RNA-binding protein 12 is a protein that in humans is encoded by the RBM12 gene. This gene encodes a protein that contains several RNA-binding motifs, potential transmembrane domains, and proline-rich regions. This gene and the gene for copine I overlap at map location 20q11.21. Alternative splicing in the 5' UTR results in two transcript variants. Both variants encode the same protein. RMB12 is a protein encoded by the RBM12 gene and it still is not entirely known the full capacity, involvement, and function of the RBM12 protein, as of early 2026. There have been some studies that have linked the RMB12 protein in the suppression of fetal hemoglobin (HbF) production. In human fetuses, fetal hemoglobin is the primary oxygen-carrying protein in their red blood cells and facilitates the exchange of oxygen between the fetus and the mother. “RBM12 is a nuclear RBP with broad tissue expression that remains unchanged between fetal and erythroid stages (Wakabayashi, et al.).”^1 When primary erythroblasts and HeLa cells are stained with immunofluorescence, the staining showed RBM12 displaying nuclear localization suggesting it functions at pre-RNA level synthesis. It also showed to display expression across multiple different types of tissue and the expression does not seem to be developmentally selective. RBM12 has shown a preference in binding at the 5’UTR of its target mRNA’s.
Sickle cell anemia Hemoglobin is made up of four different subunits. In adults, hemoglobin is made up of two alpha subunits and two beta subunits. In a fetus, hemoglobin is made up of two identical alpha subunits, but instead of the beta subunits it is made up of two gamma subunits. Sickle cell disease is caused by a mutation in the beta subunits of hemoglobin. Since fetal hemoglobin does not have the beta subunits and instead has the gamma subunits, they are not affected by sickle cell disease. HbF, fetal hemoglobin, has recently begun to be studied as a possible treatment for sickle cell disease. “Increased levels of HbF can diminish the propensity of sickle cell hemoglobin to polymerize under hypoxic conditions and thus inhibit the pathognomonic changes in cell shape (Wakabayashi, et al.).”
Mental health disorders Studies have shown the RBM12 protein to have an influence on the development of different psychiatric disorders like schizophrenia and psychosis. “RBM12 is a high-penetrance risk factor for familial schizophrenia and psychosis… (Semesta, et al.).” The RBM12 protein can suppress the G protein-coupled receptor signaling axis. Loss of RMB12 can lead to a hyperactive cAMP production which then will increase PKA activity and can alter neuronal transcriptional responses.
Other disorders RBM12 has been linked to certain cancers as well. An increase in RBM12 expression has been linked to a negative prognosis in different types of cancers. Some of those cancers include Meibomian, a rare and aggressive cancer of the oil glands in the eyelids, and hepatocellular cell carcinoma. Various mutations in RBM12 have also been linked to some endometrial, colorectal, and kidney cancer diagnoses.
References Semesta K, Garces A, Tsvetanova N. The psychosis risk factor RBM12 encodes a novel repressor of GPCR/cAMP signal transduction. Journal of Biological Chemistry, 2023; 299 Aoi Wakabayashi, Maryanne Kihiu, Malini Sharma, A. Josephine Thrasher, Megan S. Saari, Mathieu Quesnel-Vallières, Osheiza Abdulmalik, Scott A. Peslak, Eugene Khandros, Cheryl A. Keller, Belinda M. Giardine, Yoseph Barash, Ross C. Hardison, Junwei Shi, Gerd A. Blobel; Identification and characterization of RBM12 as a novel regulator of fetal hemoglobin expression. Blood Adv2022; 6 (23): 5956–5968. doi: https://doi.org/10.1182/bloodadvances.2022007904 Craig, C., Eng, S., Manzo, J., & Tkacenko, A. (2021, January). PDB101: Molecule of the Month: Fetal Hemoglobin. RCSB: PDB-101. https://pdb101.rcsb.org/motm/257 RBM12. (n.d.). The Human Protein Atlas. Retrieved May 8, 2026, from https://www.proteinatlas.org/ENSG00000244462-RBM12
Further reading
External links RBM12 human gene location in the UCSC Genome Browser. RBM12 human gene details in the UCSC Genome Browser.






