Renal ciliopathies
Gene: BBS9EnsemblGeneIds (GRCh38): ENSG00000122507
EnsemblGeneIds (GRCh37): ENSG00000122507
OMIM: 607968, Gene2Phenotype
BBS9 is in 21 panels
2 reviews
Beth Hoskins (Great Ormond Street Hospital)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Publications
Variants in this GENE are reported as part of current diagnostic practice
Ellen McDonagh (Genomics England Curator)
Comment on list classification: Gene is green on the Bardet-Biedl Syndrome panel (version 1.53).Created: 4 Aug 2016, 3:51 p.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Eligibility statement prior genetic testing
- Expert list
- Expert Review Green
- Phenotypes
-
- Bardet Biedl syndrome 9
- OMIM
- 607968
- Clinvar variants
- Variants in BBS9
- Penetrance
- None
- Publications
- Panels with this gene
-
- Ophthalmological ciliopathies
- Skeletal dysplasia
- Renal ciliopathies
- Skeletal ciliopathies
- Unexplained kidney failure in young people
- Ductal plate malformation
- Severe early-onset obesity
- Rare multisystem ciliopathy disorders
- Fetal anomalies
- Dystonia, chorea or related movement disorder, childhood onset
- Structural eye disease
- Intellectual disability
- Bardet Biedl syndrome
- DDG2P
- Glaucoma (developmental)
- Thoracic dystrophies
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Primary ciliary disorders
- Limb disorders
- Cystic kidney disease
- Retinal disorders
History Filter Activity
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Eleanor Williams (Genomics England Curator)gene: BBS9 was added gene: BBS9 was added to Renal ciliopathies. Sources: Expert Review Green,Expert list,Eligibility statement prior genetic testing Mode of inheritance for gene: BBS9 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: BBS9 were set to 16380913 Phenotypes for gene: BBS9 were set to Bardet Biedl syndrome 9