Non-syndromic familial congenital anorectal malformations
Gene: WDPCPEnsemblGeneIds (GRCh38): ENSG00000143951
EnsemblGeneIds (GRCh37): ENSG00000143951
OMIM: 613580, Gene2Phenotype
WDPCP is in 21 panels
1 review
Eleanor Williams (Genomics England Curator)
Comment on phenotypes: Phenotype added from publication PMID:23936318Created: 14 Aug 2018, 4:08 p.m.
Gene added to the panel a listed as a candidate gene in Wong et al 2013 (PMID:23936318) who performed a gene network analysis using genes identified in CNVs in an earlier paper (Wong et al 2013 (PMID: 23108157)).Created: 4 Aug 2018, 9:48 p.m.
Details
- Sources
-
- Literature
- Phenotypes
-
- anorectal malformation
- OMIM
- 613580
- Clinvar variants
- Variants in WDPCP
- Penetrance
- None
- Publications
- Panels with this gene
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- Ductal plate malformation
- Skeletal ciliopathies
- Cystic kidney disease
- Bardet Biedl syndrome
- Structural eye disease
- Skeletal dysplasia
- Fetal anomalies
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
- Rare multisystem ciliopathy disorders
- Intellectual disability
- Childhood onset dystonia, chorea or related movement disorder
- Renal ciliopathies
- Non-syndromic familial congenital anorectal malformations
- Limb disorders
- Ophthalmological ciliopathies
- Unexplained kidney failure in young people
- Retinal disorders
- DDG2P
- Severe early-onset obesity
History Filter Activity
Panel promoted to version 1.0
Eleanor Williams (Genomics England Curator)Eleanor Williams: Gene added to the panel a list
Set Phenotypes
Eleanor Williams (Genomics England Curator)Phenotypes for gene: WDPCP were set to anorectal malformation
Added New Source
Eleanor Williams (Genomics England Curator)WDPCP was added to Non-syndromic familial congenital anorectal malformations panel. Sources: Literature
Created
Eleanor Williams (Genomics England Curator)WDPCP was created by Eleanor Williams