Interleukin-6 family signaling

Pathway network for the Interleukin-6 family signaling SuperPath

Sources:
  • Reactome
  • GeneGo (Thomson Reuters)

Gene overlap in member pathways for Interleukin-6 family signaling SuperPath

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

Disorders associated with Interleukin-6 family signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT39.39
2Primary cutaneous amyloidosisEnrichmentIL31RA, OSMR5.83
3Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCBL, PTPN115.45
4Stuve-wiedemann syndrome 1EnrichmentIL6ST, LIFR5.35
5Cold-induced sweating syndromeEnrichmentCLCF1, CRLF15.35
6Stüve-wiedemann syndromeEnrichmentIL6ST, LIFR5.35
7Myeloproliferative neoplasmEnrichmentCBL, JAK25.22
8Crisponi/cold-induced sweating syndrome 1EnrichmentCLCF1, CRLF14.83
9Juvenile myelomonocytic leukemiaEnrichmentCBL, PTPN114.41
10Noonan syndrome and noonan-related syndromeEnrichmentCBL, PTPN114.20
11Acute promyelocytic leukemiaEnrichmentSTAT3, STAT5B3.84
12Noonan syndrome 1EnrichmentCBL, PTPN113.82
13RasopathyEnrichmentCBL, PTPN113.72
14Human immunodeficiency virus type 1EnrichmentCCL11, CCL23.55
15MetachondromatosisEnrichmentPTPN113.09
16Immunodeficiency 35EnrichmentTYK23.09
17Dermatitis, atopic, 4EnrichmentSOCS33.09
18Leopard syndrome 1EnrichmentPTPN113.09
19Stuve-wiedemann syndrome 2EnrichmentIL6ST3.09
20Hyper-ige syndrome 4a, autosomal dominant, with recurrent infectionsEnrichmentIL6ST3.09
21T-cell large granular lymphocyte leukemiaEnrichmentSTAT33.09
22Interleukin 6, serum level of, quantitative trait locusEnrichmentIL6R3.09
23Immunodeficiency 31aEnrichmentSTAT13.09
24Soluble interleukin-6 receptor, serum level of, quantitative trait locusEnrichmentIL6R3.09
25Hyper-ige syndrome 5, autosomal recessive, with recurrent infectionsEnrichmentIL6R3.09
26Immunodeficiency 31bEnrichmentSTAT13.09
27Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT33.09
28Hyper-ige syndrome 4b, autosomal recessive, with recurrent infectionsEnrichmentIL6ST3.09
29Immunodeficiency 94 with autoinflammation and dysmorphic faciesEnrichmentIL6ST3.09
30Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT33.09
31Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT33.09
32Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK13.09
33Malignant astrocytomaEnrichmentPTPN113.09
34Amyloidosis, primary localized cutaneous, 1EnrichmentOSMR2.90
35Craniosynostosis and dental anomaliesEnrichmentIL11RA2.90
36Amyloidosis, primary localized cutaneous, 2EnrichmentIL31RA2.90
37Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B2.85
38Microvascular complications of diabetes 1EnrichmentVEGFA2.85
39Ovarian germ cell cancerEnrichmentCBL2.79
40Thrombocythemia 3EnrichmentJAK22.79
41Immunodeficiency 31cEnrichmentSTAT12.79
42Werner syndromeEnrichmentPTPN112.79
43Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.79
44PolycythemiaEnrichmentJAK22.79
45Lymphomatoid papulosisEnrichmentTYK22.79
46Hypereosinophilic syndromeEnrichmentJAK22.79
47Malignant germ cell tumor of ovaryEnrichmentCBL2.79
48Primary cutaneous anaplastic large cell lymphomaEnrichmentTYK22.79
49Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.61
50Polycythemia veraEnrichmentJAK22.61
51Hyper ige syndromeEnrichmentSTAT32.61
52Tricuspid valve insufficiencyEnrichmentPTPN112.61
53Crisponi/cold-induced sweating syndrome 2EnrichmentCLCF12.60
54Cold-induced sweating syndrome 2EnrichmentCLCF12.60
55Cold-induced sweating syndrome including crisponi syndromeEnrichmentCRLF12.60
56Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.55
57Recessive dystrophic epidermolysis bullosaEnrichmentMMP12.55
58Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.55
59Kaposi sarcomaEnrichmentIL62.49
60Erythrocytosis, familial, 1EnrichmentJAK22.49
61Budd-chiari syndromeEnrichmentJAK22.49
62Noonan syndrome with multiple lentiginesEnrichmentPTPN112.49
63Systemic-onset juvenile idiopathic arthritisEnrichmentIL62.49
64Cone-rod dystrophy 12EnrichmentCRLF12.43
65Rheumatoid arthritis, systemic juvenileEnrichmentIL62.39
66LymphomaEnrichmentPTPN112.39
67Aggressive systemic mastocytosisEnrichmentCBL2.39
68Type 1 diabetes mellitusEnrichmentIL62.31
69Patent ductus arteriosusEnrichmentPTPN112.31
70Chronic mucocutaneous candidiasisEnrichmentSTAT12.31
71Cold-induced sweating syndrome 1EnrichmentCRLF12.30
72Idiopathic achalasiaEnrichmentCRLF12.30
73Mantle cell lymphomaEnrichmentCCND12.25
74MyelofibrosisEnrichmentJAK22.25
75Noonan syndrome 3EnrichmentPTPN112.25
76Essential thrombocythemiaEnrichmentJAK22.25
77Permanent neonatal diabetes mellitusEnrichmentSTAT32.19
78Von hippel-lindau syndromeEnrichmentCCND12.16
79Inflammatory bowel disease 1EnrichmentIL62.14
80Leukemia, acute lymphoblastic 3EnrichmentJAK22.14
81Pectus excavatumEnrichmentPTPN112.05
82Specific learning disabilityEnrichmentPTPN112.05
83EpicanthusEnrichmentPTPN112.01
84Congenital long qt syndromeEnrichmentPTPN112.01
85RhabdomyosarcomaEnrichmentCBL1.89
86Leukemia, chronic lymphocyticEnrichmentCCND11.86
87Patent foramen ovaleEnrichmentPTPN111.84
88AsthmaEnrichmentCCL111.82
89Arteriovenous malformations of the brainEnrichmentIL61.82
90Diffuse large b-cell lymphomaEnrichmentSTAT31.82
91ScoliosisEnrichmentPTPN111.71
92Hydrops fetalis, nonimmuneEnrichmentPTPN111.68
93StrabismusEnrichmentPTPN111.66
94Long qt syndrome 1EnrichmentPTPN111.62
95CraniosynostosisEnrichmentIL11RA1.61
96Non-immune hydrops fetalisEnrichmentPTPN111.60
97Leukemia, acute myeloidEnrichmentJAK21.50
98Type 2 diabetes mellitusEnrichmentIL61.47
99Hypertrophic cardiomyopathyEnrichmentPTPN111.46
100ThrombocytopeniaEnrichmentPTPN111.42
101CakutEnrichmentLIFR1.38
102Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.35
103Primary ovarian insufficiencyEnrichmentJAK21.33
104Myeloma, multipleEnrichmentCCND11.12
105Autism spectrum disorderEnrichmentPTPN111.07
106MicrocephalyEnrichmentPTPN111.02
107Inherited cancer-predisposing syndromeEnrichmentPTPN110.99
108Colorectal cancerEnrichmentCCND10.94

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