PEX19
peroxisomal biogenesis factor 19 | D1S2223E, HK33, PMP1, PMPI, PXMP1, PXF

This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]

Biological processes 35 terms
Expression (TPM)
PEX19 — as a Regulated Gene

TFs regulating PEX19 0 TFs

Transcription factors with Perturb-seq knockdown data for PEX19. 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 = PEX19 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 PEX19

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of PEX19, 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
chr1:160,031,268–160,032,381 253.2 kb Distal (>10kb) Multiome 780
chr1:160,046,290–160,047,082 238.5 kb Distal (>10kb) Multiome 540
chr1:160,069,829–160,071,049 214.7 kb Distal (>10kb) Multiome 419
chr1:160,083,809–160,084,575 200.9 kb Distal (>10kb) Multiome 327
chr1:160,095,707–160,096,231 189.1 kb Distal (>10kb) Multiome 79
chr1:160,097,214–160,099,572 186.3 kb Distal (>10kb) Multiome 659
chr1:160,100,845–160,101,543 184.0 kb Distal (>10kb) Multiome HiCAR 530
chr1:160,169,049–160,170,141 115.4 kb Distal (>10kb) Multiome 330
chr1:160,192,913–160,193,769 91.9 kb Distal (>10kb) Multiome 551
chr1:160,204,860–160,206,035 79.7 kb Distal (>10kb) Multiome 637
chr1:160,261,515–160,263,143 22.7 kb Distal (>10kb) Multiome 992
chr1:160,284,609–160,285,332 18 bp At TSS Multiome 638
chr1:160,291,386–160,291,589 6.2 kb Proximal (<10kb) 189
chr1:160,342,945–160,343,700 58.2 kb Distal (>10kb) Multiome 868
chr1:160,399,764–160,401,441 115.3 kb Distal (>10kb) Multiome 590
chr1:160,539,925–160,540,644 255.1 kb Distal (>10kb) Multiome 479

Genome Browser

Genomic view of the PEX19 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.

chr1:160,021,268 – 160,550,644
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq