Interleukin-2 family signaling

Pathway network for the Interleukin-2 family signaling SuperPath

Sources:
  • Reactome

Pathways in the Interleukin-2 family signaling SuperPath

#NameSourceGenes
1Interleukin-2 family signalingReactome
2Interleukin-3, Interleukin-5 and GM-CSF signalingReactome
3Signaling by CSF1 (M-CSF) in myeloid cellsReactome
4Interleukin receptor SHC signalingReactome
5Regulation of signaling by CBLReactome
6Interleukin-15 signalingReactome
7Interleukin-21 signalingReactome

Gene overlap in member pathways for Interleukin-2 family signaling SuperPath

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

Disorders associated with Interleukin-2 family signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome and noonan-related syndromeEnrichmentCBL, KRAS, PTPN11, SOS17.52
2Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK1, JAK2, STAT37.50
3Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCBL, PTPN11, YWHAZ6.81
4Noonan syndrome 1EnrichmentCBL, KRAS, PTPN11, SOS16.72
5RasopathyEnrichmentCBL, KRAS, PTPN11, SOS16.49
6Noonan syndrome 3EnrichmentKRAS, PTPN11, SOS16.42
7Autosomal non-syndromic agammaglobulinemiaEnrichmentBLNK, PIK3CD, PIK3R16.36
8Immunodeficiency 31cEnrichmentIL21R, STAT16.31
9Oligoarticular juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB, STAT45.96
10Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB, STAT45.96
11Juvenile myelomonocytic leukemiaEnrichmentCBL, KRAS, PTPN115.63
12Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.12
13Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R15.12
14Immunodeficiency 14EnrichmentPIK3CD, PIK3R15.12
15Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R24.82
16Acute promyelocytic leukemiaEnrichmentSTAT3, STAT5B4.42
17Hereditary pulmonary alveolar proteinosisEnrichmentCSF2RA, CSF2RB4.42
18Breast adenocarcinomaEnrichmentKRAS, PIK3CA4.12
19Lung squamous cell carcinomaEnrichmentKRAS, PIK3CA4.12
20Nevus, epidermalEnrichmentKRAS, PIK3CA3.98
21Capillary malformation-arteriovenous malformation 1EnrichmentKRAS, PIK3CA3.98
22Gallbladder cancerEnrichmentKRAS, PIK3CA3.98
23Myeloproliferative neoplasmEnrichmentCBL, JAK23.93
24Lung non-small cell carcinomaEnrichmentKRAS, PIK3CA3.56
25Nk-cell enteropathyEnrichmentJAK3, PIK3CB3.53
26Breast cancerEnrichmentIL2, PIK3CA, SHC13.36
27Lynch syndromeEnrichmentKRAS, PIK3CA3.28
28Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B3.13
29Disabling pansclerotic morphea of childhoodEnrichmentSTAT43.13
30T-cell large granular lymphocyte leukemiaEnrichmentSTAT33.13
31Systemic lupus erythematosus 11EnrichmentSTAT43.13
32Immunodeficiency 31aEnrichmentSTAT13.13
33Immunodeficiency 31bEnrichmentSTAT13.13
34Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT33.13
35T-b+ severe combined immunodeficiency due to jak3 deficiencyEnrichmentJAK33.13
36Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT33.13
37Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT33.13
38Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK13.13
39Colorectal cancerEnrichmentPIK3CA, PIK3R1, SRC3.00
40Noonan syndrome 4EnrichmentSOS12.99
41Noonan syndrome 9EnrichmentSOS22.99
42Immunodeficiency 63 with lymphoproliferation and autoimmunityEnrichmentIL2RB2.99
43Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.83
44Immunodeficiency 56EnrichmentIL21R2.83
45Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.83
46Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.83
47MacrodactylyEnrichmentPIK3CA2.79
48Megalencephaly, autosomal dominantEnrichmentPIK3CA2.79
49Cowden syndrome 5EnrichmentPIK3CA2.79
50Cerebral cavernous malformations 4EnrichmentPIK3CA2.79
51Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.79
52Short syndromeEnrichmentPIK3R12.79
53Hemifacial myohyperplasiaEnrichmentPIK3CA2.79
54Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.79
55Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.79
56Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.79
57Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.79
58Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.79
59Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.79
60Autoinflammation with pulmonary and cutaneous vasculitisEnrichmentHCK2.79
61HypospadiasEnrichmentPIK3CA2.79
62ColitisEnrichmentSYK2.79
63Rare venous malformationEnrichmentPIK3CA2.79
64Diaphragmatic eventrationEnrichmentPIK3CA2.79
65Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.79
66Rare combined vascular malformationEnrichmentPIK3CA2.79
67Cavernous lymphangiomaEnrichmentPIK3CA2.79
68Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.79
69Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.79
70Eccrine angiomatous hamartomaEnrichmentPIK3CA2.79
71Macrodactyly of toeEnrichmentPIK3CA2.79
72Bladder cancerEnrichmentKRAS, PIK3CA2.70
73Surfactant metabolism dysfunction, pulmonary, 4EnrichmentCSF2RA2.70
74Type 1 diabetes mellitus 10EnrichmentIL2RA2.70
75Surfactant metabolism dysfunction, pulmonary, 5EnrichmentCSF2RB2.70
76Vegetative pyoderma gangrenosumEnrichmentPTPN62.70
77Bullous pyoderma gangrenosumEnrichmentPTPN62.70
78Pustular pyoderma gangrenosumEnrichmentPTPN62.70
79Classic pyoderma gangrenosumEnrichmentPTPN62.70
80Fibromatosis, gingival, 1EnrichmentSOS12.69
81Pulmonic stenosisEnrichmentSOS12.69
82Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentJAK32.66
83Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.66
84Severe combined immunodeficiency, x-linkedEnrichmentIL2RG2.66
85Combined immunodeficiency, x-linkedEnrichmentIL2RG2.66
86Hyper ige syndromeEnrichmentSTAT32.66
87Immunodeficiency, common variable, 11EnrichmentIL212.66
88Non-immune hydrops fetalisEnrichmentKRAS, PTPN112.65
89MetachondromatosisEnrichmentPTPN112.64
90Oculoectodermal syndromeEnrichmentKRAS2.64
91Leopard syndrome 1EnrichmentPTPN112.64
92Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.64
93Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.64
94Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.64
95Thrombocytopenia 6EnrichmentSRC2.64
96Brain abnormalities, neurodegeneration, and dysosteosclerosisEnrichmentCSF1R2.64
97Csf1r-related disorderEnrichmentCSF1R2.64
98Congenital pulmonary airway malformationEnrichmentKRAS2.64
99Early-onset calcifying leukoencephalopathy-skeletal dysplasiaEnrichmentCSF1R2.64
100Malignant astrocytomaEnrichmentPTPN112.64
101Lung cancerEnrichmentKRAS, PIK3CA2.62
102Adenosine deaminase deficiencyEnrichmentJAK32.53
103Pediatric systemic lupus erythematosusEnrichmentSTAT42.53
104Nuchal bleb, familialEnrichmentSOS12.51
105Ovarian germ cell cancerEnrichmentCBL2.49
106Agammaglobulinemia 4, autosomal recessiveEnrichmentBLNK2.49
107Keratosis, seborrheicEnrichmentPIK3CA2.49
108Roifman-chitayat syndromeEnrichmentPIK3CD2.49
109Noonan syndrome 8EnrichmentPIK3CA2.49
110Agammaglobulinemia 4EnrichmentBLNK2.49
111Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.49
112Immune system diseaseEnrichmentPIK3CD2.49
113ArthritisEnrichmentSYK2.49
114Malignant germ cell tumor of ovaryEnrichmentCBL2.49
115Submucosal cleft palateEnrichmentUBB2.49
116Cleft hard palateEnrichmentUBB2.49
117Immunodeficiency 22EnrichmentLCK2.49
118T-cell lymphoma, subcutaneous panniculitis-likeEnrichmentHAVCR22.49
119Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.46
120Cardioacrofacial dysplasia 1EnrichmentPRKACA2.46
121Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentJAK32.43
122Schneckenbecken dysplasiaEnrichmentINPPL12.40
123Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA2.40
124Thrombocythemia 3EnrichmentJAK22.40
125PolycythemiaEnrichmentJAK22.40
126Hypereosinophilic syndromeEnrichmentJAK22.40
127Gingival fibromatosisEnrichmentSOS12.38
128Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS22.38
129Gastric cancerEnrichmentKRAS, PIK3CA2.37
130Chronic mucocutaneous candidiasisEnrichmentSTAT12.35
131Hereditary breast carcinomaEnrichmentKRAS, PIK3CA2.35
132Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.34
133Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS2.34
134Werner syndromeEnrichmentPTPN112.34
135Pompe disease, infantile-onsetEnrichmentPIK3CA2.31
136Uvula, bifidEnrichmentUBB2.31
137Cleft soft palateEnrichmentUBB2.31
138KeratoacanthomaEnrichmentPIK3CA2.31
139Severe combined immunodeficiencyEnrichmentJAK3, LCK2.29
140ThrombocytopeniaEnrichmentPTPN11, SRC2.27
141Permanent neonatal diabetes mellitusEnrichmentSTAT32.23
142OpsismodysplasiaEnrichmentINPPL12.22
143Polycythemia veraEnrichmentJAK22.22
144Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.22
145Chromosome 22q11.2 deletion syndrome, distalEnrichmentCRKL2.19
146Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R22.19
147Cerebrovascular diseaseEnrichmentPIK3CA2.19
148Familial cerebral cavernous malformationsEnrichmentPIK3CA2.19
149Leukoencephalopathy, hereditary diffuse, with spheroids 1EnrichmentCSF1R2.16
150Tricuspid valve insufficiencyEnrichmentPTPN112.16
151Fibrolamellar carcinomaEnrichmentPRKACA2.16
152Omenn syndromeEnrichmentIL2RG2.13
153Erythrocytosis, familial, 1EnrichmentJAK22.10
154Budd-chiari syndromeEnrichmentJAK22.10
155Combined immunodeficiencyEnrichmentIL2RG2.09
156Combined t cell and b cell immunodeficiencyEnrichmentIL2RG2.09
157Combined t and b cell immunodeficiencyEnrichmentIL2RG2.09
158Capillary malformations, congenitalEnrichmentPIK3CA2.09
159HemimegalencephalyEnrichmentPIK3CA2.09
160Aggressive systemic mastocytosisEnrichmentCBL2.09
161Schimmelpenning-feuerstein-mims syndromeEnrichmentKRAS2.04
162Cardiofaciocutaneous syndrome 1EnrichmentKRAS2.04
163Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS2.04
164Cardiofaciocutaneous syndromeEnrichmentKRAS2.04
165Lung sarcomatoid carcinomaEnrichmentKRAS2.04
166Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS2.04
167Noonan syndrome with multiple lentiginesEnrichmentPTPN112.04
168Pilocytic astrocytomaEnrichmentKRAS2.04
169Klippel-trenaunay-weber syndromeEnrichmentPIK3CA2.01
170Cowden syndrome 1EnrichmentPIK3CA2.01
171Hemihyperplasia, isolatedEnrichmentPIK3CA2.01
172IchthyosisEnrichmentIL2RB1.95
173Overgrowth syndromeEnrichmentPIK3R11.95
174LymphomaEnrichmentPTPN111.94
175Aortic valve disease 1EnrichmentSOS11.87
176Patent ductus arteriosusEnrichmentPTPN111.87
177MyelofibrosisEnrichmentJAK21.86
178Essential thrombocythemiaEnrichmentJAK21.86
179Behcet syndromeEnrichmentSTAT41.86
180Diffuse large b-cell lymphomaEnrichmentSTAT31.86
18146,xy partial gonadal dysgenesisEnrichmentSOS11.84
182Arteriovenous malformationEnrichmentPIK3CA1.84
183Adult hepatocellular carcinomaEnrichmentPIK3CA1.84
184Cowden syndromeEnrichmentPIK3CA1.84
185Leukemia, chronic myeloidEnrichmentKRAS1.80
186Pilomyxoid astrocytomaEnrichmentKRAS1.80
187Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.79
188Immune deficiency diseaseEnrichmentSYK1.75
189Leukemia, acute lymphoblastic 3EnrichmentJAK21.75
190MeningiomaEnrichmentPIK3CA1.71
191Lip and oral cavity carcinomaEnrichmentPIK3CA1.71
192Severe covid-19EnrichmentJAK31.67
193Ovarian cancerEnrichmentKRAS, PIK3CA1.65
194Pectus excavatumEnrichmentPTPN111.60
195Frontotemporal dementia 1EnrichmentCSF1R1.60
196Specific learning disabilityEnrichmentPTPN111.60
197RhabdomyosarcomaEnrichmentCBL1.59
198EpicanthusEnrichmentPTPN111.57
199Congenital long qt syndromeEnrichmentPTPN111.57
200Systemic lupus erythematosusEnrichmentSTAT41.55
201Alzheimer's diseaseEnrichmentCSF1R1.53
202Ellis-van creveld syndromeEnrichmentPRKACA1.51
203OsteoporosisEnrichmentSRC1.50
204Lung cancer susceptibility 3EnrichmentKRAS1.50
205Endometrial cancerEnrichmentPIK3CA1.47
206Hepatocellular carcinomaEnrichmentPIK3CA1.45
207Alzheimer disease, familial, 1EnrichmentCSF1R1.42
208Patent foramen ovaleEnrichmentPTPN111.39
209Arteriovenous malformations of the brainEnrichmentKRAS1.37
210Prostate cancerEnrichmentPIK3CA1.34
211ScoliosisEnrichmentPTPN111.27
212Pancreatic cancerEnrichmentKRAS1.25
213Hydrops fetalis, nonimmuneEnrichmentPTPN111.24
214StrabismusEnrichmentPTPN111.22
215Differentiated thyroid carcinomaEnrichmentKRAS1.19
216Long qt syndrome 1EnrichmentPTPN111.18
217Leukemia, acute myeloidEnrichmentJAK21.12
218HypertelorismEnrichmentPIK3CA1.09
219Myeloma, multipleEnrichmentPIK3R21.06
220Hypertrophic cardiomyopathyEnrichmentPTPN111.03
221Primary ovarian insufficiencyEnrichmentJAK20.95
222Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.93
223Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.92
224Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentCSF1R0.90
225Autosomal dominant non-syndromic intellectual disabilityEnrichmentYWHAZ0.80
226Autism spectrum disorderEnrichmentPTPN110.65
227MicrocephalyEnrichmentPTPN110.61
228Inherited cancer-predisposing syndromeEnrichmentPTPN110.58

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