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ATP5F1AP2 ATP synthase F1 subunit alpha pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 504, updated on 17-Sep-2024

Summary

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Official Symbol
ATP5F1AP2provided by HGNC
Official Full Name
ATP synthase F1 subunit alpha pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:828
See related
AllianceGenome:HGNC:828
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ATP5AP2; ATP5A1P2
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Genomic context

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See ATP5F1AP2 in Genome Data Viewer
Location:
2q24.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (155269631..155270037)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (155722647..155723053)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (156126143..156126549)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373698 Neighboring gene Sharpr-MPRA regulatory region 11721 Neighboring gene MT-CO1 pseudogene 45 Neighboring gene MT-ND2 pseudogene 20 Neighboring gene uncharacterized LOC124908061 Neighboring gene MT-ND4 pseudogene 28

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Comparative genomic hybridization analysis of Y79 and FISH mapping indicate the amplified human mitochondrial ATP synthase alpha-subunit gene (ATP5A) maps to chromosome 18q12-->q21. Godbout R, et al. Cytogenet Cell Genet, 1997. PMID 9284928

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 2
  • ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, 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_008671.1 

    Range
    101..507
    Download
    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    155269631..155270037
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    155722647..155723053
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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