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    GGT2P gamma-glutamyltransferase 2, pseudogene [ Homo sapiens (human) ]

    Gene ID: 728441, updated on 2-Nov-2024

    Summary

    Official Symbol
    GGT2Pprovided by HGNC
    Official Full Name
    gamma-glutamyltransferase 2, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:4251
    See related
    MIM:137181; AllianceGenome:HGNC:4251
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    GGT; GGT2; GGT 2
    Summary
    This gene (GGT2P) appears to be a human duplication of the gamma-glutamyltransferase 1 (GGT1) gene. While GGT2P and GGT1 can potentially encode proteins of the same size and with 94% identity, the ability of GGT2P to encode a stable, functional enzyme has been disputed (see PMID:23682772). Since it is also expressed at a much lower level than GGT1, GGT2P is now thought to be a processed pseudogene. [provided by RefSeq, Jan 2022]
    Expression
    Biased expression in testis (RPKM 7.1), kidney (RPKM 4.7) and 11 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See GGT2P in Genome Data Viewer
    Location:
    22q11.21
    Exon count:
    15
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (21207976..21259684, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (21617766..21669309, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (21562265..21613973, complement)

    Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene MPRA-validated peak4464 silencer Neighboring gene family with sequence similarity 230 member B Neighboring gene H3K4me1 hESC enhancer GRCh37_chr22:21555249-21555931 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr22:21555932-21556613 Neighboring gene family with sequence similarity 247 member A Neighboring gene H3K4me1 hESC enhancer GRCh37_chr22:21569798-21570298 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr22:21570299-21570799 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr22:21585968-21586526 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr22:21609011-21609708 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:21609709-21610404 Neighboring gene OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:21610405-21611102 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:21613263-21613765 Neighboring gene E2F transcription factor 6 pseudogene 3 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:21634291-21635236 Neighboring gene POM121 transmembrane nucleoporin like 8, pseudogene Neighboring gene BCR pseudogene 6

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Other Names

    • gamma-glutamyltransferase 2
    • gamma-glutamyltranspeptidase 2
    • glutathione hydrolase 2
    • inactive gamma-glutamyltranspeptidase 2
    • inactive glutathione hydrolase 2

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    NOT enables glutathione hydrolase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in glutathione catabolic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in leukotriene D4 biosynthetic process ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in peptide modification IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in regulation of immune system process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in regulation of inflammatory response IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    NOT involved_in zymogen activation IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in endoplasmic reticulum IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in extracellular exosome HDA PubMed 
    located_in perinuclear region of cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    RNA

    1. NR_172944.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AP000550, AP000551

    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_000022.11 Reference GRCh38.p14 Primary Assembly

      Range
      21207976..21259684 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060946.1 Alternate T2T-CHM13v2.0

      Range
      21617766..21669309 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001351304.1: Suppressed sequence

      Description
      NM_001351304.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.