Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template

Pathway network for the Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template SuperPath

Sources:
  • Reactome

Pathways in the Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template SuperPath

#NameSourceGenes
1Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA templateReactome
2DNA Damage BypassReactome
3Termination of translesion DNA synthesisReactome
4Recognition of DNA damage by PCNA-containing replication complexReactome
5Translesion Synthesis by POLHReactome
6Translesion synthesis by POLKReactome
7Translesion synthesis by POLIReactome
8Translesion synthesis by REV1Reactome

Gene overlap in member pathways for Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template SuperPath

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

Disorders associated with Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Polymerase proofreading-related polyposisEnrichmentPOLD1, POLE4.85
2Familial colorectal cancer type xEnrichmentPOLD1, POLE3.59
3Fanconi anemia, complementation group vEnrichmentMAD2L22.93
4Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 6EnrichmentRPA12.93
5Ataxia-telangiectasia-like disorder 2EnrichmentPCNA2.93
6Morimoto-ryu-malicdan neuromuscular syndromeEnrichmentRFC42.93
7Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1EnrichmentVCP2.85
8Ruijs-aalfs syndromeEnrichmentSPRTN2.85
9Frontotemporal dementia and/or amyotrophic lateral sclerosis 6EnrichmentVCP2.85
10Multisystem proteinopathyEnrichmentVCP2.85
11Adult-onset distal myopathy due to vcp mutationEnrichmentVCP2.85
12Colorectal cancerEnrichmentPOLD1, POLE, REV3L2.71
13Cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual developmentEnrichmentPOLE2.66
14Colorectal cancer 10EnrichmentPOLD12.66
15Colorectal cancer 12EnrichmentPOLE2.66
16White-kernohan syndromeEnrichmentDDB12.66
17Immunodeficiency 120EnrichmentPOLD12.66
18Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndromeEnrichmentPOLD12.66
19Autosomal recessive spastic paraplegia type 60EnrichmentWDR482.66
20Immunodeficiency 122EnrichmentPOLD32.66
21Cerebellar ataxia, neuropathy, and vestibular areflexia syndromeEnrichmentRFC12.63
22Submucosal cleft palateEnrichmentUBB2.63
23Cleft hard palateEnrichmentUBB2.63
24Immunodeficiency 38 with basal ganglia calcificationEnrichmentISG152.63
25Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic faciesEnrichmentPOLK2.60
26Amyotrophic lateral sclerosis 6 with or without frontotemporal dementiaEnrichmentVCP2.55
27Spastic paraplegia-paget disease of bone syndromeEnrichmentVCP2.55
28Uvula, bifidEnrichmentUBB2.45
29Cleft soft palateEnrichmentUBB2.45
30Childhood apraxia of speechEnrichmentRFC32.45
31Inclusion body myopathy with paget disease of bone and frontotemporal dementiaEnrichmentVCP2.38
32Intellectual developmental disorder, x-linked, syndromic, cabezas typeEnrichmentCUL4B2.35
33Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesEnrichmentPOLE2.35
34Pettigrew syndromeEnrichmentCUL4B2.35
35Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiencyEnrichmentPOLE2.35
36Facial dysmorphism, immunodeficiency, livedo, and short statureEnrichmentPOLE2.35
37Moebius syndromeEnrichmentREV3L2.23
38Dementia, lewy bodyEnrichmentVCP2.16
39Charcot-marie-tooth disease, axonal, type 2eEnrichmentVCP2.16
40Progressive non-fluent aphasiaEnrichmentVCP1.90
41Behavioral variant of frontotemporal dementiaEnrichmentVCP1.90
42Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentVCP1.86
43Xeroderma pigmentosum, variant typeEnrichmentPOLH1.82
44Digeorge syndromeEnrichmentUFD11.78
45Alzheimer's diseaseEnrichmentVCP1.74
46OligospermiaEnrichmentSPRTN1.74
47Parkinson's diseaseEnrichmentRFC11.65
48Williams-beuren syndromeEnrichmentRFC21.63
49Alzheimer disease, familial, 1EnrichmentVCP1.63
50Combined immunodeficiencyEnrichmentPOLD11.62
51Combined t cell and b cell immunodeficiencyEnrichmentPOLD11.62
52Combined t and b cell immunodeficiencyEnrichmentPOLD11.62
53Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentVCP1.58
54Parkinson disease, late-onsetEnrichmentRFC11.55
55Inherited cancer-predisposing syndromeEnrichmentPOLD1, POLE1.47
56Prostate cancerEnrichmentPOLK1.45
57Fanconi anemia, complementation group aEnrichmentMAD2L21.39
58Pancreatic cancerEnrichmentPOLD11.27
59Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentVCP1.11

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