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MTATP6P16 MT-ATP6 pseudogene 16 [ Homo sapiens (human) ]

Gene ID: 107075158, updated on 17-Sep-2024

Summary

Official Symbol
MTATP6P16provided by HGNC
Official Full Name
MT-ATP6 pseudogene 16provided by HGNC
Primary source
HGNC:HGNC:52061
See related
Ensembl:ENSG00000224299 AllianceGenome:HGNC:52061
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
ALS2CR3
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Genomic context

See MTATP6P16 in Genome Data Viewer
Location:
2q33.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (201550524..201551049)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (202031306..202031835)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (202415247..202415772)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene C2 calcium dependent domain containing 6 Neighboring gene MT-CO1 pseudogene 16 Neighboring gene MT-CO2 pseudogene 16 Neighboring gene MT-CO3 pseudogene 16 Neighboring gene MT-ND3 pseudogene 16

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded ATP synthase 6 pseudogene 16

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_046404.1 

    Range
    101..626
    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
    201550524..201551049
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    202031306..202031835
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)