FBRSL1 pseudogene 1 (FBRSL1P1)

Fibrosin-like protein 1 (FBRSL1) is a member of the AUTS2 gene family, encoding a poorly characterized protein with RNA-binding activity, primarily important during embryonic development and neurodevelopment. FBRSL1 interacts with chromatin regulators and Polycomb group complexes, influencing transcriptional regulation and epigenetic processes. Mutations or truncations in FBRSL1 are linked to congenital malformation and intellectual disability syndromes. There is no current evidence linking "FBRSL1 pseudogene 1" to functional roles or therapeutic targeting. Pseudogenes generally may have regulatory roles, such as acting as miRNA sponges, but such effects are not documented for FBRSL1P1[1][2][3][4][5].

None known for drugs, as neither FBRSL1 nor FBRSL1P1 is an established drug target.