The POU3F4 gene homepage

General information
Gene symbol POU3F4
Gene name POU class 3 homeobox 4
Chromosome X
Chromosomal band q21.1
Imprinted Unknown
Genomic reference NG_009936.2
Transcript reference NM_000307.4
Exon/intron information NM_000307.4 exon/intron table
Associated with diseases DFNX2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 137
Unique public DNA variants reported 81
Individuals with public variants 150
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created March 06, 2009
Date last updated December 21, 2021
Version POU3F4:211221

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_000307.4.
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 http://www.LOVD.nl/POU3F4
HGNC 9217
Entrez Gene 5456
PubMed articles POU3F4
OMIM - Gene 300039
OMIM - Diseases DFNX2 (deafness, X-linked, type 2 (DFNX-2))
HGMD POU3F4
GeneCards POU3F4
GeneTests POU3F4
Orphanet POU3F4


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024114 X POU class 3 homeobox 4 NM_000307.4 NP_000298.3 137


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