GS28 Polyclonal Antibody, 100ul Custom Peptide Synthesis Diseases associated with GPR157 include

Diseases associated with GPR157 include stromal dystrophy

Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis

This suggests that in mice this gene product plays a role in thermogenesis and lipolysis

CTNNA1 encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell

is secreted by activated T cells and displays chemotactic activity for monocytes but not for neutrophils

GS28 Polyclonal Antibody, 100ul Custom Peptide Synthesis Diseases associated with GPR157 includeGOSR1 (golgi SNAP receptor complex member 1) encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi and between Golgi compartments. This protein is considered an essential component of the Golgi SNAP receptor (SNARE) complex. Alternatively spliced transcript variants encoding distinct isoforms have been found for GOSR1.