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MTCO2P19 MT-CO2 pseudogene 19 [ Homo sapiens (human) ]

Gene ID: 107075223, updated on 10-Oct-2023

Summary

Official Symbol
MTCO2P19provided by HGNC
Official Full Name
MT-CO2 pseudogene 19provided by HGNC
Primary source
HGNC:HGNC:52035
See related
Ensembl:ENSG00000237628 AllianceGenome:HGNC:52035
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:
Xq22.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (102797531..102798128)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (101242477..101243074)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (102052459..102053056)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ARMCX5-GPRASP2 readthrough Neighboring gene long intergenic non-protein coding RNA 630 Neighboring gene MT-ND2 pseudogene 2 Neighboring gene MT-ATP6 pseudogene 19 Neighboring gene MT-CO1 pseudogene 19 Neighboring gene MT-CO3 pseudogene 19 Neighboring gene MT-ND4 pseudogene 32

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded cytochrome c oxidase II pseudogene 19

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_051995.1 

    Range
    101..698
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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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    102797531..102798128
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    101242477..101243074
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)