← Назад
🧬
SLC22A12
solute carrier family 22 member 12
gene with protein product
OMIM: 607096
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Hereditary renal hypouricemia
ORPHA:94088
→
Home
Calc.
Tools
Sign in
MEDLIB
Home
Tools
Pricing
Sign in
Language
ҚАЗ
EN
DE
RU
Главная
Инструменты
Редкие заболевания
SLC22A12
🧬
SLC22A12
solute carrier family 22 member 12
gene with protein product
OMIM: 607096
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Hereditary renal hypouricemia
ORPHA:94088
→