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