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ELOCP10 elongin C pseudogene 10 [ Homo sapiens (human) ]

Gene ID: 100462871, updated on 25-Jan-2022

Summary

Official Symbol
ELOCP10provided by HGNC
Official Full Name
elongin C pseudogene 10provided by HGNC
Primary source
HGNC:HGNC:38146
See related
Ensembl:ENSG00000234081 AllianceGenome:HGNC:38146
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
TCEB1P10
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Genomic context

See ELOCP10 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 (24006911..24007237, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (26153058..26153384, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene trafficking protein particle complex 2 pseudogene 10 Neighboring gene OFD1 pseudogene 12 Y-linked Neighboring gene chromodomain Y-linked 1B Neighboring gene chromodomain Y-linked 17 pseudogene

Genomic regions, transcripts, and products

General gene information

Other Names

  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 10
  • transcription elongation factor B subunit 1 pseudogene 10

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_021925.1 

    Range
    101..427
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    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
    24006911..24007237 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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