RNA-binding protein 12B (RBM12B)

RNA-binding protein 12B (RBM12B) is a protein encoded by the human RBM12B gene and is characterized by the presence of an RNA recognition motif (RRM) domain, classifying it as a member of the ribonucleoprotein (RNP) superfamily[1][6][8]. The protein is predicted to bind RNA and is implicated in the regulation of RNA splicing, operating as part of ribonucleoprotein complexes within the nucleoplasm[1][4][5]. Genetic studies have associated mutations in RBM12B with rare diseases such as primary cerebellar degeneration and Boucher-Neuhauser syndrome; broader roles in gene expression and disease mechanisms may be inferred due to its fundamental involvement in post-transcriptional regulation[1][3]. There are currently no documented drug-targeting interactions, clinical biomarkers, or established therapeutic safety challenges described for this protein.

Other names

RNA binding motif protein 12BMGC:33837RBM12BGC08M094813GC08M089951GC08M094743