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:

∙ 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 ENST00000425171 ENST00000433670 ENST00000447941 ENST00000453308 NP_036425


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
PF01462 LRRNT Leucine rich repeat N-terminal domain 22-51 Caenorhabditis elegans
PF03098 An_peroxidase Animal haem peroxidase 634-1188 CL0617 Peroxidase Caenorhabditis elegans
PF13855 LRR_8 Leucine rich repeat 52-112 CL0022 LRR Caenorhabditis elegans
PF13855 LRR_8 Leucine rich repeat 123-182 CL0022 LRR Caenorhabditis elegans
PF07679 I-set Immunoglobulin I-set domain 315-402 CL0011 Ig Caenorhabditis elegans
PF07679 I-set Immunoglobulin I-set domain 408-496 CL0011 Ig Caenorhabditis elegans

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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