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Genomic imprinting

Gene: WT1

Red List (low evidence)

WT1 (Wilms tumor 1)
EnsemblGeneIds (GRCh38): ENSG00000184937
EnsemblGeneIds (GRCh37): ENSG00000184937
OMIM: 607102, Gene2Phenotype
WT1 is in 21 panels

1 review

Sarah Leigh (Genomics England Curator)

I don't know

WT1-Alt transcript (listed in table S1 in PMID 30794780) does not have a match in HGNC. Known as AWT1 (PMID 14681303) and is the previous name, the HGNC approved name is WT1, which includes this alternative transcript.
Created: 22 Dec 2020, 6:10 p.m. | Last Modified: 22 Dec 2020, 6:10 p.m.
Panel Version: 0.26

History Filter Activity

22 Dec 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications

Sarah Leigh (Genomics England Curator)

gene: WT1 was added gene: WT1 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: WT1 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: WT1 were set to 30794780; 14681303; http://igc.otago.ac.nz/home.html