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Functional Annotation unavailable. Annotation Distribution unavailable. Genomic Variants unavailble for Mouse Genomic Variants unavailable. Functional Annotation.

RNA Polymerase III Accurately Initiates Transcription from RNA Polymerase II Promoters in Vitro

Annotation Distribution. Genomic Variants.

Movie 6 Transcriptional initiation by RNA Pol II

Protein-Protein Interactions unavailable. Damaging Variants unavailble for Mouse Damaging Variants unavailable. Protein-Protein Interactions. Damaging Variants. Annotation Comparison unavailable. OLGA unavailable. Annotation Comparison. Excel Download. Gene Enrichment unavailable.

Introduction

Ortholog Finder unavailable. Gene Enrichment. Ortholog Finder. Pathway Diagram:. GO TO: Genes. References Ontology path Diagram. Cardiomegaly , Cerebellofaciodental Syndrome , fibroma , intellectual disability. Hyperalgesia , pleomorphic xanthoastrocytoma , sciatic neuropathy.

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Dwarfism , Peutz-Jeghers syndrome. Kartagener syndrome , primary ciliary dyskinesia Diamond-Blackfan anemia , hypomyelinating leukodystrophy 4 , hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism , Neonatal Progeroid Syndrome. Cerebellar Hypoplasia with Endosteal Sclerosis , hypogonadotropic hypogonadism 7 with or without anosmia , hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism , hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism , intellectual disability.


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Hereditary Neoplastic Syndromes , Neurodevelopmental Disorders. Dwarfism , hemochromatosis type 2A , schizophrenia , thrombocytopenia-absent radius syndrome. Common Variable Immunodeficiency 4 , genetic disease , infantile cerebellar-retinal degeneration , Optic Atrophy 8 , Optic Atrophy 9.

Disease Progression , Stomach Neoplasms. Adams-Oliver Syndrome 5 , early infantile epileptic encephalopathy 14 , long QT syndrome.

Signaling to and from the RNA Polymerase III Transcription and Processing Machinery

Alzheimer's disease , amenorrhea , Huntington's disease , late onset Parkinson's disease , schizophrenia , sleep apnea , Spinal Cord Injuries , spinocerebellar ataxia type 17 , Spinocerebellar Ataxias , type 1 diabetes mellitus. Autosomal Recessive Nonsyndromic Deafness Brown-Vialetto-Van Laere Syndrome 2. Brf1 , Rb1.


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Cerebellar Hypoplasia with Endosteal Sclerosis. Common Variable Immunodeficiency 4. Polr2e , Polr3gl. Epidermolysis Bullosa Simplex with Nail Dystrophy. Polr2f , Polr3h. Polr3g , Rb1. Polr3a , Polr3b. Brf1 , Polr3b , Rb1. Snapc4 , Snapc5. Bdp1 , Gtf3c3 , Polr3g , Sub1. Brf2 , Rb1. Polr3c , Polr3e , Polr3gl , Tbp.


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  • Polr3c , Polr3gl. Gtf3c4 , Gtf3c5. Polr2e , Polr2f , Tbp. RNA polymerase I transcription pathway. Polr1c , Polr2e , Polr2f , Polr2k , Tbp. RNA polymerase II transcription initiation pathway. Please help to improve this article by introducing more precise citations. April Learn how and when to remove this template message. Journal of Biological Chemistry. Cell Discovery. Trends Genet. PLoS Genet. Transferases : phosphorus -containing groups EC 2. Phosphoglycerate Aspartate kinase.

    Ribose-phosphate diphosphokinase Thiamine diphosphokinase. UTP—glucosephosphate uridylyltransferase Galactosephosphate uridylyltransferase. Recombinase Integrase Transposase. N-acetylglucosaminephosphate transferase. Protein-histidine pros-kinase Protein-histidine tele-kinase Histidine kinase. Categories : Gene expression Proteins.