| ID | Type | Location (GRCh37) | Location (GRCh38) | Length | GC content |
|---|---|---|---|---|---|
| hsa_MBNL1_0001400 | Intron-Intron | chr3:151996742-151996891 | chr3:152278953-152279102 | 150 nt | 0.4333 |
| hsa_MBNL1_0001500 | Intron-Intron | chr3:152000566-152000865 | chr3:152282777-152283076 | 300 nt | 0.3800 |
| hsa_MBNL1_0001600 | Intron-Intron | chr3:152000663-152000865 | chr3:152282874-152283076 | 203 nt | 0.4335 |
| hsa_MBNL1_0001700 | Intron-Intron | chr3:152003691-152004505 | chr3:152285902-152286716 | 815 nt | 0.1779 |
| hsa_MBNL1_0001800 | Intron-Intron | chr3:152008179-152008892 | chr3:152290390-152291103 | 714 nt | 0.3417 |
| hsa_MBNL1_0001900 | Intron-Intron | chr3:152013416-152013724 | chr3:152295627-152295935 | 309 nt | 0.4369 |
| hsa_MBNL1_0002000 | Intron-Exon-Intron | chr3:152016047-152018156 | chr3:152298258-152300367 | 63 nt | 0.2857 |
| hsa_MBNL1_0002600 | Intron-Exon-Intron | chr3:152017194-152018762 | chr3:152299405-152300973 | 99 nt | 0.4545 |
| hsa_MBNL1_0002300 | Intron-Exon-Intron | chr3:152017194-152020758 | chr3:152299405-152302969 | 250 nt | 0.4000 |
| hsa_MBNL1_0002700 | Intron-Exon-Intron | chr3:152017194-152043306 | chr3:152299405-152325517 | 139 nt | 0.3813 |
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].