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XRCC6P5 X-ray repair cross complementing 6 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 442459, updated on 23-Nov-2021

Summary

Official Symbol
XRCC6P5provided by HGNC
Official Full Name
X-ray repair cross complementing 6 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:45187
See related
Ensembl:ENSG00000215070
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

See XRCC6P5 in Genome Data Viewer
Location:
Xq22.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (99719130..99721206, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (98974128..98976204, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene high mobility group box 1 pseudogene 32 Neighboring gene TEX101 pseudogene 1 Neighboring gene B3GNT2 pseudogene 1 Neighboring gene CTDSPL2 pseudogene 1

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Other Names

  • DNA repair protein
  • X-ray repair complementing defective repair in Chinese hamster cells 6 pseudogene 5
  • X-ray repair complementing defective repair pseudogene

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_061628.2 

    Range
    101..2177
    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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    99719130..99721206 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001127438.1: Suppressed sequence

    Description
    NM_001127438.1: This RefSeq was permanently suppressed because it is now thought that this gene does not encode a protein.
  2. NR_024608.1: Suppressed sequence

    Description
    NR_024608.1: This RefSeq was removed because there is insufficient evidence that this locus is transcribed.
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