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ELOCP12 elongin C pseudogene 12 [ Homo sapiens (human) ]

Gene ID: 100462874, updated on 23-Nov-2021

Summary

Official Symbol
ELOCP12provided by HGNC
Official Full Name
elongin C pseudogene 12provided by HGNC
Primary source
HGNC:HGNC:38148
See related
Ensembl:ENSG00000230412
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
TCEB1P12
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Genomic context

See ELOCP12 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 (18068483..18068810)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (20230369..20230696)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene chromodomain Y-linked 8 pseudogene Neighboring gene chromodomain Y-linked 2A Neighboring gene OFD1 pseudogene 2 Y-linked Neighboring gene trafficking protein particle complex 2 pseudogene 8

Genomic regions, transcripts, and products

General gene information

Other Names

  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 12
  • transcription elongation factor B subunit 1 pseudogene 12

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
    552388..552715
    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
    18068483..18068810
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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