FAM186B

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Description

The FAM186B (family with sequence similarity 186 member B) is a protein-coding gene located on chromosome 12.

FAM186B is also known as C12orf25.

Associated Diseases

• nephronophthisis
• substance abuse
• cholesterol-ester transfer protein deficiency
• hypertriglyceridemia 2
• hyperlipoproteinemia type V
• diabetes mellitus, permanent neonatal 4
• diabetes mellitus, transient neonatal, 3
• permanent neonatal diabetes mellitus 1
• glycogen storage disease VI