Joubert syndrome
Gene: TMEM67EnsemblGeneIds (GRCh38): ENSG00000164953
EnsemblGeneIds (GRCh37): ENSG00000164953
OMIM: 609884, Gene2Phenotype
TMEM67 is in 24 panels
2 reviews
Penny Clouston (Oxford)
Positives within our diagnostic patient cohort. Evidence in literature.Created: 15 Mar 2016, 10:37 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Variants in this GENE are reported as part of current diagnostic practice
Ellen McDonagh (Genomics England Curator)
Relevant phenotype and mode of inheritance was sourced from OMIM.Created: 8 Jan 2016, 11:36 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Other
- Eligibility statement prior genetic testing
- Phenotypes
-
- Joubert syndrome 6
- OMIM
- 609884
- Clinvar variants
- Variants in TMEM67
- Penetrance
- Complete
- Panels with this gene
-
- Ophthalmological ciliopathies
- Neurological ciliopathies
- DDG2P
- Childhood onset dystonia, chorea or related movement disorder
- Fetal anomalies
- Tubulointerstitial kidney disease
- Ocular coloboma
- Cholestasis
- Limb disorders
- Intellectual disability
- Familial Neural Tube Defects
- Unexplained kidney failure in young people
- Ductal plate malformation
- Bardet Biedl syndrome
- Retinal disorders
- Renal ciliopathies
- Rare multisystem ciliopathy disorders
- Cystic kidney disease
- Skeletal dysplasia
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
- Polycystic liver disease
- Structural eye disease
History Filter Activity
Set Phenotypes
Ellen McDonagh (Genomics England Curator)Phenotypes for gene TMEM67 were set to Joubert syndrome 6
Upload gene information
Ellen McDonagh (Genomics England Curator)TMEM67 was added to Joubert syndromepanel. Sources: Other
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Model of inheritance for gene TMEM67 was set to BIALLELIC, autosomal or pseudoautosomal
Created
Ellen McDonagh (Genomics England Curator)TMEM67 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)TMEM67 was added to Joubert syndromepanel. Sources: Eligibility statement prior genetic testing