This Panel is marked as Deleted
Leukodystrophy Victorian Clinical Genetics Services
Gene: HTRA1
HTRA1 (HtrA serine peptidase 1)
EnsemblGeneIds (GRCh38): ENSG00000166033
EnsemblGeneIds (GRCh37): ENSG00000166033
OMIM: 602194, Gene2Phenotype
HTRA1 is in 8 panels
EnsemblGeneIds (GRCh38): ENSG00000166033
EnsemblGeneIds (GRCh37): ENSG00000166033
OMIM: 602194, Gene2Phenotype
HTRA1 is in 8 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 602194
- Clinvar variants
- Variants in HTRA1
- Penetrance
- None
- Panels with this gene
-
- Retinal disorders
- Early onset dementia (encompassing fronto-temporal dementia and prion disease)
- Adult onset neurodegenerative disorder
- Inherited white matter disorders
- Familial cerebral small vessel disease
- White matter disorders and cerebral calcification - narrow panel
- Cerebral vascular malformations
- Adult onset leukodystrophy
History Filter Activity
21 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)HTRA1 was added to Leukodystrophy 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)HTRA1 was created by Sarah Leigh