Early SARS-CoV-2 Infection Events

Pathway network for the Early SARS-CoV-2 Infection Events SuperPath

Sources:
  • Reactome
  • WikiPathways

Pathways in the Early SARS-CoV-2 Infection Events SuperPath

#NameSourceGenes
1Early SARS-CoV-2 Infection EventsReactome
2SARS-CoV-2 InfectionWikiPathways
3SARS-CoV-1 InfectionWikiPathways
4Translation of Structural ProteinsReactome
5Attachment and EntryReactome
6Translation of Replicase and Assembly of the Replication Transcription ComplexReactome
7Translation of Replicase and Assembly of the Replication Transcription ComplexReactome
8Maturation of protein 3aReactome
9Maturation of protein 3aReactome
10Maturation of spike proteinReactome
11Attachment and EntryReactome
12Defective MOGS causes CDG-2bReactome

Gene overlap in member pathways for Early SARS-CoV-2 Infection Events SuperPath

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

Disorders associated with Early SARS-CoV-2 Infection Events SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Covid-19Direct
2Severe acute respiratory syndromeDirect
3Immunodeficiency 47Direct
4Progressive non-fluent aphasiaEnrichmentCHMP2B, VCP3.31
5Behavioral variant of frontotemporal dementiaEnrichmentCHMP2B, VCP3.31
6Polycystic liver diseaseEnrichmentGANAB, PRKCSH2.74
7Autosomal dominant polycystic liver diseaseEnrichmentGANAB, PRKCSH2.74
8Cataract 31, multiple typesEnrichmentCHMP4B2.42
9Intellectual developmental disorder, autosomal recessive 12EnrichmentST3GAL32.42
10Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1EnrichmentVCP2.42
11Orofacial cleft 10EnrichmentSUMO12.42
12Frontotemporal dementia and/or amyotrophic lateral sclerosis 6EnrichmentVCP2.42
13Multisystem proteinopathyEnrichmentVCP2.42
14Trilateral retinoblastomaEnrichmentRB12.42
15Adult-onset distal myopathy due to vcp mutationEnrichmentVCP2.42
16St3gal3-cdgEnrichmentST3GAL32.42
17Retinal hemangioblastomaEnrichmentVHL2.42
18Lung oat cell carcinomaEnrichmentRB12.42
19Congenital disorder of glycosylation, type iiaEnrichmentMGAT22.30
20Intellectual developmental disorder, autosomal recessive 7EnrichmentTUSC32.30
21Congenital disorder of glycosylation, type iw, autosomal recessiveEnrichmentSTT3A2.30
22Congenital disorder of glycosylation, type iccEnrichmentMAGT12.30
23Congenital disorder of glycosylation, type irEnrichmentDDOST2.30
24Congenital disorder of glycosylation iwEnrichmentSTT3A2.30
25Man1b1-congenital disorder of glycosylationEnrichmentMAN1B12.30
26Congenital disorder of glycosylation, type iibEnrichmentMOGS2.12
27Amyotrophic lateral sclerosis 6 with or without frontotemporal dementiaEnrichmentVCP2.12
28Chromosome 13q14 deletion syndromeEnrichmentRB12.12
29Developmental and epileptic encephalopathy 15EnrichmentST3GAL32.12
30Polycystic kidney disease 3EnrichmentGANAB2.12
31Acute leukemia of ambiguous lineageEnrichmentVHL2.12
32Familial retinoblastomaEnrichmentRB12.12
33Submucosal cleft palateEnrichmentUBB2.12
34Cleft hard palateEnrichmentUBB2.12
35Spastic paraplegia-paget disease of bone syndromeEnrichmentVCP2.12
36Immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection, and neoplasiaEnrichmentMAGT12.00
37Rafiq syndromeEnrichmentMAN1B12.00
38Congenital disorder of glycosylation with defective fucosylation 1EnrichmentFUT82.00
39Intellectual developmental disorder, autosomal recessive 24EnrichmentTUSC32.00
40Congenital disorder of glycosylation, type iw, autosomal dominantEnrichmentSTT3A2.00
41Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)EnrichmentRPN12.00
42RetinoblastomaEnrichmentRB11.95
43Myasthenic syndrome, congenital, 6, presynapticEnrichmentVHL1.95
44Uvula, bifidEnrichmentUBB1.95
45Osteogenic sarcomaEnrichmentRB11.95
46Cleft soft palateEnrichmentUBB1.95
47Woolly hair, autosomal recessive 3EnrichmentRB11.95
48Hypotrichosis 8EnrichmentRB11.95
49Primary polycythemiaEnrichmentVHL1.95
50Inclusion body myopathy with paget disease of bone and frontotemporal dementiaEnrichmentVCP1.95
51Squamous cell carcinomaEnrichmentRB11.95
52Bone osteosarcomaEnrichmentRB11.95
53Small cell cancer of the lungEnrichmentRB11.83
54Erythrocytosis, familial, 2EnrichmentVHL1.83
55Au-kline syndromeEnrichmentVHL1.83
56Lynch syndrome 4EnrichmentRB11.83
57Cataract 6, multiple typesEnrichmentCHMP4B1.73
58Polycystic liver disease 1 with or without kidney cystsEnrichmentPRKCSH1.73
59Dementia, lewy bodyEnrichmentVCP1.73
60Fanconi anemia, complementation group d2EnrichmentVHL1.73
61Von hippel-lindau syndromeEnrichmentVHL1.73
62Polycystic kidney disease 3 with or without polycystic liver diseaseEnrichmentGANAB1.73
63Charcot-marie-tooth disease, axonal, type 2eEnrichmentVCP1.73
64Polycystic liver disease 1EnrichmentPRKCSH1.73
65Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentCHMP2B, VCP1.70
66Sporadic pheochromocytoma/secreting paragangliomaEnrichmentVHL1.65
67Renal cell carcinoma, papillary, 1EnrichmentVHL1.58
68Multiple enchondromatosis, maffucci typeEnrichmentVHL1.58
69Semantic dementiaEnrichmentCHMP2B1.58
70Early-onset posterior polar cataractEnrichmentCHMP4B1.53
71Autosomal recessive non-syndromic intellectual disabilityEnrichmentMAN1B1, TUSC31.47
72Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentVCP1.43
73Lip and oral cavity carcinomaEnrichmentRB11.35
74Alzheimer's diseaseEnrichmentVCP1.32
75PheochromocytomaEnrichmentVHL1.29
76Lung cancer susceptibility 3EnrichmentRB11.29
77Renal cell carcinoma, nonpapillaryEnrichmentVHL1.26
78Autosomal dominant polycystic kidney diseaseEnrichmentGANAB1.26
79Alzheimer disease, familial, 1EnrichmentVCP1.21
80Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentVCP1.16
81Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentVHL1.12
82Tooth agenesisEnrichmentSUMO11.10
83Congenital disorder of glycosylation, type inEnrichmentMAGT11.09
84Inherited cancer-predisposing syndromeEnrichmentRB1, VHL1.06
85Bladder cancerEnrichmentRB10.98
86Fanconi anemia, complementation group aEnrichmentVHL0.91
87Developmental and epileptic encephalopathyEnrichmentST3GAL30.90
88Ovarian cancerEnrichmentRB10.50
89Congenital nervous system abnormalityEnrichmentTUSC30.38
90Nervous system diseaseEnrichmentTUSC30.38

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