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ELOCP14 elongin C pseudogene 14 [ Homo sapiens (human) ]

Gene ID: 100462876, updated on 23-Nov-2021

Summary

Official Symbol
ELOCP14provided by HGNC
Official Full Name
elongin C pseudogene 14provided by HGNC
Primary source
HGNC:HGNC:38150
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TCEB1P14
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Genomic context

See ELOCP14 in Genome Data Viewer
Location:
Yq11.222
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (18787665..18788326)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (20949551..20950212)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene heat shock transcription factor Y-linked 2 Neighboring gene glycoprotein M6B pseudogene 2 Neighboring gene USP9Y pseudogene 2 Neighboring gene PTPN13 like Y-linked pseudogene 6 Neighboring gene XK related, Y-linked pseudogene 2

Genomic regions, transcripts, and products

General gene information

Other Names

  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 14
  • transcription elongation factor B subunit 1 pseudogene 14

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_004636.1 

    Range
    1271570..1272231
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p13 Primary Assembly

    Range
    18787665..18788326
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_028691.1: Suppressed sequence

    Description
    NG_028691.1: This RefSeq was permanently suppressed because this pseudogene is annotated on NG_004636.
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