Cataract
Gene: HPS1EnsemblGeneIds (GRCh38): ENSG00000107521
EnsemblGeneIds (GRCh37): ENSG00000107521
OMIM: 604982, Gene2Phenotype
HPS1 is in 16 panels
1 review
Lauren Akesson (Royal Melbourne Hospital)
Some individuals with Hermansky-Pudlak syndrome have cataract (PMID: 8719678 - 3/55, genetic aetiology not identified) and these patients may benefit from cataract surgery (PMID: 27058854, genetic linkage analysis performed to determine type of albinism). Systemic steroids are thought to contribute to the lens opacities seen in this condition (PMID: 8719678). Cataract is not mentioned in the Gene Reviews article for this condition. Other articles detailing the ophthalmic findings in this condition do not mention cataract or lens opacification.Created: 6 Apr 2020, 12:04 a.m. | Last Modified: 6 Apr 2020, 12:04 a.m.
Panel Version: 0.60
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hermansky-Pudlak syndrome 1 (203300)
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Victorian Clinical Genetics Services
- Phenotypes
-
- Hermansky-Pudlak syndrome 1 (203300)
- OMIM
- 604982
- Clinvar variants
- Variants in HPS1
- Penetrance
- None
- Publications
- Panels with this gene
-
- Mackenzie's Mission_Reproductive Carrier Screening
- Ocular and Oculocutaneous Albinism
- Prepair 1000+
- Pulmonary Fibrosis_Interstitial Lung Disease
- Inflammatory bowel disease
- BabyScreen+ newborn screening
- Vasculitis
- Lysosomal Storage Disorder
- Congenital nystagmus
- Bleeding and Platelet Disorders
- Transplant Co-Morbidity Superpanel
- Additional findings_Paediatric
- Mendeliome
- Cataract
- Prepair 500+
- Interstitial Lung Disease
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: hps1 has been classified as Amber List (Moderate Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: HPS1 were changed from to Hermansky-Pudlak syndrome 1 (203300)
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: HPS1 were set to
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: HPS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: hps1 has been classified as Amber List (Moderate Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: HPS1 was added gene: HPS1 was added to Cataract_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: HPS1 was set to Unknown