FOXP1 gene homepage

General information
Gene symbol FOXP1
Gene name forkhead box P1
Chromosome 3
Chromosomal band p14.1
Imprinted Unknown
Genomic reference NG_028243.1
Transcript reference NM_032682.5
Exon/intron information NM_032682.5 exon/intron table
Associated with diseases ID, MRLIAF
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 51
Unique public DNA variants reported 47
Individuals with public variants 10
Hidden variants 12
Date created January 16, 2013
Date last updated February 26, 2019
Version FOXP1:190226

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_032682.5.
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 3823
Entrez Gene 27086
PubMed articles FOXP1
OMIM - Gene 605515
OMIM - Diseases MRLIAF (mental retardation, language impairment, autistic features (MRLIAF))
HGMD FOXP1
GeneCards FOXP1
GeneTests FOXP1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001788 3 transcript variant 1 NM_032682.5 NP_116071.2 51


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 © 2013-2019. 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.