Immune response Function of MEF2 in T lymphocytes

Pathway network for the Immune response Function of MEF2 in T lymphocytes SuperPath

Sources:
  • GeneGo (Thomson Reuters)
  • QIAGEN
  • Reactome

Pathways in the Immune response Function of MEF2 in T lymphocytes SuperPath

#NameSourceGenes
1Immune response Function of MEF2 in T lymphocytesGeneGo (Thomson Reuters)
2Development Role of HDAC and calcium/calmodulin-dependent kinase (CaMK) in control of skeletal myogenesisGeneGo (Thomson Reuters)
3Calcium Mediated T-Cell ApoptosisQIAGEN
4SARS-CoV-2 targets host intracellular signalling and regulatory pathwaysReactome

Gene overlap in member pathways for Immune response Function of MEF2 in T lymphocytes SuperPath

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

Disorders associated with Immune response Function of MEF2 in T lymphocytes SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Covid-19Direct
2HemimegalencephalyEnrichmentAKT3, MTOR, PIK3CA, RHEB8.62
3Severe combined immunodeficiencyEnrichmentCD247, CD3D, CD3E, CD3G, LCK, ZAP707.60
4T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD247, CD3D, CD3E7.27
5Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT3, PIK3CA, PIK3R26.38
6Focal cortical dysplasia, type iiEnrichmentMTOR, RHEB, TSC26.38
7Isolated focal cortical dysplasia type iiEnrichmentMTOR, RHEB, TSC26.38
8Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM1, CALM2, CALM35.53
9Long qt syndrome 1EnrichmentCALM1, CALM2, CALM3, ITPR35.31
10Celiac disease 1EnrichmentHLA-DQA1, HLA-DQB14.84
11Bullous pemphigoidEnrichmentHLA-DQB1, HLA-DRB14.84
12Pediatric multiple sclerosisEnrichmentHLA-DQB1, HLA-DRB14.84
13Multiple sclerosisEnrichmentHLA-DQB1, HLA-DRB1, ITPR14.73
14Colorectal cancerEnrichmentAKT1, EP300, IGF2, PIK3CA, PIK3R14.23
15Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.17
16Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R14.17
17Immunodeficiency 14EnrichmentPIK3CD, PIK3R14.17
18Idiopathic achalasiaEnrichmentHLA-DQA1, HLA-DQB14.07
19Immunodeficiency 7EnrichmentTRA, TRAC4.03
20Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT3, PIK3R23.87
21Narcolepsy 2EnrichmentHLA-DQB1, HLA-DRB13.84
22Insulin-like growth factor iEnrichmentIGF1, IGF1R3.65
23Myopathy, centronuclear, 1EnrichmentMYF6, MYOD13.48
24Hemihyperplasia, isolatedEnrichmentIGF2, PIK3CA3.48
25Breast adenocarcinomaEnrichmentAKT1, PIK3CA3.48
26Narcolepsy 1EnrichmentHLA-DQB1, HLA-DRB13.40
27Long qt syndromeEnrichmentCACNA1C, CALM1, CALM23.37
28Overgrowth syndromeEnrichmentMTOR, PIK3R13.33
29Adult hepatocellular carcinomaEnrichmentPIK3CA, TSC23.10
30Cowden syndromeEnrichmentAKT1, PIK3CA3.10
31Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R13.00
32MeningiomaEnrichmentAKT1, PIK3CA2.84
33Nk-cell enteropathyEnrichmentIGF1R, PIK3CB2.77
34Rare genetic intellectual disabilityEnrichmentEP300, MTOR2.64
35Anhidrosis, isolated, with normal sweat glandsEnrichmentITPR22.42
36Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.42
37Charcot-marie-tooth disease, demyelinating, type 1jEnrichmentITPR32.42
38Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.42
39Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.42
40Okt4 epitope deficiencyEnrichmentCD42.42
41Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.42
42Immunodeficiency 18EnrichmentCD3E2.42
43Pulmonary alveolar proteinosis, acquiredEnrichmentHLA-DRB12.42
44Immunodeficiency 25EnrichmentCD2472.42
45Spinocerebellar ataxia 14EnrichmentPRKCG2.42
46Long qt syndrome 16EnrichmentCALM32.42
47Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.42
48Congenital heart defects and ectodermal dysplasiaEnrichmentPRKD12.42
49Immunodeficiency 22EnrichmentLCK2.42
50Immunodeficiency 79EnrichmentCD42.42
51Immunodeficiency 19, severe combinedEnrichmentCD3D2.42
52Long qt syndrome 15EnrichmentCALM22.42
53Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathyEnrichmentITPR32.42
54Rhabdomyolysis 2EnrichmentATP2A22.42
55Immunodeficiency 19EnrichmentCD3D2.42
56Malignant epithelial tumor of salivary glandsEnrichmentPRKD12.42
57MacrodactylyEnrichmentPIK3CA2.32
58Proteus syndromeEnrichmentAKT12.32
59Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.32
60Megalencephaly, autosomal dominantEnrichmentPIK3CA2.32
61Cowden syndrome 5EnrichmentPIK3CA2.32
62Cerebral cavernous malformations 4EnrichmentPIK3CA2.32
63Chromosome 2q37 deletion syndromeEnrichmentHDAC42.32
64Auriculocondylar syndrome 4EnrichmentHDAC92.32
65Short syndromeEnrichmentPIK3R12.32
66Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.32
67Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.32
68Brugada syndrome 3EnrichmentCACNA1C2.32
69Hemifacial myohyperplasiaEnrichmentPIK3CA2.32
70Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.32
71Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.32
72Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.32
73Cowden syndrome 6EnrichmentAKT12.32
74Congenital myopathy 17EnrichmentMYOD12.32
75Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.32
76Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.32
77Developmental and epileptic encephalopathy 56EnrichmentYWHAG2.32
78Myopathy due to myoadenylate deaminase deficiencyEnrichmentAMPD12.32
79Neurodevelopmental disorder with central hypotonia and dysmorphic faciesEnrichmentHDAC42.32
80Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.32
81HypospadiasEnrichmentPIK3CA2.32
82Capillary hemangiomaEnrichmentAKT32.32
835q14.3 microdeletion syndromeEnrichmentMEF2C2.32
84Cerebral cavernous malformations 5EnrichmentMAP3K32.32
85Rare venous malformationEnrichmentPIK3CA2.32
86Diaphragmatic eventrationEnrichmentPIK3CA2.32
87Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.32
88Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.32
89Atypical timothy syndromeEnrichmentCACNA1C2.32
90Rare combined vascular malformationEnrichmentPIK3CA2.32
91Cavernous lymphangiomaEnrichmentPIK3CA2.32
92Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.32
93Timothy syndrome type 2EnrichmentCACNA1C2.32
94Mef2c-related disorderEnrichmentMEF2C2.32
95Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.32
96Verrucous hemangiomaEnrichmentMAP3K32.32
97Eccrine angiomatous hamartomaEnrichmentPIK3CA2.32
98Timothy syndrome type 1EnrichmentCACNA1C2.32
99Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.32
100Macrodactyly of toeEnrichmentPIK3CA2.32
101Cacna1c-related disordersEnrichmentCACNA1C2.32
102Akt2-related familial partial lipodystrophyEnrichmentAKT22.32
103Breast cancerEnrichmentAKT1, JUN, PIK3CA2.26
104Immunodeficiency 48EnrichmentZAP702.25
105Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.25
106Chromosome 15q24 deletion syndromeEnrichmentSIN3A2.25
107Zap70-related severe combined immunodeficiencyEnrichmentZAP702.25
108Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB2.14
109Spinocerebellar ataxia 29EnrichmentITPR12.12
110Acrokeratosis verruciformisEnrichmentATP2A22.12
111Brody diseaseEnrichmentATP2A12.12
112Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM12.12
113Creutzfeldt-jakob diseaseEnrichmentHLA-DQB12.12
114Sarcoidosis 1EnrichmentHLA-DRB12.12
115Long qt syndrome 14EnrichmentCALM12.12
116Menke-hennekam syndrome 2EnrichmentEP3002.12
117Immunodeficiency 17EnrichmentCD3G2.12
118Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.12
119Bladder cancerEnrichmentCDKN1A, PIK3CA2.07
120Scoliosis, isolated 1EnrichmentMAPK72.02
121Timothy syndromeEnrichmentCACNA1C2.02
122LymphangioleiomyomatosisEnrichmentTSC22.02
123Keratosis, seborrheicEnrichmentPIK3CA2.02
124Roifman-chitayat syndromeEnrichmentPIK3CD2.02
125Silver-russell syndrome 3EnrichmentIGF22.02
126Noonan syndrome 8EnrichmentPIK3CA2.02
127Long qt syndrome 8EnrichmentCACNA1C2.02
128Cebalid syndromeEnrichmentMTOR2.02
129Senior-loken syndrome 7EnrichmentAKT32.02
130Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.02
131Immune system diseaseEnrichmentPIK3CD2.02
132Bardet-biedl syndrome 16EnrichmentAKT32.02
133Smith-kingsmore syndromeEnrichmentMTOR2.02
134Adenosine monophosphate deaminase deficiencyEnrichmentAMPD12.02
135Growth delay due to insulin-like growth factor type 1 deficiencyEnrichmentIGF12.02
136Silver-russell syndrome due to an imprinting defect of 11p15EnrichmentIGF22.02
137Silver-russell syndrome due to 11p15 microduplicationEnrichmentIGF22.02
138Witteveen-kolk syndromeEnrichmentSIN3A1.95
139Trypsinogen deficiencyEnrichmentTRB1.95
140Immunodeficiency 52EnrichmentLAT1.95
141Darier-white diseaseEnrichmentATP2A21.94
142Gillespie syndromeEnrichmentITPR11.94
143Adult-onset myasthenia gravisEnrichmentHLA-DQA11.94
144Vogt-koyanagi-harada diseaseEnrichmentHLA-DRB11.94
145Ovarian cancerEnrichmentAKT1, PIK3CA, TSC21.90
146Pompe disease, infantile-onsetEnrichmentPIK3CA1.84
147Tuberous sclerosis 1EnrichmentTSC21.84
148Polycystic kidney disease, infantile severe, with tuberous sclerosisEnrichmentTSC21.84
149Tuberous sclerosis 2EnrichmentTSC21.84
150Miller-dieker lissencephaly syndromeEnrichmentYWHAE1.84
151Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE1.84
152Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizuresEnrichmentCACNA1C1.84
153HamartomaEnrichmentTSC21.84
154Xanthinuria, type iiEnrichmentTSC21.84
155Growth delay due to insulin-like growth factor i resistanceEnrichmentIGF1R1.84
156KeratoacanthomaEnrichmentPIK3CA1.84
157Beckwith-wiedemann syndrome due to imprinting defect of 11p15EnrichmentIGF21.84
158Temporal arteritisEnrichmentHLA-DRB11.82
159Spinocerebellar ataxia 15EnrichmentITPR11.82
160Hereditary ataxiaEnrichmentPRKCG1.82
161Systemic-onset juvenile idiopathic arthritisEnrichmentHLA-DRB11.82
162Type 2 diabetes mellitusEnrichmentAKT2, IRS11.76
163Hereditary breast carcinomaEnrichmentAKT1, PIK3CA1.73
164Rubinstein-taybi syndrome 2EnrichmentEP3001.72
165Follicular lymphomaEnrichmentHLA-DRB11.72
166Diffuse cutaneous systemic sclerosisEnrichmentHLA-DRB11.72
167Ventricular fibrillation, paroxysmal familial, 1EnrichmentCACNA1C1.72
168Glycogen storage disease xEnrichmentPGAM21.72
169Tuberous sclerosisEnrichmentTSC21.72
170Cerebrovascular diseaseEnrichmentPIK3CA1.72
171Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentYWHAZ1.72
172Familial cerebral cavernous malformationsEnrichmentPIK3CA1.72
173Silver-russell syndrome due to a point mutationEnrichmentIGF21.72
174MicrocephalyEnrichmentEP300, IGF1R, YWHAG1.67
175Rubinstein-taybi syndrome 1EnrichmentEP3001.64
176Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.64
177Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.64
178Granulomatosis with polyangiitisEnrichmentHLA-DPA11.64
179Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.64
180Limited sclerodermaEnrichmentHLA-DRB11.64
181Capillary malformations, congenitalEnrichmentPIK3CA1.62
182Heart conduction diseaseEnrichmentCACNA1C1.62
183Endometrial stromal sarcomaEnrichmentYWHAE1.62
184Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA, YWHAZ1.62
185Oligoarticular juvenile idiopathic arthritisEnrichmentCD2471.58
186Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD2471.58
187Vitamin d-dependent rickets, type 2aEnrichmentTRB1.56
188Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.55
189Cowden syndrome 1EnrichmentPIK3CA1.55
190Lung squamous cell carcinomaEnrichmentPIK3CA1.55
191Kidney clear cell sarcomaEnrichmentYWHAE1.55
192Myeloma, multipleEnrichmentHDAC4, PIK3R21.53
193Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA, YWHAG1.53
194Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.52
195Nevus, epidermalEnrichmentPIK3CA1.48
196Polycystic kidney disease 1 with or without polycystic liver diseaseEnrichmentTSC21.48
197Multiple endocrine neoplasia, type iEnrichmentCDKN1A1.48
198Silver-russell syndrome 1EnrichmentIGF21.48
199Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.48
200Renal cell carcinoma, papillary, 1EnrichmentMTOR1.48
201Polycystic kidney disease 1EnrichmentTSC21.48
202Gallbladder cancerEnrichmentPIK3CA1.48
203MegacolonEnrichmentAKT31.48
204Charge syndromeEnrichmentEP3001.47
205Inflammatory bowel disease 1EnrichmentPRKCQ1.47
206Stroke, ischemicEnrichmentPRKCH1.42
207Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentCACNA1C1.37
208Arteriovenous malformationEnrichmentPIK3CA1.37
209Congenital long qt syndromeEnrichmentITPR31.35
210Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.33
211PolymicrogyriaEnrichmentAKT31.33
212Lung non-small cell carcinomaEnrichmentPIK3CA1.29
213Specific learning disabilityEnrichmentYWHAG1.29
214Polydactyly, postaxial, type a1EnrichmentEP3001.25
215Anterior segment dysgenesisEnrichmentITPR11.25
216Cardiac conduction defectEnrichmentCACNA1C1.25
217Lip and oral cavity carcinomaEnrichmentPIK3CA1.25
218Combined immunodeficiencyEnrichmentZAP701.22
219Combined t cell and b cell immunodeficiencyEnrichmentZAP701.22
220Combined t and b cell immunodeficiencyEnrichmentZAP701.22
221Sudden infant death syndromeEnrichmentCALM21.20
222Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.16
223Wilms tumor 1EnrichmentIGF21.16
224Lynch syndromeEnrichmentPIK3CA1.16
225Autosomal dominant polycystic kidney diseaseEnrichmentTSC21.16
226Chromosome 1p36 deletion syndromeEnrichmentPRKCZ1.15
227Hereditary chronic pancreatitisEnrichmentTRB1.12
228Cardiomyopathy, dilated, 1aEnrichmentNFATC21.11
229Beckwith-wiedemann syndromeEnrichmentIGF21.08
230Pancreatitis, hereditaryEnrichmentTRB1.04
231Endometrial cancerEnrichmentPIK3CA1.02
232Autism spectrum disorderEnrichmentMEF2C, TSC21.02
233Hepatocellular carcinomaEnrichmentPIK3CA1.00
234Severe covid-19EnrichmentHLA-DQB10.98
235Cardiomyopathy, familial hypertrophic, 1EnrichmentCACNA1C0.96
236Brugada syndromeEnrichmentCACNA1C0.93
237Prostate cancerEnrichmentPIK3CA0.89
238Systemic lupus erythematosusEnrichmentHLA-DRB10.86
239Lung cancerEnrichmentPIK3CA0.85
240Fetal akinesia deformation sequence 1EnrichmentMYOD10.79
241Cerebral palsyEnrichmentCACNA1C0.77
242Distal arthrogryposisEnrichmentMYOD10.74
243Spastic ataxiaEnrichmentITPR10.73
244Gastric cancerEnrichmentPIK3CA0.73
245West syndromeEnrichmentTSC20.72
246HypertelorismEnrichmentPIK3CA0.65
247Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.61
248Congenital nervous system abnormalityEnrichmentTSC20.40
249Nervous system diseaseEnrichmentTSC20.40
250Complex neurodevelopmental disorderEnrichmentCACNA1C0.35
251Inherited cancer-predisposing syndromeEnrichmentTSC20.33

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