Moreover, a recent large-scale sequencing study additionally implicated a role for HNRNPAB (OMIM #602688), HNRNPD (OMIM #601324), HNRNPF (OMIM #601037), HNRNPH3 (OMIM #602324), HNRNPUL1 (OMIM #605800), HNRNPUL2 (currently no OMIM #), and HNRNPQ/SYNCRIP (OMIM #616686) in human neurodevelopmental disorders (Gillentine et al. 2021). The gene discussed is SYNCRIP; the disease is neurodevelopmental disorder.