T cell receptor and co-stimulatory signaling

No Pathway Network information available for T cell receptor and co-stimulatory signaling

Pathways in the T cell receptor and co-stimulatory signaling SuperPath

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

Disorders associated with T cell receptor and co-stimulatory signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Mycosis fungoidesEnrichmentCD28, CTLA44.98
2Saczary syndromeEnrichmentCD28, CTLA44.98
3Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB3.06
4Severe combined immunodeficiencyEnrichmentLCK, ZAP702.75
5Proteus syndromeEnrichmentAKT12.72
6Cystic angiomatosis of bone, diffuseEnrichmentRASA12.72
7Celiac disease 3EnrichmentCTLA42.72
8Immunodeficiency 116EnrichmentCD8A2.72
9Intellectual developmental disorder, autosomal dominant 7EnrichmentDYRK1A2.72
10Immunodeficiency 64 with lymphoproliferationEnrichmentRASGRP12.72
11Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.72
12Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.72
13Immunodeficiency 48EnrichmentZAP702.72
14Autoimmune disease, multisystem, infantile-onset, 4EnrichmentPDCD12.72
15Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.72
16Type 1 diabetes mellitus 12EnrichmentCTLA42.72
17Systemic lupus erythematosus 2EnrichmentPDCD12.72
18Cowden syndrome 6EnrichmentAKT12.72
19Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.72
20Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.72
21Immunodeficiency 22EnrichmentLCK2.72
22Vegetative pyoderma gangrenosumEnrichmentPTPN62.72
23Bullous pyoderma gangrenosumEnrichmentPTPN62.72
24Immunodeficiency 64EnrichmentRASGRP12.72
25Gorham's diseaseEnrichmentRASA12.72
26Ebv-induced lymphoproliferative disease due to rasgrp1 deficiencyEnrichmentRASGRP12.72
27Pustular pyoderma gangrenosumEnrichmentPTPN62.72
28Classic pyoderma gangrenosumEnrichmentPTPN62.72
29Zap70-related severe combined immunodeficiencyEnrichmentZAP702.72
30Systemic lupus erythematosusEnrichmentCTLA4, PDCD12.60
31Hashimoto thyroiditisEnrichmentCTLA42.42
32Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.42
33Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.42
34Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.42
35Trypsinogen deficiencyEnrichmentTRB2.42
36Common variable immunodeficiency 12EnrichmentNFKB12.42
37Nasopharyngeal carcinomaEnrichmentNFKBIA2.24
38Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.24
39Immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferationEnrichmentCTLA42.24
40Wieacker-wolff syndromeEnrichmentRASA12.24
41Asparagine synthetase deficiencyEnrichmentCTLA42.24
42Immunodeficiency 7EnrichmentTRA2.24
43Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeEnrichmentCTLA42.24
44Adult-onset myasthenia gravisEnrichmentCTLA42.24
45Immunodeficiency, common variable, 1EnrichmentCTLA42.12
46EnophthalmosEnrichmentDYRK1A2.12
47Breast cancerEnrichmentAKT1, IL22.05
48Capillary malformations, congenitalEnrichmentRASA12.02
49Vitamin d-dependent rickets, type 2aEnrichmentTRB2.02
50Klippel-trenaunay-weber syndromeEnrichmentRASA11.94
51Telangiectasia, hereditary hemorrhagic, type 1EnrichmentRASA11.94
52Hemangioma, capillary infantileEnrichmentRASA11.94
53Basal cell carcinoma 1EnrichmentRASA11.94
54Granulomatosis with polyangiitisEnrichmentCTLA41.94
55Breast adenocarcinomaEnrichmentAKT11.94
56Capillary malformation-arteriovenous malformation 1EnrichmentRASA11.87
57Hereditary hemorrhagic telangiectasiaEnrichmentRASA11.87
58Common variable immunodeficiencyEnrichmentNFKB11.87
59Arteriovenous malformationEnrichmentRASA11.77
60Cowden syndromeEnrichmentAKT11.77
61Myopathy, x-linked, with excessive autophagyEnrichmentRASA11.72
62Ciliary dyskinesia, primary, 3EnrichmentNFKB11.72
63Combined immunodeficiencyEnrichmentZAP701.68
64Combined t cell and b cell immunodeficiencyEnrichmentZAP701.68
65Combined t and b cell immunodeficiencyEnrichmentZAP701.68
66MeningiomaEnrichmentAKT11.64
67Hereditary chronic pancreatitisEnrichmentTRB1.58
68Male infertility with spermatogenesis disorderEnrichmentDYRK1A1.55
69GliosarcomaEnrichmentNFKBIA1.52
70Pancreatitis, hereditaryEnrichmentTRB1.49
71Giant cell glioblastomaEnrichmentNFKBIA1.49
72MicrophthalmiaEnrichmentDYRK1A1.38
73Hereditary breast carcinomaEnrichmentAKT11.09
74Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA1.04
75Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.99
76Colorectal cancerEnrichmentAKT10.81
77Ovarian cancerEnrichmentAKT10.75
78Autism spectrum disorderEnrichmentDYRK1A0.72
79MicrocephalyEnrichmentDYRK1A0.68
80Complex neurodevelopmental disorderEnrichmentDYRK1A0.67

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