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    PRSS59P serine protease 59, pseudogene [ Homo sapiens (human) ]

    Gene ID: 207147, updated on 10-Dec-2024

    Summary

    Official Symbol
    PRSS59Pprovided by HGNC
    Official Full Name
    serine protease 59, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:43791
    See related
    Ensembl:ENSG00000293407 AllianceGenome:HGNC:43791
    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
    TRY2P; Tryx5
    Summary
    Predicted to be located in Golgi apparatus. [provided by Alliance of Genome Resources, Dec 2024]
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    Genomic context

    See PRSS59P in Genome Data Viewer
    Location:
    7q34
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (142268284..142272249, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (143583342..143587309, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (141968101..141972068, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr7:141945363-141946562 Neighboring gene monooxygenase DBH like 2, pseudogene Neighboring gene Sharpr-MPRA regulatory region 9540 Neighboring gene serine protease 58 Neighboring gene PRSS3 pseudogene 3 Neighboring gene T cell receptor beta variable 1 (pseudogene) Neighboring gene T cell receptor beta locus

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    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_001333.2 

      Range
      60827..64794 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. NR_036483.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AW085103, BC039387, BC047233
      Related
      ENST00000616556.2

    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
      142268284..142272249 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_187562.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      230181..234148 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      143583342..143587309 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)