View 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
Associated with diseases lymphedema-distichiasis syndrome syndrome
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Michel van Geel
Total number of public variants reported 96
Unique public DNA variants reported 77
Individuals with public variants 138
Hidden variants 9
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created April 29, 2010
Date last updated December 07, 2015
Version FOXC2:151207

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
External URL Orphanet
HGNC 3801
Entrez Gene 2303
PubMed articles FOXC2
OMIM - Gene 602402
OMIM - Diseases lymphedema-distichiasis syndrome syndrome
GeneCards FOXC2
GeneTests FOXC2

Active transcripts




NCBI ID     

NCBI Protein ID     

00008070 16 forkhead box C2 (MFH-1, mesenchyme forkhead 1) NM_005251.2 NP_005242.1 96

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