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

Gene information from NCBI Gene. Variant classifications from ClinVar.