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COX11P1 COX11 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 140468, updated on 10-Oct-2023

Summary

Official Symbol
COX11P1provided by HGNC
Official Full Name
COX11 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:2262
See related
AllianceGenome:HGNC:2262
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
COX11; COX11P
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Genomic context

See COX11P1 in Genome Data Viewer
Location:
6p22.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (28446920..28447630)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (28318361..28319071)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (28414697..28415407)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene RNA, U2 small nuclear 45, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:28384184-28384684 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:28384685-28385185 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:28390954-28392153 Neighboring gene zinc finger and SCAN domain containing 23 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:28411067-28411577 Neighboring gene olfactory receptor family 2 subfamily E member 1 pseudogene Neighboring gene tRNA-Thr (anticodon TGT) 1-1

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • COX11 cytochrome c oxidase assembly homolog pseudogene 1
  • COX11 homolog, cytochrome c oxidase assembly protein pseudogene 1
  • COX11 homolog, cytochrome c oxidase assembly protein, pseudogene
  • COX11, cytochrome c oxidase copper chaperone pseudogene 1

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_007347.3 

    Range
    101..811
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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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    28446920..28447630
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    28318361..28319071
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_000031.1: Suppressed sequence

    Description
    NR_000031.1: This RefSeq was permanently suppressed because there is insufficient evidence that this pseudogene is transcribed.