This Panel is marked as Deleted
Mitochondrial disorders Victorian Clinical Genetics Services
Gene: GARS
GARS (glycyl-tRNA synthetase)
EnsemblGeneIds (GRCh38): ENSG00000106105
EnsemblGeneIds (GRCh37): ENSG00000106105
OMIM: 600287, Gene2Phenotype
GARS is in 9 panels
EnsemblGeneIds (GRCh38): ENSG00000106105
EnsemblGeneIds (GRCh37): ENSG00000106105
OMIM: 600287, Gene2Phenotype
GARS is in 9 panels
1 review
Louise Daugherty (Genomics England Curator)
Added new-gene-name tag, new approved HGNC gene symbol for GARS is GARS1Created: 6 Sep 2019, 1:49 p.m. | Last Modified: 6 Sep 2019, 1:49 p.m.
Panel Version: 0.4
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- Tags
- OMIM
- 600287
- Clinvar variants
- Variants in GARS
- Penetrance
- None
- Panels with this gene
-
- Mitochondrial disorders
- Undiagnosed metabolic disorders
- Paediatric motor neuronopathies
- Hereditary neuropathy or pain disorder
- Childhood onset dystonia, chorea or related movement disorder
- Possible mitochondrial disorder - nuclear genes
- Likely inborn error of metabolism
- Hereditary neuropathy
- Arthrogryposis
History Filter Activity
6 Sep 2019, Gel status: 3
Added Tag
Louise Daugherty (Genomics England Curator)Tag new-gene-name tag was added to gene: GARS.
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)GARS 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)GARS was created by Sarah Leigh