The 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) Global Variome, with Curator vacancy
Total number of public variants reported 101
Unique public DNA variants reported 89
Individuals with public variants 42
Hidden variants 15
Date created January 16, 2013
Date last updated April 19, 2024
Version FOXP1:240419

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
Orphanet FOXP1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001788 3 transcript variant 1 NM_032682.5 NP_116071.2 101


Copyright & disclaimer
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