Childhood solid tumours cancer susceptibility
Gene: TRIM37
TRIM37 (tripartite motif containing 37)
EnsemblGeneIds (GRCh38): ENSG00000108395
EnsemblGeneIds (GRCh37): ENSG00000108395
OMIM: 605073, Gene2Phenotype
TRIM37 is in 14 panels
EnsemblGeneIds (GRCh38): ENSG00000108395
EnsemblGeneIds (GRCh37): ENSG00000108395
OMIM: 605073, Gene2Phenotype
TRIM37 is in 14 panels
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Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Phenotypes
-
- Mulibrey nanism 253250
- OMIM
- 605073
- Clinvar variants
- Variants in TRIM37
- Penetrance
- None
- Panels with this gene
-
- IUGR and IGF abnormalities
- Clefting
- Childhood onset dystonia, chorea or related movement disorder
- DDG2P
- Likely inborn error of metabolism
- Monogenic short stature
- Fetal anomalies
- Childhood solid tumours cancer susceptibility
- Childhood solid tumours
- Undiagnosed metabolic disorders
- Peroxisomal disorders
- Osteogenesis imperfecta
- Intellectual disability
- Embryonal tumour of possible germline origin
History Filter Activity
26 Mar 2019, Gel status: 2
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: TRIM37 was added gene: TRIM37 was added to Childhood solid tumours pertinent cancer susceptibility. Sources: Expert Review Amber Mode of inheritance for gene: TRIM37 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TRIM37 were set to Mulibrey nanism 253250