Human pathology

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BTNL2

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.

Pathology

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