Species Human Entrez 7837 | Human Mouse Ensembl ENSG00000130508 | |
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Aliases PXDN, COPOA, D2S448, D2S448E, MG50, PRG2, PXN, VPO, peroxidasin External IDs MGI: 1916925 HomoloGene: 33907 GeneCards: PXDN | ||
Peroxidasin homolog is a protein that in humans is encoded by the PXDN gene.
Clinical significance
Mutations in PXDN are associated with microphthalmia .
References
PXDN Wikipedia(Text) CC BY-SA