TCR signaling (REACTOME)

Pathway network for the TCR signaling (REACTOME) SuperPath

Sources:
  • Reactome

Pathways in the TCR signaling (REACTOME) SuperPath

Gene overlap in member pathways for TCR signaling (REACTOME) SuperPath

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

Disorders associated with TCR signaling (REACTOME) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G, LCK, ZAP7010.98
2T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E8.63
3Granulomatosis with polyangiitisEnrichmentHLA-DPA1, HLA-DPB1, PTPN227.33
4Celiac disease 1EnrichmentHLA-DQA1, HLA-DQB15.73
5Bullous pemphigoidEnrichmentHLA-DQB1, HLA-DRB15.73
6Pediatric multiple sclerosisEnrichmentHLA-DQB1, HLA-DRB15.73
7Vogt-koyanagi-harada diseaseEnrichmentHLA-DRB1, PTPN225.25
8Temporal arteritisEnrichmentHLA-DRB1, PTPN224.95
9Idiopathic achalasiaEnrichmentHLA-DQA1, HLA-DQB14.95
10Narcolepsy 2EnrichmentHLA-DQB1, HLA-DRB14.73
11Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.46
12Oligoarticular juvenile idiopathic arthritisEnrichmentCD247, PTPN224.41
13Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD247, PTPN224.41
14Narcolepsy 1EnrichmentHLA-DQB1, HLA-DRB14.29
15Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R13.99
16Multiple sclerosisEnrichmentHLA-DQB1, HLA-DRB13.78
17Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R23.69
18HemimegalencephalyEnrichmentPIK3CA, PTEN3.47
19Cowden syndrome 1EnrichmentPIK3CA, PTEN3.29
20Isolated split hand-split foot malformationEnrichmentBTRC, SEM13.03
21Cowden syndromeEnrichmentPIK3CA, PTEN2.92
22Systemic lupus erythematosusEnrichmentHLA-DRB1, PTPN222.87
23Immunodeficiency 48EnrichmentZAP702.85
24Okt4 epitope deficiencyEnrichmentCD42.85
25Immunodeficiency 18EnrichmentCD3E2.85
26Pulmonary alveolar proteinosis, acquiredEnrichmentHLA-DRB12.85
27Immunodeficiency 25EnrichmentCD2472.85
28Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.85
29Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.85
30Immunodeficiency 22EnrichmentLCK2.85
31BerylliosisEnrichmentHLA-DPB12.85
32Immunodeficiency 79EnrichmentCD42.85
33Immunodeficiency 19, severe combinedEnrichmentCD3D2.85
34Immunodeficiency 19EnrichmentCD3D2.85
35Zap70-related severe combined immunodeficiencyEnrichmentZAP702.85
36MeningiomaEnrichmentPIK3CA, PTEN2.66
37Creutzfeldt-jakob diseaseEnrichmentHLA-DQB12.55
38Sarcoidosis 1EnrichmentHLA-DRB12.55
39Immunodeficiency 17EnrichmentCD3G2.55
40Adult-onset myasthenia gravisEnrichmentHLA-DQA12.38
41Patent foramen ovaleEnrichmentPSMC3, TAB22.31
42Systemic-onset juvenile idiopathic arthritisEnrichmentHLA-DRB12.25
43MacrodactylyEnrichmentPIK3CA2.23
44Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.23
45Vacterl association with hydrocephalusEnrichmentPTEN2.23
46Incontinentia pigmentiEnrichmentIKBKG2.23
47Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.23
48Megalencephaly, autosomal dominantEnrichmentPIK3CA2.23
49Cowden syndrome 5EnrichmentPIK3CA2.23
50Fetal encasement syndromeEnrichmentCHUK2.23
51Frontometaphyseal dysplasia 2EnrichmentMAP3K72.23
52Cerebral cavernous malformations 4EnrichmentPIK3CA2.23
53Immunodeficiency 15bEnrichmentIKBKB2.23
54Neurodevelopmental disorder with microcephaly, hypotonia, and absent languageEnrichmentPSMB12.23
55Immunodeficiency 15aEnrichmentIKBKB2.23
56Short syndromeEnrichmentPIK3R12.23
57Neurodevelopmental, jaw, eye, and digital syndromeEnrichmentFBXW112.23
58Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.23
59Stankiewicz-isidor syndromeEnrichmentPSMD122.23
60Papillary tumor of the pineal regionEnrichmentPTEN2.23
61Deafness, cataract, impaired intellectual development, and polyneuropathyEnrichmentPSMC32.23
62Hemifacial myohyperplasiaEnrichmentPIK3CA2.23
63Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.23
64Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.23
65Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.23
66Glioma susceptibility 2EnrichmentPTEN2.23
67Bartsocas-papas syndrome 2EnrichmentCHUK2.23
68Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.23
69HypospadiasEnrichmentPIK3CA2.23
70Rare venous malformationEnrichmentPIK3CA2.23
71Diaphragmatic eventrationEnrichmentPIK3CA2.23
72Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.23
73Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.23
74Rare combined vascular malformationEnrichmentPIK3CA2.23
75Cavernous lymphangiomaEnrichmentPIK3CA2.23
76Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.23
77Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeEnrichmentPTEN2.23
78Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.23
79Eccrine angiomatous hamartomaEnrichmentPIK3CA2.23
80Macrodactyly of toeEnrichmentPIK3CA2.23
81Polyvalvular heart disease syndromeEnrichmentTAB22.23
82Endometrial cancerEnrichmentPIK3CA, PTEN2.17
83Follicular lymphomaEnrichmentHLA-DRB12.16
84Diffuse cutaneous systemic sclerosisEnrichmentHLA-DRB12.16
85Thrombocytopenia 1EnrichmentWAS2.12
86Intellectual developmental disorder, x-linked 30EnrichmentPAK32.12
87Immunodeficiency 81EnrichmentLCP22.12
88Knobloch syndrome 2EnrichmentPAK22.12
89Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.12
90Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.12
91Thrombocytopenia 3EnrichmentFYB12.12
92Lymphoproliferative syndrome 1EnrichmentITK2.12
93Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.12
94Immunodeficiency 105, severe combinedEnrichmentPTPRC2.12
95Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.12
96Was-related disordersEnrichmentWAS2.12
97Congenital autosomal recessive small-platelet thrombocytopeniaEnrichmentFYB12.12
98Cd45 deficiencyEnrichmentPTPRC2.12
99Thrombocytopenia 10EnrichmentPTPRJ2.12
100Limited sclerodermaEnrichmentHLA-DRB12.08
101Immunodeficiency 33EnrichmentIKBKG1.93
102Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA1.93
103Keratosis, seborrheicEnrichmentPIK3CA1.93
104Noonan syndrome 8EnrichmentPIK3CA1.93
105Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB11.93
106Birk-aharoni syndromeEnrichmentPSMC11.93
107Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA1.93
108Proteasome-associated autoinflammatory syndrome 3EnrichmentPSMB41.93
109Rela fusion-positive ependymomaEnrichmentRELA1.93
110Rosette-forming glioneuronal tumorEnrichmentPIK3CA1.93
111Congenital heart defects, multiple types, 2EnrichmentTAB21.93
112Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG1.93
11317q24.2 microdeletion syndromeEnrichmentPSMD121.93
114Vacterl with hydrocephalusEnrichmentPTEN1.93
115Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB21.93
116Common variable immunodeficiency 12EnrichmentNFKB11.93
117Juvenile polyposis of infancyEnrichmentPTEN1.93
118Submucosal cleft palateEnrichmentUBB1.93
119Cleft hard palateEnrichmentUBB1.93
120Bladder cancerEnrichmentPIK3CA, PTEN1.90
121Prostate cancerEnrichmentPIK3CA, PTEN1.90
122Neutropenia, severe congenital, x-linkedEnrichmentWAS1.82
123Wiskott-aldrich syndromeEnrichmentWAS1.82
124Lymphoproliferative syndromeEnrichmentITK1.82
125Immunodeficiency 104, severe combinedEnrichmentPTPRC1.82
126Immunodeficiency 52EnrichmentLAT1.82
127Combined immunodeficiencyEnrichmentZAP701.82
128Combined t cell and b cell immunodeficiencyEnrichmentZAP701.82
129Combined t and b cell immunodeficiencyEnrichmentZAP701.82
130Pelvic organ prolapseEnrichmentTAB21.75
131Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB41.75
132Pompe disease, infantile-onsetEnrichmentPIK3CA1.75
133Uvula, bifidEnrichmentUBB1.75
134Cleft soft palateEnrichmentUBB1.75
135Nasopharyngeal carcinomaEnrichmentNFKBIA1.75
136Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R11.75
137Proteosome-associated autoinflammatory syndromeEnrichmentPSMB41.75
138Frontometaphyseal dysplasiaEnrichmentMAP3K71.75
139Immunodeficiency 14EnrichmentPIK3R11.75
140Laryngeal squamous cell carcinomaEnrichmentPTEN1.75
141Thyroid hemiagenesisEnrichmentPSMD31.75
142KeratoacanthomaEnrichmentPIK3CA1.75
143Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.63
144Cerebrovascular diseaseEnrichmentPIK3CA1.63
145Familial cerebral cavernous malformationsEnrichmentPIK3CA1.63
146GliomaEnrichmentPTEN1.63
147Gastric cancerEnrichmentPIK3CA, PTEN1.58
148Hereditary breast carcinomaEnrichmentPIK3CA, PTEN1.56
149Colorectal cancerEnrichmentPIK3CA, PIK3R1, PTPRJ1.56
150Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.54
151Capillary malformations, congenitalEnrichmentPIK3CA1.54
152Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.54
153Macrocephaly/autism syndromeEnrichmentPTEN1.54
154HemangiomaEnrichmentPTEN1.54
155Acute megakaryocytic leukemiaEnrichmentPTEN1.54
156Knobloch syndromeEnrichmentPAK21.53
157Developmental dysplasia of the hip 1EnrichmentPSMC31.46
158Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.46
159Hemihyperplasia, isolatedEnrichmentPIK3CA1.46
160Patent ductus arteriosusEnrichmentPSMC31.46
161Breast adenocarcinomaEnrichmentPIK3CA1.46
162Lung squamous cell carcinomaEnrichmentPIK3CA1.46
163Knobloch syndrome 1EnrichmentPAK21.43
164Severe covid-19EnrichmentHLA-DQB11.40
165Nevus, epidermalEnrichmentPIK3CA1.39
166Thyroid cancer, nonmedullary, 2EnrichmentPTEN1.39
167Squamous cell carcinoma, head and neckEnrichmentPTEN1.39
168Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.39
169Gallbladder cancerEnrichmentPIK3CA1.39
170Common variable immunodeficiencyEnrichmentNFKB11.39
171Follicular thyroid carcinomaEnrichmentPTEN1.39
172Overgrowth syndromeEnrichmentPIK3R11.39
173Coronary heart disease 5EnrichmentIKBKG1.29
174Arteriovenous malformationEnrichmentPIK3CA1.29
175Adult hepatocellular carcinomaEnrichmentPIK3CA1.29
176Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.24
177Ciliary dyskinesia, primary, 3EnrichmentNFKB11.24
178PolymicrogyriaEnrichmentPSMC31.24
179MelanomaEnrichmentPTEN1.24
180Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.24
181Migraine with or without aura 1EnrichmentTAB21.20
182Meningioma, familialEnrichmentPTEN1.20
183Lung non-small cell carcinomaEnrichmentPIK3CA1.20
184Uterine corpus cancerEnrichmentPTEN1.20
185Complex neurodevelopmental disorderEnrichmentFBXW11, PAK3, PSMD121.18
186Lip and oral cavity carcinomaEnrichmentPIK3CA1.16
187Breast cancerEnrichmentPIK3CA, PTEN1.14
188Aortic valve disease 1EnrichmentTAB21.13
189Nk-cell enteropathyEnrichmentPIK3CB1.13
190Lynch syndromeEnrichmentPIK3CA1.07
191RhabdomyosarcomaEnrichmentPTEN1.04
192GliosarcomaEnrichmentNFKBIA1.04
193Giant cell glioblastomaEnrichmentNFKBIA1.02
194Diffuse large b-cell lymphomaEnrichmentPTEN0.97
195Ovarian cancerEnrichmentPIK3CA, PTEN0.92
196Hepatocellular carcinomaEnrichmentPIK3CA0.91
197Myocardial infarctionEnrichmentPSMA60.91
198MalariaEnrichmentIKBKG0.90
199Lung cancerEnrichmentPIK3CA0.76
200MicrocephalyEnrichmentPAK3, PSMC30.63
201HypertelorismEnrichmentPIK3CA0.58
202Hereditary breast ovarian cancer syndromeEnrichmentPTEN0.56
203Myeloma, multipleEnrichmentPIK3R20.55
204ThrombocytopeniaEnrichmentWAS0.52
205Dilated cardiomyopathyEnrichmentTAB20.42
206Congenital nervous system abnormalityEnrichmentPTEN0.33
207Nervous system diseaseEnrichmentPTEN0.33
208Autism spectrum disorderEnrichmentPTEN0.32
209Inherited cancer-predisposing syndromeEnrichmentPTEN0.26

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