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MTATP6P15 MT-ATP6 pseudogene 15 [ Homo sapiens (human) ]

Gene ID: 107075273, updated on 25-Jan-2022

Summary

Official Symbol
MTATP6P15provided by HGNC
Official Full Name
MT-ATP6 pseudogene 15provided by HGNC
Primary source
HGNC:HGNC:52060
See related
Ensembl:ENSG00000254931 AllianceGenome:HGNC:52060
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 MTATP6P15 in Genome Data Viewer
Location:
11q22.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (103402588..103403422, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (103273316..103274150, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene defective in cullin neddylation 1 domain containing 5 Neighboring gene dynein cytoplasmic 2 heavy chain 1 Neighboring gene MT-CO3 pseudogene 15 Neighboring gene MT-CO2 pseudogene 15 Neighboring gene MT-CO1 pseudogene 15

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded ATP synthase 6 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_046403.1 

    Range
    101..935
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    103402588..103403422 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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