CDK-mediated phosphorylation and removal of Cdc6

Pathway network for the CDK-mediated phosphorylation and removal of Cdc6 SuperPath

Sources:
  • Reactome

Pathways in the CDK-mediated phosphorylation and removal of Cdc6 SuperPath

#NameSourceGenes
1CDK-mediated phosphorylation and removal of Cdc6Reactome
2S PhaseReactome
3Synthesis of DNAReactome
4Switching of origins to a post-replicative stateReactome
5Regulation of mitotic cell cycleReactome
6APC/C-mediated degradation of cell cycle proteinsReactome
7Regulation of APC/C activators between G1/S and early anaphaseReactome
8Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteinsReactome
9APC/C:Cdc20 mediated degradation of mitotic proteinsReactome
10APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpointReactome
11APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1Reactome
12Cdc20:Phospho-APC/C mediated degradation of Cyclin AReactome
13Orc1 removal from chromatinReactome
14APC/C:Cdc20 mediated degradation of SecurinReactome
15Autodegradation of Cdh1 by Cdh1:APC/CReactome
16Phosphorylation of the APC/CReactome
17Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphaseReactome
18Establishment of Sister Chromatid CohesionReactome

Gene overlap in member pathways for CDK-mediated phosphorylation and removal of Cdc6 SuperPath

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

Disorders associated with CDK-mediated phosphorylation and removal of Cdc6 SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Meier-gorlin syndrome 1EnrichmentCDC45, CDC6, CDT1, GMNN, MCM7, ORC1, ORC4, ORC616.00
2Cornelia de lange syndrome 1EnrichmentRAD21, SMC1A, SMC37.48
3Cornelia de lange syndromeEnrichmentRAD21, SMC1A, SMC37.48
4Wiedemann-steiner syndromeEnrichmentSMC1A, SMC35.05
5Semilobar holoprosencephalyEnrichmentSMC1A, STAG24.04
6Polymerase proofreading-related polyposisEnrichmentPOLD1, POLE3.73
7Mosaic variegated aneuploidy syndromeEnrichmentBUB1B, BUB33.28
8Isolated split hand-split foot malformationEnrichmentBTRC, SEM13.17
9Developmental and epileptic encephalopathy 85 with or without midline brain defectsEnrichmentSMC1A3.09
10Roberts-sc phocomelia syndromeEnrichmentESCO23.09
11Holoprosencephaly 13, x-linkedEnrichmentSTAG23.09
12Cornelia de lange syndrome 3 with or without midline brain defectsEnrichmentSMC33.09
13Cornelia de lange syndrome 4 with or without midline brain defectsEnrichmentRAD213.09
14Juberg-hayward syndromeEnrichmentESCO23.09
15Mullegama-klein-martinez syndromeEnrichmentSTAG23.09
16Intellectual developmental disorder, autosomal dominant 47EnrichmentSTAG13.09
17Mungan syndromeEnrichmentRAD213.09
18Xq25 microduplication syndromeEnrichmentSTAG23.09
19Ferguson-bonni neurodevelopmental syndromeEnrichmentANAPC72.83
20Rothmund-thomson syndrome, type 1EnrichmentANAPC12.83
21Deafness, autosomal recessive 32, with or without immotile spermEnrichmentCDC14A2.83
22Oocyte/zygote/embryo maturation arrest 14EnrichmentCDC202.83
23Developmental and epileptic encephalopathy 109EnrichmentFZR12.83
24Autosomal recessive nonsyndromic deafness 32EnrichmentCDC14A2.83
25Cornelia de lange syndrome 2EnrichmentSMC1A2.79
26Multiple endocrine neoplasia, type iEnrichmentCDKN1A, CDKN1B2.61
27Trichorhinophalangeal syndrome, type iiEnrichmentRAD212.49
28Familial colorectal cancer type xEnrichmentPOLD1, POLE2.48
29Inherited cancer-predisposing syndromeEnrichmentCDK4, CDKN1B, MAX, POLD1, POLE, RB12.46
30Neurodevelopmental disorder with microcephaly, hypotonia, and absent languageEnrichmentPSMB12.40
31Stankiewicz-isidor syndromeEnrichmentPSMD122.40
32Deafness, cataract, impaired intellectual development, and polyneuropathyEnrichmentPSMC32.40
33Lactose intolerance, adult typeEnrichmentMCM62.37
34Meier-gorlin syndrome 3EnrichmentORC62.37
35Meier-gorlin syndrome 2EnrichmentORC42.37
36Meier-gorlin syndrome 4EnrichmentCDT12.37
37AnisometropiaEnrichmentMCM72.37
38Immunodeficiency 54EnrichmentMCM42.37
39Deafness, autosomal dominant 70EnrichmentMCM22.37
40Meier-gorlin syndrome 8EnrichmentMCM52.37
41Premature ovarian failure 10EnrichmentMCM82.37
42Meier-gorlin syndrome 5EnrichmentCDC62.37
43Premature chromatid separation traitEnrichmentBUB1B2.35
44Retinitis pigmentosa 67EnrichmentNEK22.35
45Trilateral retinoblastomaEnrichmentRB12.35
46Lung oat cell carcinomaEnrichmentRB12.35
47PolymicrogyriaEnrichmentAKT3, PSMC32.29
48Seckel syndromeEnrichmentDNA2, PRIM12.27
49Meier-gorlin syndrome 6EnrichmentGMNN2.23
50Rett syndrome, congenital variantEnrichmentSMC1A2.19
51Deafness, autosomal recessive 63EnrichmentANAPC152.13
52Birk-aharoni syndromeEnrichmentPSMC12.10
53Proteasome-associated autoinflammatory syndrome 3EnrichmentPSMB42.10
5417q24.2 microdeletion syndromeEnrichmentPSMD122.10
55Submucosal cleft palateEnrichmentUBB2.10
56Cleft hard palateEnrichmentUBB2.10
57Cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual developmentEnrichmentPOLE2.10
58Van esch-o'driscoll syndromeEnrichmentPOLA12.10
59Colorectal cancer 10EnrichmentPOLD12.10
60Seckel syndrome 8EnrichmentDNA22.10
61Colorectal cancer 12EnrichmentPOLE2.10
62Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 6EnrichmentRPA12.10
63Pigmentary disorder, reticulate, with systemic manifestations, x-linkedEnrichmentPOLA12.10
64Immunodeficiency 120EnrichmentPOLD12.10
65Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 6EnrichmentDNA22.10
66Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndromeEnrichmentPOLD12.10
67Ataxia-telangiectasia-like disorder 2EnrichmentPCNA2.10
68Immunodeficiency 96EnrichmentLIG12.10
69Meier-gorlin syndrome 7EnrichmentCDC452.10
70Rothmund-thomson syndrome, type 4EnrichmentDNA22.10
71Morimoto-ryu-malicdan neuromuscular syndromeEnrichmentRFC42.10
72Immunodeficiency 122EnrichmentPOLD32.10
73Chromosome 13q14 deletion syndromeEnrichmentRB12.05
74Familial retinoblastomaEnrichmentRB12.05
75Proteus syndromeEnrichmentAKT11.96
76Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT21.96
77Melanoma, cutaneous malignant 3EnrichmentCDK41.96
78Brunet-wagner neurodevelopmental syndromeEnrichmentRBL21.96
79Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT31.96
80Neuroendocrine tumorEnrichmentCDKN1B1.96
81Polydactyly-macrocephaly syndromeEnrichmentMAX1.96
82Cowden syndrome 6EnrichmentAKT11.96
83Capillary hemangiomaEnrichmentAKT31.96
84Akt2-related familial partial lipodystrophyEnrichmentAKT21.96
85Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB41.92
86Uvula, bifidEnrichmentUBB1.92
87Cleft soft palateEnrichmentUBB1.92
88Proteosome-associated autoinflammatory syndromeEnrichmentPSMB41.92
89Thyroid hemiagenesisEnrichmentPSMD31.92
90RetinoblastomaEnrichmentRB11.87
91Osteogenic sarcomaEnrichmentRB11.87
92Woolly hair, autosomal recessive 3EnrichmentRB11.87
93Hypotrichosis 8EnrichmentRB11.87
94Squamous cell carcinomaEnrichmentRB11.87
95Bone osteosarcomaEnrichmentRB11.87
96Alobar holoprosencephalyEnrichmentSTAG21.86
97Colorectal cancerEnrichmentAKT1, CCND1, POLD1, POLE1.80
98Rothmund-thomson syndrome, type 2EnrichmentDNA21.80
99Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesEnrichmentPOLE1.80
100Cerebellar ataxia, neuropathy, and vestibular areflexia syndromeEnrichmentRFC11.80
101Immunodeficiency 55EnrichmentGINS11.80
102Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiencyEnrichmentPOLE1.80
103Primordial dwarfism-immunodeficiency-lipodystrophy syndromeEnrichmentPRIM11.80
104Facial dysmorphism, immunodeficiency, livedo, and short statureEnrichmentPOLE1.80
105AstigmatismEnrichmentMCM71.77
106EnophthalmosEnrichmentMCM71.77
107Small cell cancer of the lungEnrichmentRB11.75
108Lynch syndrome 4EnrichmentRB11.75
1092q23.1 microduplication syndromeEnrichmentORC41.67
110FarsightednessEnrichmentMCM71.67
111Mosaic variegated aneuploidy syndrome 1EnrichmentBUB1B1.66
112Burkitt lymphomaEnrichmentMYC1.66
113Multiple endocrine neoplasia, type ivEnrichmentCDKN1B1.66
114Senior-loken syndrome 7EnrichmentAKT31.66
115Bardet-biedl syndrome 16EnrichmentAKT31.66
116Developmental dysplasia of the hip 1EnrichmentPSMC31.63
117Patent ductus arteriosusEnrichmentPSMC31.63
118Partington syndromeEnrichmentPOLA11.63
119Childhood apraxia of speechEnrichmentRFC31.63
120Wieacker-wolff syndromeEnrichmentCCNH1.48
121High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC1.48
122Dedifferentiated liposarcomaEnrichmentCDK41.48
123Well-differentiated liposarcomaEnrichmentCDK41.48
124Ear malformationEnrichmentCDC14A1.46
125Bladder cancerEnrichmentCDKN1A, RB11.39
126Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT31.36
127Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT31.36
128Mantle cell lymphomaEnrichmentCCND11.36
129Primary hyperparathyroidismEnrichmentCDKN1B1.36
130Lip and oral cavity carcinomaEnrichmentRB11.28
131Capillary malformations, congenitalEnrichmentCCNH1.27
132Von hippel-lindau syndromeEnrichmentCCND11.27
133HemimegalencephalyEnrichmentAKT31.27
134Nk-cell enteropathyEnrichmentAURKB1.24
135Lung cancer susceptibility 3EnrichmentRB11.21
136Isolated growth hormone deficiency, type iaEnrichmentDNA21.21
137Klippel-trenaunay-weber syndromeEnrichmentCCNH1.19
138Telangiectasia, hereditary hemorrhagic, type 1EnrichmentCCNH1.19
139Hemangioma, capillary infantileEnrichmentCCNH1.19
140Basal cell carcinoma 1EnrichmentCCNH1.19
141Breast adenocarcinomaEnrichmentAKT11.19
142Sensorineural hearing lossEnrichmentCDC14A1.16
143Patent foramen ovaleEnrichmentPSMC31.16
144Capillary malformation-arteriovenous malformation 1EnrichmentCCNH1.13
145Hereditary hemorrhagic telangiectasiaEnrichmentCCNH1.13
146MegacolonEnrichmentAKT31.13
147Undetermined early-onset epileptic encephalopathyEnrichmentFZR11.10
148AzoospermiaEnrichmentMCM81.09
149Congenital nervous system abnormalityEnrichmentSMC1A1.08
150Nervous system diseaseEnrichmentSMC1A1.08
151Myocardial infarctionEnrichmentPSMA61.08
152Combined immunodeficiencyEnrichmentPOLD11.07
153Combined t cell and b cell immunodeficiencyEnrichmentPOLD11.07
154Combined t and b cell immunodeficiencyEnrichmentPOLD11.07
155Autism spectrum disorderEnrichmentSMC31.07
156MicrophthalmiaEnrichmentMCM71.05
157Arteriovenous malformationEnrichmentCCNH1.02
158Cowden syndromeEnrichmentAKT11.02
159MicrocephalyEnrichmentSMC1A1.02
160Ovarian cancerEnrichmentAKT1, CDKN1B, RB10.99
161Leukemia, chronic lymphocyticEnrichmentCCND10.98
162Myopathy, x-linked, with excessive autophagyEnrichmentCCNH0.98
163Rare genetic deafnessEnrichmentCDC14A0.96
164Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentCDC14A0.91
165MeningiomaEnrichmentAKT10.90
166Primary autosomal recessive microcephalyEnrichmentMCM70.89
167Parkinson's diseaseEnrichmentRFC10.85
168PheochromocytomaEnrichmentMAX0.84
169Williams-beuren syndromeEnrichmentRFC20.83
170Melanoma, cutaneous malignant 1EnrichmentCDK40.76
171Polycystic liver diseaseEnrichmentCDC25A0.76
172Autosomal dominant polycystic liver diseaseEnrichmentCDC25A0.76
173Parkinson disease, late-onsetEnrichmentRFC10.76
174Pancreatic cancerEnrichmentPOLD10.74
175Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentMCM20.70
176Breast cancerEnrichmentAKT1, CKS1B0.70
177Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentMAX0.68
178Myeloma, multipleEnrichmentAURKA0.65
179Precursor t-cell acute lymphoblastic leukemiaEnrichmentMYC0.65
180Type 2 diabetes mellitusEnrichmentAKT20.43
181Gastric cancerEnrichmentCDK40.42
182Hereditary breast carcinomaEnrichmentAKT10.41
183Complex neurodevelopmental disorderEnrichmentPSMD120.41
184Retinitis pigmentosaEnrichmentNEK20.21
185Hereditary retinal dystrophyEnrichmentNEK20.13
186Fundus dystrophyEnrichmentNEK20.13

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