FOXL2 @ medgen.ugent.be/LOVD/

When using or discussing LOVD please refer to:
Fokkema IFAC, Den Dunnen JT and Taschner PEM (2005). LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-Box" approach.
Hum Mutat. 2005 Aug;26(2):63-8.

FOXL2 @ medgen.ugent.be/LOVD/

General information
Gene name:	forkhead box L2
Gene symbol:	FOXL2
Chromosome Location:	3q23
Database location:	medgen.ugent.be/LOVD/
Curators:	Diane Beysen and Elfride De Baere
Date of creation:	November 25, 2005
*Last update*:	*January 25, 2011*
*Version*:	*FOXL2 110125*
*Add allelic variant*:	Submit an allelic variant
First time submitters:	Register here
Genomic reference sequence:	FOXL2 reference sequence for describing allelic variants
*Total number of allelic variants*:	271
*Number of unique allelic variants*:	144
*NOTE*:	This database is dedicated to all BPES patients.

Allelic variant tables
Complete allelic variant table:	Listing of all allelic variants in the FOXL2 database
Summary tables:	Summary of all allelic variants in the FOXL2 database, sorted by type of variant (with graphical displays and statistics)
Polymorphism table:	Listing of all FOXL2 variants reported to have no noticeable phenotypic effect

Search the database
By type of variant:	View allelic variant table after selecting one type of variant
Simple search:	Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search:	Query the database by selecting a combination of variables

Links to other resources:
Homepage	http://medgen.ugent.be/CMGG
Other link	Winged Helix Proteins
Other link	FOXL2 Orthologues
Other link	BPES in Genetests
Entrez Gene (LocusLink)	668
OMIM - gene	605597
OMIM - disease	110100 (BPES)
HGMD	129025
GDB	129025