← Назад
🧬

HNRNPA1

heterogeneous nuclear ribonucleoprotein A1

gene with protein productOMIM: 1640173 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3
Amyotrophic lateral sclerosisORPHA:803
→
HNRNPA1-related adult-onset distal myopathyORPHA:399086
→
Inclusion body myopathy with Paget disease of bone and frontotemporal dementiaORPHA:52430
→
Данные: Orphadata (CC-BY-4.0)