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ELOCP13 elongin C pseudogene 13 [ Homo sapiens (human) ]

Gene ID: 100462875, updated on 23-Nov-2021

Summary

Official Symbol
ELOCP13provided by HGNC
Official Full Name
elongin C pseudogene 13provided by HGNC
Primary source
HGNC:HGNC:38149
See related
Ensembl:ENSG00000225716
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
TCEB1P13
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Genomic context

See ELOCP13 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 (18440797..18441125)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (20602683..20603011)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377220 Neighboring gene RNA, 5S ribosomal pseudogene 523 Neighboring gene tubulin beta 1 class VI pseudogene 1 Neighboring gene family with sequence similarity 41 member A, Y-linked 2 Neighboring gene OFD1 pseudogene 4 Y-linked Neighboring gene USP9Y pseudogene 14 Neighboring gene RNA, U1 small nuclear 48, pseudogene

Genomic regions, transcripts, and products

General gene information

Other Names

  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 13
  • transcription elongation factor B subunit 1 pseudogene 13

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
    924702..925030
    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
    18440797..18441125
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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