Enables signaling receptor activity. Predicted to be involved in negative regulation of axon regeneration. Located in cell surface and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Transcription factors with Perturb-seq knockdown data for RTN4RL1. 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 = RTN4RL1 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 RTN4RL1, 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 |
|---|---|---|---|---|
| chr17:1,829,368–1,830,287 | 195.4 kb | Distal (>10kb) Multiome | 660 | |
| chr17:1,931,964–1,932,566 | 93.0 kb | Distal (>10kb) Multiome | 198 | |
| chr17:1,960,870–1,961,658 | 64.0 kb | Distal (>10kb) Multiome | 192 | |
| chr17:1,997,556–1,998,757 | 27.2 kb | Distal (>10kb) Multiome | 543 | |
| chr17:2,023,483–2,024,229 | 1.5 kb | Proximal (<10kb) Multiome | 281 | |
| chr17:2,024,335–2,024,664 | 669 bp | At TSS | 163 | |
| chr17:2,024,769–2,026,284 | 136 bp | At TSS Multiome | 459 | |
| chr17:2,029,741–2,030,885 | 5.5 kb | Proximal (<10kb) Multiome | 871 | |
| chr17:2,041,423–2,042,366 | 16.6 kb | Distal (>10kb) Multiome | 834 | |
| chr17:2,048,764–2,051,218 | 23.7 kb | Distal (>10kb) Multiome | 658 | |
| chr17:2,054,616–2,055,766 | 29.7 kb | Distal (>10kb) Multiome | 544 | |
| chr17:2,058,401–2,059,503 | 33.5 kb | Distal (>10kb) Multiome | 366 | |
| chr17:2,302,778–2,304,288 | 278.4 kb | Distal (>10kb) Multiome | 770 |
Genomic view of the RTN4RL1 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.