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SLC16A1
solute carrier family 16 member 1
gene with protein product
OMIM: 600682
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Exercise-induced hyperinsulinism
ORPHA:165991
→
Metabolic myopathy due to lactate transporter defect
ORPHA:171690
→
Disease-causing germline mutation(s) (loss of function) in
1
Ketoacidosis due to monocarboxylate transporter-1 deficiency
ORPHA:438075
→
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Редкие заболевания
SLC16A1
🧬
SLC16A1
solute carrier family 16 member 1
gene with protein product
OMIM: 600682
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Exercise-induced hyperinsulinism
ORPHA:165991
→
Metabolic myopathy due to lactate transporter defect
ORPHA:171690
→
Disease-causing germline mutation(s) (loss of function) in
1
Ketoacidosis due to monocarboxylate transporter-1 deficiency
ORPHA:438075
→