PXDN

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Peroxidasin homolog is a protein that in humans is encoded by the PXDN gene.[5][6][7]

AliasesPXDN, COPOA, D2S448, D2S448E, MG50, PRG2, PXN, VPO, peroxidasin, ASGD7
End1,744,852 bp[1]
Quick facts Identifiers, Aliases ...
PXDN
Identifiers
AliasesPXDN, COPOA, D2S448, D2S448E, MG50, PRG2, PXN, VPO, peroxidasin, ASGD7
External IDsOMIM: 605158; MGI: 1916925; HomoloGene: 33907; GeneCards: PXDN; OMA:PXDN - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012293

NM_181395
NM_177804

RefSeq (protein)

NP_036425

NP_852060

Location (UCSC)Chr 2: 1.63 – 1.74 MbChr 12: 29.99 – 30.07 Mb
PubMed search[3][4]
Wikidata
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Peroxidasin requires ionic bromine as a co-factor, making bromine an essential element for human life.[8]

Clinical significance

Mutations in PXDN are associated with microphthalmia.[9]

References

Further reading

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