RNA Polymerase II Transcription Initiation And Promoter Clearance

Pathway network for the RNA Polymerase II Transcription Initiation And Promoter Clearance SuperPath

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

Pathways in the RNA Polymerase II Transcription Initiation And Promoter Clearance SuperPath

#NameSourceGenes
1RNA Polymerase II Transcription Initiation And Promoter ClearanceReactome
2Transcription Ligand-Dependent Transcription of Retinoid-Target genesGeneGo (Thomson Reuters)
3Crosstalk Between CARM1 and ESRsQIAGEN
4Protein Acetylation and DeacetylationQIAGEN
5RNA Polymerase II Transcription InitiationReactome
6RNA Polymerase II Promoter EscapeReactome
7HIV Transcription InitiationReactome
8RNA Polymerase II Transcription Pre-Initiation And Promoter OpeningReactome
9RNA Polymerase II HIV Promoter EscapeReactome
10Transcription of mRNAQIAGEN
11Assembly of RNA Polymerase-II Initiation ComplexQIAGEN
12Eukaryotic transcription initiationWikiPathways

Gene overlap in member pathways for RNA Polymerase II Transcription Initiation And Promoter Clearance SuperPath

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

Disorders associated with RNA Polymerase II Transcription Initiation And Promoter Clearance SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Human immunodeficiency virus infectious diseaseDirect
2TrichothiodystrophyEnrichmentERCC2, ERCC3, GTF2E2, GTF2H57.80
3Witteveen-kolk syndromeEnrichmentSIN3A, SIN3B4.79
4Tessadori-bicknell-van haaften neurodevelopmental syndrome 1EnrichmentH4C1, H4C34.40
5Tessadori-bicknell-van haaften neurodevelopmental syndrome 2EnrichmentH4C1, H4C114.40
6Bryant-li-bhoj neurodevelopmental syndrome 2EnrichmentH3-3A, H3-3B4.40
7Xeroderma pigmentosum-cockayne syndrome complexEnrichmentERCC2, ERCC34.05
8Tessadori-bicknell-van haaften neurodevelopmental syndrome 4EnrichmentH4C1, H4C93.93
9Tessadori-bicknell-van haaften neurodevelopmental syndrome 3EnrichmentH4C1, H4C53.93
10Treacher collins syndrome 1EnrichmentPOLR1B, POLR1D3.73
11Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3003.62
12Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3003.62
13Corpus callosum, agenesis ofEnrichmentCREBBP, ERCC2, MED123.45
14Isolated corpus callosum agenesisEnrichmentCREBBP, ERCC2, MED123.45
15Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP, ERCC2, MED123.45
16Xeroderma pigmentosum, variant typeEnrichmentERCC2, ERCC33.32
17Cornelia de lange syndrome 1EnrichmentHDAC8, TAF63.24
18Cornelia de lange syndromeEnrichmentHDAC8, TAF63.24
19Glioma susceptibility 1EnrichmentH3-3A, H3C12.96
20LeukodystrophyEnrichmentERCC2, POLR3B2.79
21Rare genetic intellectual disabilityEnrichmentCREBBP, EP3002.79
22Intellectual developmental disorder, x-linked, syndromic 33EnrichmentTAF12.52
23Dystonia 3, torsion, x-linkedEnrichmentTAF12.52
24Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformityEnrichmentTAF22.52
25Trichothiodystrophy 6, nonphotosensitiveEnrichmentGTF2E22.52
26Trichothiodystrophy 3, photosensitiveEnrichmentGTF2H52.52
27Alazami-yuan syndromeEnrichmentTAF62.52
28Intellectual developmental disorder, autosomal recessive 60EnrichmentTAF132.52
29X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndromeEnrichmentTAF12.52
30Xeroderma pigmentosum, complementation group bEnrichmentERCC32.52
31Leukodystrophy, hypomyelinating, 27EnrichmentPOLR1A2.52
32Treacher collins syndrome 4EnrichmentPOLR1B2.52
33Xeroderma pigmentosum, complementation group dEnrichmentERCC22.52
34Leukodystrophy, hypomyelinating, 21EnrichmentPOLR3K2.52
35Trichothiodystrophy 2, photosensitiveEnrichmentERCC32.52
36Xeroderma pigmentosum group bEnrichmentERCC32.52
37Treacher collins syndrome 2EnrichmentPOLR1D2.52
38Cerebrooculofacioskeletal syndrome 2EnrichmentERCC22.52
39Xeroderma pigmentosum group dEnrichmentERCC22.52
40Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB2.51
41Spermatogenic failure 13EnrichmentTAF4B2.46
42Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmiaEnrichmentHDAC62.39
43Auriculocondylar syndrome 4EnrichmentHDAC92.39
44Cornelia de lange syndrome 5EnrichmentHDAC82.39
45Menke-hennekam syndrome 1EnrichmentCREBBP2.39
46Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.39
47Chromosome 15q24 deletion syndromeEnrichmentSIN3A2.39
48Menke-hennekam syndromeEnrichmentCREBBP2.39
49Spinocerebellar ataxia 17EnrichmentTBP2.22
50Waardenburg syndrome, type 4cEnrichmentPOLR2F2.22
51Intellectual developmental disorder, autosomal dominant 73EnrichmentTAF42.22
52Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung diseaseEnrichmentPOLR2F2.22
53Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadismEnrichmentPOLR3B2.22
54Charcot-marie-tooth disease, demyelinating, type 1iEnrichmentPOLR3B2.22
55Acrofacial dysostosis, cincinnati typeEnrichmentPOLR1A2.22
56Nephrotic syndrome, type 8EnrichmentARHGDIA2.20
57Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.20
58Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.20
59Ovarian dysgenesis 8EnrichmentESR22.20
60Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.20
61Bryant-li-bhoj neurodevelopmental syndrome 1EnrichmentH3-3A2.20
62Fraser syndrome 3EnrichmentGRIP12.20
63Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.20
64Immunodeficiency 129EnrichmentRHOH2.20
65T-cell immunodeficiency with epidermodysplasia verruciformisEnrichmentRHOH2.20
665q14.3 microdeletion syndromeEnrichmentMEF2C2.20
67Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.20
68Mef2c-related disorderEnrichmentMEF2C2.20
69Complex neurodevelopmental disorderEnrichmentCDK8, MED13, MED27, PSMD12, TAF42.18
70Thumb deformityEnrichmentCREBBP2.09
71Syndactyly, type iiiEnrichmentHDAC82.09
72Menke-hennekam syndrome 2EnrichmentEP3002.09
73Wilson-turner syndromeEnrichmentHDAC82.09
74Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.09
75Waardenburg syndrome, type 2aEnrichmentPOLR2F2.04
76Trichothiodystrophy 1, photosensitiveEnrichmentERCC22.04
77Burn-mckeown syndromeEnrichmentPOLR1A2.04
78Infantile cerebellar-retinal degenerationEnrichmentPOLR3H2.04
79Optic atrophy 9EnrichmentPOLR3H2.04
80Viss syndromeEnrichmentPOLR3B2.04
81Wieacker-wolff syndromeEnrichmentCCNH2.04
82Polr3-related leukodystrophyEnrichmentPOLR3B2.04
83Spermatogenic failure, x-linked, 9EnrichmentRBBP72.02
84Intellectual developmental disorder, autosomal recessive 18, with or without epilepsyEnrichmentMED232.02
85Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasiaEnrichmentMED272.02
86Neurodevelopmental disorder with microcephaly, hypotonia, and absent languageEnrichmentPSMB12.02
87Stankiewicz-isidor syndromeEnrichmentPSMD122.02
88Cardioacrofacial dysplasia 2EnrichmentPRKACB2.02
89Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophyEnrichmentTAF82.02
90Deafness, cataract, impaired intellectual development, and polyneuropathyEnrichmentPSMC32.02
91Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.02
92Cardioacrofacial dysplasia 1EnrichmentPRKACA2.02
93Guillouet-gordon syndromeEnrichmentMED162.02
94Hydrocephalus, congenital, 1EnrichmentCDK8, MED122.01
95Syndromic intellectual disabilityEnrichmentMED16, TAF61.95
96Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalitiesEnrichmentPOLR2A1.92
97Hypomyelinating leukodystrophy 7EnrichmentPOLR3B1.92
98CraniopharyngiomaEnrichmentERCC21.92
99Tethered spinal cord syndromeEnrichmentCREBBP1.92
100Intraocular pressure quantitative trait locusEnrichmentCREBBP1.92
101Hypogonadotropic hypogonadism 1 with or without anosmiaEnrichmentPOLR2F1.82
102Chondrosarcoma, extraskeletal myxoidEnrichmentTAF151.82
103Capillary malformations, congenitalEnrichmentCCNH1.82
104Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadismEnrichmentPOLR3B1.82
105Myeloma, multipleEnrichmentCREBBP, NCOR2, RXRA1.79
106Waardenburg syndrome, type 4aEnrichmentPOLR2F1.74
107Waardenburg syndromeEnrichmentPOLR2F1.74
108Klippel-trenaunay-weber syndromeEnrichmentCCNH1.74
109Cerebrooculofacioskeletal syndrome 1EnrichmentERCC21.74
110Telangiectasia, hereditary hemorrhagic, type 1EnrichmentCCNH1.74
111Hemangioma, capillary infantileEnrichmentCCNH1.74
112Basal cell carcinoma 1EnrichmentCCNH1.74
113Thyroid carcinoma, familial medullaryEnrichmentESR21.72
114Estrogen resistanceEnrichmentESR11.72
115Migraine without auraEnrichmentESR11.72
116ArgininemiaEnrichmentMED231.72
117Ebstein anomalyEnrichmentCDK81.72
118Hardikar syndromeEnrichmentMED121.72
119Opitz-kaveggia syndromeEnrichmentMED121.72
120Bleeding disorder, platelet-type, 19EnrichmentPRKACG1.72
121Birk-aharoni syndromeEnrichmentPSMC11.72
122Ohdo syndrome, x-linkedEnrichmentMED121.72
123Proteasome-associated autoinflammatory syndrome 3EnrichmentPSMB41.72
124Fibrolamellar carcinomaEnrichmentPRKACA1.72
12517q24.2 microdeletion syndromeEnrichmentPSMD121.72
126Cholestasis-pigmentary retinopathy-cleft palate syndromeEnrichmentMED121.72
127Intellectual developmental disorder with hypotonia and behavioral abnormalitiesEnrichmentCDK81.72
128Med12-related disordersEnrichmentMED121.72
129Blepharophimosis - intellectual disability syndrome, mkb typeEnrichmentMED121.72
130Rubinstein-taybi syndrome 2EnrichmentEP3001.70
131Waardenburg syndrome, type 1EnrichmentPOLR2F1.68
132Waardenburg syndrome, type 2eEnrichmentPOLR2F1.68
133Capillary malformation-arteriovenous malformation 1EnrichmentCCNH1.68
134Hereditary hemorrhagic telangiectasiaEnrichmentCCNH1.68
135HypertrichosisEnrichmentCREBBP1.62
136Arthrogryposis multiplex congenita 3, myogenic typeEnrichmentESR11.60
137Inflammatory bowel disease 1EnrichmentERCC21.57
138Arteriovenous malformationEnrichmentCCNH1.57
139Hypotrichosis simplexEnrichmentERCC21.57
140Cleidocranial dysplasia 1EnrichmentSUPT3H1.55
141Proteasome-associated autoinflammatory syndrome 1EnrichmentPSMB41.55
142Intellectual developmental disorder, x-linked, syndromic, lujan-fryns typeEnrichmentMED121.55
143Microcephaly, postnatal progressive, with seizures and brain atrophyEnrichmentMED171.55
144Anus, imperforateEnrichmentMED121.55
145Intellectual developmental disorder, autosomal dominant 61EnrichmentMED131.55
146Proteosome-associated autoinflammatory syndromeEnrichmentPSMB41.55
147Cleidocranial dysplasiaEnrichmentSUPT3H1.55
148Thyroid hemiagenesisEnrichmentPSMD31.55
149MicrocephalyEnrichmentEP300, MED12, PSMC3, TAF81.53
150Myopathy, x-linked, with excessive autophagyEnrichmentCCNH1.53
151Fanconi anemia, complementation group cEnrichmentHDAC81.50
15246 xx gonadal dysgenesisEnrichmentPOLR3H1.45
153Charge syndromeEnrichmentEP3001.44
154Ovarian cancerEnrichmentERCC2, ERCC31.43
155Fraser syndrome 1EnrichmentGRIP11.43
156Hemihyperplasia, isolatedEnrichmentRHOA1.43
157Isolated growth hormone deficiency, type iiEnrichmentMED131.43
158Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentPOLR3B1.38
159Atrial heart septal defectEnrichmentHDAC81.36
160Interatrial communicationEnrichmentHDAC81.36
161Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C, TAF151.28
162Heart diseaseEnrichmentCREBBP1.26
163Developmental dysplasia of the hip 1EnrichmentPSMC31.25
164Patent ductus arteriosusEnrichmentPSMC31.25
165Esophageal atresia/tracheoesophageal fistulaEnrichmentPOLR2B1.25
166Parkinson's diseaseEnrichmentTBP1.25
167Polydactyly, postaxial, type a1EnrichmentEP3001.23
168HepatoblastomaEnrichmentERCC21.21
169Williams-beuren syndromeEnrichmentGTF2I1.19
170Kallmann syndromeEnrichmentPOLR2F1.17
171Migraine with or without aura 1EnrichmentESR11.17
172Parkinson disease, late-onsetEnrichmentTBP1.15
173Polycystic kidney diseaseEnrichmentHDAC81.15
174Diffuse large b-cell lymphomaEnrichmentCREBBP1.13
175Hirschsprung disease 1EnrichmentPOLR2F1.08
176Bladder cancerEnrichmentERCC21.08
177PolymicrogyriaEnrichmentPSMC31.04
178Primary autosomal recessive microcephalyEnrichmentTAF131.03
179ScoliosisEnrichmentCREBBP1.03
180Diaphragmatic hernia, congenitalEnrichmentCDK80.93
181Acute promyelocytic leukemiaEnrichmentRARA0.93
182Optic atrophy plus syndromeEnrichmentPOLR3H0.90
183Myocardial infarctionEnrichmentESR10.88
184Cardiomyopathy, dilated, 1eEnrichmentMED120.82
185Heart, malformation ofEnrichmentCDK80.80
186Patent foramen ovaleEnrichmentPSMC30.80
187Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentTAF4B0.75
188Familial isolated dilated cardiomyopathyEnrichmentTAF1A0.71
189Genetic steroid-resistant nephrotic syndromeEnrichmentARHGDIA0.71
190Rare genetic deafnessEnrichmentPOLR2F0.67
191Hereditary breast carcinomaEnrichmentESR10.61
192AutismEnrichmentCREBBP0.59
193Non-syndromic x-linked intellectual disabilityEnrichmentMED120.54
194Colorectal cancerEnrichmentEP3000.52
195Inherited cancer-predisposing syndromeEnrichmentERCC30.48
196Familial thoracic aortic aneurysm and aortic dissectionEnrichmentMED120.46
197Congenital nervous system abnormalityEnrichmentCREBBP0.45
198Nervous system diseaseEnrichmentCREBBP0.45
199Breast cancerEnrichmentESR10.42
200Autosomal recessive non-syndromic intellectual disabilityEnrichmentMED230.37
201Autism spectrum disorderEnrichmentMEF2C0.30

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