IL-17 Family Signaling Pathways

Pathway network for the IL-17 Family Signaling Pathways SuperPath

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

Pathways in the IL-17 Family Signaling Pathways SuperPath

Gene overlap in member pathways for IL-17 Family Signaling Pathways SuperPath

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

Disorders associated with IL-17 Family Signaling Pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chronic mucocutaneous candidiasisEnrichmentIL17F, IL17RA, IL17RC, TRAF3IP29.45
2Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT37.97
3Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.07
4Metaphyseal anadysplasiaEnrichmentMMP13, MMP94.46
5Histiocytoid hemangiomaEnrichmentFOS, FOSB4.07
6Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.75
7Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K23.69
8Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K23.69
9Herpes simplex virus encephalitisEnrichmentTBK1, TRAF33.47
10Proteus syndromeEnrichmentAKT12.64
11Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.64
12Incontinentia pigmentiEnrichmentIKBKG2.64
13Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.64
14Candidiasis, familial, 6EnrichmentIL17F2.64
15Frontometaphyseal dysplasia 2EnrichmentMAP3K72.64
16Immunodeficiency 15bEnrichmentIKBKB2.64
17Noonan syndrome 13EnrichmentMAPK12.64
18Immunodeficiency 15aEnrichmentIKBKB2.64
19Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.64
20Immunodeficiency 132aEnrichmentTRAF32.64
21Immunodeficiency 132bEnrichmentTRAF32.64
22T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.64
23Cowden syndrome 6EnrichmentAKT12.64
24Hypogonadotropic hypogonadism 18 with or without anosmiaEnrichmentIL17RD2.64
25Candidiasis, familial, 9EnrichmentIL17RC2.64
26Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.64
27PsoriasisEnrichmentIL17RA2.64
28Immunodeficiency 112EnrichmentMAP3K142.64
29Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.64
30Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.64
31Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.64
32Nik deficiencyEnrichmentMAP3K142.64
33Leprosy 3EnrichmentTLR22.53
34Legionnaire diseaseEnrichmentTLR52.53
35Fetal encasement syndromeEnrichmentCHUK2.53
36Stuve-wiedemann syndrome 2EnrichmentIL6ST2.53
37Hyper-ige syndrome 4a, autosomal dominant, with recurrent infectionsEnrichmentIL6ST2.53
38Immunodeficiency 92EnrichmentREL2.53
39Systemic lupus erythematosus 1EnrichmentTLR52.53
40Immunodeficiency 42EnrichmentRORC2.53
41Interleukin 6, serum level of, quantitative trait locusEnrichmentIL6R2.53
42Soluble interleukin-6 receptor, serum level of, quantitative trait locusEnrichmentIL6R2.53
43Hyper-ige syndrome 5, autosomal recessive, with recurrent infectionsEnrichmentIL6R2.53
44MelioidosisEnrichmentTLR52.53
45Hyper-ige syndrome 4b, autosomal recessive, with recurrent infectionsEnrichmentIL6ST2.53
46Immunodeficiency 94 with autoinflammation and dysmorphic faciesEnrichmentIL6ST2.53
47Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.53
48Immunodeficiency 53EnrichmentRELB2.53
49Bartsocas-papas syndrome 2EnrichmentCHUK2.53
50Aquagenic palmoplantar keratodermaEnrichmentCFTR2.53
51Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.53
52Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.53
53Extrinsic allergic alveolitisEnrichmentMUC5B2.53
54Noonan syndrome and noonan-related syndromeEnrichmentMAP2K1, MAP2K22.46
55Immunodeficiency 33EnrichmentIKBKG2.34
56Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.34
57Thrombocythemia 3EnrichmentJAK22.34
58Immunodeficiency 51EnrichmentIL17RA2.34
59Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.34
60Rela fusion-positive ependymomaEnrichmentRELA2.34
61Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.34
62Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.34
63PolycythemiaEnrichmentJAK22.34
64Hypereosinophilic syndromeEnrichmentJAK22.34
65Common variable immunodeficiency 12EnrichmentNFKB12.34
66Discoid lupus erythematosusEnrichmentTRAF3IP22.34
67Spermatogenic failure, y-linked, 2EnrichmentCFTR2.23
68Panbronchiolitis, diffuseEnrichmentMUC5B2.23
69Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.23
70Immunodeficiency, common variable, 10EnrichmentNFKB22.23
71Immunodeficiency 108 with autoinflammationEnrichmentCEBPE2.23
72Caspase 8 deficiencyEnrichmentCASP82.23
73Melorheostosis, isolatedEnrichmentMAP2K12.23
74Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.23
75Autoimmune lymphoproliferative syndrome, type iiaEnrichmentCASP102.23
76MelorheostosisEnrichmentMAP2K12.23
77Coronary heart disease 6EnrichmentMMP32.23
78Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.23
79Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.23
80Autoinflammation with arthritis and vasculitisEnrichmentTBK12.23
81Corticobasal syndromeEnrichmentTBK12.23
82Encephalopathy, acute, infection-induced 8EnrichmentTBK12.23
83Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP22.23
84Epilepsy, idiopathic generalized 19EnrichmentUSP252.23
85Cebpe-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndromeEnrichmentCEBPE2.23
86Acute myeloid leukemia with mutated cebpaEnrichmentCEBPA2.23
87Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.16
88Polycythemia veraEnrichmentJAK22.16
89Psoriasis 13EnrichmentTRAF3IP22.16
90Hyper ige syndromeEnrichmentSTAT32.16
91Candidiasis, familial, 8EnrichmentTRAF3IP22.16
92Frontometaphyseal dysplasiaEnrichmentMAP3K72.16
93Noonan syndrome 1EnrichmentMAP2K1, MAP2K22.10
94Stuve-wiedemann syndrome 1EnrichmentIL6ST2.05
95Nuchal bleb, familialEnrichmentCFTR2.05
96Nasopharyngeal carcinomaEnrichmentNFKBIA2.05
97Stüve-wiedemann syndromeEnrichmentIL6ST2.05
98Erythrocytosis, familial, 1EnrichmentJAK22.04
99Budd-chiari syndromeEnrichmentJAK22.04
100Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.04
101RasopathyEnrichmentMAP2K1, MAP2K21.99
102Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.94
103Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.94
104Myeloproliferative neoplasmEnrichmentJAK21.94
105Kaposi sarcomaEnrichmentIL61.93
106Immunodeficiency, common variable, 1EnrichmentNFKB21.93
107Congenital generalized lipodystrophyEnrichmentFOS1.93
108Idiopathic bronchiectasisEnrichmentCFTR1.93
109Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.93
110Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.93
111Metaphyseal dysplasia, spahr typeEnrichmentMMP131.93
112Specific granule deficiency 1EnrichmentCEBPE1.93
113Spondyloepimetaphyseal dysplasia, missouri typeEnrichmentMMP131.93
114Neurodevelopmental disorder with dysmorphic facies and behavioral abnormalitiesEnrichmentSRSF11.93
115Immunodeficiency 127EnrichmentTNF1.93
116Recessive dystrophic epidermolysis bullosaEnrichmentMMP11.93
117Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK11.93
118Metaphyseal anadysplasia 2EnrichmentMMP91.93
119Tafro syndromeEnrichmentMAP2K21.93
120Oculootodental syndromeEnrichmentFADD1.93
121Specific granule deficiencyEnrichmentCEBPE1.93
122Breast adenocarcinomaEnrichmentAKT11.87
123Rheumatoid arthritis, systemic juvenileEnrichmentIL61.83
124MyelofibrosisEnrichmentJAK21.80
125Essential thrombocythemiaEnrichmentJAK21.80
126Type 1 diabetes mellitusEnrichmentIL61.76
127Pulmonary fibrosisEnrichmentMUC5B1.76
128Langerhans cell histiocytosisEnrichmentMAP2K11.75
129Psoriatic arthritisEnrichmentTNF1.75
130Migraine without auraEnrichmentTNF1.75
131Permanent neonatal diabetes mellitusEnrichmentSTAT31.74
132Coronary heart disease 5EnrichmentIKBKG1.69
133Leukemia, acute lymphoblastic 3EnrichmentJAK21.69
134Cowden syndromeEnrichmentAKT11.69
135Ciliary dyskinesia, primary, 3EnrichmentNFKB11.65
136Autoimmune lymphoproliferative syndromeEnrichmentCASP101.63
137Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.63
138Cerebral malariaEnrichmentTNF1.63
139Specific learning disabilityEnrichmentMAPK11.60
140Bronchiectasis with or without elevated sweat chloride 1EnrichmentCFTR1.58
141Vas deferens, congenital bilateral aplasia ofEnrichmentCFTR1.58
142Inflammatory bowel disease 1EnrichmentIL61.58
143MeningiomaEnrichmentAKT11.57
144Vascular dementiaEnrichmentTNF1.54
145Inherited acute myeloid leukemiaEnrichmentCEBPA1.54
146Acute myeloid leukemia with t(8;21)(q22;q22) translocationEnrichmentCEBPA1.54
147Acute promyelocytic leukemiaEnrichmentSTAT31.53
148Heart, malformation ofEnrichmentMAPK11.39
149Hereditary chronic pancreatitisEnrichmentCFTR1.39
150Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.39
151Motor neuron diseaseEnrichmentTBK11.39
152Arteriovenous malformations of the brainEnrichmentIL17RD1.37
153Diffuse large b-cell lymphomaEnrichmentSTAT31.37
154Lynch syndromeEnrichmentCFTR1.36
155GliosarcomaEnrichmentNFKBIA1.34
156Lymphoma, non-hodgkin, familialEnrichmentCASP101.34
157Lennox-gastaut syndromeEnrichmentMAPK101.34
158Pancreatitis, hereditaryEnrichmentCFTR1.31
159Interstitial lung disease 2EnrichmentMUC5B1.31
160Giant cell glioblastomaEnrichmentNFKBIA1.31
161Multisystem inflammatory syndrome in childrenEnrichmentTRAF31.31
162MalariaEnrichmentIKBKG1.29
163Kallmann syndromeEnrichmentIL17RD1.29
164Arteriovenous malformationEnrichmentMAP2K11.29
165Adult hepatocellular carcinomaEnrichmentCASP81.29
166Progressive non-fluent aphasiaEnrichmentTBK11.29
167Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.24
168Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.24
169AsthmaEnrichmentTNF1.20
170Lung non-small cell carcinomaEnrichmentMAP2K11.20
171Severe combined immunodeficiencyEnrichmentIKBKB1.14
172Alzheimer's diseaseEnrichmentTNF1.13
173Severe covid-19EnrichmentMUC5B1.09
174Leukemia, acute myeloidEnrichmentJAK21.06
175Cystic fibrosisEnrichmentCFTR1.04
176Male infertilityEnrichmentCFTR1.02
177Hereditary breast carcinomaEnrichmentAKT11.02
178Human immunodeficiency virus type 1EnrichmentCCL21.00
179Type 2 diabetes mellitusEnrichmentIL60.93
180Hepatocellular carcinomaEnrichmentCASP80.91
181Primary ovarian insufficiencyEnrichmentJAK20.90
182Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentCFTR0.82
183Breast cancerEnrichmentAKT10.80
184Lung cancerEnrichmentCASP80.76
185Colorectal cancerEnrichmentAKT10.74
186Systemic lupus erythematosusEnrichmentTNF0.69
187Ovarian cancerEnrichmentAKT10.68
188Gastric cancerEnrichmentCASP100.65
189MicrocephalyEnrichmentMAPK10.61
190Myeloma, multipleEnrichmentTRAF50.55
191Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK10.54
192Autism spectrum disorderEnrichmentMAP2K10.32
193Inherited cancer-predisposing syndromeEnrichmentCEBPA0.26

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