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    POLR1D RNA polymerase I and III subunit D [ Homo sapiens (human) ]

    Gene ID: 51082, updated on 10-Dec-2024

    Summary

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    Official Symbol
    POLR1Dprovided by HGNC
    Official Full Name
    RNA polymerase I and III subunit Dprovided by HGNC
    Primary source
    HGNC:HGNC:20422
    See related
    Ensembl:ENSG00000186184 MIM:613715; AllianceGenome:HGNC:20422
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    AC19; RPA9; TCS2; RPA16; RPAC2; RPC16; POLR1C; RPO1-3
    Summary
    The protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011]
    Expression
    Ubiquitous expression in testis (RPKM 19.3), adrenal (RPKM 13.6) and 25 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See POLR1D in Genome Data Viewer
    Location:
    13q12.2
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (27620743..27667411)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (26841857..26888521)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (28194880..28241548)

    Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr13:28008622-28009821 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_32805 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:28023938-28024852 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7506 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7507 Neighboring gene general transcription factor IIIA Neighboring gene Sharpr-MPRA regulatory region 13742 Neighboring gene mitochondrial translational initiation factor 3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7508 Neighboring gene RNA, U6 small nuclear 63, pseudogene Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_32806 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_32807 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_32809 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:28107144-28107644 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:28107645-28108145 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_32810 Neighboring gene ligand of numb-protein X 2 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:28194694-28195422 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5204 Neighboring gene nucleophosmin 1 pseudogene 4 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr13:28302713-28303912 Neighboring gene uncharacterized LOC105370129

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. POLR1D silencing suppresses lung cancer cells proliferation and migration via inhibition of PI3K-Akt pathway. Yuan Z, et al. J Cardiothorac Surg, 2024 Jun 6. PMID 38844975, Free PMC Article
    2. Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes. Giampietro PF, et al. Am J Med Genet A, 2015 Jan. PMID 25348728
    3. Association of survival and disease progression with chromosomal instability: a genomic exploration of colorectal cancer. Sheffer M, et al. Proc Natl Acad Sci U S A, 2009 Apr 28. PMID 19359472, Free PMC Article
    4. POLR1D promotes colorectal cancer progression and predicts poor prognosis of patients. Wang M, et al. Mol Carcinog, 2019 May. PMID 30582221
    5. Expression and Clinical Significance of POLR1D in Colorectal Cancer. Tian Y, et al. Oncology, 2020. PMID 31722331

    See all (75) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. POLR1D silencing suppresses lung cancer cells proliferation and migration via inhibition of PI3K-Akt pathway.
      Title: POLR1D silencing suppresses lung cancer cells proliferation and migration via inhibition of PI3K-Akt pathway.
    2. A clinically-relevant residue of POLR1D is required for Drosophila development.
      Title: A clinically-relevant residue of POLR1D is required for Drosophila development.
    3. POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4.
      Title: POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4.
    4. Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer.
      Title: Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer.
    5. High POLR1D expression is an independent prognostic factor for poor overall survival in colorectal cancer.
      Title: Expression and Clinical Significance of POLR1D in Colorectal Cancer.
    6. High POLR1D expression is associated with colorectal cancer progression.
      Title: POLR1D promotes colorectal cancer progression and predicts poor prognosis of patients.
    7. We report a clinical and extensive molecular study, including TCOF1, POLR1D, POLR1C, and EFTUD2 genes, in a series of 146 patients with TCS.
      Title: Treacher Collins syndrome: a clinical and molecular study based on a large series of patients.
    8. Whole exome sequencing identified a nonsynonymous mutation in POLR1D (subunit of RNA polymerase I and II): exon2:c.T332C:p.L111P.
      Title: Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes.
    9. Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome.
      Title: Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome.
    10. Mutations in TCOF1, POLR1C and POLR1D have all been implicated in causing TCS
      Title: Treacher Collins Syndrome: the genetics of a craniofacial disease.
    Submit: New GeneRIF Correction See all GeneRIFs (14)

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    Associated conditions

    Description Tests
    Treacher Collins syndrome 2
    MedGen: C3150983 OMIM: 613717 GeneReviews: Treacher Collins Syndrome
    		Compare labs

    Copy number response

    Description
    Copy number response
    Triplosensitivity

    No evidence available (Last evaluated 2021-06-23)

    ClinGen Genome Curation Page
    Haploinsufficency

    Sufficient evidence for dosage pathogenicity (Last evaluated 2021-06-23)

    ClinGen Genome Curation PagePubMed

    EBI GWAS Catalog

    Description
    Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.
    EBI GWAS Catalog

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Pathways from PubChem

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    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • MGC9850, FLJ20616

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables DNA binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    contributes_to RNA polymerase I activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    contributes_to RNA polymerase III activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    enables protein dimerization activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    Process Evidence Code Pubs
    involved_in transcription by RNA polymerase III IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in transcription elongation by RNA polymerase I IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    Component Evidence Code Pubs
    part_of RNA polymerase I complex IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    part_of RNA polymerase I complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of RNA polymerase III complex IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    part_of RNA polymerase III complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in cytosol TAS
    Traceable Author Statement
    more info
    		  
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
    		  

    General protein information

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    Preferred Names
    DNA-directed RNA polymerases I and III subunit RPAC2; Protein POLR1D
    Names
    DNA-directed RNA polymerase I subunit D
    RNA polymerase I subunit D
    RNA polymerases I and III subunit AC2
    polymerase (RNA) I polypeptide D, 16kDa
    polymerase (RNA) I subunit D

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_028908.1 RefSeqGene

      Range
      6150..7707
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001206559.2 → NP_001193488.1  DNA-directed RNA polymerases I and III subunit RPAC2 isoform 3

      See identical proteins and their annotated locations for NP_001193488.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in both UTRs and in the coding region, compared to variant 1. The encoded isoform (3) shares identity with isoform 2 but is distinct and shorter, compared to isoform 1.
      Source sequence(s)
      AK307356, BC015319, BQ004736, DB123903, DR156229
      Consensus CDS
      CCDS73555.1
      UniProtKB/TrEMBL
      A0A087WTY1, A0A8I5QL02
      Related
      ENSP00000478213.1, ENST00000621089.2

    2. NM_001374407.1 → NP_001361336.1  DNA-directed RNA polymerases I and III subunit RPAC2 isoform 1

      Status: REVIEWED

      Source sequence(s)
      AL136439
      Consensus CDS
      CCDS9325.1
      UniProtKB/Swiss-Prot
      P0DPB6, Q5TBX2, Q96BR3, Q9Y2S0
      UniProtKB/TrEMBL
      A0A0R4J2F3
      Conserved Domains (1) summary
      cd07029
      Location:30 → 114
      RNAP_I_III_AC19; AC19 subunit of Eukaryotic RNA polymerase (RNAP) I and RNAP III

    3. NM_015972.4 → NP_057056.1  DNA-directed RNA polymerases I and III subunit RPAC2 isoform 1

      See identical proteins and their annotated locations for NP_057056.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the shortest transcript but encodes the longest isoform (1).
      Source sequence(s)
      BC000889
      Consensus CDS
      CCDS9325.1
      UniProtKB/Swiss-Prot
      P0DPB6, Q5TBX2, Q96BR3, Q9Y2S0
      UniProtKB/TrEMBL
      A0A0R4J2F3
      Related
      ENSP00000302478.4, ENST00000302979.5
      Conserved Domains (1) summary
      cd07029
      Location:30 → 114
      RNAP_I_III_AC19; AC19 subunit of Eukaryotic RNA polymerase (RNAP) I and RNAP III

    4. NM_152705.3 → NP_689918.1  Protein POLR1D isoform 2

      See identical proteins and their annotated locations for NP_689918.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 3' coding region and 3' UTR, compared to variant 1. The encoded isoform (2) has a distinct and shorter C-terminus, compared to isoform 1.
      Source sequence(s)
      BC015319, BQ004736
      Consensus CDS
      CCDS9324.1
      UniProtKB/Swiss-Prot
      P0DPB5
      Related
      ENSP00000382604.3, ENST00000399697.7

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000013.11 Reference GRCh38.p14 Primary Assembly

      Range
      27620743..27667411
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047430381.1 → XP_047286337.1  Protein POLR1D isoform X2

      UniProtKB/Swiss-Prot
      P0DPB5

    2. XM_017020622.2 → XP_016876111.1  DNA-directed RNA polymerases I and III subunit RPAC2 isoform X1

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060937.1 Alternate T2T-CHM13v2.0

      Range
      26841857..26888521
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054374597.1 → XP_054230572.1  Protein POLR1D isoform X2

      UniProtKB/Swiss-Prot
      P0DPB5

    2. XM_054374596.1 → XP_054230571.1  DNA-directed RNA polymerases I and III subunit RPAC2 isoform X1

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    P0DPB5.1 GenPept UniProtKB/Swiss-Prot:P0DPB5
    P0DPB6.1 GenPept UniProtKB/Swiss-Prot:P0DPB6

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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