| ID | Type | Location (GRCh37) | Location (GRCh38) | Length | GC content |
|---|---|---|---|---|---|
| hsa_MBNL1_0013100 | Exon-Exon | chr3:152132790-152150709 | chr3:152415001-152432920 | 315 nt | 0.5143 |
| hsa_MBNL1_0013200 | Exon-Exon | chr3:152132790-152164546 | chr3:152415001-152446757 | 117 nt | 0.4957 |
| hsa_MBNL1_0013300 | Intron-Intron | chr3:152133483-152133703 | chr3:152415694-152415914 | 221 nt | 0.3122 |
| hsa_chr3_0290900 | Intergenic-Intergenic | chr3:152135258-152136484 | chr3:152417469-152418695 | 1227 nt | 0.4262 |
| hsa_MBNL1_0013400 | Intron-Intron | chr3:152135476-152135813 | chr3:152417687-152418024 | 338 nt | 0.4290 |
| hsa_MBNL1_0013500 | Intron-Intron | chr3:152141078-152141290 | chr3:152423289-152423501 | 213 nt | 0.3944 |
| hsa_MBNL1_0013600 | Intron-Exon-Intron | chr3:152149476-152165562 | chr3:152431687-152447773 | 148 nt | 0.3378 |
| hsa_MBNL1_0013800 | Exon-Exon | chr3:152150506-152150709 | chr3:152432717-152432920 | 204 nt | 0.5294 |
| hsa_MBNL1_0013700 | Intron-Exon-Intron | chr3:152150506-152155235 | chr3:152432717-152437446 | 250 nt | 0.3440 |
| hsa_MBNL1_0013900 | Exon-Exon | chr3:152150506-152163328 | chr3:152432717-152445539 | 462 nt | 0.5152 |
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].