The FOXC2 gene homepage

General information
Gene symbol FOXC2
Gene name forkhead box C2 (MFH-1, mesenchyme forkhead 1)
Chromosome 16
Chromosomal band q24.1
Imprinted Unknown
Genomic reference NG_012025.1
Transcript reference NM_005251.2
Exon/intron information NM_005251.2 exon/intron table
Associated with diseases LPHDST
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (3) Michel van Geel, Élodie Fastré, and Pascal Brouillard
Total number of public variants reported 127
Unique public DNA variants reported 103
Individuals with public variants 146
Hidden variants 10
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 April 10, 2010
Date last updated May 09, 2022
Version FOXC2:220509

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_005251.2.
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 https://www.LOVD.nl/FOXC2
HGNC 3801
Entrez Gene 2303
PubMed articles FOXC2
OMIM - Gene 602402
OMIM - Diseases LPHDST (Lymphedema-distichiasis syndrome)
HGMD FOXC2
GeneCards FOXC2
GeneTests FOXC2
Orphanet FOXC2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008070 16 forkhead box C2 (MFH-1, mesenchyme forkhead 1) NM_005251.2 NP_005242.1 127


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