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ATP5MGL ATP synthase membrane subunit g like [ Homo sapiens (human) ]

Gene ID: 267020, updated on 22-May-2022

Summary

Official Symbol
ATP5MGLprovided by HGNC
Official Full Name
ATP synthase membrane subunit g likeprovided by HGNC
Primary source
HGNC:HGNC:13213
See related
Ensembl:ENSG00000249222 AllianceGenome:HGNC:13213
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ATP5K2; ATP5L2
Summary
Predicted to enable proton transmembrane transporter activity. Predicted to be involved in ATP synthesis coupled proton transport. Located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]
Orthologs
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Genomic context

See ATP5MGL in Genome Data Viewer
Location:
22q13.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (42639803..42640601, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (43120674..43121476, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (43035809..43036607, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene DNA polymerase delta interacting protein 3 Neighboring gene uncharacterized LOC124905127 Neighboring gene RNA, U12 small nuclear Neighboring gene cytochrome b5 reductase 3 Neighboring gene alpha 1,4-galactosyltransferase (P blood group) Neighboring gene ribosomal protein L5 pseudogene 34

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General protein information

Preferred Names
putative ATP synthase subunit g 2, mitochondrial
Names
ATP synthase membrane subunit g-like protein
ATP synthase subunit g 2, mitochondrial
ATP synthase, H+ transporting, mitochondrial F0 complex, subunit G2 pseudogene
ATP synthase, H+ transporting, mitochondrial F1F0, subunit g
ATP synthase, H+ transporting, mitochondrial Fo complex subunit G2
ATPase subunit g 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.

mRNA and Protein(s)

  1. NM_001165877.1NP_001159349.1  putative ATP synthase subunit g 2, mitochondrial

    See identical proteins and their annotated locations for NP_001159349.1

    Status: VALIDATED

    Source sequence(s)
    AF092923
    Consensus CDS
    CCDS54534.1
    UniProtKB/Swiss-Prot
    Q7Z4Y8
    Related
    ENSP00000421076.1, ENST00000505920.1
    Conserved Domains (1) summary
    pfam04718
    Location:16100
    ATP-synt_G; Mitochondrial ATP synthase g subunit

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    42639803..42640601 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    43120674..43121476 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_004718.4: Suppressed sequence

    Description
    NG_004718.4: This RefSeq was permanently suppressed because it is now thought that this gene does encode a protein.
  2. NM_198822.1: Suppressed sequence

    Description
    NM_198822.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.