Unexplained kidney failure in young people
Gene: ARL6
ARL6 (ADP ribosylation factor like GTPase 6)
EnsemblGeneIds (GRCh38): ENSG00000113966
EnsemblGeneIds (GRCh37): ENSG00000113966
OMIM: 608845, Gene2Phenotype
ARL6 is in 20 panels
EnsemblGeneIds (GRCh38): ENSG00000113966
EnsemblGeneIds (GRCh37): ENSG00000113966
OMIM: 608845, Gene2Phenotype
ARL6 is in 20 panels
0 reviews
Details
- Sources
-
- Expert
- Expert Review Red
- Phenotypes
-
- 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
- Limb disorders
- Dystonia, chorea or related movement disorder, childhood onset
- Structural eye disease
- Unexplained kidney failure in young people
- Ductal plate malformation
- Skeletal dysplasia
- Severe early-onset obesity
- Rare multisystem ciliopathy disorders
- Bardet Biedl syndrome
- DDG2P
- Intellectual disability
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
- Cystic kidney disease
- Retinal disorders
- Fetal anomalies
- Skeletal ciliopathies
History Filter Activity
17 Aug 2016, Gel status: 1
panel promoted to version 1
Sarah Leigh (Genomics England Curator)Promoted to version 1 17th August 2016
16 May 2016, Gel status: 0
Created
Sarah Leigh (Genomics England Curator)ARL6 was created by sleigh
16 May 2016, Gel status: 1
Added New Source
Sarah Leigh (Genomics England Curator)ARL6 was added to Unexplained kidney failure in young peoplepanel. Sources: Expert,Expert Review Red