FOXR2 gene homepage

General information
Gene symbol FOXR2
Gene name forkhead box R2
Chromosome X
Chromosomal band p11
Imprinted Unknown
Genomic reference NG_021325.1
Transcript reference NM_198451.3
Associated with diseases -
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 7
Unique public DNA variants reported 6
Individuals with public variants 2
Hidden variants 0
Notes This gene sequence variant database has been initiated based on the data reported by Tarpey et al. (2009) A systematic, large-scale resequencing screen of the X-chromosome coding exons in mental retardation. Nat.Genet. 41: 535-543. Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created November 10, 2009
Date last updated October 24, 2015
Version FOXR2:151024

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
HGNC 30469
Entrez Gene 139628
PubMed articles FOXR2
OMIM - Gene 300949
HGMD FOXR2
GeneCards FOXR2
GeneTests FOXR2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000327 X forkhead box R2 NM_198451.3 NP_940853.1 7


Copyright & disclaimer
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