Cystic kidney disease
Gene: WDPCPEnsemblGeneIds (GRCh38): ENSG00000143951
EnsemblGeneIds (GRCh37): ENSG00000143951
OMIM: 613580, Gene2Phenotype
WDPCP is in 21 panels
1 review
Miranda Durkie (Genetics)
Details
- Sources
-
- Expert Review Red
- Expert
- Phenotypes
-
- Ciliopathy genes associated with cystic kidney disease
- OMIM
- 613580
- Clinvar variants
- Variants in WDPCP
- Penetrance
- Complete
- Panels with this gene
-
- Skeletal ciliopathies
- Non-syndromic familial congenital anorectal malformations
- Ophthalmological ciliopathies
- Childhood onset dystonia, chorea or related movement disorder
- Intellectual disability
- Skeletal dysplasia
- Retinal disorders
- Structural eye disease
- Severe early-onset obesity
- Fetal anomalies
- Cystic kidney disease
- Bardet Biedl syndrome
- Unexplained kidney failure in young people
- Ductal plate malformation
- DDG2P
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
- Limb disorders
- Renal ciliopathies
- Rare multisystem ciliopathy disorders
History Filter Activity
Gene classified by Genomics England curator
Ellen Thomas (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)WDPCP was added to Cystic kidney diseasepanel. Sources: Expert