- Human pathology

Home > A. Molecular pathology > BTNL2


Sunday 3 April 2005

The BTNL2 gene is a member of the B7 receptor family that probably functions as a T-cell costimulatory molecule. It resides in the class II major histocompatibility complex (MHC) region of chromosome 6p.


- truncating splice site mutation in BTNL2 gene in sarcoidosis (15735647, 16080124)