FBXW7 - Gene browser | 3billion

FBXW7

FBXW7

F-box and WD repeat domain containing 7

HCNC Approved Symbol: FBXW7 (HGNC:16712)
Genomic Coordinates: 4:152,320,544 - 152,536,092 (4q31.3)
Synonyms: AGO, FLJ11071, SEL-10, SEL10, FBW7, FBX30, CDC4, FBXW6
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the FBXW7 gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

01
Patient count

Global developmental delay: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Intellectual disability: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

FBXW7 - Gene browser | 3billion