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COX5BP2 cytochrome c oxidase subunit 5B pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 1331, updated on 23-Nov-2021

Summary

Official Symbol
COX5BP2provided by HGNC
Official Full Name
cytochrome c oxidase subunit 5B pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:2271
See related
Ensembl:ENSG00000213111
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
COX5BL2
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Genomic context

See COX5BP2 in Genome Data Viewer
Location:
6q23.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (136034515..136034886, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (136355653..136356024, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101928326 Neighboring gene uncharacterized LOC101928373 Neighboring gene phosphodiesterase 7B Neighboring gene uncharacterized LOC644135 Neighboring gene mitochondrial fission regulator 2

Genomic regions, transcripts, and products

General gene information

Other Names

  • cytochrome c oxidase subunit Vb pseudogene 2
  • cytochrome c oxidase subunit Vb-like 2

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_028814.1 

    Range
    101..472
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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_000006.12 Reference GRCh38.p13 Primary Assembly

    Range
    136034515..136034886 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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