This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 14. [provided by RefSeq, Jun 2010]
Modules significantly affected by knockdown. ↑ Up = module upregulated upon KD; ↓ Down = module downregulated upon KD.
| Cluster | Dir | NES | padj | Bind | OR | padj (bind) |
|---|
| Module | Dir | NES | #gRNA | padj | Bind | OR | padj (bind) |
|---|
| Submodule | Module | Dir | NES | #gRNA | Bind | OR | padj (bind) |
|---|
Genes likely regulated by MYNN through linked binding evidence in open chromatin. The chart ranks TF-linked genes by their mean Perturb-seq response to MYNN knockdown, with negative coefficients indicating downregulation and positive coefficients indicating upregulation upon knockdown.
Open chromatin elements (ATAC-seq) where MYNN has ChIP-seq or motif footprint binding evidence and which are linked to at least one target gene region.
| Element | Size | Linked genes |
|---|
Transcription factors with Perturb-seq knockdown data for MYNN. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = MYNN upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.
| TF | Mean coef | Binding | Outlier | TF→Gene link |
|---|
Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of MYNN, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.
| Accessibility | Element | Dist. to TSS | Link type | TFs |
|---|---|---|---|---|
| chr3:169,509,784–169,511,185 | 262.8 kb | Distal (>10kb) Multiome | 338 | |
| chr3:169,658,211–169,659,014 | 114.6 kb | Distal (>10kb) Multiome | 212 | |
| chr3:169,661,423–169,664,653 | 109.8 kb | Distal (>10kb) Multiome | 840 | |
| chr3:169,668,169–169,669,789 | 104.2 kb | Distal (>10kb) Multiome | 655 | |
| chr3:169,762,996–169,763,428 | 10.0 kb | Proximal (<10kb) | 459 | |
| chr3:169,764,381–169,765,564 | 8.3 kb | Proximal (<10kb) Multiome | 782 | |
| chr3:169,769,273–169,770,082 | 3.8 kb | Proximal (<10kb) Multiome | 566 | |
| chr3:169,771,800–169,773,839 | 1.4 kb | Proximal (<10kb) Multiome | 1077 | |
| chr3:169,811,873–169,814,235 | 39.2 kb | Distal (>10kb) Multiome | 581 | |
| chr3:169,966,015–169,967,550 | 193.4 kb | Distal (>10kb) Multiome | 1017 | |
| chr3:170,037,354–170,039,248 | 264.6 kb | Distal (>10kb) Multiome | 804 |
Genomic view of the MYNN locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.