POU2F3 POU class 2 homeobox 3

Information
Symbol
POU2F3
Type
protein-coding
Description
POU class 2 homeobox 3
Entrez Gene ID
25833
Genome
hg19
Position
chr11:120,107,349-120,190,653
Genome
hg38
Position
chr11:120,236,640-120,319,944
MIM
607394 OMIM
HGNC
HGNC:19864 HGNC
Ensembl
ENSG00000137709 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
40
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
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 Epoc-1
SYNONYM OCT-11
SYNONYM OCT11
SYNONYM OTF-11
SYNONYM PLA-1
SYNONYM PLA1
SYNONYM Skn-1a
MIM 607394 OMIM
HGNC HGNC:19864 HGNC
Ensembl ENSG00000137709 Ensembl
AllianceGenome HGNC:19864
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000260264.8 hg38 chr11 120,236,640 120,319,944 83,305
ENST00000543440.7 hg38 chr11 120,240,140 120,319,945 79,806
ENST00000260264.8 hg19 chr11 120,107,349 120,190,653 83,305
ENST00000543440.7 hg19 chr11 120,110,849 120,190,654 79,806
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