Interactions between immune cells and microRNAs in tumor microenvironment

No Pathway Network information available for Interactions between immune cells and microRNAs in tumor microenvironment

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

Disorders associated with Interactions between immune cells and microRNAs in tumor microenvironment SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Loeys-dietz syndromeEnrichmentTGFB2, TGFB3, TGFBR25.46
2Systemic lupus erythematosusEnrichmentCTLA4, PDCD1, SOCS1, TLR74.98
3Loeys-dietz syndrome 4EnrichmentTGFB2, TGFB34.91
4Anemia, autoimmune hemolyticEnrichmentSOCS1, TLR84.14
5Immunodeficiency, common variable, 1EnrichmentCTLA4, NFKB24.14
6Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.59
7Oligoarticular juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.59
8Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.59
9Familial thoracic aortic aneurysm and aortic dissectionEnrichmentTGFB2, TGFB3, TGFBR23.30
10Marfan syndromeEnrichmentTGFB2, TGFBR23.27
11Human immunodeficiency virus type 1EnrichmentCCL2, CCL52.74
12Diffuse large b-cell lymphomaEnrichmentSOCS1, STAT32.70
13Ehlers-danlos syndromeEnrichmentTGFB2, TGFBR22.70
14Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB2.53
15Type 1 diabetes mellitus 10EnrichmentIL2RA2.45
16Celiac disease 3EnrichmentCTLA42.45
17Hyper-ige syndrome 6, autosomal dominant, with recurrent infectionsEnrichmentSTAT62.45
18Immunodeficiency 63 with lymphoproliferation and autoimmunityEnrichmentIL2RB2.45
19Immunodeficiency 74, covid19-related, x-linkedEnrichmentTLR72.45
20Autoimmune disease, multisystem, infantile-onset, 4EnrichmentPDCD12.45
21X-linked immunodeficiency 74EnrichmentTLR72.45
22Systemic lupus erythematosus 17EnrichmentTLR72.45
23T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.45
24Type 1 diabetes mellitus 12EnrichmentCTLA42.45
25Camurati-engelmann disease 2EnrichmentTGFB22.45
26Systemic lupus erythematosus 2EnrichmentPDCD12.45
27Immunodeficiency 67EnrichmentIRAK42.45
28Colorectal cancer, hereditary nonpolyposis, type 6EnrichmentTGFBR22.45
29Macular degeneration, age-related, 10EnrichmentTLR42.45
30Loeys-dietz syndrome 5EnrichmentTGFB32.45
31Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.45
32Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.45
33Autoimmune disease, multisystem, infantile-onset, 5EnrichmentCD2742.45
34Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.45
35Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.45
36Hashimoto thyroiditisEnrichmentCTLA42.15
37Camurati-engelmann disease 1EnrichmentTGFB12.15
38Hemangiopericytoma, malignantEnrichmentSTAT62.15
39Immunodeficiency 33EnrichmentIRAK42.15
40Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA2.15
41Loeys-dietz syndrome 2EnrichmentTGFBR22.15
42Microvascular complications of diabetes 5EnrichmentTGFBR22.15
43Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.15
44Immunodeficiency, common variable, 10EnrichmentNFKB22.15
45Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.15
46Camurati-engelmann diseaseEnrichmentTGFB12.15
47Congenital dyserythropoietic anemiaEnrichmentIRAK42.15
48Trypsinogen deficiencyEnrichmentTRB2.15
49Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK42.15
50Common variable immunodeficiency 12EnrichmentNFKB12.15
51Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT31.98
52Immune thrombocytopeniaEnrichmentSOCS11.98
53Mycosis fungoidesEnrichmentCTLA41.98
54Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentTLR81.98
55Severe combined immunodeficiency, x-linkedEnrichmentIL2RG1.98
56Combined immunodeficiency, x-linkedEnrichmentIL2RG1.98
57Immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferationEnrichmentCTLA41.98
58Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS11.98
59Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT31.98
60Hyper ige syndromeEnrichmentSTAT31.98
61Loeys-dietz syndrome 1EnrichmentTGFBR21.98
62Asparagine synthetase deficiencyEnrichmentCTLA41.98
63Immunodeficiency 7EnrichmentTRA1.98
64Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeEnrichmentCTLA41.98
65Adult-onset myasthenia gravisEnrichmentCTLA41.98
66Saczary syndromeEnrichmentCTLA41.98
67Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.76
68Arrhythmogenic right ventricular dysplasia, familial, 1EnrichmentTGFB31.76
69Vitamin d-dependent rickets, type 2aEnrichmentTRB1.76
70Arrhythmogenic right ventricular dysplasia 1EnrichmentTGFB31.76
71Atrial septal defect 1EnrichmentTGFB21.68
72Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB11.68
73Granulomatosis with polyangiitisEnrichmentCTLA41.68
74Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB11.68
75Esophageal cancerEnrichmentTGFBR21.61
76Permanent neonatal diabetes mellitusEnrichmentSTAT31.55
77Omenn syndromeEnrichmentIL2RG1.46
78Ciliary dyskinesia, primary, 3EnrichmentNFKB11.46
79Combined immunodeficiencyEnrichmentIL2RG1.42
80IchthyosisEnrichmentIL2RB1.42
81Combined t cell and b cell immunodeficiencyEnrichmentIL2RG1.42
82Combined t and b cell immunodeficiencyEnrichmentIL2RG1.42
83Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variantEnrichmentTGFB31.38
84Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variantEnrichmentTGFB31.38
85Acute promyelocytic leukemiaEnrichmentSTAT31.35
86Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variantEnrichmentTGFB31.31
87Hereditary chronic pancreatitisEnrichmentTRB1.31
88Lynch syndromeEnrichmentTGFBR21.29
89Pancreatitis, hereditaryEnrichmentTRB1.23
90Behcet syndromeEnrichmentTLR41.19
91Cystic fibrosisEnrichmentTGFB10.97
92Connective tissue diseaseEnrichmentTGFBR20.97

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