URAD
ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase | PRHOXNB

Predicted to enable 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase activity. Predicted to be involved in amide catabolic process; nucleobase-containing small molecule metabolic process; and urate catabolic process. Predicted to be active in peroxisome. [provided by Alliance of Genome Resources, Jul 2025]

Biological processes 5 terms
Expression (TPM)
URAD — as a Regulated Gene

TFs regulating URAD 0 TFs

Transcription factors with Perturb-seq knockdown data for URAD. 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 = URAD upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to URAD

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of URAD, 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
chr13:27,968,317–27,969,555 9.2 kb Proximal (<10kb) 369
chr13:27,978,000–27,978,930 at TSS At TSS 128
chr13:27,984,348–27,984,546 5.6 kb Proximal (<10kb) 133

Genome Browser

Genomic view of the URAD 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.

chr13:27,958,317 – 27,994,546
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq