SYCN

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Description

The SYCN (syncollin) is a protein-coding gene located on chromosome 19.

SYCN is also known as INSSA1, SYL.

Associated Diseases

• bronchiectasis with or without elevated sweat chloride 1
• hereditary chronic pancreatitis
• GCGR-related hyperglucagonemia
• hyperinsulinemic hypoglycemia, familial, 2
• pancreatic agenesis 2
• benign recurrent intrahepatic cholestasis type 1
• cancer
• pancreatic ductal adenocarcinoma
• pachyonychia congenita