GPR6 Polyclonal Antibody, 100ul Cell Function Analysis Abnormal recombination between PRKX and

Abnormal recombination between PRKX and a related pseudogene on chromosome Y is a frequent cause of sex reversal disorder in XX males and XY females

which may be partly responsible for the protection against cell death

The protein encoded by this gene belongs to the SMAD| a family of proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C

particularly capillaries

Also found in the colon

GPR6 Polyclonal Antibody, 100ul Cell Function Analysis Abnormal recombination between PRKX andReceptor for the lysosphingolipid sphingosine 1 phosphate (S1P). S1P is a bioactive lysophospholipid that elicits diverse physiological effect on most types of cells and tissues. This receptor mediates its action by association with G proteins that activate a phosphatidylinositol calcium second messenger system.,Belongs to the G protein coupled receptor 1 family.,