The FOXE3 gene homepage

General information
Gene symbol FOXE3
Gene name forkhead box E3
Chromosome 1
Chromosomal band p32
Imprinted Unknown
Genomic reference NG_016192.1
Transcript reference NM_012186.2
Exon/intron information NM_012186.2 exon/intron table
Associated with diseases AAT11, AAT11, ASGD1, ASGD2, CTRCT34
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 126
Unique public DNA variants reported 65
Individuals with public variants 503
Hidden variants 6
Download all this gene's data Download all data
Date created May 03, 2013
Date last updated February 26, 2024
Version FOXE3:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_012186.2.
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 http://www.LOVD.nl/FOXE3
HGNC 3808
Entrez Gene 2301
PubMed articles FOXE3
OMIM - Gene 601094
OMIM - Diseases AAT11 ({Aortic aneurysm, familial thoracic 11, susceptibility to})
ASGD1 (dysgenesis, anterior segment, type 1 (ASGD1))
ASGD2 (dysgenesis, anterior segment, type 2 (ASGD-2, aphakia, congenital primary))
CTRCT34 (cataract, multiple types, type 34 (CTRCT-34))
HGMD FOXE3
GeneCards FOXE3
GeneTests FOXE3
Orphanet FOXE3


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008083 1 forkhead box E3 NM_012186.2 NP_036318.1 126


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