DNA Methylation and Transcriptional Repression

No Pathway Network information available for DNA Methylation and Transcriptional Repression

Pathways in the DNA Methylation and Transcriptional Repression SuperPath

#NameSourceGenes
1DNA Methylation and Transcriptional RepressionQIAGEN

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

Disorders associated with DNA Methylation and Transcriptional Repression SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmiaEnrichmentHDAC62.77
2Spermatogenic failure, x-linked, 9EnrichmentRBBP72.77
3Facial hypertrichosisEnrichmentMECP22.77
4Intellectual developmental disorder, x-linked, syndromic, lubs typeEnrichmentMECP22.77
5Auriculocondylar syndrome 4EnrichmentHDAC92.77
6Autism x-linked 3EnrichmentMECP22.77
7Cornelia de lange syndrome 5EnrichmentHDAC82.77
8Heyn-sproul-jackson syndromeEnrichmentDNMT3A2.77
9Syndromic x-linked intellectual disability lubs typeEnrichmentMECP22.77
10Chromosome 15q24 deletion syndromeEnrichmentSIN3A2.77
11Immunodeficiency-centromeric instability-facial anomalies syndrome 1EnrichmentDNMT3B2.47
12Encephalopathy, neonatal severe, due to mecp2 mutationsEnrichmentMECP22.47
13Sifrim-hitz-weiss syndromeEnrichmentCHD42.47
14Syndactyly, type iiiEnrichmentHDAC82.47
15Intellectual developmental disorder, x-linked, syndromic 13EnrichmentMECP22.47
16Wilson-turner syndromeEnrichmentHDAC82.47
17Facioscapulohumeral muscular dystrophy 4, digenicEnrichmentDNMT3B2.47
18Cerebellar ataxia, deafness, and narcolepsy, autosomal dominantEnrichmentDNMT12.47
19X-linked intellectual disability-psychosis-macroorchidism syndromeEnrichmentMECP22.47
20Witteveen-kolk syndromeEnrichmentSIN3A2.47
21Tatton-brown-rahman syndromeEnrichmentDNMT3A2.47
22Progressive bulbar palsyEnrichmentMECP22.47
23BruxismEnrichmentMECP22.47
24LaryngomalaciaEnrichmentMECP22.29
25Neuropathy, hereditary sensory, type ieEnrichmentDNMT12.29
26Sick sinus syndromeEnrichmentMECP22.17
27Myeloproliferative neoplasmEnrichmentDNMT3A2.07
28GlioblastomaEnrichmentDNMT3A2.07
29Angelman syndromeEnrichmentMECP21.99
30Facioscapulohumeral muscular dystrophy 1EnrichmentDNMT3B1.99
31Immunodeficiency-centromeric instability-facial anomalies syndromeEnrichmentDNMT3B1.99
32Sporadic pheochromocytoma/secreting paragangliomaEnrichmentDNMT3A1.99
33Rett syndromeEnrichmentMECP21.93
34Hereditary sensory and autonomic neuropathy type 1EnrichmentDNMT11.93
35Focal epilepsyEnrichmentMECP21.93
36Fanconi anemia, complementation group cEnrichmentHDAC81.87
37Rett syndrome, congenital variantEnrichmentMECP21.87
38Congenital nervous system abnormalityEnrichmentDNMT3A, MECP21.86
39Nervous system diseaseEnrichmentDNMT3A, MECP21.86
40Autism spectrum disorderEnrichmentDNMT3A, MECP21.84
41Cornelia de lange syndrome 1EnrichmentHDAC81.82
42Cornelia de lange syndromeEnrichmentHDAC81.82
43MelanomaEnrichmentDNMT3A1.77
44MicrocephalyEnrichmentHDAC8, MECP21.74
45Atrial heart septal defectEnrichmentHDAC81.73
46Interatrial communicationEnrichmentHDAC81.73
47Specific learning disabilityEnrichmentDNMT3A1.73
48Stereotypic movement disorderEnrichmentMECP21.66
49Pituitary stalk interruption syndromeEnrichmentDNMT11.63
50Rare genetic intellectual disabilityEnrichmentDNMT3A1.60
51GliosarcomaEnrichmentDNMT3A1.57
52Giant cell glioblastomaEnrichmentDNMT3A1.55
53Polycystic kidney diseaseEnrichmentHDAC81.52
54Diffuse large b-cell lymphomaEnrichmentDNMT3A1.50
55Attention deficit-hyperactivity disorderEnrichmentMECP21.44
56DystoniaEnrichmentMECP21.24
57Non-syndromic x-linked intellectual disabilityEnrichmentMECP21.23
58Systemic lupus erythematosusEnrichmentMECP21.19
59Leukemia, acute myeloidEnrichmentDNMT3A1.18
60EpilepsyEnrichmentMECP21.18
61Body mass index quantitative trait locus 11EnrichmentDNMT3A1.09
62Spastic ataxiaEnrichmentDNMT11.06
63Myeloma, multipleEnrichmentDNMT3A1.04
64AutismEnrichmentMECP20.94

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