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MTATP6P2 MT-ATP6 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100287745, updated on 23-Nov-2021

Summary

Official Symbol
MTATP6P2provided by HGNC
Official Full Name
MT-ATP6 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:44576
See related
Ensembl:ENSG00000270307
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 MTATP6P2 in Genome Data Viewer
Location:
5q21.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 5 NC_000005.10 (100051917..100052597, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (99387621..99388301, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene MT-ND4 pseudogene 35 Neighboring gene MT-ND3 pseudogene 19 Neighboring gene MT-CO3 pseudogene 22 Neighboring gene MT-ATP8 pseudogene 3 Neighboring gene MT-CO2 pseudogene 22 Neighboring gene MT-CO1 pseudogene 22

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • mitochondrially encoded ATP synthase 6 pseudogene 2

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_027709.1 

    Range
    101..781
    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_000005.10 Reference GRCh38.p13 Primary Assembly

    Range
    100051917..100052597 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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