The FBXW7 gene homepage

General information
Gene symbol FBXW7
Gene name F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
Chromosome 4
Chromosomal band q31.23
Imprinted Unknown
Genomic reference NC_000004.11
Transcript reference NM_001349798.2
Associated with diseases DEDHIL
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 62
Unique public DNA variants reported 47
Individuals with public variants 36
Hidden variants 3
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated March 27, 2026
Version FBXW7:260327

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/FBXW7
HGNC HGNC:16712
Entrez Gene 55294
PubMed articles FBXW7
OMIM - Gene 606278
OMIM - Diseases DEDHIL (developmental delay, hypotonia, and impaired language)
HGMD FBXW7
GeneCards FBXW7
NIH Genetic Testing Registry FBXW7
Orphanet FBXW7


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00025830 4 transcript variant 5 NM_001349798.2 NP_001336727.1 62


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