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ELOCP36 elongin C pseudogene 36 [ Homo sapiens (human) ]

Gene ID: 101059905, updated on 10-Oct-2023

Summary

Official Symbol
ELOCP36provided by HGNC
Official Full Name
elongin C pseudogene 36provided by HGNC
Primary source
HGNC:HGNC:54973
See related
AllianceGenome:HGNC:54973
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
TCEB1P26
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Genomic context

Location:
Yq11.222
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (17726652..17727180)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (18633204..18633732)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (19838532..19839060)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124905302 Neighboring gene chromodomain Y-linked 5 pseudogene Neighboring gene PTPN13 like Y-linked pseudogene 1 Neighboring gene actin gamma 1 pseudogene 2

Genomic regions, transcripts, and products

General gene information

Other Names

  • elongin C pseudogene 26
  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 36
  • transcription elongation factor B subunit 1 pseudogene 36

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_084004.1 

    Range
    101..629
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    17726652..17727180
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    18633204..18633732
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_033276.1: Suppressed sequence

    Description
    NG_033276.1: This RefSeq was permanently suppressed because this pseudogene is now annotated on NG_004636.1