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    ATP6V0E2 ATPase H+ transporting V0 subunit e2 [ Homo sapiens (human) ]

    Gene ID: 155066, updated on 10-Dec-2024

    Summary

    Official Symbol
    ATP6V0E2provided by HGNC
    Official Full Name
    ATPase H+ transporting V0 subunit e2provided by HGNC
    Primary source
    HGNC:HGNC:21723
    See related
    Ensembl:ENSG00000171130 MIM:611019; AllianceGenome:HGNC:21723
    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
    C7orf32; ATP6V0E2L
    Summary
    Multisubunit vacuolar-type proton pumps, or H(+)-ATPases, acidify various intracellular compartments, such as vacuoles, clathrin-coated and synaptic vesicles, endosomes, lysosomes, and chromaffin granules. H(+)-ATPases are also found in plasma membranes of specialized cells, where they play roles in urinary acidification, bone resorption, and sperm maturation. Multiple subunits form H(+)-ATPases, with proteins of the V1 class hydrolyzing ATP for energy to transport H+, and proteins of the V0 class forming an integral membrane domain through which H+ is transported. ATP6V0E2 encodes an isoform of the H(+)-ATPase V0 e subunit, an essential proton pump component (Blake-Palmer et al., 2007 [PubMed 17350184]).[supplied by OMIM, Mar 2008]
    Expression
    Broad expression in brain (RPKM 57.2), kidney (RPKM 22.7) and 14 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See ATP6V0E2 in Genome Data Viewer
    Location:
    7q36.1
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (149872964..149880713)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (151055071..151062678)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (149570053..149577802)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:149479128-149479704 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:149480282-149480858 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:149480859-149481434 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:149482621-149483120 Neighboring gene Sharpr-MPRA regulatory region 4172 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:149484857-149485446 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:149487626-149488414 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:149496913-149497414 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:149497415-149497914 Neighboring gene zinc finger protein 467 Neighboring gene SCO-spondin, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18769 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:149552405-149552958 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:149552959-149553510 Neighboring gene ATP6V0E2 antisense RNA 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18770 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:149570857-149571825 Neighboring gene zinc finger protein 862 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:149604113-149604612 Neighboring gene actin related protein 3C Neighboring gene uncharacterized LOC124901772 Neighboring gene ReSE screen-validated silencer GRCh37_chr7:149697909-149698096 Neighboring gene NANOG hESC enhancer GRCh37_chr7:149721691-149722215 Neighboring gene NANOG hESC enhancer GRCh37_chr7:149728774-149729275 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:149732655-149733170 Neighboring gene uncharacterized LOC100134040

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables ATPase-coupled ion transmembrane transporter activity ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables proton-transporting ATPase activity, rotational mechanism IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in proton transmembrane transport IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in regulation of macroautophagy NAS
    Non-traceable Author Statement
    more info
    PubMed 
    involved_in transmembrane transport IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in vacuolar acidification ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    Component Evidence Code Pubs
    located_in clathrin-coated vesicle membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in endosome membrane TAS
    Traceable Author Statement
    more info
     
    located_in lysosomal membrane TAS
    Traceable Author Statement
    more info
     
    located_in membrane NAS
    Non-traceable Author Statement
    more info
    PubMed 
    located_in phagocytic vesicle membrane TAS
    Traceable Author Statement
    more info
     
    located_in synaptic vesicle membrane IEA
    Inferred from Electronic Annotation
    more info
     
    part_of vacuolar proton-transporting V-type ATPase, V0 domain ISS
    Inferred from Sequence or Structural Similarity
    more info
     

    General protein information

    Preferred Names
    V-type proton ATPase subunit e 2
    Names
    H+-ATPase e2 subunit
    V-ATPase subunit e 2
    V-ATPase subunit e1
    lysosomal 9 kDa H(+)-transporting ATPase V0 subunit e2
    vacuolar proton pump subunit e 2
    vacuolar proton-ATPase subunit

    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_001100592.3NP_001094062.2  V-type proton ATPase subunit e 2 isoform 2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an alternate segment in the 3' coding region, compared to variant 1, that causes a frameshift. The resulting protein (isoform 2) has a longer and distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AC093458
      Consensus CDS
      CCDS47742.2
      Related
      ENSP00000411672.3, ENST00000421974.7
      Conserved Domains (1) summary
      pfam05493
      Location:951
      ATP_synt_H; ATP synthase subunit H
    2. NM_001289990.2NP_001276919.2  V-type proton ATPase subunit e 2 isoform 3

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) uses an alternate splice site in the 3' coding region, which results in a frameshift, compared to variant 1. The encoded protein (isoform 3) has a longer and distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AC093458
      Consensus CDS
      CCDS94229.1
      Related
      ENSP00000417939.1, ENST00000479613.5
      Conserved Domains (1) summary
      pfam05493
      Location:967
      ATP_synt_H; ATP synthase subunit H
    3. NM_001367788.1NP_001354717.1  V-type proton ATPase subunit e 2 isoform 4

      Status: VALIDATED

      Source sequence(s)
      AC093458
    4. NM_001367789.2NP_001354718.2  V-type proton ATPase subunit e 2 isoform 1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6), as well as variant 1, encodes isoform 1.
      Source sequence(s)
      AC093458
      Consensus CDS
      CCDS55181.2
      UniProtKB/Swiss-Prot
      A2T863, A2T8L7, B5MDP5, J3KQW7, Q6MZW1, Q75L47, Q7Z4R7, Q8N7I8, Q8NHE4
      Related
      ENSP00000475645.1, ENST00000464662.5
      Conserved Domains (1) summary
      pfam05493
      Location:967
      ATP_synt_H; ATP synthase subunit H
    5. NM_001367791.1NP_001354720.1  V-type proton ATPase subunit e 2 isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (7), as well as variants 8-13, encodes isoform 5.
      Source sequence(s)
      AC093458
    6. NM_001367792.1NP_001354721.1  V-type proton ATPase subunit e 2 isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (8), as well as variants 7 and 9-13, encodes isoform 5.
      Source sequence(s)
      AC093458
    7. NM_001367793.1NP_001354722.1  V-type proton ATPase subunit e 2 isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (9), as well as variants 7, 8, and 10-13, encodes isoform 5.
      Source sequence(s)
      AC093458
    8. NM_001367794.1NP_001354723.1  V-type proton ATPase subunit e 2 isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (10), as well as variants 7-9 and 11-13, encodes isoform 5.
      Source sequence(s)
      AC093458, HY134292
    9. NM_001367795.1NP_001354724.1  V-type proton ATPase subunit e 2 isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (11), as well as variants 7-10, 12, and 13, encodes isoform 5.
      Source sequence(s)
      AC093458
    10. NM_001367796.1NP_001354725.1  V-type proton ATPase subunit e 2 isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (12), as well as variants 7-11 and 13, encodes isoform 5.
      Source sequence(s)
      AC093458, BX488744
    11. NM_001367797.1NP_001354726.1  V-type proton ATPase subunit e 2 isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (13), as well as variants 7-12, encodes isoform 5.
      Source sequence(s)
      AC093458, DA066294
    12. NM_145230.4NP_660265.3  V-type proton ATPase subunit e 2 isoform 1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the predominantly occurring transcript and it encodes isoform 1. Variants 1 and 6 both encode the same isoform (1).
      Source sequence(s)
      AC093458
      Consensus CDS
      CCDS55181.2
      UniProtKB/Swiss-Prot
      A2T863, A2T8L7, B5MDP5, J3KQW7, Q6MZW1, Q75L47, Q7Z4R7, Q8N7I8, Q8NHE4
      Related
      ENSP00000396148.2, ENST00000425642.3
      Conserved Domains (1) summary
      pfam05493
      Location:967
      ATP_synt_H; ATP synthase subunit H

    RNA

    1. NR_110612.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) contains an alternate 3' exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AK057700, AK094602, AK172725, BE677432

    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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      149872964..149880713
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      151055071..151062678
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)