Immune response IL-2 activation and signaling pathway

Pathway network for the Immune response IL-2 activation and signaling pathway SuperPath

Sources:
  • GeneGo (Thomson Reuters)
  • WikiPathways

Pathways in the Immune response IL-2 activation and signaling pathway SuperPath

Gene overlap in member pathways for Immune response IL-2 activation and signaling pathway SuperPath

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

Disorders associated with Immune response IL-2 activation and signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RasopathyEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS1, SOS216.00
2Noonan syndrome and noonan-related syndromeEnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS111.34
3Noonan syndrome 1EnrichmentHRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS1, SOS211.12
4Noonan syndrome 3EnrichmentHRAS, PTPN11, RAF1, SOS18.60
5Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT3, PIK3CA, PIK3R26.38
6Arteriovenous malformationEnrichmentHRAS, MAP2K1, PIK3CA5.06
7Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K1, PIK3CA4.91
8Lung non-small cell carcinomaEnrichmentHRAS, MAP2K1, PIK3CA4.77
9Breast cancerEnrichmentAKT1, IL2, JUN, PIK3CA, SHC14.54
10Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K24.27
11Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K24.27
12Noonan syndrome with multiple lentiginesEnrichmentPTPN11, RAF14.27
13Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.17
14Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R14.17
15Immunodeficiency 14EnrichmentPIK3CD, PIK3R14.17
16Histiocytoid hemangiomaEnrichmentFOS, FOSB4.05
17Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT3, PIK3R23.87
18Type 1 diabetes mellitus 10EnrichmentIL2RA3.83
19Phakomatosis pigmentokeratoticaEnrichmentHRAS3.83
20HemimegalencephalyEnrichmentAKT3, PIK3CA3.65
21Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.61
22Costello syndromeEnrichmentHRAS3.53
23Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA3.53
24Wooly hair nevusEnrichmentHRAS3.53
25Breast adenocarcinomaEnrichmentAKT1, PIK3CA3.48
26Large congenital melanocytic nevusEnrichmentHRAS3.35
27SpermatocytomaEnrichmentHRAS3.35
28Nevus, epidermalEnrichmentHRAS, PIK3CA3.33
29Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K1, PIK3CA3.33
30Gallbladder cancerEnrichmentPIK3CA, SMAD43.33
31Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.33
32Oligoarticular juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.33
33Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.33
34Specific learning disabilityEnrichmentMAPK1, PTPN113.32
35Severe combined immunodeficiencyEnrichmentIKBKB, JAK3, LCK3.29
36Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS3.23
37Epidermolytic nevusEnrichmentHRAS3.23
38Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R1, SMAD43.10
39Cowden syndromeEnrichmentAKT1, PIK3CA3.10
40Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R13.00
41Thyroid cancer, nonmedullary, 2EnrichmentHRAS2.99
42Follicular thyroid carcinomaEnrichmentHRAS2.99
43MeningiomaEnrichmentAKT1, PIK3CA2.84
44Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA2.84
45Nk-cell enteropathyEnrichmentJAK3, PIK3CB2.77
46RhabdomyosarcomaEnrichmentHRAS2.63
47Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.56
48MetachondromatosisEnrichmentPTPN112.52
49Noonan syndrome 5EnrichmentRAF12.52
50Noonan syndrome 4EnrichmentSOS12.52
51Melorheostosis, isolatedEnrichmentMAP2K12.52
52Dermatitis, atopic, 4EnrichmentSOCS32.52
53Leopard syndrome 1EnrichmentPTPN112.52
54Cardiomyopathy, dilated, 1nnEnrichmentRAF12.52
55Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.52
56Noonan syndrome 9EnrichmentSOS22.52
57Noonan syndrome 13EnrichmentMAPK12.52
58Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B2.52
59Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.52
60Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.52
61MelorheostosisEnrichmentMAP2K12.52
62Leopard syndrome 2EnrichmentRAF12.52
63Surfactant metabolism dysfunction, pulmonary, 5EnrichmentCSF2RB2.52
64Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.52
65TrigonitisEnrichmentRAF12.52
66Vegetative pyoderma gangrenosumEnrichmentPTPN62.52
67Bullous pyoderma gangrenosumEnrichmentPTPN62.52
68Pustular pyoderma gangrenosumEnrichmentPTPN62.52
69Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.52
70Classic pyoderma gangrenosumEnrichmentPTPN62.52
71Malignant astrocytomaEnrichmentPTPN112.52
72Non-immune hydrops fetalisEnrichmentHRAS, PTPN112.41
73Bladder cancerEnrichmentHRAS2.37
74Differentiated thyroid carcinomaEnrichmentHRAS2.37
75MacrodactylyEnrichmentPIK3CA2.32
76Proteus syndromeEnrichmentAKT12.32
77Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.32
78Megalencephaly, autosomal dominantEnrichmentPIK3CA2.32
79Cowden syndrome 5EnrichmentPIK3CA2.32
80Fetal encasement syndromeEnrichmentCHUK2.32
81Cerebral cavernous malformations 4EnrichmentPIK3CA2.32
82Immunodeficiency 15bEnrichmentIKBKB2.32
83Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.32
84Immunodeficiency 15aEnrichmentIKBKB2.32
85Immunodeficiency 92EnrichmentREL2.32
86Immunodeficiency 63 with lymphoproliferation and autoimmunityEnrichmentIL2RB2.32
87Short syndromeEnrichmentPIK3R12.32
88Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.32
89Hemifacial myohyperplasiaEnrichmentPIK3CA2.32
90Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.32
91Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.32
92Cowden syndrome 6EnrichmentAKT12.32
93Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.32
94Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.32
95Immunodeficiency 22EnrichmentLCK2.32
96Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.32
97Immunodeficiency 53EnrichmentRELB2.32
98Bartsocas-papas syndrome 2EnrichmentCHUK2.32
99Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.32
100T-b+ severe combined immunodeficiency due to jak3 deficiencyEnrichmentJAK32.32
101Heritable thoracic aortic diseaseEnrichmentSMAD42.32
102HypospadiasEnrichmentPIK3CA2.32
103Capillary hemangiomaEnrichmentAKT32.32
104ColitisEnrichmentSYK2.32
105Rare venous malformationEnrichmentPIK3CA2.32
106Diaphragmatic eventrationEnrichmentPIK3CA2.32
107Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.32
108Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.32
109Rare combined vascular malformationEnrichmentPIK3CA2.32
110Cavernous lymphangiomaEnrichmentPIK3CA2.32
111Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.32
112Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.32
113Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.32
114Eccrine angiomatous hamartomaEnrichmentPIK3CA2.32
115Macrodactyly of toeEnrichmentPIK3CA2.32
116Akt2-related familial partial lipodystrophyEnrichmentAKT22.32
117Fibromatosis, gingival, 1EnrichmentSOS12.22
118Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.22
119Pulmonic stenosisEnrichmentSOS12.22
120Thrombocythemia 3EnrichmentJAK22.22
121Werner syndromeEnrichmentPTPN112.22
122PolycythemiaEnrichmentJAK22.22
123Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.22
124Hypereosinophilic syndromeEnrichmentJAK22.22
125Tafro syndromeEnrichmentMAP2K22.22
126Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.22
127Immune thrombocytopeniaEnrichmentSOCS12.04
128Polycythemia veraEnrichmentJAK22.04
129Nuchal bleb, familialEnrichmentSOS12.04
130Langerhans cell histiocytosisEnrichmentMAP2K12.04
131Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.04
132Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS12.04
133Bacteremia 2EnrichmentCISH2.04
134Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK22.04
135Tricuspid valve insufficiencyEnrichmentPTPN112.04
136Burkitt lymphomaEnrichmentMYC2.02
137Myhre syndromeEnrichmentSMAD42.02
138Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.02
139Juvenile polyposis/hereditary hemorrhagic telangiectasia syndromeEnrichmentSMAD42.02
140Keratosis, seborrheicEnrichmentPIK3CA2.02
141Roifman-chitayat syndromeEnrichmentPIK3CD2.02
142Noonan syndrome 8EnrichmentPIK3CA2.02
143Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.02
144Immunodeficiency, common variable, 10EnrichmentNFKB22.02
145Loeys-dietz syndrome 3EnrichmentSMAD32.02
146Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.02
147Rela fusion-positive ependymomaEnrichmentRELA2.02
148Senior-loken syndrome 7EnrichmentAKT32.02
149Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.02
150Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.02
151Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.02
152Immune system diseaseEnrichmentPIK3CD2.02
153Bardet-biedl syndrome 16EnrichmentAKT32.02
154ArthritisEnrichmentSYK2.02
155Common variable immunodeficiency 12EnrichmentNFKB12.02
156Erythrocytosis, familial, 1EnrichmentJAK21.92
157Anemia, autoimmune hemolyticEnrichmentSOCS11.92
158Budd-chiari syndromeEnrichmentJAK21.92
159Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.92
160Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.92
161Congenital generalized lipodystrophyEnrichmentFOS1.92
162TuberculosisEnrichmentCISH1.92
163Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN111.92
164Gingival fibromatosisEnrichmentSOS11.92
165Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.92
166Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.92
167Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentJAK31.84
168Juvenile polyposis syndromeEnrichmentSMAD41.84
169Pompe disease, infantile-onsetEnrichmentPIK3CA1.84
170Severe combined immunodeficiency, x-linkedEnrichmentIL2RG1.84
171Combined immunodeficiency, x-linkedEnrichmentIL2RG1.84
172Nasopharyngeal carcinomaEnrichmentNFKBIA1.84
173High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC1.84
174KeratoacanthomaEnrichmentPIK3CA1.84
175LymphomaEnrichmentPTPN111.82
176Myeloproliferative neoplasmEnrichmentJAK21.82
177Hereditary pulmonary alveolar proteinosisEnrichmentCSF2RB1.82
178Type 2 diabetes mellitusEnrichmentAKT2, HMGA11.76
179Gastric cancerEnrichmentPIK3CA, SMAD41.74
180Patent ductus arteriosusEnrichmentPTPN111.74
181Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD3, SMAD41.73
182Hereditary breast carcinomaEnrichmentAKT1, PIK3CA1.73
183Immunodeficiency, common variable, 1EnrichmentNFKB21.72
184Cerebrovascular diseaseEnrichmentPIK3CA1.72
185Aortic aneurysmEnrichmentSMAD31.72
186Familial cerebral cavernous malformationsEnrichmentPIK3CA1.72
187Adenosine deaminase deficiencyEnrichmentJAK31.72
188MyelofibrosisEnrichmentJAK21.68
189Essential thrombocythemiaEnrichmentJAK21.68
190Pilomyxoid astrocytomaEnrichmentRAF11.68
191ThrombocytopeniaEnrichmentPTPN11, SMAD41.65
192Capillary malformations, congenitalEnrichmentPIK3CA1.62
193Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentJAK31.62
194Generalized juvenile polyposis/juvenile polyposis coliEnrichmentSMAD41.62
195Leukemia, acute lymphoblastic 3EnrichmentJAK21.57
196Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.55
197Cowden syndrome 1EnrichmentPIK3CA1.55
198Hemihyperplasia, isolatedEnrichmentPIK3CA1.55
199Lung squamous cell carcinomaEnrichmentPIK3CA1.55
200Pectus excavatumEnrichmentPTPN111.48
201Hereditary hemorrhagic telangiectasiaEnrichmentSMAD41.48
202MegacolonEnrichmentAKT31.48
203Overgrowth syndromeEnrichmentPIK3R11.48
204EpicanthusEnrichmentPTPN111.45
205Juvenile myelomonocytic leukemiaEnrichmentPTPN111.45
206Congenital long qt syndromeEnrichmentPTPN111.45
207Aortic valve disease 1EnrichmentSOS11.41
208Acute promyelocytic leukemiaEnrichmentSTAT5B1.41
20946,xy partial gonadal dysgenesisEnrichmentSOS11.38
210Loeys-dietz syndromeEnrichmentSMAD31.37
211Adult hepatocellular carcinomaEnrichmentPIK3CA1.37
212Familial thoracic aortic aneurysm and dissectionEnrichmentSMAD31.37
213Autism spectrum disorderEnrichmentMAP2K1, PTPN111.37
214Omenn syndromeEnrichmentIL2RG1.33
215Ciliary dyskinesia, primary, 3EnrichmentNFKB11.33
216PolymicrogyriaEnrichmentAKT31.33
217Immune deficiency diseaseEnrichmentSYK1.29
218Combined immunodeficiencyEnrichmentIL2RG1.29
219IchthyosisEnrichmentIL2RB1.29
220Combined t cell and b cell immunodeficiencyEnrichmentIL2RG1.29
221Combined t and b cell immunodeficiencyEnrichmentIL2RG1.29
222Heart, malformation ofEnrichmentMAPK11.28
223Patent foramen ovaleEnrichmentPTPN111.28
224MicrocephalyEnrichmentMAPK1, PTPN111.27
225Diffuse large b-cell lymphomaEnrichmentSOCS11.25
226Cardiomyopathy, dilated, 1aEnrichmentNFATC21.21
227Aortic aneurysm, familial thoracic 1EnrichmentSMAD31.19
228MalariaEnrichmentCISH1.17
229Lynch syndromeEnrichmentPIK3CA1.16
230Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.15
231ScoliosisEnrichmentPTPN111.15
232GliosarcomaEnrichmentNFKBIA1.13
233Giant cell glioblastomaEnrichmentNFKBIA1.11
234StrabismusEnrichmentPTPN111.10
235Ovarian cancerEnrichmentAKT1, PIK3CA1.07
236Long qt syndrome 1EnrichmentPTPN111.06
237Ehlers-danlos syndromeEnrichmentSMAD31.06
238Familial hypertrophic cardiomyopathyEnrichmentRAF11.02
239Endometrial cancerEnrichmentPIK3CA1.02
240Hepatocellular carcinomaEnrichmentPIK3CA1.00
241Left ventricular noncompactionEnrichmentRAF11.00
242Precursor t-cell acute lymphoblastic leukemiaEnrichmentMYC0.98
243Systemic lupus erythematosusEnrichmentSOCS10.95
244Pancreatic cancerEnrichmentSMAD40.95
245Leukemia, acute myeloidEnrichmentJAK20.94
246Hypertrophic cardiomyopathyEnrichmentPTPN110.91
247Prostate cancerEnrichmentPIK3CA0.89
248Severe covid-19EnrichmentJAK30.89
249Inherited cancer-predisposing syndromeEnrichmentPTPN11, SMAD40.88
250Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.85
251Lung cancerEnrichmentPIK3CA0.85
252Connective tissue diseaseEnrichmentSMAD30.85
253Familial isolated dilated cardiomyopathyEnrichmentRAF10.83
254Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.81
255Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.81
256Primary ovarian insufficiencyEnrichmentJAK20.79
257Dilated cardiomyopathyEnrichmentRAF10.67
258HypertelorismEnrichmentPIK3CA0.65
259Myeloma, multipleEnrichmentPIK3R20.63

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