ACOT2 Polyclonal Antibody, 50ul Pathway and Network Analysis Mutations in this gene are

Mutations in this gene are the cause of brachydactyly type A1

HTR4 is a member of the family of serotonin receptors

These genes may be overexpressed in tumors

The protein bears a characteristic V-type domain and two potential N-glycosylation sites in the extracellular domain

The protein is regulated by intracellular calcium ions and is found in both the plasma membrane and intracellular organellar membranes

ACOT2 Polyclonal Antibody, 50ul Pathway and Network Analysis Mutations in this gene areACOT2 encodes a member of the acyl CoA thioesterase protein family, and is one of four acyl CoA hydrolase genes located in a cluster on chromosome 14. Alternative splicing results in multiple transcript variants.