This Panel is marked as Deleted
Arthrogryposis Victorian Clinical Genetics Services
Gene: DPM2
DPM2 (dolichyl-phosphate mannosyltransferase subunit 2, regulatory)
EnsemblGeneIds (GRCh38): ENSG00000136908
EnsemblGeneIds (GRCh37): ENSG00000136908
OMIM: 603564, Gene2Phenotype
DPM2 is in 10 panels
EnsemblGeneIds (GRCh38): ENSG00000136908
EnsemblGeneIds (GRCh37): ENSG00000136908
OMIM: 603564, Gene2Phenotype
DPM2 is in 10 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 603564
- Clinvar variants
- Variants in DPM2
- Penetrance
- None
- Panels with this gene
-
- Congenital disorders of glycosylation
- Likely inborn error of metabolism
- Childhood onset dystonia, chorea or related movement disorder
- Undiagnosed metabolic disorders
- Intellectual disability
- Fetal anomalies
- Early onset or syndromic epilepsy
- Skeletal dysplasia
- Arthrogryposis
- Congenital muscular dystrophy
History Filter Activity
21 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)DPM2 was added to Arthrogryposis Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
21 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)DPM2 was created by Sarah Leigh