T cell modulation in pancreatic cancer

No Pathway Network information available for T cell modulation in pancreatic cancer

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

Disorders associated with T cell modulation in pancreatic cancer SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Systemic lupus erythematosusEnrichmentCTLA4, IL10, PDCD1, TNFSF45.10
2Loeys-dietz syndrome 4EnrichmentTGFB2, TGFB34.97
3Mycosis fungoidesEnrichmentCD28, CTLA44.49
4Saczary syndromeEnrichmentCD28, CTLA44.49
5Autoimmune lymphoproliferative syndromeEnrichmentFAS, FASLG4.19
6Immunodeficiency, common variable, 1EnrichmentCTLA4, ICOS4.19
7Loeys-dietz syndromeEnrichmentTGFB2, TGFB33.42
8Human immunodeficiency virus type 1EnrichmentCXCL12, IL102.80
9Behcet syndromeEnrichmentFAS, IL102.75
10Calcification of joints and arteriesEnrichmentNT5E2.48
11Celiac disease 3EnrichmentCTLA42.48
12Immunodeficiency 16EnrichmentTNFRSF42.48
13Immunodeficiency 43EnrichmentB2M2.48
14Immunodeficiency with hyper-igm, type 1EnrichmentCD40LG2.48
15Autoimmune disease, multisystem, infantile-onset, 4EnrichmentPDCD12.48
16Hereditary lymphedema idEnrichmentVEGFC2.48
17Graft-versus-host diseaseEnrichmentIL102.48
18Type 1 diabetes mellitus 12EnrichmentCTLA42.48
19Lymphatic malformation 4EnrichmentVEGFC2.48
20Dialysis-related amyloidosisEnrichmentB2M2.48
21Microvascular complications of diabetes 1EnrichmentVEGFA2.48
22Camurati-engelmann disease 2EnrichmentTGFB22.48
23Systemic lupus erythematosus 2EnrichmentPDCD12.48
24Immunodeficiency with hyper-igm, type 3EnrichmentCD402.48
25Birdshot chorioretinopathyEnrichmentHLA-A2.48
26Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.48
27Loeys-dietz syndrome 5EnrichmentTGFB32.48
28T-cell lymphoma, subcutaneous panniculitis-likeEnrichmentHAVCR22.48
29Amyloidosis, hereditary systemic 6EnrichmentB2M2.48
30Immunodeficiency 109 with lymphoproliferationEnrichmentTNFRSF92.48
31Autoimmune disease, multisystem, infantile-onset, 5EnrichmentCD2742.48
32Cd40 ligand deficiencyEnrichmentCD40LG2.48
33Congenital primary lymphedema of gordonEnrichmentVEGFC2.48
34Lung cancerEnrichmentFAS, FASLG2.30
35Hashimoto thyroiditisEnrichmentCTLA42.18
36ArgininemiaEnrichmentARG12.18
37Severe cutaneous adverse reactionEnrichmentHLA-A2.18
38Spastic paraplegia 64, autosomal recessiveEnrichmentENTPD12.18
39Familial thoracic aortic aneurysm and aortic dissectionEnrichmentTGFB2, TGFB32.03
40Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.00
41Immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferationEnrichmentCTLA42.00
42Asparagine synthetase deficiencyEnrichmentCTLA42.00
43Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeEnrichmentCTLA42.00
44Adult-onset myasthenia gravisEnrichmentCTLA42.00
45Vogt-koyanagi-harada diseaseEnrichmentFAS2.00
46Kaposi sarcomaEnrichmentIL61.88
47Immunodeficiency by defective expression of mhc class iEnrichmentB2M1.88
48Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.88
49Amyloidosis, hereditary systemic 2EnrichmentB2M1.78
50Arrhythmogenic right ventricular dysplasia, familial, 1EnrichmentTGFB31.78
51Rheumatoid arthritis, systemic juvenileEnrichmentIL61.78
52Arrhythmogenic right ventricular dysplasia 1EnrichmentTGFB31.78
53Atrial septal defect 1EnrichmentTGFB21.70
54Type 1 diabetes mellitusEnrichmentIL61.70
55Granulomatosis with polyangiitisEnrichmentCTLA41.70
56Il10-related early-onset inflammatory bowel diseaseEnrichmentIL101.70
57Common variable immunodeficiencyEnrichmentCD40LG1.64
58Narcolepsy 1EnrichmentTNFSF41.58
59Lymphoma, non-hodgkin, familialEnrichmentB2M1.58
60Rheumatoid arthritisEnrichmentIL101.53
61Inflammatory bowel disease 1EnrichmentIL61.53
62Marfan syndromeEnrichmentTGFB21.49
63Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variantEnrichmentTGFB31.41
64Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variantEnrichmentTGFB31.41
65Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variantEnrichmentTGFB31.34
66Arteriovenous malformations of the brainEnrichmentIL61.21
67Ehlers-danlos syndromeEnrichmentTGFB21.21
68Myocardial infarctionEnrichmentTNFSF41.15
69Severe covid-19EnrichmentHLA-A1.04
70Type 2 diabetes mellitusEnrichmentIL60.88

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