Cataract
Gene: NDPEnsemblGeneIds (GRCh38): ENSG00000124479
EnsemblGeneIds (GRCh37): ENSG00000124479
OMIM: 300658, Gene2Phenotype
NDP is in 12 panels
1 review
Ain Roesley (Victorian Clinical Genetics Services)
Classified as "definitive" for Norrie Disease by ClinGen working group (https://search.clinicalgenome.org/kb/gene-validity/9611)
Progressive cataract is a feature of Norrie Disease (Genereviews, OMIM)Created: 8 Jul 2020, 5:41 a.m. | Last Modified: 8 Jul 2020, 6:30 a.m.
Panel Version: 0.191
Mode of inheritance
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Norrie disease (MIM# 310600)
Details
- Mode of Inheritance
- X-LINKED: hemizygous mutation in males, biallelic mutations in females
- Sources
-
- Expert Review Green
- Victorian Clinical Genetics Services
- Phenotypes
-
- Norrie disease (MIM# 310600)
- OMIM
- 300658
- Clinvar variants
- Variants in NDP
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: ndp has been classified as Green List (High Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: NDP were changed from to Norrie disease (MIM# 310600)
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: NDP was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: NDP was added gene: NDP was added to Cataract_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: NDP was set to Unknown