This Panel is marked as Deleted
Polydactyly Victorian Clinical Genetics Services
Gene: TRIM32
TRIM32 (tripartite motif containing 32)
EnsemblGeneIds (GRCh38): ENSG00000119401
EnsemblGeneIds (GRCh37): ENSG00000119401
OMIM: 602290, Gene2Phenotype
TRIM32 is in 20 panels
EnsemblGeneIds (GRCh38): ENSG00000119401
EnsemblGeneIds (GRCh37): ENSG00000119401
OMIM: 602290, Gene2Phenotype
TRIM32 is in 20 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 602290
- Clinvar variants
- Variants in TRIM32
- Penetrance
- None
- Panels with this gene
-
- Ophthalmological ciliopathies
- Severe early-onset obesity
- Retinal disorders
- Arthrogryposis
- DDG2P
- Structural eye disease
- Limb disorders
- Intellectual disability
- Fetal anomalies
- Unexplained kidney failure in young people
- Bardet Biedl syndrome
- Skeletal dysplasia
- Renal ciliopathies
- Rare multisystem ciliopathy disorders
- Cystic kidney disease
- Glaucoma (developmental)
- Thoracic dystrophies
- Primary ciliary disorders
- Skeletal ciliopathies
- Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)TRIM32 was added to Polydactyly Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)TRIM32 was created by Sarah Leigh