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CBX1P5 chromobox 1 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 100133259, updated on 10-Oct-2023

Summary

Official Symbol
CBX1P5provided by HGNC
Official Full Name
chromobox 1 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:21006
See related
AllianceGenome:HGNC:21006
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
CBX9
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Genomic context

Location:
3q26.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (166810829..166812743)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (169594009..169595930)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (166528617..166530531)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene RN7SK pseudogene 298 Neighboring gene phosphoserine aminotransferase 1 pseudogene 4 Neighboring gene uncharacterized LOC124909498 Neighboring gene uncharacterized LOC105374194 Neighboring gene uncharacterized LOC105374193

Genomic regions, transcripts, and products

General gene information

Other Names

  • chromobox homolog 1 (HP1 beta homolog Drosophila ) pseudogene
  • chromobox homolog 1 pseudogene 5
  • chromobox homolog 9

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_007645.4 

    Range
    101..2015
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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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    166810829..166812743
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    169594009..169595930
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)