Unexplained kidney failure in young people
Gene: SDCCAG8EnsemblGeneIds (GRCh38): ENSG00000054282
EnsemblGeneIds (GRCh37): ENSG00000054282
OMIM: 613524, Gene2Phenotype
SDCCAG8 is in 20 panels
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Details
- Sources
-
- Expert Review Red
- Expert
- Phenotypes
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- Ciliopathy genes associated with cystic kidney disease
- OMIM
- 613524
- Clinvar variants
- Variants in SDCCAG8
- Penetrance
- Complete
- Panels with this gene
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- Ophthalmological ciliopathies
- Severe early-onset obesity
- DDG2P
- Childhood onset dystonia, chorea or related movement disorder
- Fetal anomalies
- Limb disorders
- Intellectual disability
- Unexplained kidney failure in young people
- Ductal plate malformation
- Bardet Biedl syndrome
- Retinal disorders
- Renal ciliopathies
- Rare multisystem ciliopathy disorders
- Cystic kidney disease
- Skeletal dysplasia
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
- Structural eye disease
- Skeletal ciliopathies
History Filter Activity
panel promoted to version 1
Sarah Leigh (Genomics England Curator)Promoted to version 1 17th August 2016
Created
Sarah Leigh (Genomics England Curator)SDCCAG8 was created by sleigh
Added New Source
Sarah Leigh (Genomics England Curator)SDCCAG8 was added to Unexplained kidney failure in young peoplepanel. Sources: Expert,Expert Review Red