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