This Panel is marked as Deleted
Kidneyome_SuperPanel_KidGen_VCGS
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
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- KidGen_CilioNephronop v38.1.0
- OMIM
- 608151
- Clinvar variants
- Variants in WDR19
- Penetrance
- None
- Panels with this gene
-
- Fetal anomalies
- Skeletal ciliopathies
- Retinal disorders
- Clefting
- Ophthalmological ciliopathies
- Tubulointerstitial kidney disease
- Ectodermal dysplasia
- Cystic kidney disease
- Renal ciliopathies
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Intellectual disability
- Childhood onset dystonia, chorea or related movement disorder
- Unexplained kidney failure in young people
- DDG2P
- Rare multisystem ciliopathy disorders
- Ectodermal dysplasia without a known gene mutation
- Skeletal dysplasia
- Thoracic dystrophies
- Primary ciliary disorders
- Limb disorders
History Filter Activity
23 Dec 2019, Gel status: 3
Created, Added New Source, Set mode of inheritance
Ivone Leong (Genomics England Curator)gene: WDR19 was added gene: WDR19 was added to Kidneyome_SuperPanel_KidGen_VCGS. Sources: KidGen_CilioNephronop v38.1.0,Expert Review Green Mode of inheritance for gene: WDR19 was set to Unknown