| ID | Sequence | Length | GC content |
|---|---|---|---|
| GUUGGGAAACAGCCCAGUGGUAUAAGGAUGAGGAAACUGAAGCCCAGAG… | 26911 nt | 0.3934 | |
| GCACUGCCAGGACUUACCGUACAACACUCCUUGGCUUCUGGAAUUUUAU… | 27373 nt | 0.3934 | |
| AGUCAGGGACGGAUUAUUGAAUAUGCAAGUUAGAAGAAAAAUCACAGGA… | 27167 nt | 0.3927 | |
| AGUCAGGGACGGAUUAUUGAAUAUGCAAGUUAGAAGAAAAAUCACAGGA… | 27121 nt | 0.3926 | |
| ACUUGUUGCUUACGGUACAGUCCAGCAUGAGCUGGAAAUGUAGGAACCU… | 26930 nt | 0.3932 | |
| GCAGGGAGCUUAACAGCCAGGCCUGGACACCCUCAAGAGACUGUGUGCU… | 26952 nt | 0.3935 | |
| CUUCUGCCGAAGAAGUAGGGGCGGGGGGAAGUUUAGGAGUUGAGGAAAG… | 27503 nt | 0.3943 | |
| CUUCUGCCGAAGAAGUAGGGGCGGGGGGAAGUUUAGGAGUUGAGGAAAG… | 27229 nt | 0.3934 | |
| CUUCUGCCGAAGAAGUAGGGGCGGGGGGAAGUUUAGGAGUUGAGGAAAG… | 27238 nt | 0.3935 | |
| CUUCUGCCGAAGAAGUAGGGGCGGGGGGAAGUUUAGGAGUUGAGGAAAG… | 27626 nt | 0.3945 |
This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]
A study in mice demonstrated that the ZBTB20 is a differentially expressed RNA marker involved in chromatin remodeling in type 2 alveolar cells during radiation pneumonitis [Yang et al. DOI:10.3390/antiox11081457]. In a separate investigation of acute myocardial infarction in mice, the ZBTB20 was identified as a target mRNA for multiple downregulated cardioprotective miRNAs, including miR-142a-3p, and its expression was negatively correlated with miR-142a-3p, indicating its role in post-infarction molecular regulation [Tuerxun et al. DOI:10.1007/s12013-024-01528-x].