BT3A1 Polyclonal Antibody, 100ul Custom DNA Oligos Mutations in this gene have

Mutations in this gene have been associated with antenatal Bartter syndrome

where it colocalizes with protein tyrosine kinase 2-beta (PYK2)

The exact function of this gene is not known but studies in rat suggest a role in cellular proliferation and c-Myc-mediated transformation

They contain ankyrin repeat sequence and a SOCS box domain

also known as SDR25C1 or HEP27

BT3A1 Polyclonal Antibody, 100ul Custom DNA Oligos Mutations in this gene haveThe butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC) associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30. 2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single copy BTN1A1 gene (MIM 601610) and the BTN2 (e. g., BTN2A1; MIM 613590) and BTN3 (e. g., BNT3A1) genes, which have undergone tandem