Format

Send to:

Choose Destination

PRSS30P serine protease 30, pseudogene [ Homo sapiens (human) ]

Gene ID: 124221, updated on 23-Nov-2021

Summary

Official Symbol
PRSS30Pprovided by HGNC
Official Full Name
serine protease 30, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:28753
See related
Ensembl:ENSG00000172460
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
Disp; TMPRSS8; TMPRSS8P
Expression
Biased expression in testis (RPKM 2.9), placenta (RPKM 0.7) and 8 other tissues See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See PRSS30P in Genome Data Viewer
Location:
16p13.3
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 16 NC_000016.10 (2839573..2842751, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (2889574..2892752, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene eukaryotic translation initiation factor 1 pseudogene 4 Neighboring gene zymogen granule protein 16B Neighboring gene serine protease 22 Neighboring gene uncharacterized LOC101929566

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

General gene information

Other Names

  • protease, serine, 30 homolog, pseudogene
  • protease, serine, 30 pseudogene
  • transmembrane protease, serine 8 homolog, pseudogene
  • transmembrane protease, serine pseudogene

Clone Names

  • FLJ16659, MGC52282

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_026864.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC003965, AC005361, KF459802
    Related
    ENST00000476276.5

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p13 Primary Assembly

    Range
    2839573..2842751 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 PATCHES

Genomic

  1. NW_013171812.1 Reference GRCh38.p13 PATCHES

    Range
    19035..22213 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_178453.2: Suppressed sequence

    Description
    NM_178453.2: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
Support Center