Telomere C-strand (Lagging Strand) Synthesis

Pathway network for the Telomere C-strand (Lagging Strand) Synthesis SuperPath

Sources:
  • Reactome

Pathways in the Telomere C-strand (Lagging Strand) Synthesis SuperPath

#NameSourceGenes
1Telomere C-strand (Lagging Strand) SynthesisReactome
2Extension of TelomeresReactome
3Polymerase switching on the C-strand of the telomereReactome
4Telomere Extension By TelomeraseReactome
5Processive synthesis on the C-strand of the telomereReactome
6Removal of the Flap Intermediate from the C-strandReactome
7Leading Strand SynthesisReactome
8Polymerase switchingReactome
9Telomere C-strand synthesis initiationReactome

Gene overlap in member pathways for Telomere C-strand (Lagging Strand) Synthesis SuperPath

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

Disorders associated with Telomere C-strand (Lagging Strand) Synthesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hoyeraal-hreidarsson syndromeEnrichmentACD, DKC1, RTEL1, TERT, TINF211.20
2Dyskeratosis congenitaEnrichmentCTC1, DKC1, NHP2, NOP10, POT1, RTEL1, TERT, TINF2, WRAP5311.00
3Melanoma, cutaneous malignant 1EnrichmentACD, POT1, TERF2IP, TERT7.83
4Cerebroretinal microangiopathy with calcifications and cysts 1EnrichmentCTC1, STN15.59
5Dyskeratosis congenita, x-linkedEnrichmentDKC1, RTEL15.08
6Interstitial lung disease 2EnrichmentRTEL1, STN1, TERT4.48
7Dyskeratosis congenita, autosomal dominant 1EnrichmentTERT, TINF24.39
8Pulmonary fibrosisEnrichmentRTEL1, TERT4.39
9Dyskeratosis congenita, autosomal dominant 2EnrichmentTERT, TINF24.24
10Seckel syndromeEnrichmentDNA2, PRIM13.26
11Inherited cancer-predisposing syndromeEnrichmentBLM, POLD1, POT13.11
12Van esch-o'driscoll syndromeEnrichmentPOLA13.02
13Tumor predisposition syndrome 3EnrichmentPOT13.02
14Pigmentary disorder, reticulate, with systemic manifestations, x-linkedEnrichmentPOLA13.02
15Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8EnrichmentPOT13.02
16High-grade astrocytoma with piloid featuresEnrichmentPOT13.02
17Cerebroretinal microangiopathy with calcifications and cysts 3EnrichmentPOT13.02
18Cerebroretinal microangiopathy with calcifications and cysts 2EnrichmentSTN13.02
19Colorectal cancer 10EnrichmentPOLD12.99
20Immunodeficiency 120EnrichmentPOLD12.99
21Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndromeEnrichmentPOLD12.99
22Ataxia-telangiectasia-like disorder 2EnrichmentPCNA2.99
23Morimoto-ryu-malicdan neuromuscular syndromeEnrichmentRFC42.99
24Immunodeficiency 122EnrichmentPOLD32.99
25Seckel syndrome 8EnrichmentDNA22.90
26Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 6EnrichmentRPA12.90
27Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 6EnrichmentDNA22.90
28Rothmund-thomson syndrome, type 4EnrichmentDNA22.90
29Bloom syndromeEnrichmentBLM2.85
30Immunodeficiency 96EnrichmentLIG12.85
31Dyskeratosis congenita, autosomal recessive 1EnrichmentNOP102.77
32Dyskeratosis congenita, autosomal recessive 3EnrichmentWRAP532.77
33Neurodevelopmental disorder with dystonia and seizuresEnrichmentSHQ12.77
34Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2EnrichmentNOP102.77
35Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1EnrichmentDKC12.77
36Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9EnrichmentNOP102.77
37Autosomal recessive dyskeratosis congenita 4EnrichmentTERT2.77
38Dystonia 35, childhood-onsetEnrichmentSHQ12.77
39Revesz syndromeEnrichmentTINF22.72
40Dyskeratosis congenita, autosomal dominant 3EnrichmentTINF22.72
41OligodendrogliomaEnrichmentPOT12.72
42Primordial dwarfism-immunodeficiency-lipodystrophy syndromeEnrichmentPRIM12.72
43Anaplastic oligodendrogliomaEnrichmentPOT12.72
44Leukemia, acute myeloidEnrichmentRTEL1, TERT2.69
45Cerebellar ataxia, neuropathy, and vestibular areflexia syndromeEnrichmentRFC12.69
46Rothmund-thomson syndrome, type 2EnrichmentDNA22.60
47Werner syndromeEnrichmentWRN2.60
48Partington syndromeEnrichmentPOLA12.54
49Dyskeratosis congenita, autosomal dominant 6EnrichmentACD2.54
50Childhood apraxia of speechEnrichmentRFC32.51
51Polymerase proofreading-related polyposisEnrichmentPOLD12.51
52Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 1EnrichmentTERT2.47
53Dyskeratosis congenita, autosomal recessive 5EnrichmentRTEL12.47
54Dyskeratosis congenita, autosomal recessive 2EnrichmentNHP22.47
55Immunodeficiency, common variable, 15EnrichmentRUVBL12.47
56Autosomal dominant dyskeratosis congenita 4EnrichmentRTEL12.47
57Melanoma, cutaneous malignant 9EnrichmentTERT2.47
58Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 3EnrichmentRTEL12.47
59Idiopathic interstitial pneumoniaEnrichmentTERT2.47
60Neurodevelopmental disorder with progressive spasticity and brain abnormalitiesEnrichmentRUVBL12.29
61Torsion dystonia 1EnrichmentSHQ12.29
62Interstitial lung diseaseEnrichmentTERT2.29
63Macrocytic anemiaEnrichmentTERT2.29
64Colorectal cancerEnrichmentBLM, POLD12.19
65Epilepsy, progressive myoclonic, 4, with or without renal failureEnrichmentRTEL12.17
66Lung sarcomatoid carcinomaEnrichmentTERT2.17
67Combined oxidative phosphorylation deficiency 24EnrichmentRTEL12.17
68Idiopathic aplastic anemiaEnrichmentTERT2.07
69Ovarian cancerEnrichmentBLM, WRN2.06
70Leukemia, chronic lymphocyticEnrichmentPOT12.02
71Isolated growth hormone deficiency, type iaEnrichmentDNA22.00
72Li-fraumeni syndromeEnrichmentWRAP531.99
73Adrenocortical carcinomaEnrichmentTERT1.99
74Kidney clear cell sarcomaEnrichmentTERT1.99
75Combined immunodeficiencyEnrichmentPOLD11.95
76Combined t cell and b cell immunodeficiencyEnrichmentPOLD11.95
77Familial colorectal cancer type xEnrichmentPOLD11.95
78Combined t and b cell immunodeficiencyEnrichmentPOLD11.95
79Aplastic anemiaEnrichmentTERT1.77
80MedulloblastomaEnrichmentWRN1.76
81CataractEnrichmentWRN1.76
82Parkinson's diseaseEnrichmentRFC11.71
83MeningiomaEnrichmentTERT1.70
84Williams-beuren syndromeEnrichmentRFC21.69
85Parkinson disease, late-onsetEnrichmentRFC11.61
86Pancreatic cancerEnrichmentPOLD11.59
87Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delayEnrichmentDKC11.57
88Polycystic liver diseaseEnrichmentRUVBL11.55
89Autosomal dominant polycystic liver diseaseEnrichmentRUVBL11.55
90Endometrial cancerEnrichmentBLM1.54
91HepatoblastomaEnrichmentTERT1.46
92Hepatocellular carcinomaEnrichmentTERT1.44
93Bladder cancerEnrichmentTERT1.32
94Differentiated thyroid carcinomaEnrichmentTERT1.32
95Type 2 diabetes mellitusEnrichmentWRN1.29
96Hereditary breast carcinomaEnrichmentBLM1.22
97Hereditary breast ovarian cancer syndromeEnrichmentBLM1.13
98Breast cancerEnrichmentBLM1.00

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