Cystic kidney disease
Gene: BBS9EnsemblGeneIds (GRCh38): ENSG00000122507
EnsemblGeneIds (GRCh37): ENSG00000122507
OMIM: 607968, Gene2Phenotype
BBS9 is in 21 panels
2 reviews
Ellen Thomas (Genomics England Curator)
Comment on list classification: BBS gene - not including syndromic genes on this panel.Created: 10 May 2016, 10:08 a.m.
Miranda Durkie (Genetics)
No current test experience but this gene is on the list for an extended panel.
Created: 22 Oct 2015, 10:48 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome type 9
Publications
Details
- Sources
-
- Expert Review Red
- Expert
- Phenotypes
-
- Ciliopathy genes associated with cystic kidney disease
- OMIM
- 607968
- Clinvar variants
- Variants in BBS9
- Penetrance
- Complete
- Panels with this gene
-
- Rare multisystem ciliopathy disorders
- Cystic kidney disease
- Renal ciliopathies
- Ophthalmological ciliopathies
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Childhood onset dystonia, chorea or related movement disorder
- Skeletal ciliopathies
- Limb disorders
- Structural eye disease
- Skeletal dysplasia
- Severe early-onset obesity
- Retinal disorders
- Bardet Biedl syndrome
- Unexplained kidney failure in young people
- Intellectual disability
- Ductal plate malformation
- Fetal anomalies
- DDG2P
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
History Filter Activity
Gene classified by Genomics England curator
Ellen Thomas (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Gene classified by Genomics England curator
Ellen Thomas (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)BBS9 was added to Cystic kidney diseasepanel. Sources: Expert