×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
Biomarker
disease
GENOMICS_ENGLAND
Identification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case report.
28784167
2017
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
Biomarker
disease
GENOMICS_ENGLAND
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
27604308
2016
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
GeneticVariation
disease
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159
2015
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
GeneticVariation
disease
CLINVAR
High prevalence of primary adrenal insufficiency in Zellweger spectrum disorders.
25179809
2014
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder.
21031596
2011
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
GeneticVariation
disease
CLINVAR
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder.
21031596
2011
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
Biomarker
disease
GENOMICS_ENGLAND
Mutations in PEX10 are a cause of autosomal recessive ataxia.
20695019
2010
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Mutations in PEX10 are a cause of autosomal recessive ataxia.
20695019
2010
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Rational diagnostic strategy for Zellweger syndrome spectrum patients.
19142205
2009
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Zellweger syndrome resulting from maternal isodisomy of chromosome 1.
17702006
2007
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.
17041890
2006
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.
15542397
2004
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.
12794690
2003
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients.
10862081
2000
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
GeneticVariation
disease
CLINVAR
Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients.
10862081
2000
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
GeneticVariation
disease
CLINVAR
Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.
9683594
1998
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
CausalMutation
disease
CLINVAR
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
9700193
1998
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
GeneticVariation
disease
CLINVAR
Formation of the peroxisome lumen is abolished by loss of Pichia pastoris Pas7p, a zinc-binding integral membrane protein of the peroxisome.
7565793
1995
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
5192
Gene Symbol:
PEX10
PEX10
0.600
Biomarker
disease
CTD_human