HOXB9 homeobox B9

Information
Symbol
HOXB9
Type
protein-coding
Description
homeobox B9
Entrez Gene ID
3219
Genome
hg19
Position
chr17:46,698,518-46,703,720
Genome
hg38
Position
chr17:48,621,156-48,626,358
MIM
142964 OMIM
HGNC
HGNC:5120 HGNC
Ensembl
ENSG00000170689 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
38
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 HOX-2.5
SYNONYM HOX2
SYNONYM HOX2E
MIM 142964 OMIM
HGNC HGNC:5120 HGNC
Ensembl ENSG00000170689 Ensembl
AllianceGenome HGNC:5120
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000311177.7 hg38 chr17 48,621,156 48,626,358 5,203
ENST00000311177.7 hg19 chr17 46,698,518 46,703,720 5,203
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