Mitochondrial immune response to SARS-CoV-2

No Pathway Network information available for Mitochondrial immune response to SARS-CoV-2

Pathways in the Mitochondrial immune response to SARS-CoV-2 SuperPath

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

Disorders associated with Mitochondrial immune response to SARS-CoV-2 SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Herpes simplex virus encephalitisEnrichmentTBK1, TICAM1, TRAF37.37
2Mitochondrial complex i deficiency, nuclear type 1EnrichmentACAD9, NDUFAF1, NDUFB94.46
3Renal tubular dysgenesisEnrichmentACE, AGTR14.39
4Common variable immunodeficiencyEnrichmentNFKB1, NFKB24.24
5Multisystem inflammatory syndrome in childrenEnrichmentIRF3, TRAF33.21
6Immunodeficiency 39 viral infectionsEnrichmentIRF72.77
7Encephalopathy, acute, infection-induced 7EnrichmentIRF32.77
8Microvascular complications of diabetes 3EnrichmentACE2.77
9Encephalopathy, acute, infection-induced 6EnrichmentTICAM12.77
10Bjornstad syndromeEnrichmentBCS1L2.77
11Mitochondrial complex i deficiency, nuclear type 11EnrichmentNDUFAF12.77
12Immunodeficiency 132aEnrichmentTRAF32.77
13Immunodeficiency 132bEnrichmentTRAF32.77
14Immunodeficiency 39EnrichmentIRF72.77
15Gracile syndromeEnrichmentBCS1L2.77
16Autoinflammation with arthritis and vasculitisEnrichmentTBK12.77
17Mitochondrial complex i deficiency, nuclear type 24EnrichmentNDUFB92.77
18Singleton-merten syndrome 2EnrichmentRIGI2.77
19Corticobasal syndromeEnrichmentTBK12.77
20Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.77
21Encephalopathy, acute, infection-induced 8EnrichmentTBK12.77
22Renal tubulopathy-encephalopathy-liver failure syndromeEnrichmentBCS1L2.77
23Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.47
24Immunodeficiency, common variable, 10EnrichmentNFKB22.47
25Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.47
26Singleton-merten syndromeEnrichmentRIGI2.47
27Common variable immunodeficiency 12EnrichmentNFKB12.47
28Mitochondrial complex iii deficiency, nuclear type 1EnrichmentBCS1L2.29
29Mitochondrial complex i deficiency, nuclear type 20EnrichmentACAD92.29
30Immunodeficiency, common variable, 1EnrichmentNFKB22.17
31Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.07
32Hemorrhage, intracerebralEnrichmentACE1.99
33Motor neuron diseaseEnrichmentTBK11.93
34Progressive non-fluent aphasiaEnrichmentTBK11.82
35Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.77
36Stroke, ischemicEnrichmentACE1.77
37Ciliary dyskinesia, primary, 3EnrichmentNFKB11.77
38Movement diseaseEnrichmentBCS1L1.73
39Isolated complex iii deficiencyEnrichmentBCS1L1.73
40Hypertension, essentialEnrichmentAGTR11.55
41Myocardial infarctionEnrichmentACE1.44
42CakutEnrichmentACE1.25
43Non-syndromic x-linked intellectual disabilityEnrichmentAGTR21.23
44Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK11.03
45Leigh syndrome, nuclearEnrichmentBCS1L0.96
46Leigh diseaseEnrichmentBCS1L0.92
47MicrocephalyEnrichmentBCS1L0.72

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