Property Summary

NCBI Gene PubMed Count 21
PubMed Score 21.20
PubTator Score 19.39

Knowledge Summary


No data available


  Differential Expression (4)

Disease log2 FC p
psoriasis -1.500 1.2e-04
osteosarcoma -2.107 1.1e-09
non primary Sjogren syndrome sicca 1.100 2.3e-02
subependymal giant cell astrocytoma 1.291 1.9e-02

Gene RIF (4)

25636090 abnormal expression of PEX10 gene resulting from copy number variations of 1p36 region may be associated with the epilepsy phenotype
20695019 child and an adult of normal intelligence with progressive ataxia, axonal motor neuropathy, decreased vibration sense and cerebellar atrophy; 2 mutations in PEX10 found in child, c.992G>A and c.764_765insA, and in the adult, c.2T>C and c.790C>T
19105186 the relative fraction of disease-causing alleles that occur in the coding and splice junction sequences of PEX10 gene.
14713216 Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.

AA Sequence


Text Mined References (19)

PMID Year Title
25636090 2015 [Abnormal expression of PEX10 gene may be related to epilepsy associated with 1p36 copy number variations].
22197933 2011 A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
21525035 2011 PEX14 is required for microtubule-based peroxisome motility in human cells.
20695019 2010 Mutations in PEX10 are a cause of autosomal recessive ataxia.
19105186 2009 Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
16710414 2006 The DNA sequence and biological annotation of human chromosome 1.
16344560 2006 Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.
15489334 2004 The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
14713216 2003 Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.
14702039 2004 Complete sequencing and characterization of 21,243 full-length human cDNAs.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
11390669 2001 Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences.
10862081 2000 Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients.
10837480 2000 Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p.
10704444 2000 PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis.
10562279 1999 PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import.
9922452 1999 Peroxisome synthesis in the absence of preexisting peroxisomes.
9700193 1998 Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
9683594 1998 Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.