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PXDN
This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis.
Protein class
Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets
Predicted location
Intracellular, Secreted (different isoforms)
Single cell type specificity
Cell type enhanced (Skeletal myocytes, Endometrial stromal cells, Endothelial cells, Adipocytes, Hepatic stellate cells)
Immune cell specificity
Not detected in immune cells
Cell line specificity
Cell line enhanced (EFO-21)
Interaction
Homotrimer; disulfide-linked (PubMed:25708780, 25713063, 29982533, 31295557, 32543734). The homotrimer form is predominant (PubMed:25708780). Homooligomer; disulfide-linked (PubMed:22842973, 25708780, 25713063, 29982533, 31295557). Oligomerization occurs intracellularly before C-terminal proteolytic cleavage (PubMed:31295557). Interacts with PXDNL; this interaction inhibits the peroxidase activity of PXDN (PubMed:24253521).
Molecular function
Oxidoreductase, Peroxidase
More Types Infomation
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- Species Reactivity: Human
- Application: ELISA, WB
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For Research Use Only. Not For Clinical Use.