MRPL51
Description
The MRPL51 (mitochondrial ribosomal protein L51) is a protein-coding gene located on chromosome 12.
MRPL51 is also known as CDA09, HSPC241, MRP64, bMRP64, mL51.
Associated Diseases
- dicarboxylic aminoaciduria
- ketoacidosis due to monocarboxylate transporter-1 deficiency
- exercise-induced hyperinsulinism
- 3-hydroxy-3-methylglutaryl-CoA synthase deficiency
- Dent disease
- glycogen storage disorder due to hepatic glycogen synthase deficiency
- medullary sponge kidney
- phosphoenolpyruvate carboxykinase deficiency, mitochondrial
- hyperinsulinism due to INSR deficiency
- hyperinsulinism-hyperammonemia syndrome
- congenital lipoid adrenal hyperplasia due to STAR deficency