This may be connected to etiology of some UBAP2L-associated genetic diseases such as UBAP2L-deficiency syndrome, a rare autosomal dominant neurodevelopmental disorder caused by loss-of-function mutations in UBAP2L, characterized by impaired language development, intellectual disability, behavioral abnormalities, and dysmorphic facial features (Jia et al., 2022; Yang et al., 2024). Here, UBAP2L is linked to hereditary disease.