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ELOCP11 elongin C pseudogene 11 [ Homo sapiens (human) ]

Gene ID: 100462872, updated on 25-Jan-2022

Summary

Official Symbol
ELOCP11provided by HGNC
Official Full Name
elongin C pseudogene 11provided by HGNC
Primary source
HGNC:HGNC:38147
See related
Ensembl:ENSG00000227867 AllianceGenome:HGNC:38147
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
TCEB1P11
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Genomic context

See ELOCP11 in Genome Data Viewer
Location:
Yq11.23
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (25991241..25991572, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (28137388..28137719, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene XK related, Y-linked pseudogene 6 Neighboring gene PTPN13 like Y-linked pseudogene 4 Neighboring gene chromodomain Y-linked 23 pseudogene Neighboring gene USP9Y pseudogene 26

Genomic regions, transcripts, and products

General gene information

Other Names

  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 11
  • transcription elongation factor B subunit 1 pseudogene 11

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_021932.1 

    Range
    101..432
    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
    25991241..25991572 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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