Ebstein-Barr virus LMP1 signaling

No Pathway Network information available for Ebstein-Barr virus LMP1 signaling

Pathways in the Ebstein-Barr virus LMP1 signaling SuperPath

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

Disorders associated with Ebstein-Barr virus LMP1 signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.56
2Common variable immunodeficiencyEnrichmentNFKB1, NFKB24.24
3MalariaEnrichmentIKBKG, TNF3.17
4Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.77
5Incontinentia pigmentiEnrichmentIKBKG2.77
6Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.77
7Fetal encasement syndromeEnrichmentCHUK2.77
8Frontometaphyseal dysplasia 2EnrichmentMAP3K72.77
9Immunodeficiency 15bEnrichmentIKBKB2.77
10Noonan syndrome 13EnrichmentMAPK12.77
11Immunodeficiency 15aEnrichmentIKBKB2.77
12Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.77
13Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.77
14Bartsocas-papas syndrome 2EnrichmentCHUK2.77
15Immunodeficiency 112EnrichmentMAP3K142.77
16Cerebral cavernous malformations 5EnrichmentMAP3K32.77
17Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.77
18Verrucous hemangiomaEnrichmentMAP3K32.77
19Nik deficiencyEnrichmentMAP3K142.77
20Systemic lupus erythematosusEnrichmentIRAK1, TNF2.71
21Immunodeficiency 33EnrichmentIKBKG2.47
22Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.47
23Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.47
24Immunodeficiency, common variable, 10EnrichmentNFKB22.47
25Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.47
26Immunodeficiency 127EnrichmentTNF2.47
27Rela fusion-positive ependymomaEnrichmentRELA2.47
28Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.47
29Common variable immunodeficiency 12EnrichmentNFKB12.47
30Psoriatic arthritisEnrichmentTNF2.29
31Nasopharyngeal carcinomaEnrichmentNFKBIA2.29
32Frontometaphyseal dysplasiaEnrichmentMAP3K72.29
33Migraine without auraEnrichmentTNF2.29
34Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.17
35Immunodeficiency, common variable, 1EnrichmentNFKB22.17
36Cerebral malariaEnrichmentTNF2.17
37Pediatric systemic lupus erythematosusEnrichmentIRAK12.17
38Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.07
39Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.07
40Vascular dementiaEnrichmentTNF2.07
41Coronary heart disease 5EnrichmentIKBKG1.82
42Ciliary dyskinesia, primary, 3EnrichmentNFKB11.77
43AsthmaEnrichmentTNF1.73
44Specific learning disabilityEnrichmentMAPK11.73
45Alzheimer's diseaseEnrichmentTNF1.66
46GliosarcomaEnrichmentNFKBIA1.57
47Giant cell glioblastomaEnrichmentNFKBIA1.55
48Heart, malformation ofEnrichmentMAPK11.52
49Human immunodeficiency virus type 1EnrichmentCCL51.52
50Multisystem inflammatory syndrome in childrenEnrichmentIFNB11.44
51Severe combined immunodeficiencyEnrichmentIKBKB1.26
52MicrocephalyEnrichmentMAPK10.72

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