This Panel is marked as Deleted
Polydactyly Victorian Clinical Genetics Services
Gene: WDR19
WDR19 (WD repeat domain 19)
EnsemblGeneIds (GRCh38): ENSG00000157796
EnsemblGeneIds (GRCh37): ENSG00000157796
OMIM: 608151, Gene2Phenotype
WDR19 is in 20 panels
EnsemblGeneIds (GRCh38): ENSG00000157796
EnsemblGeneIds (GRCh37): ENSG00000157796
OMIM: 608151, Gene2Phenotype
WDR19 is in 20 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 608151
- Clinvar variants
- Variants in WDR19
- Penetrance
- None
- Panels with this gene
-
- Tubulointerstitial kidney disease
- Ophthalmological ciliopathies
- Retinal disorders
- DDG2P
- Ectodermal dysplasia
- Limb disorders
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Intellectual disability
- Fetal anomalies
- Unexplained kidney failure in young people
- Skeletal dysplasia
- Renal ciliopathies
- Rare multisystem ciliopathy disorders
- Cystic kidney disease
- Ectodermal dysplasia without a known gene mutation
- Childhood onset dystonia, chorea or related movement disorder
- Clefting
- Thoracic dystrophies
- Primary ciliary disorders
- Skeletal ciliopathies
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)WDR19 was added to Polydactyly Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)WDR19 was created by Sarah Leigh