FBXW11 - Gene browser | 3billion

FBXW11

FBXW11

F-box and WD repeat domain containing 11

HCNC Approved Symbol: FBXW11 (HGNC:13607)
Genomic Coordinates: 5:171,861,549 - 172,006,638 (5q35.1)
Synonyms: KIAA0696, Fbw1b, BTRCP2, BTRC2, Hos, Fbw11, FBXW1B
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 FBXW11 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

Hypoplasia of corpus callosum: 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

FBXW11 - Gene browser | 3billion