IL-2 Gene Expression in Activated and Quiescent T-Cells

No Pathway Network information available for IL-2 Gene Expression in Activated and Quiescent T-Cells

Pathways in the IL-2 Gene Expression in Activated and Quiescent T-Cells SuperPath

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

Disorders associated with IL-2 Gene Expression in Activated and Quiescent T-Cells SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Loeys-dietz syndromeEnrichmentSMAD2, SMAD3, TGFB2, TGFBR1, TGFBR216.00
2Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD2, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR211.58
3Loeys-dietz syndrome 1EnrichmentSMAD2, TGFBR1, TGFBR28.37
4T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E8.37
5Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G6.60
6Marfan syndromeEnrichmentTGFB2, TGFBR1, TGFBR26.29
7Loeys-dietz syndrome 2EnrichmentTGFBR1, TGFBR25.56
8Loeys-dietz syndrome 4EnrichmentTGFB2, TGFB35.56
9Ehlers-danlos syndromeEnrichmentSMAD3, TGFB2, TGFBR25.39
10Aortic aneurysmEnrichmentSMAD3, TGFBR14.78
11Connective tissue diseaseEnrichmentSMAD3, TGFBR22.88
12Inherited cancer-predisposing syndromeEnrichmentCDKN1B, RB1, SMAD42.86
13Multiple self-healing squamous epitheliomaEnrichmentTGFBR12.77
14Immunodeficiency 18EnrichmentCD3E2.77
15Immunodeficiency 25EnrichmentCD2472.77
16Camurati-engelmann disease 2EnrichmentTGFB22.77
17Neuroendocrine tumorEnrichmentCDKN1B2.77
18Colorectal cancer, hereditary nonpolyposis, type 6EnrichmentTGFBR22.77
19Loeys-dietz syndrome 6EnrichmentSMAD22.77
20Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.77
21Loeys-dietz syndrome 5EnrichmentTGFB32.77
22Trilateral retinoblastomaEnrichmentRB12.77
23Immunodeficiency 19, severe combinedEnrichmentCD3D2.77
24Congenital heart defects, multiple types, 8, with or without heterotaxyEnrichmentSMAD22.77
25Heritable thoracic aortic diseaseEnrichmentSMAD42.77
26Immunodeficiency 19EnrichmentCD3D2.77
27Lung oat cell carcinomaEnrichmentRB12.77
28Noonan syndrome 13EnrichmentMAPK12.72
29Inflammatory bowel disease-recurrent sinopulmonary infections syndromeEnrichmentNFAT52.72
30Myhre syndromeEnrichmentSMAD42.47
31Camurati-engelmann disease 1EnrichmentTGFB12.47
32Juvenile polyposis/hereditary hemorrhagic telangiectasia syndromeEnrichmentSMAD42.47
33Microvascular complications of diabetes 5EnrichmentTGFBR22.47
34Chromosome 13q14 deletion syndromeEnrichmentRB12.47
35Multiple endocrine neoplasia, type ivEnrichmentCDKN1B2.47
36Loeys-dietz syndrome 3EnrichmentSMAD32.47
37Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.47
38Camurati-engelmann diseaseEnrichmentTGFB12.47
39Immunodeficiency 17EnrichmentCD3G2.47
40Familial retinoblastomaEnrichmentRB12.47
41Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.42
42Immunodeficiency 52EnrichmentLAT2.42
43Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.42
44Common variable immunodeficiency 12EnrichmentNFKB12.42
45RetinoblastomaEnrichmentRB12.29
46Juvenile polyposis syndromeEnrichmentSMAD42.29
47Mycosis fungoidesEnrichmentCD282.29
48Osteogenic sarcomaEnrichmentRB12.29
49Woolly hair, autosomal recessive 3EnrichmentRB12.29
50Hypotrichosis 8EnrichmentRB12.29
51Squamous cell carcinomaEnrichmentRB12.29
52Bone osteosarcomaEnrichmentRB12.29
53Saczary syndromeEnrichmentCD282.29
54Small cell cancer of the lungEnrichmentRB12.17
55Lynch syndrome 4EnrichmentRB12.17
56Mantle cell lymphomaEnrichmentCCND12.17
57Primary hyperparathyroidismEnrichmentCDKN1B2.17
58Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.12
59Arrhythmogenic right ventricular dysplasia, familial, 1EnrichmentTGFB32.07
60Von hippel-lindau syndromeEnrichmentCCND12.07
61Arrhythmogenic right ventricular dysplasia 1EnrichmentTGFB32.07
62Generalized juvenile polyposis/juvenile polyposis coliEnrichmentSMAD42.07
63Colorectal cancerEnrichmentCCND1, SMAD42.03
64Atrial septal defect 1EnrichmentTGFB21.99
65Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB11.99
66Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB11.99
67Classic ehlers-danlos syndromeEnrichmentTGFBR11.99
68Esophageal cancerEnrichmentTGFBR21.93
69Multiple endocrine neoplasia, type iEnrichmentCDKN1B1.93
70Gallbladder cancerEnrichmentSMAD41.93
71Hereditary hemorrhagic telangiectasiaEnrichmentSMAD41.93
72Oligoarticular juvenile idiopathic arthritisEnrichmentCD2471.93
73Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD2471.93
74Ovarian cancerEnrichmentCDKN1B, RB11.90
75Common variable immunodeficiencyEnrichmentNFKB11.87
76Familial thoracic aortic aneurysm and dissectionEnrichmentSMAD31.82
77Lennox-gastaut syndromeEnrichmentMAPK101.82
78Leukemia, chronic lymphocyticEnrichmentCCND11.77
79Pectus excavatumEnrichmentTGFBR11.73
80Ciliary dyskinesia, primary, 3EnrichmentNFKB11.72
81Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variantEnrichmentTGFB31.70
82Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variantEnrichmentTGFB31.70
83Lip and oral cavity carcinomaEnrichmentRB11.70
84Specific learning disabilityEnrichmentMAPK11.68
85Aortic aneurysm, familial thoracic 1EnrichmentSMAD31.63
86Lung cancer susceptibility 3EnrichmentRB11.63
87Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variantEnrichmentTGFB31.63
88Lynch syndromeEnrichmentTGFBR21.60
89Heart, malformation ofEnrichmentMAPK11.47
90Visceral heterotaxyEnrichmentLEFTY21.44
91Cardiomyopathy, dilated, 1aEnrichmentNFATC21.40
92Pancreatic cancerEnrichmentSMAD41.38
93Bladder cancerEnrichmentRB11.32
94Cystic fibrosisEnrichmentTGFB11.28
95Gastric cancerEnrichmentSMAD41.15
96ThrombocytopeniaEnrichmentSMAD41.11
97Myeloma, multipleEnrichmentCCND11.04
98MicrocephalyEnrichmentMAPK10.68

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