METTL22
Description
The METTL22 (methyltransferase 22, Kin17 lysine) is a protein-coding gene located on chromosome 16.
METTL22 acts as a protein N-lysine methyltransferase, specifically trimethylating KIN at lysine residue 135 in laboratory settings.
METTL22 is also known as C16orf68.
Associated Diseases
- refractive error
- hypertriglyceridemia 2
- cholesterol-ester transfer protein deficiency
- thyroid hormone metabolism, abnormal, 2
- sitosterolemia
- homozygous familial hypercholesterolemia
- hypercholesterolemia, autosomal dominant, 3
- hyperlipoproteinemia type V
- hyperlipidemia due to hepatic triglyceride lipase deficiency
- hypercholesterolemia, autosomal dominant, type B
- pancreatic triacylglycerol lipase deficiency
- familial apolipoprotein C-II deficiency
- glycogen storage disease VI
