Malformations of cortical development
Gene: PEX10EnsemblGeneIds (GRCh38): ENSG00000157911
EnsemblGeneIds (GRCh37): ENSG00000157911
OMIM: 602859, Gene2Phenotype
PEX10 is in 20 panels
1 review
Helen Brittain (Genomics England Curator)
personal communication with Clinical Genetics team in North Thames GMC noting the association between Zellweger syndrome and cortical malformations inc band heterotopiaCreated: 23 Apr 2018, 11:42 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Literature
- Expert Review Green
- Phenotypes
-
- Disorders of peroxisome biogenesis
- Peroxisome biogenesis disorder 6A (Zellweger), 614870
- Peroxisome biogenesis disorder 6B, 614871
- OMIM
- 602859
- Clinvar variants
- Variants in PEX10
- Penetrance
- None
- Publications
- Panels with this gene
-
- Peroxisomal disorders
- Hereditary neuropathy or pain disorder
- Likely inborn error of metabolism
- Undiagnosed metabolic disorders
- Intellectual disability
- Inherited white matter disorders
- Fetal hydrops
- Adult onset leukodystrophy
- Structural eye disease
- Fetal anomalies
- Childhood onset dystonia, chorea or related movement disorder
- Ductal plate malformation
- DDG2P
- Bilateral congenital or childhood onset cataracts
- Neonatal cholestasis
- White matter disorders and cerebral calcification - narrow panel
- Hereditary neuropathy
- Arthrogryposis
- Malformations of cortical development
- Early onset or syndromic epilepsy
History Filter Activity
Set Phenotypes
Louise Daugherty (Genomics England Curator)Phenotypes for PEX10 were set to Disorders of peroxisome biogenesis; Peroxisome biogenesis disorder 6A (Zellweger), 614870; Peroxisome biogenesis disorder 6B, 614871
Added New Source
Louise Daugherty (Genomics England Curator)PEX10 was added to Malformations of cortical development panel. Sources: Expert Review Green,Literature
Created
Louise Daugherty (Genomics England Curator)PEX10 was created by Louise Daugherty