This Panel is marked as Deleted
Immunological disorders_SuperPanel_PanelAppAustralia
Gene: LYST
LYST (lysosomal trafficking regulator)
EnsemblGeneIds (GRCh38): ENSG00000143669
EnsemblGeneIds (GRCh37): ENSG00000143669
OMIM: 606897, Gene2Phenotype
LYST is in 24 panels
EnsemblGeneIds (GRCh38): ENSG00000143669
EnsemblGeneIds (GRCh37): ENSG00000143669
OMIM: 606897, Gene2Phenotype
LYST is in 24 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- Melbourne Genomics Health Alliance Immunology Flagship
- OMIM
- 606897
- Clinvar variants
- Variants in LYST
- Penetrance
- None
- Panels with this gene
-
- Cytopenia - NOT Fanconi anaemia
- DDG2P
- Hereditary neuropathy or pain disorder
- COVID-19 research
- Infantile nystagmus
- Vici Syndrome and other autophagy disorders
- Fetal anomalies
- Early onset or syndromic epilepsy
- Childhood onset hereditary spastic paraplegia
- Albinism or congenital nystagmus
- Hereditary spastic paraplegia
- Adult onset neurodegenerative disorder
- Pigmentary skin disorders
- Bleeding and platelet disorders
- Rare genetic inflammatory skin disorders
- Intellectual disability
- Inherited bleeding disorders
- Parkinson Disease and Complex Parkinsonism
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Optic neuropathy
- Hereditary neuropathy
- Adult onset dystonia, chorea or related movement disorder
- Ocular and oculo-cutaneous albinism
- Adult onset hereditary spastic paraplegia
History Filter Activity
7 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: LYST was added gene: LYST was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Melbourne Genomics Health Alliance Immunology Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: LYST was set to Unknown