This Panel is marked as Deleted
Mitochondrial disorders Victorian Clinical Genetics Services
Gene: SERAC1
SERAC1 (serine active site containing 1)
EnsemblGeneIds (GRCh38): ENSG00000122335
EnsemblGeneIds (GRCh37): ENSG00000122335
OMIM: 614725, Gene2Phenotype
SERAC1 is in 16 panels
EnsemblGeneIds (GRCh38): ENSG00000122335
EnsemblGeneIds (GRCh37): ENSG00000122335
OMIM: 614725, Gene2Phenotype
SERAC1 is in 16 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 614725
- Clinvar variants
- Variants in SERAC1
- Penetrance
- None
- Panels with this gene
-
- Adult onset hereditary spastic paraplegia
- Structural basal ganglia disorders
- DDG2P
- Undiagnosed metabolic disorders
- Childhood onset dystonia, chorea or related movement disorder
- Mitochondrial disorders
- Hyperammonaemia
- Childhood onset hereditary spastic paraplegia
- Early onset dystonia
- Likely inborn error of metabolism
- Hereditary spastic paraplegia
- Adult onset neurodegenerative disorder
- Intellectual disability
- Possible mitochondrial disorder - nuclear genes
- Monogenic hearing loss
- Adult onset dystonia, chorea or related movement disorder
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)SERAC1 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)SERAC1 was created by Sarah Leigh