Wilms tumour with features suggestive of predisposition
Gene: TRIM28EnsemblGeneIds (GRCh38): ENSG00000130726
EnsemblGeneIds (GRCh37): ENSG00000130726
OMIM: 601742, Gene2Phenotype
TRIM28 is in 2 panels
2 reviews
Arina Puzriakova (Genomics England Curator)
Comment on phenotypes: OMIM phenotype accessed on 20-03-2026Created: 20 Mar 2026, 11:34 a.m. | Last Modified: 20 Mar 2026, 11:34 a.m.
Panel Version: 1.5
Eleanor Williams (Genomics England Curator)
This gene has been added to the panel on the recommendation of the NHS Genomic Medicine Service.Created: 8 Mar 2022, 2:29 p.m. | Last Modified: 8 Mar 2022, 2:29 p.m.
Panel Version: 0.2
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Phenotypes
-
- Wilms tumor 7, OMIM:621332
- OMIM
- 601742
- Clinvar variants
- Variants in TRIM28
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Arina Puzriakova (Genomics England Curator)Phenotypes for gene: TRIM28 were changed from Wilms tumor; Familial Wilms tumor to Wilms tumor 7, OMIM:621332
Removed Tag
Arina Puzriakova (Genomics England Curator)Tag gene-checked was removed from gene: TRIM28.
Added Tag
Eleanor Williams (Genomics England Curator)Tag gene-checked tag was added to gene: TRIM28.
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Eleanor Williams (Genomics England Curator)gene: TRIM28 was added gene: TRIM28 was added to Wilms tumour with features suggestive of predisposition. Sources: Expert Review Green Mode of inheritance for gene: TRIM28 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TRIM28 were set to 30885698; 29912901; 30694527 Phenotypes for gene: TRIM28 were set to Wilms tumor; Familial Wilms tumor