RNA Polymerase III Transcription Initiation

Pathway network for the RNA Polymerase III Transcription Initiation SuperPath

Sources:
  • Reactome
  • QIAGEN

Pathways in the RNA Polymerase III Transcription Initiation SuperPath

#NameSourceGenes
1RNA Polymerase III Transcription InitiationReactome
2RNA Polymerase III Abortive And Retractive InitiationReactome
3RNA Polymerase III TranscriptionReactome
4RNA Polymerase III Transcription Initiation From Type 3 PromoterReactome
5RNA Polymerase III Transcription Initiation From Type 1 PromoterReactome
6RNA Polymerase III Transcription Initiation From Type 2 PromoterReactome
7RNA Polymerase III Transcription TerminationReactome
8Transcription of tRNAQIAGEN
9Assembly of RNA Polymerase-III Initiation ComplexQIAGEN
10RNA Polymerase III Chain ElongationReactome

Gene overlap in member pathways for RNA Polymerase III Transcription Initiation SuperPath

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

Disorders associated with RNA Polymerase III Transcription Initiation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadismEnrichmentPOLR1C, POLR3A, POLR3B7.71
2Polr3-related leukodystrophyEnrichmentPOLR3A, POLR3B5.30
3Hypomyelinating leukodystrophy 7EnrichmentPOLR3A, POLR3B5.00
4Treacher collins syndrome 1EnrichmentPOLR1C, POLR1D4.46
5Pontocerebellar hypoplasia, type 2eEnrichmentTSEN2, TSEN344.36
6LeukodystrophyEnrichmentPOLR3A, POLR3B3.51
7Immunodeficiency 101EnrichmentPOLR3F2.88
8Leukodystrophy, hypomyelinating, 21EnrichmentPOLR3K2.88
9Treacher collins syndrome 2EnrichmentPOLR1D2.88
10OdontoleukodystrophyEnrichmentPOLR3A2.88
11Cerebellofaciodental syndromeEnrichmentBRF12.85
12Neurodevelopmental disorder with dysmorphic facies, brain anomalies, and seizuresEnrichmentGTF3C32.85
13Deafness, autosomal recessive 112EnrichmentBDP12.85
14Inner ear diseaseEnrichmentBRF12.85
15Pontocerebellar hypoplasia, type 2bEnrichmentTSEN22.83
16Pontocerebellar hypoplasia, type 2cEnrichmentTSEN342.83
17Macrocephaly, acquired, with impaired intellectual developmentEnrichmentNFIB2.77
18Marshall-smith syndromeEnrichmentNFIX2.77
19Malan syndromeEnrichmentNFIX2.77
20Brain malformations with or without urinary tract defectsEnrichmentNFIA2.77
2119p13.3 microduplication syndromeEnrichmentNFIX2.77
22Sotos syndrome 2EnrichmentNFIX2.77
23Bilateral polymicrogyriaEnrichmentNFIA2.77
24Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunctionEnrichmentSNAPC42.69
25Treacher collins syndrome 3EnrichmentPOLR1C2.58
26Leukodystrophy, hypomyelinating, 4EnrichmentPOLR3A2.58
27Waardenburg syndrome, type 4cEnrichmentPOLR2F2.58
28Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadismEnrichmentPOLR3B2.58
29Leukoencephalopathy, progressive, with ovarian failureEnrichmentPOLR1C2.58
30Charcot-marie-tooth disease, demyelinating, type 1iEnrichmentPOLR3B2.58
31Short stature, oligodontia, dysmorphic facies, and motor delayEnrichmentPOLR3GL2.58
32Leukodystrophy, hypomyelinating, 11EnrichmentPOLR1C2.58
33Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung diseaseEnrichmentPOLR2F2.58
34HyperostosisEnrichmentPOLR3GL2.58
35Spinocerebellar ataxia 17EnrichmentTBP2.55
36Hemolytic-uremic syndromeEnrichmentTSEN22.53
37Waardenburg syndrome, type 2aEnrichmentPOLR2F2.40
38Wiedemann-rautenstrauch syndromeEnrichmentPOLR3A2.40
39Infantile cerebellar-retinal degenerationEnrichmentPOLR3H2.40
40Optic atrophy 9EnrichmentPOLR3H2.40
41Viss syndromeEnrichmentPOLR3B2.40
42Neonatal pseudo-hydrocephalic progeroid syndromeEnrichmentPOLR3A2.40
43Glass syndromeEnrichmentGTF3C32.38
44LaryngomalaciaEnrichmentNFIX2.29
45MegalocorneaEnrichmentNFIX2.29
46Adenoid cystic carcinomaEnrichmentNFIB2.29
47Hypogonadotropic hypogonadism 1 with or without anosmiaEnrichmentPOLR2F2.18
48Waardenburg syndrome, type 4aEnrichmentPOLR2F2.10
49Waardenburg syndromeEnrichmentPOLR2F2.10
50Waardenburg syndrome, type 1EnrichmentPOLR2F2.03
51Waardenburg syndrome, type 2eEnrichmentPOLR2F2.03
52Movement diseaseEnrichmentPOLR3A1.84
5346 xx gonadal dysgenesisEnrichmentPOLR3H1.80
54Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentPOLR3B1.73
55Isolated congenital microcephalyEnrichmentBRF11.65
56Heart, malformation ofEnrichmentBRF11.60
57Pontocerebellar hypoplasiaEnrichmentTSEN21.58
58Esophageal atresia/tracheoesophageal fistulaEnrichmentGTF3C11.58
59Parkinson's diseaseEnrichmentTBP1.58
60Cleft palate, isolatedEnrichmentNFIA1.55
61Tooth agenesisEnrichmentPOLR3GL1.54
62Kallmann syndromeEnrichmentPOLR2F1.52
63Parkinson disease, late-onsetEnrichmentTBP1.48
64Hirschsprung disease 1EnrichmentPOLR2F1.42
65StrabismusEnrichmentNFIX1.35
66Optic atrophy plus syndromeEnrichmentPOLR3H1.25
67Sensorineural hearing lossEnrichmentBRF11.19
68Spastic ataxiaEnrichmentPOLR3A1.17
69Rare genetic deafnessEnrichmentPOLR2F1.00
70Colorectal cancerEnrichmentBRF10.94
71Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentBDP10.93

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