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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for TPSB2 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID64499
Official gene symbolTPSB2
Full nametryptase beta 2 (gene/pseudogene)
Aliases,TPS2,tryptaseB,tryptaseC,
Gene summaryTryptases 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, whereas in basophils, alpha-tryptases predominate. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. [provided by RefSeq]
LocationChromosome: 16   Locus: 16p13.3
Gene position1280185 - 1278336  Map Viewer
Gene orientationminus
Gene size1850 bp
Gene sequence
OMIM ID191081