| ID | Type | Location (GRCh37) | Location (GRCh38) | Length | GC content |
|---|---|---|---|---|---|
| hsa_MBNL1_0002400 | Intron-Exon-Intron | chr3:152017194-152048731 | chr3:152299405-152330942 | 250 nt | 0.3720 |
| hsa_MBNL1_0002800 | Intron-Exon-Intron | chr3:152017194-152053019 | chr3:152299405-152335230 | 120 nt | 0.4333 |
| hsa_MBNL1_0002500 | Intron-Exon-Intron | chr3:152017194-152056462 | chr3:152299405-152338673 | 250 nt | 0.3920 |
| hsa_MBNL1_0002900 | Exon-Exon | chr3:152017194-152132900 | chr3:152299405-152415111 | 171 nt | 0.4912 |
| hsa_MBNL1_0003000 | Exon-Exon | chr3:152017194-152150709 | chr3:152299405-152432920 | 375 nt | 0.5120 |
| hsa_MBNL1_0003100 | Exon-Exon | chr3:152017194-152164546 | chr3:152299405-152446757 | 54 nt | 0.5556 |
| hsa_MBNL1_0003300 | Exon-Intron | chr3:152017249-152018762 | chr3:152299460-152300973 | 1514 nt | 0.3930 |
| hsa_chr3_0288700 | Intergenic-Intergenic | chr3:152017308-152017756 | chr3:152299519-152299967 | 449 nt | 0.4187 |
| hsa_chr3_0288800 | Intergenic-Intergenic | chr3:152017315-152017740 | chr3:152299526-152299951 | 426 nt | 0.4178 |
| hsa_chr3_0288900 | Intergenic-Intergenic | chr3:152017315-152017756 | chr3:152299526-152299967 | 442 nt | 0.4140 |
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].