The protein encoded by this gene is a member of the RNase A superfamily though it has relatively weak ribonucleolytic activity. This protein is a potent mediator of new blood vessel formation and thus, in addition to the name RNase5, is commonly called angiogenin. This protein induces angiogenesis after binding to actin on the surface of endothelial cells. This protein also accumulates at the nucleolus where it stimulates ribosomal transcription. Under stress conditions this protein translocates to the cytosol where it hydrolyzes cellular tRNAs and influences protein synthesis. A signal peptide is cleaved from the precursor protein to produce a mature protein which contains a nuclear localization signal, a cell binding motif, and a catalytic domain. This protein has been shown to be both neurotrophic and neuroprotective and the mature protein has antimicrobial activity against some bacteria and fungi, including S. pneumoniae and C. albicans. Due to its effect on rRNA production and angiogenesis this gene plays important roles in cell growth and tumor progression. Mutations in this gene are associated with progression of amyotrophic lateral sclerosis (ALS). This gene and the neighboring RNase4 gene share promoters and 5' exons though each gene then splices to a distinct 3' exon containing the complete coding region of each gene. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2020]
Transcription factors with Perturb-seq knockdown data for ANG. 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 = ANG 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 ANG, 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 |
|---|---|---|---|---|
| chr14:20,412,688–20,413,758 | 271.3 kb | Distal (>10kb) Multiome | 865 | |
| chr14:20,454,384–20,455,825 | 229.5 kb | Distal (>10kb) Multiome | 1012 | |
| chr14:20,460,777–20,462,259 | 223.0 kb | Distal (>10kb) Multiome | 995 | |
| chr14:20,468,846–20,470,856 | 215.2 kb | Distal (>10kb) Multiome | 950 | |
| chr14:20,494,584–20,495,486 | 189.6 kb | Distal (>10kb) Multiome | 201 | |
| chr14:20,609,147–20,610,547 | 74.5 kb | Distal (>10kb) Multiome | 852 | |
| chr14:20,612,915–20,614,464 | 70.9 kb | Distal (>10kb) Multiome | 1003 | |
| chr14:20,624,684–20,626,122 | 59.2 kb | Distal (>10kb) Multiome | 728 | |
| chr14:20,630,325–20,631,286 | 53.9 kb | Distal (>10kb) Multiome HiCAR | 507 | |
| chr14:20,631,700–20,633,862 | 51.4 kb | Distal (>10kb) Multiome HiCAR | 757 | |
| chr14:20,642,696–20,643,499 | 41.6 kb | Distal (>10kb) Multiome | 52 | |
| chr14:20,644,459–20,645,301 | 39.8 kb | Distal (>10kb) Multiome | 52 | |
| chr14:20,652,905–20,654,391 | 31.3 kb | Distal (>10kb) Multiome HiCAR | 320 | |
| chr14:20,657,425–20,658,132 | 26.8 kb | Distal (>10kb) Multiome HiCAR | 320 | |
| chr14:20,662,835–20,663,940 | 21.3 kb | Distal (>10kb) Multiome | 587 | |
| chr14:20,681,216–20,685,294 | 197 bp | At TSS Multiome | 1181 | |
| chr14:20,691,096–20,691,328 | 6.5 kb | Proximal (<10kb) | 285 | |
| chr14:20,705,982–20,707,066 | 21.8 kb | Distal (>10kb) Multiome | 110 | |
| chr14:20,732,350–20,732,945 | 48.0 kb | Distal (>10kb) Multiome | 51 | |
| chr14:20,815,630–20,816,752 | 131.5 kb | Distal (>10kb) Multiome | 75 | |
| chr14:20,820,324–20,820,826 | 136.0 kb | Distal (>10kb) Multiome | 204 | |
| chr14:20,970,757–20,971,991 | 286.8 kb | Distal (>10kb) Multiome | 745 |
Genomic view of the ANG 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.