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

Gene ID: 207147, updated on 14-May-2022

Summary

Official Symbol
PRSS59Pprovided by HGNC
Official Full Name
serine protease 59, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:43791
See related
Ensembl:ENSG00000186163 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, Apr 2022]
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Genomic context

See PRSS59P in Genome Data Viewer
Location:
7q34
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (142268284..142272249, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (143583342..143587309, complement)
105.20220307 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 monooxygenase DBH like 2, pseudogene Neighboring gene serine protease 58 Neighboring gene PRSS3 pseudogene 3 Neighboring gene Sharpr-MPRA regulatory region 9540

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

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
    ENST00000616556.1

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_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)