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ELOA3CP elongin A3 family member C, pseudogene [ Homo sapiens (human) ]

Gene ID: 107983955, updated on 29-Mar-2023

Summary

Official Symbol
ELOA3CPprovided by HGNC
Official Full Name
elongin A3 family member C, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:52410
See related
AllianceGenome:HGNC:52410
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ELOA3B; ELOA3C; TCEB3CL
Summary
Predicted to be involved in transcription elongation from RNA polymerase II promoter. Predicted to be part of elongin complex. [provided by Alliance of Genome Resources, Apr 2022]
Annotation information
Annotation category: suggests misassembly
not in current annotation release
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Genomic context

Location:
18q21.1
Annotation release Status Assembly Chr Location
109.20200522 latest, but not current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (46968695..46969912, complement)

General gene information

Other Names

  • EloA3-like-1
  • Elongin-A3 member B
  • Elongin-A3-like-1
  • RNA polymerase II transcription factor SIII subunit A3-like-1
  • Transcription elongation factor B polypeptide 3C-like-1
  • putative elongin-A3 member C

Clone Names

  • MGC119353

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_070699.1 

    Range
    101..1941
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001354366.1: Suppressed sequence

    Description
    NM_001354366.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.