Unexplained kidney failure in young people
Gene: ARL6EnsemblGeneIds (GRCh38): ENSG00000113966
EnsemblGeneIds (GRCh37): ENSG00000113966
OMIM: 608845, Gene2Phenotype
ARL6 is in 20 panels
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Details
- Sources
-
- Expert
- Expert Review Red
- Phenotypes
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- Ciliopathy genes associated with cystic kidney disease
- OMIM
- 608845
- Clinvar variants
- Variants in ARL6
- Penetrance
- Complete
- Panels with this gene
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- Renal ciliopathies
- Ophthalmological ciliopathies
- Unexplained kidney failure in young people
- Limb disorders
- DDG2P
- Intellectual disability
- Severe early-onset obesity
- Retinal disorders
- Ductal plate malformation
- Skeletal ciliopathies
- Cystic kidney disease
- Bardet Biedl syndrome
- Structural eye disease
- Fetal anomalies
- Glaucoma (developmental)
- Thoracic dystrophies
- Skeletal dysplasia
- Primary ciliary disorders
- Rare multisystem ciliopathy disorders
- Childhood onset dystonia, chorea or related movement disorder
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)ARL6 was created by sleigh
Added New Source
Sarah Leigh (Genomics England Curator)ARL6 was added to Unexplained kidney failure in young peoplepanel. Sources: Expert,Expert Review Red