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PRSS29P serine protease 29, pseudogene [ Homo sapiens (human) ]

Gene ID: 123787, updated on 5-Jan-2022

Summary

Official Symbol
PRSS29Pprovided by HGNC
Official Full Name
serine protease 29, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:17542
See related
Ensembl:ENSG00000196364
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ISP2
Summary
Predicted to enable serine-type endopeptidase activity. Predicted to be involved in proteolysis. Predicted to act upstream of or within blastocyst hatching and embryo implantation. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Nov 2021]
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Genomic context

See PRSS29P in Genome Data Viewer
Location:
16p13.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 16 NC_000016.10 (1261003..1264004, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (1311004..1314005, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene tryptase alpha/beta 1 Neighboring gene tryptase delta 1 Neighboring gene tryptase pseudogene 1 Neighboring gene tryptase pseudogene 2

Genomic regions, transcripts, and products

General gene information

Other Names

  • ISP2-like protein
  • implantation serine proteinase 2
  • implantation serine proteinase 2-like protein
  • protease, serine 29, pseudogene
  • putative serine protease 29

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables serine-type endopeptidase activity IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Process Evidence Code Pubs
involved_in proteolysis IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
is_active_in extracellular space IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

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_002329.2 

    Range
    101..3102
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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
    1261003..1264004 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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