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IGF2

insulin like growth factor 2

gene with protein productOMIM: 1474705 заболеваний
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Роль в фенотипе3
Silver-Russell syndrome due to an imprinting defect of 11p15ORPHA:231140
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Silver-Russell syndrome due to 11p15 microduplicationORPHA:231144
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Beckwith-Wiedemann syndrome due to imprinting defect of 11p15ORPHA:231117
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Герминативная мутация (причина)2
Isolated hemihyperplasiaORPHA:2128
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Silver-Russell syndrome due to a point mutationORPHA:397590
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Данные: Orphadata (CC-BY-4.0)