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COX7BP2 COX7B pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 140692, updated on 17-Sep-2024

Summary

Official Symbol
COX7BP2provided by HGNC
Official Full Name
COX7B pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:16601
See related
AllianceGenome:HGNC:16601
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
dJ901O8.2
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Genomic context

See COX7BP2 in Genome Data Viewer
Location:
20q11.23
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (35850501..35850958, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (37571479..37571935, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (34438423..34438880, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene MPRA-validated peak4202 silencer Neighboring gene ribosome production factor 2 homolog pseudogene 1 Neighboring gene uncharacterized LOC124904972 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12864 Neighboring gene Sharpr-MPRA regulatory region 2555 Neighboring gene PHD finger protein 20 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17798 Neighboring gene MPRA-validated peak4203 silencer Neighboring gene PHF20 intron CAGE-defined high expression enhancer Neighboring gene HIG1 hypoxia inducible domain family member 1A pseudogene 16 Neighboring gene RNA, U4 small nuclear 40, pseudogene

Genomic regions, transcripts, and products

General gene information

Other Names

  • cytochrome c oxidase subunit 7B pseudogene 2
  • cytochrome c oxidase subunit VIIb (COX7B) pseudogene 2
  • cytochrome c oxidase subunit VIIb pseudogene 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_005370.3 

    Range
    101..558
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    35850501..35850958 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    37571479..37571935 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_000032.1: Suppressed sequence

    Description
    NR_000032.1: This RefSeq was permanently suppressed because it is now thought that this gene is an untranscribed pseudogene. The locus is represented by NG_005370.1.