This Panel is marked as Deleted
Mitochondrial disorders Victorian Clinical Genetics Services
Gene: HSPD1
HSPD1 (heat shock protein family D (Hsp60) member 1)
EnsemblGeneIds (GRCh38): ENSG00000144381
EnsemblGeneIds (GRCh37): ENSG00000144381
OMIM: 118190, Gene2Phenotype
HSPD1 is in 15 panels
EnsemblGeneIds (GRCh38): ENSG00000144381
EnsemblGeneIds (GRCh37): ENSG00000144381
OMIM: 118190, Gene2Phenotype
HSPD1 is in 15 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 118190
- Clinvar variants
- Variants in HSPD1
- Penetrance
- None
- Panels with this gene
-
- Adult onset neurodegenerative disorder
- Undiagnosed metabolic disorders
- Intellectual disability
- Inherited white matter disorders
- Childhood onset dystonia, chorea or related movement disorder
- Fetal anomalies
- Childhood onset hereditary spastic paraplegia
- Mitochondrial disorders
- Hereditary spastic paraplegia
- Early onset or syndromic epilepsy
- DDG2P
- Adult onset hereditary spastic paraplegia
- White matter disorders and cerebral calcification - narrow panel
- Possible mitochondrial disorder - nuclear genes
- Likely inborn error of metabolism
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)HSPD1 was added to Mitochondrial disorders Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)HSPD1 was created by Sarah Leigh