TPSB2
Description
The TPSB2 (tryptase beta 2) is a protein-coding gene located on chromosome 16.
Tryptase beta-2, also known as tryptase II, is a proteolytic enzyme that in humans is encoded by the TPSB2 gene. Formerly, the enzyme was known as Tryptase Clara.
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. These 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. The alleles of this gene exhibit an unusual amount of sequence variation, such that the alleles were once thought to represent two separate genes, beta II and beta III.
Beta tryptases appear to be the main isoenzymes expressed in mast cells and club cells, whereas in basophils, alpha-tryptases predominate.
TPSB2 is also known as TPS2, tryptaseB, tryptaseC.
Associated Diseases
- immunodeficiency 28
- varicella, severe recurrent
- systemic mastocytosis
- recurrent Neisseria infections due to factor D deficiency
- candidiasis, familial, 4
- eosinophil peroxidase deficiency
- type II complement component 8 deficiency
- mannose-binding lectin deficiency
- neutropenia, severe congenital, 1, autosomal dominant
- immunodeficiency due to ficolin3 deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
