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MTCO2P27 MT-CO2 pseudogene 27 [ Homo sapiens (human) ]

Gene ID: 107075291, updated on 10-Oct-2023

Summary

Official Symbol
MTCO2P27provided by HGNC
Official Full Name
MT-CO2 pseudogene 27provided by HGNC
Primary source
HGNC:HGNC:52156
See related
Ensembl:ENSG00000230321 AllianceGenome:HGNC:52156
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:
19p13.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (12504905..12505976)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (12633311..12634382)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (12615719..12616790)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene MT-ND2 pseudogene 40 Neighboring gene MT-CO1 pseudogene 27 Neighboring gene MT-ATP6 pseudogene 27 Neighboring gene peptidylprolyl isomerase A pseudogene 20

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded cytochrome c oxidase II pseudogene 27

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_046458.1 

    Range
    101..1172
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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_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    12504905..12505976
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    12633311..12634382
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)