Phosphatidylinositol 3-kinase phosphorylates the inositol ring of phosphatidylinositol at the 3-prime position. The enzyme comprises a 110 kD catalytic subunit and a regulatory subunit of either 85, 55, or 50 kD. This gene encodes the 85 kD regulatory subunit. Phosphatidylinositol 3-kinase plays an important role in the metabolic actions of insulin, and a mutation in this gene has been associated with insulin resistance. Alternative splicing of this gene results in four transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]
Transcription factors with Perturb-seq knockdown data for PIK3R1. 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 = PIK3R1 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 PIK3R1, 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 |
|---|---|---|---|---|
| chr5:67,957,179–67,957,871 | 258.3 kb | Distal (>10kb) Multiome | 259 | |
| chr5:68,054,246–68,055,439 | 161.1 kb | Distal (>10kb) Multiome | 168 | |
| chr5:68,187,337–68,188,243 | 28.1 kb | Distal (>10kb) Multiome | 245 | |
| chr5:68,214,631–68,216,837 | 125 bp | At TSS Multiome | 962 | |
| chr5:68,287,871–68,289,169 | 72.7 kb | Distal (>10kb) Multiome | 613 | |
| chr5:68,353,260–68,354,829 | 138.1 kb | Distal (>10kb) Multiome | 255 | |
| chr5:68,436,487–68,437,544 | 221.1 kb | Distal (>10kb) Multiome | 122 | |
| chr5:68,922,292–68,922,890 | 706.8 kb | Distal (>10kb) Multiome HiCAR | 63 |
Genomic view of the PIK3R1 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.