H19
H19 imprinted maternally expressed transcript
Ассоциированные заболевания
Роль в фенотипе5
NephroblastomaORPHA:654
→Silver-Russell syndrome due to an imprinting defect of 11p15ORPHA:231140
→Silver-Russell syndrome due to 11p15 microduplicationORPHA:231144
→Beckwith-Wiedemann syndrome due to 11p15 microdeletionORPHA:231127
→Beckwith-Wiedemann syndrome due to imprinting defect of 11p15ORPHA:231117
→Герминативная мутация (причина)1