Unexplained kidney failure in young people
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
-
- Expert Review Red
- Expert
- Phenotypes
-
- Ciliopathy genes associated with cystic kidney disease
- OMIM
- 608151
- Clinvar variants
- Variants in WDR19
- Penetrance
- Complete
- Panels with this gene
-
- Limb disorders
- Ophthalmological ciliopathies
- Childhood onset dystonia, chorea or related movement disorder
- Skeletal dysplasia
- Intellectual disability
- Unexplained kidney failure in young people
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Renal ciliopathies
- DDG2P
- Tubulointerstitial kidney disease
- Rare multisystem ciliopathy disorders
- Cystic kidney disease
- Ectodermal dysplasia without a known gene mutation
- Retinal disorders
- Ectodermal dysplasia
- Thoracic dystrophies
- Primary ciliary disorders
- Fetal anomalies
- Skeletal ciliopathies
- Clefting
History Filter Activity
17 Aug 2016, Gel status: 1
panel promoted to version 1
Sarah Leigh (Genomics England Curator)Promoted to version 1 17th August 2016
16 May 2016, Gel status: 0
Created
Sarah Leigh (Genomics England Curator)WDR19 was created by sleigh
16 May 2016, Gel status: 1
Added New Source
Sarah Leigh (Genomics England Curator)WDR19 was added to Unexplained kidney failure in young peoplepanel. Sources: Expert,Expert Review Red