MSS51
Description
The MSS51 (MSS51 mitochondrial translational activator) is a protein-coding gene located on chromosome 10.
MSS51 is also known as ZMYND17.
Associated Diseases
- long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- PLIN1-related familial partial lipodystrophy
- autosomal dominant mitochondrial myopathy with exercise intolerance
- LIPE-related familial partial lipodystrophy
- carnitine palmitoyl transferase II deficiency, severe infantile form
- familial partial lipodystrophy, Dunnigan type
- hyperinsulinism due to INSR deficiency
- AKT2-related familial partial lipodystrophy
- CIDEC-related familial partial lipodystrophy
- PPARG-related familial partial lipodystrophy
- familial partial lipodystrophy, Kobberling type
- phosphoenolpyruvate carboxykinase deficiency, mitochondrial
- 3-hydroxyacyl-CoA dehydrogenase deficiency
- hypoinsulinemic hypoglycemia and body hemihypertrophy
- type 2 diabetes mellitus
- schizophrenia
