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Multiple Tumours

Gene: FOXO3

Red List (low evidence)
FOXO3 (forkhead box O3)
EnsemblGeneIds (GRCh38): ENSG00000118689
EnsemblGeneIds (GRCh37): ENSG00000118689
OMIM: 602681, Gene2Phenotype
FOXO3 is in 1 panel

1 review

Ellen McDonagh (Genomics England Curator)

Gene from the Peutz-Jeghers syndrome gene panel.
Created: 3 May 2017, 12:18 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Hamartomatous polyposis syndromes including Peutz-Jeghers and PTEN hamartoma tumor syndromes

Publications

Created: 3 May 2017, 12:18 p.m.

Panel version: 1.76

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Other
Phenotypes
  • Hamartomatous polyposis syndromes including Peutz-Jeghers and PTEN hamartoma tumor syndromes
OMIM
602681
Clinvar variants
Variants in FOXO3
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

3 May 2017, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

FOXO3 was created by ellenmcdonagh

3 May 2017, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

FOXO3 was added to Multiple Tumourspanel. Sources: Other