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MTATP6P11 MT-ATP6 pseudogene 11 [ Homo sapiens (human) ]

Gene ID: 107075311, updated on 10-Oct-2023

Summary

Official Symbol
MTATP6P11provided by HGNC
Official Full Name
MT-ATP6 pseudogene 11provided by HGNC
Primary source
HGNC:HGNC:52057
See related
Ensembl:ENSG00000228097 AllianceGenome:HGNC:52057
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 MTATP6P11 in Genome Data Viewer
Location:
9p24.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (5099560..5100229)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (5104646..5105315)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (5099560..5100229)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene Janus kinase 2 Neighboring gene insulin like 6 Neighboring gene MT-CO1 pseudogene 11 Neighboring gene MT-CO2 pseudogene 11 Neighboring gene MT-CO3 pseudogene 11 Neighboring gene MT-ND3 pseudogene 14

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded ATP synthase 6 pseudogene 11

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_068468.1 

    Range
    101..770
    Download
    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    5099560..5100229
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    5104646..5105315
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)