Regulation of T cell activation by CD28 family

Pathway network for the Regulation of T cell activation by CD28 family SuperPath

Sources:
  • Reactome
  • QIAGEN

Pathways in the Regulation of T cell activation by CD28 family SuperPath

#NameSourceGenes
1Regulation of T cell activation by CD28 familyReactome
2CTLA4 SignalingQIAGEN
3Co-stimulation by CD28Reactome
4CD28 dependent PI3K/Akt signalingReactome
5Co-inhibition by CTLA4Reactome
6CD28 dependent Vav1 pathwayReactome
7Co-stimulation by ICOSReactome
8Co-inhibition by BTLAReactome
9Activation of AKT2Reactome

Gene overlap in member pathways for Regulation of T cell activation by CD28 family SuperPath

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

Disorders associated with Regulation of T cell activation by CD28 family SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G, LCK, ZAP707.78
2Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT3, PIK3CA, PIK3R27.55
3HemimegalencephalyEnrichmentAKT3, MTOR, PIK3CA7.15
4T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E6.86
5Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.75
6Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R15.75
7Immunodeficiency 14EnrichmentPIK3CD, PIK3R15.75
8Granulomatosis with polyangiitisEnrichmentCTLA4, HLA-DPA1, PTPN225.57
9Immune system diseaseEnrichmentCDC42, PIK3CD4.91
10Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT3, PIK3R24.64
11Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R14.57
12Celiac disease 1EnrichmentHLA-DQA1, HLA-DQB14.57
13Bullous pemphigoidEnrichmentHLA-DQB1, HLA-DRB14.57
14Pediatric multiple sclerosisEnrichmentHLA-DQB1, HLA-DRB14.57
15Mycosis fungoidesEnrichmentCD28, CTLA44.44
16Saczary syndromeEnrichmentCD28, CTLA44.44
17Breast adenocarcinomaEnrichmentAKT1, PIK3CA4.24
18Overgrowth syndromeEnrichmentMTOR, PIK3R14.10
19Mednik syndromeEnrichmentAP1B1, AP1S14.09
20Adult-onset myasthenia gravisEnrichmentCTLA4, HLA-DQA14.09
21Vogt-koyanagi-harada diseaseEnrichmentHLA-DRB1, PTPN224.09
22Cowden syndromeEnrichmentAKT1, PIK3CA3.87
23Temporal arteritisEnrichmentHLA-DRB1, PTPN223.79
24Idiopathic achalasiaEnrichmentHLA-DQA1, HLA-DQB13.79
25Immunodeficiency, common variable, 1EnrichmentCTLA4, ICOS3.76
26Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC42, PTPN113.76
27Lung cancerEnrichmentMAP3K8, PIK3CA, PPP2R1B3.72
28Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R1, SRC3.61
29MeningiomaEnrichmentAKT1, PIK3CA3.60
30Narcolepsy 2EnrichmentHLA-DQB1, HLA-DRB13.57
31Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT23.53
32Akt2-related familial partial lipodystrophyEnrichmentAKT23.53
33MetachondromatosisEnrichmentPTPN113.43
34Leopard syndrome 1EnrichmentPTPN113.43
35Vegetative pyoderma gangrenosumEnrichmentPTPN63.43
36Bullous pyoderma gangrenosumEnrichmentPTPN63.43
37Pustular pyoderma gangrenosumEnrichmentPTPN63.43
38Classic pyoderma gangrenosumEnrichmentPTPN63.43
39Malignant astrocytomaEnrichmentPTPN113.43
40Oligoarticular juvenile idiopathic arthritisEnrichmentCD247, PTPN223.25
41Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD247, PTPN223.25
42Werner syndromeEnrichmentPTPN113.13
43Narcolepsy 1EnrichmentHLA-DQB1, HLA-DRB13.13
44MacrodactylyEnrichmentPIK3CA3.09
45Megalencephaly, autosomal dominantEnrichmentPIK3CA3.09
46Cowden syndrome 5EnrichmentPIK3CA3.09
47Ataxia-oculomotor apraxia 3EnrichmentPIK3R53.09
48Cerebral cavernous malformations 4EnrichmentPIK3CA3.09
49Short syndromeEnrichmentPIK3R13.09
50Immunodeficiency 119EnrichmentICOSLG3.09
51Hemifacial myohyperplasiaEnrichmentPIK3CA3.09
52Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA3.09
53Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R13.09
54Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD3.09
55Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R13.09
56Immunodeficiency 97 with autoinflammationEnrichmentPIK3CG3.09
57Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA3.09
58HypospadiasEnrichmentPIK3CA3.09
59Rare venous malformationEnrichmentPIK3CA3.09
60Diaphragmatic eventrationEnrichmentPIK3CA3.09
61Pik3ca-related overgrowth spectrumEnrichmentPIK3CA3.09
62Rare combined vascular malformationEnrichmentPIK3CA3.09
63Cavernous lymphangiomaEnrichmentPIK3CA3.09
64Pik3ca-related overgrowth syndromeEnrichmentPIK3CA3.09
65Late-onset combined immunodeficiency due to icosl deficiencyEnrichmentICOSLG3.09
66Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA3.09
67Eccrine angiomatous hamartomaEnrichmentPIK3CA3.09
68Macrodactyly of toeEnrichmentPIK3CA3.09
69Intellectual developmental disorder, x-linked 30EnrichmentPAK33.05
70Knobloch syndrome 2EnrichmentPAK23.05
71Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK13.05
72Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD283.05
73Immunodeficiency 22EnrichmentLCK3.05
74Takenouchi-kosaki syndromeEnrichmentCDC423.05
75Nocarh syndromeEnrichmentCDC423.05
76Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC13.05
77Systemic lupus erythematosusEnrichmentCTLA4, HLA-DRB1, PTPN222.96
78Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.96
79Tricuspid valve insufficiencyEnrichmentPTPN112.96
80Noonan syndrome with multiple lentiginesEnrichmentPTPN112.83
81Proteus syndromeEnrichmentAKT12.81
82Celiac disease 3EnrichmentCTLA42.81
83Houge-janssens syndrome 4EnrichmentPPP2R5C2.81
84Type 1 diabetes mellitus 12EnrichmentCTLA42.81
85Houge-janssens syndrome 2EnrichmentPPP2R1A2.81
86Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.81
87Cowden syndrome 6EnrichmentAKT12.81
88Thrombocytopenia 6EnrichmentSRC2.81
89Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.81
90Capillary hemangiomaEnrichmentAKT32.81
91Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A2.81
92Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2EnrichmentPIK3R52.79
93Keratosis, seborrheicEnrichmentPIK3CA2.79
94Roifman-chitayat syndromeEnrichmentPIK3CD2.79
95Noonan syndrome 8EnrichmentPIK3CA2.79
96Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.79
97Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.75
98LymphomaEnrichmentPTPN112.73
99Immunodeficiency 112EnrichmentMAP3K142.70
100Nik deficiencyEnrichmentMAP3K142.70
101Patent ductus arteriosusEnrichmentPTPN112.66
102Multiple sclerosisEnrichmentHLA-DQB1, HLA-DRB12.63
103Pompe disease, infantile-onsetEnrichmentPIK3CA2.61
104KeratoacanthomaEnrichmentPIK3CA2.61
105ThrombocytopeniaEnrichmentPTPN11, SRC2.61
106Noonan syndrome 3EnrichmentPTPN112.59
107Hashimoto thyroiditisEnrichmentCTLA42.51
108Houge-janssens syndrome 1EnrichmentPPP2R5D2.51
109Senior-loken syndrome 7EnrichmentAKT32.51
110Bardet-biedl syndrome 16EnrichmentAKT32.51
111Houge-janssens syndrome 3EnrichmentPPP2CA2.51
112Cerebrovascular diseaseEnrichmentPIK3CA2.49
113Familial cerebral cavernous malformationsEnrichmentPIK3CA2.49
114Hereditary breast carcinomaEnrichmentAKT1, PIK3CA2.46
115Knobloch syndromeEnrichmentPAK22.45
116Cebalid syndromeEnrichmentMTOR2.40
117Smith-kingsmore syndromeEnrichmentMTOR2.40
118Capillary malformations, congenitalEnrichmentPIK3CA2.39
119Pectus excavatumEnrichmentPTPN112.39
120Specific learning disabilityEnrichmentPTPN112.39
121Knobloch syndrome 1EnrichmentPAK22.35
122EpicanthusEnrichmentPTPN112.35
123Juvenile myelomonocytic leukemiaEnrichmentPTPN112.35
124Congenital long qt syndromeEnrichmentPTPN112.35
125Immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferationEnrichmentCTLA42.33
126Asparagine synthetase deficiencyEnrichmentCTLA42.33
127Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeEnrichmentCTLA42.33
128Klippel-trenaunay-weber syndromeEnrichmentPIK3CA2.31
129Cowden syndrome 1EnrichmentPIK3CA2.31
130Hemihyperplasia, isolatedEnrichmentPIK3CA2.31
131Lung squamous cell carcinomaEnrichmentPIK3CA2.31
132Keratitis-ichthyosis-deafness syndrome, autosomal recessiveEnrichmentAP1B12.28
133Hypocalciuric hypercalcemia, familial, type iiiEnrichmentAP2S12.28
134Spinocerebellar ataxia 12EnrichmentPPP2R2B2.28
135Immunodeficiency 116EnrichmentCD8A2.28
136Immunodeficiency 81EnrichmentLCP22.28
137Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.28
138Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual developmentEnrichmentPTPA2.28
139Immunodeficiency 48EnrichmentZAP702.28
140Okt4 epitope deficiencyEnrichmentCD42.28
141Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.28
142Immunodeficiency 18EnrichmentCD3E2.28
143Usmani-riazuddin syndrome, autosomal recessiveEnrichmentAP1G12.28
144Pulmonary alveolar proteinosis, acquiredEnrichmentHLA-DRB12.28
145Immunodeficiency 25EnrichmentCD2472.28
146Dystonia 25EnrichmentGNAL2.28
147Psoriasis 15, pustularEnrichmentAP1S32.28
148Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.28
149Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.28
150Usmani-riazuddin syndrome, autosomal dominantEnrichmentAP1G12.28
151Immunodeficiency 79EnrichmentCD42.28
152Immunodeficiency 19, severe combinedEnrichmentCD3D2.28
153ColitisEnrichmentSYK2.28
154Immunodeficiency 19EnrichmentCD3D2.28
155Zap70-related severe combined immunodeficiencyEnrichmentZAP702.28
156Autoimmune disease, multisystem, infantile-onset, 4EnrichmentPDCD12.26
157Systemic lupus erythematosus 2EnrichmentPDCD12.26
158BerylliosisEnrichmentHLA-DPB12.26
159Autoimmune disease, multisystem, infantile-onset, 5EnrichmentCD2742.26
160Noonan syndrome and noonan-related syndromeEnrichmentPTPN112.26
161Nevus, epidermalEnrichmentPIK3CA2.25
162Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA2.25
163Gallbladder cancerEnrichmentPIK3CA2.25
164Patent foramen ovaleEnrichmentPTPN112.18
165Arteriovenous malformationEnrichmentPIK3CA2.14
166Adult hepatocellular carcinomaEnrichmentPIK3CA2.14
167Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC12.10
168Focal cortical dysplasia, type iiEnrichmentMTOR2.10
169Isolated focal cortical dysplasia type iiEnrichmentMTOR2.10
170Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA2.09
171Noonan syndrome 1EnrichmentPTPN112.07
172ScoliosisEnrichmentPTPN112.05
173Combined immunodeficiencyEnrichmentICOSLG2.05
174Lung non-small cell carcinomaEnrichmentPIK3CA2.05
175Combined t cell and b cell immunodeficiencyEnrichmentICOSLG2.05
176Combined t and b cell immunodeficiencyEnrichmentICOSLG2.05
177Hydrops fetalis, nonimmuneEnrichmentPTPN112.02
178RasopathyEnrichmentPTPN112.02
179Breast cancerEnrichmentAKT1, PIK3CA2.01
180Lip and oral cavity carcinomaEnrichmentPIK3CA2.01
181StrabismusEnrichmentPTPN112.00
182Creutzfeldt-jakob diseaseEnrichmentHLA-DQB11.98
183Sarcoidosis 1EnrichmentHLA-DRB11.98
184Psoriasis 14, pustularEnrichmentAP1S31.98
185Pettigrew syndromeEnrichmentAP1S21.98
186Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentAP2M11.98
187Immunodeficiency 17EnrichmentCD3G1.98
188Immunodeficiency 52EnrichmentLAT1.98
189ArthritisEnrichmentSYK1.98
190Nk-cell enteropathyEnrichmentPIK3CB1.98
191MyelofibrosisEnrichmentSRC1.97
192MegacolonEnrichmentAKT31.97
193Long qt syndrome 1EnrichmentPTPN111.96
194Non-immune hydrops fetalisEnrichmentPTPN111.94
195Lynch syndromeEnrichmentPIK3CA1.92
196Type 2 diabetes mellitusEnrichmentAKT21.91
197Renal cell carcinoma, papillary, 1EnrichmentMTOR1.86
198PolymicrogyriaEnrichmentAKT31.81
199Intellectual developmental disorder, autosomal dominant 56EnrichmentCLTC1.81
200Hypertrophic cardiomyopathyEnrichmentPTPN111.80
201Endometrial cancerEnrichmentPIK3CA1.77
202Ovarian cancerEnrichmentAKT1, PIK3CA1.77
203Hepatocellular carcinomaEnrichmentPIK3CA1.75
204Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.69
205Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1EnrichmentCLTC1.68
206Systemic-onset juvenile idiopathic arthritisEnrichmentHLA-DRB11.68
207OsteoporosisEnrichmentSRC1.67
208Bladder cancerEnrichmentPIK3CA1.63
209Prostate cancerEnrichmentPIK3CA1.63
210Follicular lymphomaEnrichmentHLA-DRB11.59
211Diffuse cutaneous systemic sclerosisEnrichmentHLA-DRB11.59
212Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.53
213Rare genetic intellectual disabilityEnrichmentMTOR1.53
214Inflammatory myofibroblastic tumorEnrichmentCLTC1.51
215Limited sclerodermaEnrichmentHLA-DRB11.51
216Gastric cancerEnrichmentPIK3CA1.46
217Renal cell carcinoma with mit translocationsEnrichmentCLTC1.44
218Autism spectrum disorderEnrichmentPTPN111.40
219HypertelorismEnrichmentPIK3CA1.38
220Myeloma, multipleEnrichmentPIK3R21.35
221MicrocephalyEnrichmentPTPN111.35
222Tracheoesophageal fistula with or without esophageal atresiaEnrichmentAP1G21.34
223Myoclonic-atonic epilepsyEnrichmentAP2M11.34
224Inherited cancer-predisposing syndromeEnrichmentPTPN111.32
225Isolated tracheo-esophageal fistulaEnrichmentAP1G21.29
226Immune deficiency diseaseEnrichmentSYK1.25
227Complex neurodevelopmental disorderEnrichmentPAK3, PPP2CA1.15
228Esophageal atresia/tracheoesophageal fistulaEnrichmentAP1G21.02
229Primary ovarian insufficiencyEnrichmentRICTOR0.95
230Severe covid-19EnrichmentHLA-DQB10.85
231DystoniaEnrichmentGNAL0.77
232Autosomal dominant non-syndromic intellectual disabilityEnrichmentCLTC0.64
233Undetermined early-onset epileptic encephalopathyEnrichmentCLTC0.59

Loading...
Loading...
Loading...