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    PTP4A2 protein tyrosine phosphatase 4A2 [ Homo sapiens (human) ]

    Gene ID: 8073, updated on 5-Mar-2024

    Summary

    Official Symbol
    PTP4A2provided by HGNC
    Official Full Name
    protein tyrosine phosphatase 4A2provided by HGNC
    Primary source
    HGNC:HGNC:9635
    See related
    Ensembl:ENSG00000184007 MIM:601584; AllianceGenome:HGNC:9635
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HH13; OV-1; PRL2; HH7-2; PRL-2; PTP4A; HU-PP-1; PTPCAAX2; ptp-IV1a; ptp-IV1b
    Summary
    The protein encoded by this gene belongs to a small class of the protein tyrosine phosphatase (PTP) family. PTPs are cell signaling molecules that play regulatory roles in a variety of cellular processes. PTPs in this class contain a protein tyrosine phosphatase catalytic domain and a characteristic C-terminal prenylation motif. This PTP has been shown to primarily associate with plasmic and endosomal membrane through its C-terminal prenylation. This PTP was found to interact with the beta-subunit of Rab geranylgeranyltransferase II (beta GGT II), and thus may function as a regulator of GGT II activity. Overexpression of this gene in mammalian cells conferred a transformed phenotype, which suggested its role in tumorigenesis. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 11, 12 and 17. [provided by RefSeq, Aug 2010]
    Expression
    Ubiquitous expression in thyroid (RPKM 58.0), bone marrow (RPKM 56.7) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    Location:
    1p35.2
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (31906421..31938368, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (31764401..31796321, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (32372022..32403969, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 576 Neighboring gene uncharacterized LOC124903930 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:32253763-32254538 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 578 Neighboring gene SPOC domain containing 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 653 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 654 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 579 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:32303933-32304116 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 655 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 656 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 657 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 658 Neighboring gene uncharacterized LOC128031832 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:32389035-32389578 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 659 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 660 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:32403472-32403643 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 581 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 661 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:32409768-32410302 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:32419864-32420642 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:32420643-32421419 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:32421420-32422197 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 665 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 666 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 667 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr1:32473819-32474378 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:32479704-32480274 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 583 Neighboring gene KH RNA binding domain containing, signal transduction associated 1 Neighboring gene VISTA enhancer hs645 Neighboring gene NANOG hESC enhancer GRCh37_chr1:32526442-32527054 Neighboring gene Sharpr-MPRA regulatory region 15509 Neighboring gene Sharpr-MPRA regulatory region 7843 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:32532900-32533694 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:32537939-32538544 Neighboring gene transmembrane protein 39B Neighboring gene microRNA 5585

    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

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables prenylated protein tyrosine phosphatase activity TAS
    Traceable Author Statement
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables protein tyrosine phosphatase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Process Evidence Code Pubs
    involved_in dephosphorylation IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    is_active_in cytoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytosol TAS
    Traceable Author Statement
    more info
     
    located_in early endosome IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    protein tyrosine phosphatase type IVA 2
    Names
    PTP(CAAXII)
    phosphatase of regenerating liver 2
    protein tyrosine phosphatase IVA
    protein tyrosine phosphatase IVA2
    protein tyrosine phosphatase type IVA, member 2
    protein-tyrosine phosphatase of regenerating liver 2
    NP_001182029.1
    NP_001182030.1
    NP_001356787.1
    NP_001356788.1
    NP_001356789.1
    NP_536316.1

    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.

    mRNA and Protein(s)

    1. NM_001195100.2 → NP_001182029.1  protein tyrosine phosphatase type IVA 2 isoform 3

      See identical proteins and their annotated locations for NP_001182029.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) lacks an alternate in-frame exon in the 3' coding region, compared to variant 1. This results in a shorter protein (isoform 3), compared to isoform 1.
      Source sequence(s)
      AL136115, BC018662, BC070181
      Consensus CDS
      CCDS59193.1
      UniProtKB/Swiss-Prot
      Q12974
      Related
      ENSP00000473490.1, ENST00000602683.5
      Conserved Domains (1) summary
      cl28904
      Location:1 → 130
      PTP_DSP_cys; cys-based protein tyrosine phosphatase and dual-specificity phosphatase superfamily
    2. NM_001195101.2 → NP_001182030.1  protein tyrosine phosphatase type IVA 2 isoform 4

      See identical proteins and their annotated locations for NP_001182030.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) lacks an alternate in-frame exon in the 5' coding region, compared to variant 1. This results in a shorter protein (isoform 4), compared to isoform 1. Variants 4 and 5 encode the same isoform.
      Source sequence(s)
      AL136115, BC018662, BC070181
      Consensus CDS
      CCDS53292.1
      UniProtKB/Swiss-Prot
      Q12974
      Conserved Domains (1) summary
      cl28904
      Location:1 → 124
      PTP_DSP_cys; cys-based protein tyrosine phosphatase and dual-specificity phosphatase superfamily
    3. NM_001369858.1 → NP_001356787.1  protein tyrosine phosphatase type IVA 2 isoform 4

      Status: REVIEWED

      Source sequence(s)
      AL136115, BC070181
      Consensus CDS
      CCDS53292.1
      Related
      ENSP00000409260.2, ENST00000457805.6
      Conserved Domains (1) summary
      cl28904
      Location:1 → 124
      PTP_DSP_cys; cys-based protein tyrosine phosphatase and dual-specificity phosphatase superfamily
    4. NM_001369859.1 → NP_001356788.1  protein tyrosine phosphatase type IVA 2 isoform 1

      Status: REVIEWED

      Source sequence(s)
      AL136115, BC070181, BI549454, DB503104
      Consensus CDS
      CCDS348.1
      UniProtKB/Swiss-Prot
      A8K9I8, B4DM39, D3DPP0, E9PGJ6, O00649, Q12974, Q15197, Q15259, Q15260, Q15261, R4GN50
      Related
      ENSP00000497092.1, ENST00000649841.1
      Conserved Domains (1) summary
      cd18536
      Location:1 → 155
      PTP-IVa2; protein tyrosine phosphatase type IVA 2
    5. NM_001369860.1 → NP_001356789.1  protein tyrosine phosphatase type IVA 2 isoform 1

      Status: REVIEWED

      Source sequence(s)
      AL136115, BC070181, DB503104
      Consensus CDS
      CCDS348.1
      UniProtKB/Swiss-Prot
      A8K9I8, B4DM39, D3DPP0, E9PGJ6, O00649, Q12974, Q15197, Q15259, Q15260, Q15261, R4GN50
      Related
      ENSP00000473259.1, ENST00000602725.5
      Conserved Domains (1) summary
      cd18536
      Location:1 → 155
      PTP-IVa2; protein tyrosine phosphatase type IVA 2
    6. NM_080391.4 → NP_536316.1  protein tyrosine phosphatase type IVA 2 isoform 1

      See identical proteins and their annotated locations for NP_536316.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1). Variants 1, 6 and 7 encode the same isoform.
      Source sequence(s)
      AL136115, BC018662, BC070182, BM996809
      Consensus CDS
      CCDS348.1
      UniProtKB/Swiss-Prot
      A8K9I8, B4DM39, D3DPP0, E9PGJ6, O00649, Q12974, Q15197, Q15259, Q15260, Q15261, R4GN50
      Related
      ENSP00000493688.1, ENST00000647444.2
      Conserved Domains (1) summary
      cd18536
      Location:1 → 155
      PTP-IVa2; protein tyrosine phosphatase type IVA 2

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      31906421..31938368 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      31764401..31796321 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_003479.2: Suppressed sequence

      Description
      NM_003479.2: This RefSeq was permanently suppressed because it is a nonsense-mediated decay (NMD) candidate.
    2. NM_080392.2: Suppressed sequence

      Description
      NM_080392.2: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.