Amyloidosis
Gene: LYZEnsemblGeneIds (GRCh38): ENSG00000090382
EnsemblGeneIds (GRCh37): ENSG00000090382
OMIM: 153450, Gene2Phenotype
LYZ is in 5 panels
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Amyloidosis, renal, MIM#105200
- OMIM
- 153450
- Clinvar variants
- Variants in LYZ
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: lyz has been classified as Green List (High Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: LYZ were changed from Amyloidosis, renal to Amyloidosis, renal, MIM#105200
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: lyz has been classified as Green List (High Evidence).
Removed Source, Added New Source, Set mode of inheritance, Set Phenotypes, Set publications
Chirag Patel (Genetic Health Queensland)Source KidGen_Amyloidosis v38.1.0 was removed from LYZ. Source Expert list was added to LYZ. Mode of inheritance for gene LYZ was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: LYZ were changed from to Amyloidosis, renal Publications for gene LYZ were changed from PubMed: 1808634; 8464497; 15745733, to PubMed: 1808634; 8464497; 15745733,
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: LYZ was added gene: LYZ was added to Amyloidosis_KidGen. Sources: KidGen_Amyloidosis v38.1.0 Mode of inheritance for gene: LYZ was set to Unknown