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MTCO2P15 MT-CO2 pseudogene 15 [ Homo sapiens (human) ]

Gene ID: 107075147, updated on 17-Sep-2024

Summary

Official Symbol
MTCO2P15provided by HGNC
Official Full Name
MT-CO2 pseudogene 15provided by HGNC
Primary source
HGNC:HGNC:52031
See related
Ensembl:ENSG00000255417 AllianceGenome:HGNC:52031
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

See MTCO2P15 in Genome Data Viewer
Location:
11q22.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (103403512..103404167, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (103407408..103408063, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (103274240..103274895, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene dynein cytoplasmic 2 heavy chain 1 Neighboring gene MT-ATP6 pseudogene 15 Neighboring gene MT-CO3 pseudogene 15 Neighboring gene MT-CO1 pseudogene 15 Neighboring gene MT-ND2 pseudogene 26

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded cytochrome c oxidase II pseudogene 15

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_046449.1 

    Range
    101..756
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    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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    103403512..103404167 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    103407408..103408063 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)