| ID | Type | Location (GRCh37) | Location (GRCh38) | Length | GC content |
|---|---|---|---|---|---|
| hsa_MBNL1_0004300 | Exon-Exon | chr3:152018042-152174150 | chr3:152300253-152456361 | 829 nt | 0.4982 |
| hsa_MBNL1_0004500 | Exon-Exon | chr3:152018108-152174150 | chr3:152300319-152456361 | 220 nt | 0.4727 |
| hsa_MBNL1_0004600 | Intron-Exon-Intron | chr3:152018670-152165562 | chr3:152300881-152447773 | 247 nt | 0.4656 |
| hsa_MBNL1_0004700 | Intron-Intron | chr3:152019166-152019389 | chr3:152301377-152301600 | 224 nt | 0.3170 |
| hsa_MBNL1_0004800 | Intron-Intron | chr3:152019781-152020470 | chr3:152301992-152302681 | 690 nt | 0.2942 |
| hsa_MBNL1_0004900 | Intron-Intron | chr3:152021335-152022056 | chr3:152303546-152304267 | 722 nt | 0.3116 |
| hsa_MBNL1_0005000 | Intron-Intron | chr3:152021952-152022622 | chr3:152304163-152304833 | 671 nt | 0.3458 |
| hsa_MBNL1_0005100 | Intron-Intron | chr3:152021987-152022496 | chr3:152304198-152304707 | 510 nt | 0.3431 |
| hsa_chr3_0289000 | Intergenic-Intergenic | chr3:152025009-152025793 | chr3:152307220-152308004 | 785 nt | 0.3452 |
| hsa_MBNL1_0005200 | Intron-Intron | chr3:152025264-152025654 | chr3:152307475-152307865 | 391 nt | 0.3248 |
A study in mice and Drosophila demonstrated that the circMBNL1 regulates the production of its linear mRNA counterpart in cis through competition with canonical splicing [Patop et al. DOI:10.15252/embj.2018100836]. A separate review confirmed its role as a splicing competitor that adversely affects canonical pre-mRNA splicing [Misir et al. DOI:10.1038/s41418-022-00948-7]. Research in mammalian neural tissue indicates that the circMBNL1 is synaptically-enriched and abundant in the dendritic arbor, suggesting a role in synaptic function [Mehta et al. DOI:10.1016/j.pneurobio.2020.101746].