Family with sequence similarity 47 member C (FAM47C)

Family with sequence similarity 47 member C (FAM47C) is a protein-coding gene in Homo sapiens whose function is currently unknown[1][3][7][8]. The protein belongs to a family with several tandemly repeated regions, but there is no established molecular classification such as receptor, enzyme, channel, transporter, or transcription factor[1][5][8]. There are no reported therapeutic applications, drug interactions, or well-characterized physiological roles. However, variations in the FAM47C gene have been associated with certain male reproductive disorders, specifically varicocele and oligospermia, although the mechanisms remain undefined[3]. The product is typically annotated as "putative protein FAM47C," reflecting the uncertain status of its biological and clinical significance[8].

Other names

Putative protein FAM47CFAM47C