Erythrocyte Lactate Transporter Defect, also known as metabolic myopathy due to lactate transporter defect,is related to monocarboxylate transporter 1 deficiency and hyperinsulinemic hypoglycemia, familial, 7,and has symptoms including elevated serum creatine phosphokinase, exercise-induced muscle cramps and exercise-induced muscle stiffness. An important gene associated with Erythrocyte Lactate Transporter Defect is SLC16A1 (Solute Carrier Family 16 Member 1)
Disease Interacts with Genes
Disease Interacts with Substances
Processes Associated With Trait
Molecular Function Associated With Trait
Biological Processes Associated With Trait
Pathways Associated With Trait
Symptoms Associated With Trait
Selected genes are highlighted in orange, bookmarked
genes are green
- Chemical increases gene,
- Chemical decreases gene,
- Chemical increases and decreases gene simultaneosly,
No arrows - gene doesn't interact with the chemical.
- Gene should be increased/decreased most of the time and the chemical does it.
- Gene should be increased/decreased most of the time but the chemical does the opposite.