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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- Skeletal ciliopathies
- Renal ciliopathies
- Ophthalmological ciliopathies
- Limb disorders
- Unexplained kidney failure in young people
- Ductal plate malformation
- Skeletal dysplasia
- Severe early-onset obesity
- Rare multisystem ciliopathy disorders
- Dystonia, chorea or related movement disorder, childhood onset
- Structural eye disease
- Bardet Biedl syndrome
- DDG2P
- Intellectual disability
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
- Cystic kidney disease
- Retinal disorders
- Fetal anomalies
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