Cytopenias and congenital anaemias
Gene: FBXW7EnsemblGeneIds (GRCh38): ENSG00000109670
EnsemblGeneIds (GRCh37): ENSG00000109670
OMIM: 606278, Gene2Phenotype
FBXW7 is in 4 panels
2 reviews
Ellen McDonagh (Genomics England Curator)
Comment on list classification: The COSMIC census gene list indicates that variants are somatic for colorectal, endometrial and T-cell acute lymphoblastic leukaemia. Information on OMIM indicates that somatic variants have been identified in cancer cell lines. Not associated with a disorder in OMIM or Gene2Phenotype. Literature search confirmed this is a somatic gene.Created: 7 Mar 2017, 3:18 p.m.
BRIDGE consortium (NIHRBR-RD)
Mode of inheritance
Unknown
Phenotypes
Acute lymphoblastic leukemia (ALL)
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- BRIDGE consortium (NIHRBR-RD)
- Phenotypes
-
- Acute lymphoblastic leukemia (ALL)
- Tags
- OMIM
- 606278
- Clinvar variants
- Variants in FBXW7
- Penetrance
- Complete
- Mode of Pathogenicity
- Other - please provide details in the comments
- Panels with this gene
History Filter Activity
panel promoted to version 1
Arianna Tucci (Genomics England Curator)Promoted to V1 on 11 March 2017, after internal review and discussion with the clinical team.
Set mode of pathogenicity
Ellen McDonagh (Genomics England Curator)Mode of pathogenicity for FBXW7 was changed to Other - please provide details in the comments
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Created
Louise Daugherty (Genomics England Curator)FBXW7 was created by LouiseD
Added New Source
Louise Daugherty (Genomics England Curator)FBXW7 was added to Cytopaenias and congenital anaemiaspanel. Sources: BRIDGE consortium (NIHRBR-RD)