PXDN (GeneID: 7837) | Homo sapiens
Description: peroxidasin [Source:HGNC Symbol;Acc:HGNC:14966]
Synonyms: VPO, D2S448E, ASGD7, PRG2, D2S448, XN, MG50, COPOA
Other ID(s): ENSG00000130508, HGNC:14966
Protein Accession Numbers: ENST00000447941, ENST00000252804.4, NP_036425, ENST00000433670, ENST00000252804, ENST00000453308, ENST00000425171
Statistics: ClinVar(118) COSMIC(1448) PTM(23)
ClinVar Pathogenicity of Variations help

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000252804 You are here now! ENST00000425171 ENST00000433670 ENST00000447941 ENST00000453308 NP_036425 You are here now!


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00093 VWC von Willebrand factor type C domain 1415-1470 CL0451 FnI-like Homo sapiens
PF03098 An_peroxidase Animal haem peroxidase 741-1289 CL0617 Peroxidase Homo sapiens
PF13855 LRR_8 Leucine rich repeat 86-146 CL0022 LRR Homo sapiens
PF13855 LRR_8 Leucine rich repeat 62-117 CL0022 LRR Homo sapiens
PF13855 LRR_8 Leucine rich repeat 139-194 CL0022 LRR Homo sapiens
PF07679 I-set Immunoglobulin I-set domain 433-519 CL0011 Ig Homo sapiens
PF07679 I-set Immunoglobulin I-set domain 525-611 CL0011 Ig Homo sapiens
PF07679 I-set Immunoglobulin I-set domain 342-429 CL0011 Ig Homo sapiens
PF07679 I-set Immunoglobulin I-set domain 246-334 CL0011 Ig Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Leukemia, Myelocytic, Acute Neoplasms ; 0.707 0.31
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.707 0.31
Acute Myeloid Leukemia, M1 Neoplasms ; 0.707 0.31
Cataract Eye Diseases ; 0.707 0.31
Anterior segment mesenchymal dysgenesis Eye Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.707 0.31
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.707 0.31
ANTERIOR SEGMENT DYSGENESIS 7 N/A 0.707 0.31
NO RESULT FOUND
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