LOVD PEX10 homepage

General information
Gene name Peroxisome Biogenesis Factor 10
Gene symbol PEX10
Chromosome Location 1p36.32
Database location www.dbpex.org
Curator Nancy Braverman and Steven Steinberg
PubMed references View all (unique) PubMed references in the PEX10 database
Date of creation May 07, 2006
Last update October 15, 2010
Version PEX10 101015
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Reference sequence file coding DNA reference sequence for describing sequence variants
Total number of unique DNA variants reported 19
Total number of individuals with variant(s) 28
Total number of variants reported 50
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Graphical displays and utilities
Summary tables Summary of all sequence variants in the PEX10 database, sorted by type of variant (with graphical displays and statistics)

Sequence variant tables
Unique sequence variants Listing of all unique sequence variants in the PEX10 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the PEX10 database
Variants with no known pathogenicity Listing of all PEX10 variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)
Download table Download the full sequence variant table of the PEX10 database in tab-delimited text format.

Search the database
By type of variant View all sequence variants of a certain type
Simple search Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search Query the database by selecting a combination of variables
Based on patient origin View all variants based on your patient origin search terms

Links to other resources
Entrez Gene 5192
OMIM - Disease #1 (ZELLWEGER SYNDROME)
OMIM - Disease #2 (ADRENOLEUKODYSTROPHY AUTOSOMAL NEONATAL FORM)
OMIM - Disease #3 (REFSUM DISEASE INFANTILE FORM)
HGMD PEX10