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ATP6V0A2
ATPase H+ transporting V0 subunit a2
gene with protein product
OMIM: 611716
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Wrinkly skin syndrome
ORPHA:2834
→
Autosomal recessive cutis laxa type 2, classic type
ORPHA:357074
→
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Редкие заболевания
ATP6V0A2
🧬
ATP6V0A2
ATPase H+ transporting V0 subunit a2
gene with protein product
OMIM: 611716
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Wrinkly skin syndrome
ORPHA:2834
→
Autosomal recessive cutis laxa type 2, classic type
ORPHA:357074
→