Hepatitis, fulminant viralEnrichmentIL18BP2.35
94Inflammatory bowel disease 31, autosomal recessiveEnrichmentIL372.35
95Inflammatory bowel diseaseEnrichmentIL372.35
96Asthma-related traits 5EnrichmentIRAK32.34
97Achromatopsia 7EnrichmentATF62.34
98MetachondromatosisEnrichmentPTPN112.29
99Immunodeficiency 103 fungal infectionsEnrichmentCARD92.29
100Oculoectodermal syndromeEnrichmentKRAS2.29
101Leopard syndrome 1EnrichmentPTPN112.29
102Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.29
103Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.29
104Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.29
105Isolated growth hormone deficiency type iiiEnrichmentBTK2.29
106Candidiasis, familial, 4EnrichmentCLEC7A2.29
107Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.29
108Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.29
109Dengue virusEnrichmentCD2092.29
110Immunodeficiency 12EnrichmentMALT12.29
111Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.29
112Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.29
113Menke-hennekam syndrome 1EnrichmentCREBBP2.29
114Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.29
115Sezary's diseaseEnrichmentBCL102.29
116Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.29
117ColitisEnrichmentSYK2.29
118Congenital pulmonary airway malformationEnrichmentKRAS2.29
119Vegetative pyoderma gangrenosumEnrichmentPTPN62.29
120Bullous pyoderma gangrenosumEnrichmentPTPN62.29
121Pustular pyoderma gangrenosumEnrichmentPTPN62.29
122Menke-hennekam syndromeEnrichmentCREBBP2.29
123Classic pyoderma gangrenosumEnrichmentPTPN62.29
124Mucosa-associated lymphomaEnrichmentBCL102.29
125Malignant astrocytomaEnrichmentPTPN112.29
126Autoinflammatory diseaseEnrichmentIL1RN, IL36RN2.29
127Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.21
128Rela fusion-positive ependymomaEnrichmentRELA2.21
129Congenital dyserythropoietic anemiaEnrichmentIRAK42.21
130Congenital heart defects, multiple types, 2EnrichmentTAB22.21
131Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.21
132Tafro syndromeEnrichmentMAP2K22.21
133ScoliosisEnrichmentCREBBP, PTPN112.18
134Bladder cancerEnrichmentEGFR, HRAS2.14
135Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.09
136Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.09
137Hermansky-pudlak syndrome 3EnrichmentCP2.09
138Immunodeficiency 31cEnrichmentSTAT12.09
139Immunodeficiency 127EnrichmentTNF2.09
140Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.09
141Immunodeficiency 117EnrichmentIRF12.09
142Common variable immunodeficiency 12EnrichmentNFKB12.09
143Submucosal cleft palateEnrichmentUBB2.09
144Cleft hard palateEnrichmentUBB2.09
145Fibromatosis, gingival, 1EnrichmentSOS12.05
146Costello syndromeEnrichmentHRAS2.05
147Spermatogenic failure, y-linked, 2EnrichmentCFTR2.05
148Panbronchiolitis, diffuseEnrichmentMUC5B2.05
149Pulmonic stenosisEnrichmentSOS12.05
150Immunodeficiency, common variable, 10EnrichmentNFKB22.05
151Wooly hair nevusEnrichmentHRAS2.05
152Pelvic organ prolapseEnrichmentTAB22.03
153Langerhans cell histiocytosisEnrichmentMAP2K12.03
154Frontometaphyseal dysplasiaEnrichmentMAP3K72.03
155Colorectal cancerEnrichmentBCL10, EP300, SRC2.01
156Long qt syndrome 1EnrichmentCALM1, PTPN111.99
157Thumb deformityEnrichmentCREBBP1.99
158Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK1.99
159Agammaglobulinemia 4, autosomal recessiveEnrichmentBLNK1.99
160Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM11.99
161Encephalocraniocutaneous lipomatosisEnrichmentKRAS1.99
162Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS1.99
163Immunodeficiency 37EnrichmentBCL101.99
164AspergillosisEnrichmentCLEC7A1.99
165Long qt syndrome 14EnrichmentCALM11.99
166Agammaglobulinemia, x-linkedEnrichmentBTK1.99
167Werner syndromeEnrichmentPTPN111.99
168Menke-hennekam syndrome 2EnrichmentEP3001.99
169Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP1.99
170Agammaglobulinemia 4EnrichmentBLNK1.99
171Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC21.99
172ArthritisEnrichmentSYK1.99
173Non-immune hydrops fetalisEnrichmentKRAS, PTPN111.97
174Systemic lupus erythematosusEnrichmentIRAK1, TNF1.96
175Uvula, bifidEnrichmentUBB1.92
176Psoriatic arthritisEnrichmentTNF1.92
177Cleft soft palateEnrichmentUBB1.92
178Nasopharyngeal carcinomaEnrichmentNFKBIA1.92
179Migraine without auraEnrichmentTNF1.92
180Severe combined immunodeficiencyEnrichmentIKBKB, MALT11.91
181Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.91
182Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.91
183Congenital generalized lipodystrophyEnrichmentFOS1.91
184Pediatric systemic lupus erythematosusEnrichmentIRAK11.91
185Gastric cancerEnrichmentIL1B, IRF11.88
186Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR1.88
187Large congenital melanocytic nevusEnrichmentHRAS1.88
188SpermatocytomaEnrichmentHRAS1.88
189Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR1.88
190Melanoma of soft tissueEnrichmentATF11.86
191Mesothelioma, malignantEnrichmentBCL101.82
192Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentTLR81.82
193Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK1.82
194Neutrophilic dermatosis, acute febrileEnrichmentPTPN61.82
195Agammaglobulinemia 1EnrichmentBTK1.82
196Tethered spinal cord syndromeEnrichmentCREBBP1.82
197T-cell acute lymphoblastic leukemiaEnrichmentBCL101.82
198Intraocular pressure quantitative trait locusEnrichmentCREBBP1.82
199Tricuspid valve insufficiencyEnrichmentPTPN111.82
200Testicular cancerEnrichmentBCL101.82
201Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.81
202Kaposi sarcomaEnrichmentIL61.79
203Auriculocondylar syndrome 1EnrichmentEDN11.79
204Cerebral malariaEnrichmentTNF1.79
205Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.79
206Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.76
207Immunodeficiency, common variable, 1EnrichmentNFKB21.76
208Epidermolytic nevusEnrichmentHRAS1.76
209Idiopathic bronchiectasisEnrichmentCFTR1.76
210Gingival fibromatosisEnrichmentSOS11.76
211Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.76
212Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.70
213Rheumatoid arthritis, systemic juvenileEnrichmentIL61.70
214Vascular dementiaEnrichmentTNF1.70
215Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS1.69
216Anemia, autoimmune hemolyticEnrichmentTLR81.69
217Lung sarcomatoid carcinomaEnrichmentKRAS1.69
218Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS1.69
219Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN111.69
220Pilocytic astrocytomaEnrichmentKRAS1.69
221Type 1 diabetes mellitusEnrichmentIL61.62
222Chronic mucocutaneous candidiasisEnrichmentSTAT11.62
223MicrocephalyEnrichmentEP300, MAPK1, PTPN111.61
224ThrombocytopeniaEnrichmentPTPN11, SRC1.61
225Rubinstein-taybi syndrome 2EnrichmentEP3001.60
226Follicular lymphomaEnrichmentBCL101.60
227LymphomaEnrichmentPTPN111.60
228Cowden syndrome 1EnrichmentEGFR1.58
229Pulmonary fibrosisEnrichmentMUC5B1.58
230Lung squamous cell carcinomaEnrichmentEGFR1.58
231Hemihyperplasia, isolatedEnrichmentRHOA1.52
232Testicular germ cell tumorEnrichmentBCL101.52
233Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.52
234Patent ductus arteriosusEnrichmentPTPN111.52
235Breast adenocarcinomaEnrichmentKRAS1.52
236HypertrichosisEnrichmentCREBBP1.52
237Nevus, epidermalEnrichmentHRAS1.51
238Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.51
239MyelofibrosisEnrichmentSRC1.51
240Squamous cell carcinoma, head and neckEnrichmentEGFR1.51
241Follicular thyroid carcinomaEnrichmentHRAS1.51
242Lennox-gastaut syndromeEnrichmentMAPK101.50
243Myeloma, multipleEnrichmentCREBBP, KRAS1.48
244Migraine with or without aura 1EnrichmentTAB21.47
24546,xy complete gonadal dysgenesisEnrichmentMAP3K11.47
246Leukemia, chronic myeloidEnrichmentKRAS1.45
247Gallbladder cancerEnrichmentKRAS1.45
248Inflammatory bowel disease 1EnrichmentIL61.44
249Coronary heart disease 5EnrichmentIKBKG1.44
250Bronchiectasis with or without elevated sweat chloride 1EnrichmentCFTR1.41
251Vas deferens, congenital bilateral aplasia ofEnrichmentCFTR1.41
252Ciliary dyskinesia, primary, 3EnrichmentNFKB11.40
253Neurodegeneration with brain iron accumulationEnrichmentCP1.40
254Lymphoma, non-hodgkin, familialEnrichmentBCL101.40
255Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.40
256Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM11.40
257Breast cancerEnrichmentJUN, SHC11.36
258AsthmaEnrichmentTNF1.36
259AchromatopsiaEnrichmentATF61.35
260Charge syndromeEnrichmentEP3001.35
261Dilated cardiomyopathyEnrichmentRAF1, TAB21.31
262Autosomal non-syndromic agammaglobulinemiaEnrichmentBLNK1.30
263Pulmonary disease, chronic obstructiveEnrichmentHMOX11.29
264Alzheimer's diseaseEnrichmentTNF1.29
265Heart, malformation ofEnrichmentMAPK11.27
266Patent foramen ovaleEnrichmentTAB21.27
267Pectus excavatumEnrichmentPTPN111.26
268Immune deficiency diseaseEnrichmentSYK1.26
269Combined immunodeficiencyEnrichmentMALT11.26
270Combined t cell and b cell immunodeficiencyEnrichmentMALT11.26
271Combined t and b cell immunodeficiencyEnrichmentMALT11.26
272Hermansky-pudlak syndromeEnrichmentCP1.23
273EpicanthusEnrichmentPTPN111.23
274Congenital long qt syndromeEnrichmentPTPN111.23
275OsteoporosisEnrichmentSRC1.22
276Lung cancer susceptibility 3EnrichmentEGFR1.22
277Hereditary chronic pancreatitisEnrichmentCFTR1.22
278Hermansky-pudlak syndrome 1EnrichmentCP1.20
279Lynch syndromeEnrichmentCFTR1.19
280RhabdomyosarcomaEnrichmentHRAS1.16
281Heart diseaseEnrichmentCREBBP1.16
282Pancreatitis, hereditaryEnrichmentCFTR1.14
283Interstitial lung disease 2EnrichmentMUC5B1.14
284Ovarian cancerEnrichmentEGFR, MAP3K11.13
285Polydactyly, postaxial, type a1EnrichmentEP3001.13
286Corpus callosum, agenesis ofEnrichmentCREBBP1.13
287Isolated corpus callosum agenesisEnrichmentCREBBP1.13
288Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.13
289Human immunodeficiency virus type 1EnrichmentCD2091.06
290Tooth agenesisEnrichmentTGFA1.03
291Lung cancerEnrichmentMAP3K81.02
292Multisystem inflammatory syndrome in childrenEnrichmentIRAK31.02
293Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.00
294Cardiomyopathy, dilated, 1aEnrichmentNFATC20.99
295Autism spectrum disorderEnrichmentMAP2K1, PTPN110.97
296Hydrops fetalis, nonimmuneEnrichmentHRAS0.96
297Pancreatic cancerEnrichmentKRAS0.92
298Severe covid-19EnrichmentMUC5B0.92
299Differentiated thyroid carcinomaEnrichmentHRAS0.92
300Cystic fibrosisEnrichmentHMOX10.91
301StrabismusEnrichmentPTPN110.89
302Familial hypertrophic cardiomyopathyEnrichmentRAF10.87
303Male infertilityEnrichmentCFTR0.85
304Left ventricular noncompactionEnrichmentRAF10.84
305Long qt syndromeEnrichmentCALM10.83
306Type 2 diabetes mellitusEnrichmentIL60.80
307Leukemia, acute myeloidEnrichmentKRAS0.73
308Hypertrophic cardiomyopathyEnrichmentPTPN110.71
309Hereditary breast carcinomaEnrichmentKRAS0.70
310Familial isolated dilated cardiomyopathyEnrichmentRAF10.68
311Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentCFTR0.66
312Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.65
313Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.61
314Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.60
315Cone-rod dystrophy 2EnrichmentATF60.57
316AutismEnrichmentCREBBP0.51
317Congenital nervous system abnormalityEnrichmentCREBBP0.38
318Nervous system diseaseEnrichmentCREBBP0.38
319Inherited cancer-predisposing syndromeEnrichmentEGFR0.35
320Hereditary retinal dystrophyEnrichmentATF60.13
321Fundus dystrophyEnrichmentATF60.13

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