FOXG1 gene homepage

General information
Gene symbol FOXG1
Gene name forkhead box G1
Chromosome 14
Chromosomal band q11-q13
Imprinted Not imprinted
Genomic reference NG_009367.1
Transcript reference NM_005249.4
Exon/intron information NM_005249.4 exon/intron table
Associated with diseases ID, Rett syndrome, congenital variant
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 117
Unique public DNA variants reported 88
Individuals with public variants 78
Hidden variants 6
Download all this gene's data Download all data
Notes NOTE: the data displayed here derive from the RettBASE FOXG1 gene variant database and are shown only to link directly to their original source.
The establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nÂș 200754 - the GEN2PHEN project.
Date created October 31, 2012
Date last updated December 02, 2019
Version FOXG1:191202

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_005249.4.
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 RettBASE
HGNC 3811
Entrez Gene 2290
PubMed articles FOXG1
OMIM - Gene 164874
OMIM - Diseases Rett syndrome, congenital variant
GeneCards FOXG1
GeneTests FOXG1

Active transcripts




NCBI ID     

NCBI Protein ID     

00001723 14 forkhead box G1 NM_005249.4 NP_005240.3 117

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2012-2019. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.

NOTE: the data displayed here derive from the RettBASE FOXG1 gene variant database and are shown only to link directly to their original source.