Activation of the pre-replicative complex

Pathway network for the Activation of the pre-replicative complex SuperPath

Sources:
  • Reactome
  • QIAGEN
  • GeneGo (Thomson Reuters)
  • WikiPathways
  • PubChem

Pathways in the Activation of the pre-replicative complex SuperPath

#NameSourceGenes
1Activation of the pre-replicative complexReactome
2Cell Cycle Control of Chromosomal ReplicationQIAGEN
3Cell cycle Start of DNA replication in early S phaseGeneGo (Thomson Reuters)
4DNA replicationWikiPathways
5Activation of ATR in response to replication stressReactome
6ATR signaling pathwayPubChem
7DNA strand elongationReactome
8Lagging Strand SynthesisReactome
9Processive synthesis on the lagging strandReactome
10Removal of the Flap IntermediateReactome
11Unwinding of DNAReactome
12CDC6 association with the ORC:origin complexReactome
13DNA replication initiationReactome

Gene overlap in member pathways for Activation of the pre-replicative complex SuperPath

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

Disorders associated with Activation of the pre-replicative complex SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Meier-gorlin syndrome 1EnrichmentCDC45, CDC6, CDT1, MCM7, ORC1, ORC4, ORC616.00
2Familial colorectal cancer type xEnrichmentCHEK2, POLD1, POLE5.32
3Polymerase proofreading-related polyposisEnrichmentPOLD1, POLE4.55
4Seckel syndromeEnrichmentDNA2, PRIM14.05
5Fanconi anemia, complementation group aEnrichmentBRCA2, FANCD2, RAD513.94
6Hereditary breast carcinomaEnrichmentBRCA2, NBN, RAD513.64
7Hereditary breast ovarian cancer syndromeEnrichmentBRCA2, NBN, RAD513.35
8Breast-ovarian cancer, familial 1EnrichmentBRCA2, NBN3.26
9Meier-gorlin syndrome 3EnrichmentORC63.23
10Meier-gorlin syndrome 2EnrichmentORC43.23
11Premature ovarian failure 10EnrichmentMCM83.23
12Meier-gorlin syndrome 5EnrichmentCDC63.23
13Cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual developmentEnrichmentPOLE3.23
14Van esch-o'driscoll syndromeEnrichmentPOLA13.23
15Colorectal cancer 12EnrichmentPOLE3.23
16Pigmentary disorder, reticulate, with systemic manifestations, x-linkedEnrichmentPOLA13.23
17Inherited cancer-predisposing syndromeEnrichmentCDK4, CHEK2, POLD1, POLE3.10
18Lactose intolerance, adult typeEnrichmentMCM63.05
19AnisometropiaEnrichmentMCM73.05
20Immunodeficiency 54EnrichmentMCM43.05
21Deafness, autosomal dominant 70EnrichmentMCM23.05
22Meier-gorlin syndrome 8EnrichmentMCM53.05
23Meier-gorlin syndrome 7EnrichmentCDC453.05
24Colorectal cancer 10EnrichmentPOLD12.99
25Seckel syndrome 8EnrichmentDNA22.99
26Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 6EnrichmentRPA12.99
27Immunodeficiency 120EnrichmentPOLD12.99
28Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 6EnrichmentDNA22.99
29Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndromeEnrichmentPOLD12.99
30Ataxia-telangiectasia-like disorder 2EnrichmentPCNA2.99
31Rothmund-thomson syndrome, type 4EnrichmentDNA22.99
32Immunodeficiency 122EnrichmentPOLD32.99
33Breast cancerEnrichmentBRCA2, NBN, RAD512.96
34Immunodeficiency 96EnrichmentLIG12.96
35Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesEnrichmentPOLE2.93
36Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiencyEnrichmentPOLE2.93
37Primordial dwarfism-immunodeficiency-lipodystrophy syndromeEnrichmentPRIM12.93
38Facial dysmorphism, immunodeficiency, livedo, and short statureEnrichmentPOLE2.93
39Diffuse large b-cell lymphomaEnrichmentBRCA2, NBN2.92
40Morimoto-ryu-malicdan neuromuscular syndromeEnrichmentRFC42.83
41Partington syndromeEnrichmentPOLA12.75
42Immunodeficiency 55EnrichmentGINS12.75
43Rothmund-thomson syndrome, type 2EnrichmentDNA22.69
44Pancreatic cancerEnrichmentBRCA2, NBN2.68
45Immunodeficiency 80 with or without congenital cardiomyopathyEnrichmentMCM102.61
46Meier-gorlin syndrome 4EnrichmentCDT12.61
47Meier-gorlin syndrome 6EnrichmentGMNN2.61
48Ovarian cancerEnrichmentBRCA2, FANCD2, NBN2.59
49Colorectal cancerEnrichmentCHEK2, POLD1, POLE2.58
50Seckel syndrome 1EnrichmentATR2.56
51Cutaneous telangiectasia and cancer syndrome, familialEnrichmentATR2.56
52Oocyte/zygote/embryo maturation arrest 21EnrichmentCHEK12.56
53Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndromeEnrichmentATR2.56
54Spinocerebellar ataxia 12EnrichmentPPP2R2B2.56
55Glioma susceptibility 3EnrichmentBRCA22.56
56Mirror movements 2EnrichmentRAD512.56
57Schimke immunoosseous dysplasiaEnrichmentSMARCAL12.56
58Accelerated tumor formationEnrichmentMDM22.56
59Fanconi anemia, complementation group rEnrichmentRAD512.56
60Lessel-kubisch syndromeEnrichmentMDM22.56
61Pancreatic cancer 2EnrichmentBRCA22.56
62Houge-janssens syndrome 2EnrichmentPPP2R1A2.56
63Advanced sleep phase syndrome, familial, 4EnrichmentTIMELESS2.56
64Nephronophthisis 15EnrichmentCEP1642.56
65Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A2.56
66Prostate cancerEnrichmentBRCA2, NBN2.55
672q23.1 microduplication syndromeEnrichmentORC42.53
68Cerebellar ataxia, neuropathy, and vestibular areflexia syndromeEnrichmentRFC12.53
69Melanoma, cutaneous malignant 3EnrichmentCDK42.50
70Microcephaly 12, primary, autosomal recessiveEnrichmentCDK62.50
71Lissencephaly 7 with cerebellar hypoplasiaEnrichmentCDK52.50
72Leukodystrophy, hypomyelinating, 27EnrichmentPOLR1A2.50
73Tumor predisposition syndrome 4EnrichmentCHEK22.50
74LeiomyosarcomaEnrichmentCHEK22.50
75Childhood myocerebrohepatopathy spectrumEnrichmentPOLG2.50
76Spinocerebellar ataxia with epilepsyEnrichmentPOLG2.50
77Recessive mitochondrial ataxia syndromeEnrichmentPOLG2.50
78Rahman syndromeEnrichmentH1-42.50
79AstigmatismEnrichmentMCM72.45
80EnophthalmosEnrichmentMCM72.45
81FarsightednessEnrichmentMCM72.35
82Childhood apraxia of speechEnrichmentRFC32.35
83MicrocephalyEnrichmentMCM7, NBN, SMARCAL12.35
84Primary autosomal recessive microcephalyEnrichmentCDK6, MCM72.34
85Diffuse midline glioma, h3 k27m-mutantEnrichmentBRCA22.26
86Fanconi anemia, complementation group d1EnrichmentBRCA22.26
87Inflammatory breast carcinomaEnrichmentBRCA22.26
88Houge-janssens syndrome 3EnrichmentPPP2CA2.26
89Bilateral breast cancerEnrichmentBRCA22.26
90Neuroendocrine tumor of pancreasEnrichmentBRCA22.26
91Gastric cancerEnrichmentBRCA2, NBN2.22
92Ebstein anomalyEnrichmentCDK82.20
93Fanconi anemia, complementation group iEnrichmentPOLG2.20
94Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic faciesEnrichmentPOLK2.20
95Congenital heart defects, multiple types, 3EnrichmentCHEK22.20
96Developmental and epileptic encephalopathy 87EnrichmentCDK192.20
97Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 1EnrichmentPOLG2.20
98Al kaissi syndromeEnrichmentCDK102.20
99Li-fraumeni syndrome 1EnrichmentCHEK22.20
100SarcomaEnrichmentCHEK22.20
101Acrofacial dysostosis, cincinnati typeEnrichmentPOLR1A2.20
102Polg-related disordersEnrichmentPOLG2.20
103Autosomal recessive progressive external ophthalmoplegiaEnrichmentPOLG2.20
104Intellectual developmental disorder with hypotonia and behavioral abnormalitiesEnrichmentCDK82.20
105Vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestationsEnrichmentATRIP2.09
106Chilblain lupus 1EnrichmentATRIP2.09
107Chilblain lupusEnrichmentATRIP2.09
108Nijmegen breakage syndromeEnrichmentNBN2.09
109Tumor predisposition syndrome 1EnrichmentBRCA22.09
110Dedifferentiated liposarcomaEnrichmentMDM22.09
111Bap1 tumor predisposition syndromeEnrichmentBRCA22.09
112Well-differentiated liposarcomaEnrichmentMDM22.09
113Isolated growth hormone deficiency, type iaEnrichmentDNA22.08
114Burn-mckeown syndromeEnrichmentPOLR1A2.02
115Osteogenic sarcomaEnrichmentCHEK22.02
116Bone osteosarcomaEnrichmentCHEK22.02
117Idiopathic camptocormiaEnrichmentPOLG2.02
118Aicardi-goutieres syndrome 1EnrichmentATRIP1.96
119Thrombotic microangiopathyEnrichmentATRIP1.96
120Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentCHEK11.96
121Mirror movements 1EnrichmentRAD511.96
122ChordomaEnrichmentBRCA21.96
123Erythrocytosis, familial, 2EnrichmentFANCD21.96
124Polyposis syndrome, hereditary mixed, 1EnrichmentBRCA21.96
125CholangiocarcinomaEnrichmentBRCA21.96
126Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentYWHAZ1.96
127Combined immunodeficiencyEnrichmentPOLD11.95
128Combined t cell and b cell immunodeficiencyEnrichmentPOLD11.95
129Combined t and b cell immunodeficiencyEnrichmentPOLD11.95
130AzoospermiaEnrichmentMCM81.93
131Generalized epilepsyEnrichmentPOLG1.90
132Hemoglobin c diseaseEnrichmentCHEK21.90
133Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1EnrichmentATRIP1.87
134Vascular dementiaEnrichmentATRIP1.87
135Fanconi anemia, complementation group d2EnrichmentFANCD21.87
136Von hippel-lindau syndromeEnrichmentFANCD21.87
137Atrioventricular septal defectEnrichmentSMARCAL11.87
138Breast-ovarian cancer, familial 2EnrichmentBRCA21.87
139Primary ovarian insufficiencyEnrichmentCHEK2, POLG1.82
140Sensory ataxic neuropathy, dysarthria, and ophthalmoparesisEnrichmentPOLG1.80
141Li-fraumeni syndromeEnrichmentMDM21.79
142Kabuki syndrome 1EnrichmentBRCA21.79
143Machado-joseph diseaseEnrichmentPOLG1.72
144Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1EnrichmentPOLG1.72
145Wilms tumor 5EnrichmentCHEK21.72
146Mitochondrial dna depletion syndrome 1EnrichmentPOLG1.72
147Mitochondrial dna depletion syndromeEnrichmentPOLG1.72
148MicrophthalmiaEnrichmentMCM71.71
149Mitochondrial dna depletion syndrome 4aEnrichmentPOLG1.66
150Tracheoesophageal fistula with or without esophageal atresiaEnrichmentBRCA21.61
151PolydactylyEnrichmentBRCA21.61
152Mitochondrial dna depletion syndrome 4bEnrichmentPOLG1.60
153Aicardi-goutieres syndromeEnrichmentATRIP1.57
154Aplastic anemiaEnrichmentNBN1.57
155Isolated tracheo-esophageal fistulaEnrichmentBRCA21.57
156Parkinson's diseaseEnrichmentRFC11.56
157Colonic benign neoplasmEnrichmentCHEK21.55
158Autosomal dominant cerebellar ataxiaEnrichmentPOLG1.55
159Mitochondrial neurogastrointestinal encephalomyopathyEnrichmentPOLG1.55
160Williams-beuren syndromeEnrichmentRFC21.54
161Leukemia, acute lymphoblasticEnrichmentNBN1.53
162Uterine corpus cancerEnrichmentBRCA21.53
163Lynch syndrome 1EnrichmentCHEK21.50
164MelanomaEnrichmentCHEK21.50
165Xeroderma pigmentosum, variant typeEnrichmentPOLH1.46
166Parkinson disease, late-onsetEnrichmentRFC11.46
167Neural tube defectsEnrichmentRAD9B1.46
168Senior-loken syndrome 1EnrichmentCEP1641.46
169Premature menopauseEnrichmentNBN1.46
170MedulloblastomaEnrichmentBRCA21.43
171Wilms tumor 1EnrichmentBRCA21.40
172Atypical hemolytic-uremic syndromeEnrichmentSMARCAL11.40
173Diaphragmatic hernia, congenitalEnrichmentCDK81.39
174Nk-cell enteropathyEnrichmentCHEK21.39
175RhabdomyosarcomaEnrichmentBRCA21.37
176Isolated congenital microcephalyEnrichmentSMARCAL11.37
177Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentMCM21.35
178Polycystic liver diseaseEnrichmentCDC25A1.34
179Autosomal dominant polycystic liver diseaseEnrichmentCDC25A1.34
180Lynch syndromeEnrichmentCHEK21.33
181Hydrocephalus, congenital, 1EnrichmentCDK81.30
182Esophageal atresia/tracheoesophageal fistulaEnrichmentBRCA21.30
183Melanoma, cutaneous malignant 1EnrichmentCDK41.28
184Focal segmental glomerulosclerosisEnrichmentSMARCAL11.27
185Heart, malformation ofEnrichmentCDK81.26
186Endometrial cancerEnrichmentBRCA21.25
187LissencephalyEnrichmentNBN1.25
188HepatoblastomaEnrichmentBRCA21.25
189Hepatocellular carcinomaEnrichmentNBN1.23
190Bladder cancerEnrichmentBRCA21.12
191Auditory neuropathyEnrichmentH1-41.10
192Lung cancerEnrichmentCHEK21.01
193Systemic lupus erythematosusEnrichmentATRIP0.99
194Cerebral palsyEnrichmentBRCA20.99
195Leukemia, acute myeloidEnrichmentFANCD20.98
196Nephrotic syndromeEnrichmentSMARCAL10.95
197Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodesEnrichmentPOLG0.94
198Hereditary spastic paraplegiaEnrichmentPOLG0.90
199Hypertrophic cardiomyopathyEnrichmentPOLG0.89
200Autosomal dominant non-syndromic intellectual disabilityEnrichmentYWHAZ0.89
201Myeloma, multipleEnrichmentBRCA20.85
202Body mass index quantitative trait locus 11EnrichmentPOLG0.83
203Undetermined early-onset epileptic encephalopathyEnrichmentCDK190.79
204Hereditary retinal dystrophyEnrichmentATRIP, CEP1640.73
205Fundus dystrophyEnrichmentATRIP, CEP1640.73
206Leigh syndrome, nuclearEnrichmentPOLG0.71
207Mitochondrial diseaseEnrichmentPOLG0.62
208Congenital nervous system abnormalityEnrichmentPOLG0.54
209Nervous system diseaseEnrichmentPOLG0.54
210Complex neurodevelopmental disorderEnrichmentPPP2CA0.54

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