Identity
HGNC
LOCATION
2p25.3
LOCUSID
ALIAS
ASGD7,COPOA,D2S448,D2S448E,MG50,PRG2,PXN,VPO
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 7837
MIM: 605158
HGNC: 14966
Ensembl: ENSG00000130508
Variants:
dbSNP: 7837
ClinVar: 7837
TCGA: ENSG00000130508
COSMIC: PXDN
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37801286 | 2023 | The role of peroxidasin in solid cancer progression. | 2 |
| 37801286 | 2023 | The role of peroxidasin in solid cancer progression. | 2 |
| 35093588 | 2022 | Peroxidasin Deficiency Re-programs Macrophages Toward Pro-fibrolysis Function and Promotes Collagen Resolution in Liver. | 9 |
| 35317099 | 2022 | Differential DNA methylation analysis of SUMF2, ADAMTS5, and PXDN provides novel insights into colorectal cancer prognosis prediction in Taiwan. | 3 |
| 35093588 | 2022 | Peroxidasin Deficiency Re-programs Macrophages Toward Pro-fibrolysis Function and Promotes Collagen Resolution in Liver. | 9 |
| 35317099 | 2022 | Differential DNA methylation analysis of SUMF2, ADAMTS5, and PXDN provides novel insights into colorectal cancer prognosis prediction in Taiwan. | 3 |
| 32813143 | 2021 | Vascular peroxidase 1 is independently associated with worse kidney function in patients with peripheral artery disease. | 1 |
| 33903591 | 2021 | PXDN reduces autophagic flux in insulin-resistant cardiomyocytes via modulating FoxO1. | 5 |
| 33985410 | 2021 | Novel heterozygous variants in PXDN cause different anterior segment dysgenesis phenotypes in monozygotic twins. | 3 |
| 32813143 | 2021 | Vascular peroxidase 1 is independently associated with worse kidney function in patients with peripheral artery disease. | 1 |
| 33903591 | 2021 | PXDN reduces autophagic flux in insulin-resistant cardiomyocytes via modulating FoxO1. | 5 |
| 33985410 | 2021 | Novel heterozygous variants in PXDN cause different anterior segment dysgenesis phenotypes in monozygotic twins. | 3 |
| 31295557 | 2020 | Monomeric and homotrimeric solution structures of truncated human peroxidasin 1 variants. | 5 |
| 31953133 | 2020 | Reaction of human peroxidasin 1 compound I and compound II with one-electron donors. | 7 |
| 32015378 | 2020 | Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis. | 3 |
Citation
Dessen P
PXDN (peroxidasin)
Atlas Genet Cytogenet Oncol Haematol. 2003-02-01
Online version: http://atlasgeneticsoncology.org/gene/40257/pxdn
