POU3F4 POU class 3 homeobox 4

Information
Symbol
POU3F4
Type
protein-coding
Description
POU class 3 homeobox 4
Entrez Gene ID
5456
Genome
hg19
Position
chrX:82,763,298-82,767,135
Genome
hg38
Position
chrX:83,508,290-83,512,127
MIM
300039 OMIM
HGNC
HGNC:9217 HGNC
Ensembl
ENSG00000196767 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 14 66
Likely pathogenic 0 30
Benign 0 21
Likely benign 0 40
Conflicting classifications of pathogenicity 0 10
not provided 6 4
Uncertain significance 0 76
Ranking
ClinVar
0
0
18
165
40
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM BRAIN-4
SYNONYM BRN-4
SYNONYM BRN4
SYNONYM DFN3
SYNONYM DFNX2
SYNONYM OCT-9
SYNONYM OTF-9
SYNONYM OTF9
MIM 300039 OMIM
HGNC HGNC:9217 HGNC
Ensembl ENSG00000196767 Ensembl
AllianceGenome HGNC:9217
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000644024.2 hg38 chrX 83,508,290 83,512,127 3,838
ENST00000644024.2 hg19 chrX 82,763,298 82,767,135 3,838
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