Maturation of protein E

Pathway network for the Maturation of protein E SuperPath

Sources:
  • Reactome

Pathways in the Maturation of protein E SuperPath

Gene overlap in member pathways for Maturation of protein E SuperPath

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

Disorders associated with Maturation of protein E SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe acute respiratory syndromeDirect
2Covid-19Direct
3Parkinson's diseaseEnrichmentATXN3, PRKN3.91
4Parkinson disease, late-onsetEnrichmentATXN3, PRKN3.71
5Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1EnrichmentVCP3.05
6Leprosy 2EnrichmentPRKN3.05
7Frontotemporal dementia and/or amyotrophic lateral sclerosis 6EnrichmentVCP3.05
8Multisystem proteinopathyEnrichmentVCP3.05
9Adult-onset distal myopathy due to vcp mutationEnrichmentVCP3.05
10Parkinson disease 12EnrichmentPRKN2.75
11Amyotrophic lateral sclerosis 6 with or without frontotemporal dementiaEnrichmentVCP2.75
12Submucosal cleft palateEnrichmentUBB2.75
13Cleft hard palateEnrichmentUBB2.75
14Spastic paraplegia-paget disease of bone syndromeEnrichmentVCP2.75
15Uvula, bifidEnrichmentUBB2.58
16Cleft soft palateEnrichmentUBB2.58
17Inclusion body myopathy with paget disease of bone and frontotemporal dementiaEnrichmentVCP2.58
18Complex hereditary spastic paraplegiaEnrichmentPRKN2.45
19Dementia, lewy bodyEnrichmentVCP2.35
20Parkinson disease 2, autosomal recessive juvenileEnrichmentPRKN2.35
21Charcot-marie-tooth disease, axonal, type 2eEnrichmentVCP2.35
22Parkin type of early-onset parkinson diseaseEnrichmentPRKN2.35
23Machado-joseph diseaseEnrichmentATXN32.28
24Progressive non-fluent aphasiaEnrichmentVCP2.10
25Behavioral variant of frontotemporal dementiaEnrichmentVCP2.10
26Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentVCP2.05
27Early-onset parkinson's diseaseEnrichmentPRKN1.98
28Alzheimer's diseaseEnrichmentVCP1.94
29Lung cancer susceptibility 3EnrichmentPRKN1.91
30Alzheimer disease, familial, 1EnrichmentVCP1.83
31Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentVCP1.78
32Lung cancerEnrichmentPRKN1.55
33Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentVCP1.30
34SchizophreniaEnrichmentPRKN1.29
35AutismEnrichmentPRKN1.21
36Ovarian cancerEnrichmentPRKN1.07
37Autism spectrum disorderEnrichmentPRKN1.03

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