C16orf89

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Description

The C16ORF89 (chromosome 16 open reading frame 89) is a protein-coding gene located on chromosome 16.

C16ORF89 is also known as -.

Associated Diseases

• 22q11.2 deletion syndrome
• 8p23.1 microdeletion syndrome
• hypoparathyroidism, familial isolated, 2
• dilated cardiomyopathy 1I
• colorectal cancer