TPSD1

tryptase delta 1

Summary

Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. These genes are characterized by several distinct features. They have a highly conserved 3' UTR and contain tandem repeat sequences at the 5' flank and 3' UTR which are thought to play a role in regulation of the mRNA stability. Although this gene may be an exception, most of the tryptase genes have an intron immediately upstream of the initiator Met codon, which separates the site of transcription initiation from protein coding sequence. This feature is characteristic of tryptases but is unusual in other genes. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. This gene was once considered to be a pseudogene, although it is now believed to be a functional gene that encodes a protein. [provided by RefSeq, Jul 2008]

Known Variants33 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37643395216:1,306,295C/T—uncertain significance
rs20149483216:1,306,310G/A—uncertain significance
rs20024372516:1,306,333G/A—uncertain significance
rs75413868916:1,306,538A/G—likely benign
rs6175343316:1,306,541C/T—uncertain significance
rs203097149716:1,306,552G/T—uncertain significance
rs74752561416:1,306,609G/A—uncertain significance
rs143243717716:1,306,633G/C—uncertain significance
rs75561120116:1,306,640C/T—uncertain significance
rs254876449416:1,306,646T/A—uncertain significance
rs77557243516:1,306,670C/T—uncertain significance
rs18527563716:1,306,746G/Adownstream gene variant—
rs75435783816:1,306,825G/C—uncertain significance
rs203098160816:1,306,841C/A—uncertain significance
rs254876462316:1,306,898C/G—uncertain significance
rs146539491616:1,306,914A/G—uncertain significance
rs20056328116:1,306,919G/A—uncertain significance
rs76196126716:1,306,937C/A—uncertain significance
rs20218163316:1,306,964T/A—uncertain significance
rs7277546716:1,306,986C/A—uncertain significance
rs77276541816:1,307,039G/A—uncertain significance
rs74712884616:1,307,046G/C—uncertain significance
rs36807111016:1,307,048G/A—uncertain significance
rs20093848416:1,307,051G/A—uncertain significance
rs224260016:1,307,676A/Gdownstream gene variant—
rs76841530716:1,308,081C/T—uncertain significance
rs77921674016:1,308,143G/A—uncertain significance
rs11304545816:1,308,154G/A—benign
rs20163761016:1,308,173G/A—uncertain significance
rs14178153216:1,308,177G/A—uncertain significance
rs37296319416:1,308,182G/T—uncertain significance
rs76099690616:1,308,187G/T—uncertain significance
rs14299882016:1,308,333G/A—benign

Gene information from NCBI Gene. Variant classifications from ClinVar.