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Thromboxane-A synthase

TBXAS1
Identifiers
Aliases TBXAS1, BDPLT14, CYP5, CYP5A1, GHOSAL, THAS, TS, TXAS, TXS, thromboxane A synthase 1
External IDs OMIM: 274180 MGI: 98497 HomoloGene: 130979 GeneCards: TBXAS1
Genetically Related Diseases
amyotrophic lateral sclerosis, obesity,
RNA expression pattern
PBB GE TBXAS1 208130 s at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_011539

RefSeq (protein)

NP_035669.3
NP_035669

Location (UCSC) Chr 7: 139.78 – 140.02 Mb Chr 6: 38.88 – 39.08 Mb
PubMed search

NM_030984

NM_011539

NP_112246

NP_035669.3
NP_035669

Thromboxane A synthase 1 (platelet, cytochrome P450, family 5, subfamily A), also known as TBXAS1, is a enzyme that, in humans, is encoded by the TBXAS1 gene.

This gene encodes a member of the cytochrome P450 superfamily of enzymes. The proteins are monooxygenases that catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids, and other lipids. However, this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity. This endoplasmic reticulum membrane protein catalyzes the conversion of prostaglandin H2 to thromboxane A2, a potent vasoconstrictor and inducer of platelet aggregation and 12-Hydroxyheptadecatrienoic acid (i.e. 12-(S)-hydroxy-5Z,8E,10E-heptadecatrienoic acid or 12-HHT) and agonist of Leukotriene B4 receptors (i.e. BLT2 receptors) and mediator of certain BLT2 receptor]] actions. The enzyme plays a role in several pathophysiological processes including hemostasis, cardiovascular disease, and stroke. The gene expresses two transcript variants.


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