Ciliopathies
Gene: PKHD1EnsemblGeneIds (GRCh38): ENSG00000170927
EnsemblGeneIds (GRCh37): ENSG00000170927
OMIM: 606702, Gene2Phenotype
PKHD1 is in 13 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Included due to phenotypic overlap with nephronophthisis.Created: 5 Jul 2021, 10:43 p.m. | Last Modified: 5 Jul 2021, 10:43 p.m.
Panel Version: 0.408
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Polycystic kidney disease 4, with or without hepatic disease, MIM# 263200
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Victorian Clinical Genetics Services
- Phenotypes
-
- Polycystic kidney disease 4, with or without hepatic disease, MIM# 263200
- OMIM
- 606702
- Clinvar variants
- Variants in PKHD1
- Penetrance
- None
- Panels with this gene
-
- Polycystic liver disease
- Ciliopathies
- Mackenzie's Mission_Reproductive Carrier Screening
- Skeletal dysplasia
- Fetal anomalies
- Additional findings_Paediatric
- Prepair 1000+
- Cholestasis
- Renal Macrocystic Disease
- Mendeliome
- BabyScreen+ newborn screening
- Renal Ciliopathies and Nephronophthisis
- Prepair 500+
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: pkhd1 has been classified as Green List (High Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: PKHD1 were changed from to Polycystic kidney disease 4, with or without hepatic disease, MIM# 263200
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: PKHD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: PKHD1 was added gene: PKHD1 was added to Ciliopathies_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: PKHD1 was set to Unknown