IUGR and IGF abnormalities
Gene: TRIM37EnsemblGeneIds (GRCh38): ENSG00000108395
EnsemblGeneIds (GRCh37): ENSG00000108395
OMIM: 605073, Gene2Phenotype
TRIM37 is in 14 panels
2 reviews
Philip Murray (University of Manchester)
Peter Clayton (University of Manchester)
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Emory Genetics Laboratory
- Phenotypes
-
- Mulibery Nanism
- OMIM
- 605073
- Clinvar variants
- Variants in TRIM37
- Penetrance
- Complete
- Panels with this gene
-
- Fetal anomalies
- Childhood solid tumours cancer susceptibility
- Childhood solid tumours
- Clefting
- Monogenic short stature
- Childhood onset dystonia, chorea or related movement disorder
- Peroxisomal disorders
- Osteogenesis imperfecta
- Intellectual disability
- Likely inborn error of metabolism
- Embryonal tumour of possible germline origin
- IUGR and IGF abnormalities
- Undiagnosed metabolic disorders
- DDG2P
History Filter Activity
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Set Phenotypes
emma baple (Genomics England Curator)Phenotypes for TRIM37 were set to Mulibery Nanism
Set Mode of Inheritance
emma baple (Genomics England Curator)Mode of inheritance for TRIM37 was changed to BIALLELIC, autosomal or pseudoautosomal
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
GEL ()TRIM37 was added to IUGR and IGF abnormalitiespanel. Sources: Emory Genetics Laboratory