MAGEL2
MAGE family member L2
Ассоциированные заболевания
Роль в фенотипе4
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1ORPHA:177901
→Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2ORPHA:177904
→Prader-Willi syndrome due to imprinting mutationORPHA:177910
→Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15ORPHA:98754
→Герминативная мутация (причина)1
Disease-causing germline mutation(s) (loss of function) in1