U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

    • Showing Current items.

    ELOA3P elongin A3, pseudogene [ Homo sapiens (human) ]

    Gene ID: 162699, updated on 10-Dec-2024

    Summary

    Go to the top of the page Help
    Official Symbol
    ELOA3Pprovided by HGNC
    Official Full Name
    elongin A3, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:24617
    See related
    AllianceGenome:HGNC:24617
    Gene type
    pseudo
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ELOA3; ELOA3A; HsT829; TCEB3C; ELOA3AP; TCEB3L2
    Summary
    The SIII (or elongin) transcription elongation factor complex stimulates the rate of transcription elongation by RNA polymerase II by suppressing the transient pausing of the polymerase at many sites along the DNA template. This gene represents a likely pseudogene of ELOA (GeneID: 6924). [provided by RefSeq, Jun 2020]
    Annotation information
    not in current annotation release
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    Go to the top of the page Help
    See ELOA3P in Genome Data Viewer
    Location:
    18q21.1
    Annotation release Status Assembly Chr Location
    109.20211119 latest, but not current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (47028021..47030461, complement)

    Bibliography

    Go to the top of the pageHelp

    Related articles in PubMed

    1. A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes. Strichman-Almashanu LZ, et al. Genome Res, 2002 Apr. PMID 11932239, Free PMC Article
    2. Identification and biochemical characterization of a novel transcription elongation factor, Elongin A3. Yamazaki K, et al. J Biol Chem, 2002 Jul 19. PMID 11994304
    3. Analysis of phosphatase and tensin homolog tumor suppressor interacting proteins by in vitro and in silico proteomics. Crockett DK, et al. Proteomics, 2005 Apr. PMID 15717329
    4. Paralog knockout profiling identifies DUSP4 and DUSP6 as a digenic dependence in MAPK pathway-driven cancers. Ito T, et al. Nat Genet, 2021 Dec. PMID 34857952
    5. In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker. Gao H, et al. Anal Chem, 2022 May 31. PMID 35575683

    See all (7) citations in PubMed

    GeneRIFs: Gene References Into Functions

    Phenotypes

    Go to the top of the page Help

    Copy number response

    Description
    Copy number response
    Haploinsufficency

    No evidence available (Last evaluated 2012-02-22)

    ClinGen Genome Curation Page
    Triplosensitivity

    No evidence available (Last evaluated 2012-02-22)

    ClinGen Genome Curation Page

    Variation

    Go to the top of the page Help

    See studies and variants in dbVar

    See Variation Viewer (GRCh38)

    Interactions

    Go to the top of the page Help
    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Go to the top of the page Help

    Markers

    Other Names

    • RNA polymerase II transcription factor SIII subunit A3
    • elongin A3 family member A
    • transcription elongation factor B polypeptide 3C (elongin A3)
    • transcription elongation factor B subunit 3C

    NCBI Reference Sequences (RefSeq)

    Go to the top of the page Help

    NEW Try the new Transcript table

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_016749.1: Suppressed sequence

      Description
      NG_016749.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.

    2. NM_145653.3: Suppressed sequence

      Description
      NM_145653.3: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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

    Chemical Information
    Molecular Biology Databases
    Research Materials
    Tools