Enables several functions, including phosphatidylinositol phosphate binding activity; phosphatidylinositol-3,4-bisphosphate binding activity; and protein homodimerization activity. Involved in several processes, including positive regulation of signal transduction; protein stabilization; and regulation of organelle organization. Located in clathrin-coated vesicle; cytosol; and ruffle membrane. [provided by Alliance of Genome Resources, Apr 2025]
Transcription factors with Perturb-seq knockdown data for HIP1R. 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 = HIP1R 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 HIP1R, 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 |
|---|---|---|---|---|
| chr12:122,751,194–122,751,767 | 84.1 kb | Distal (>10kb) Multiome | 128 | |
| chr12:122,752,332–122,753,299 | 82.7 kb | Distal (>10kb) Multiome | 978 | |
| chr12:122,774,223–122,774,865 | 60.9 kb | Distal (>10kb) Multiome | 445 | |
| chr12:122,834,656–122,836,128 | 51 bp | At TSS Multiome | 514 | |
| chr12:122,895,832–122,896,391 | 60.6 kb | Distal (>10kb) Multiome | 774 | |
| chr12:122,965,963–122,966,953 | 131.1 kb | Distal (>10kb) Multiome | 576 | |
| chr12:122,974,115–122,975,704 | 139.4 kb | Distal (>10kb) Multiome | 889 | |
| chr12:122,980,138–122,981,155 | 145.2 kb | Distal (>10kb) Multiome | 817 | |
| chr12:123,049,639–123,050,104 | 214.3 kb | Distal (>10kb) Multiome | 45 |
Genomic view of the HIP1R 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.