HOXB7 homeobox B7

Information
Symbol
HOXB7
Type
protein-coding
Description
homeobox B7
Entrez Gene ID
3217
Genome
hg19
Position
chr17:46,684,594-46,688,379
Genome
hg38
Position
chr17:48,607,232-48,611,017
MIM
142962 OMIM
HGNC
HGNC:5118 HGNC
Ensembl
ENSG00000260027 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
30
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 HHO.C1
SYNONYM HOX2
SYNONYM HOX2C
SYNONYM Hox-2.3
MIM 142962 OMIM
HGNC HGNC:5118 HGNC
Ensembl ENSG00000260027 Ensembl
AllianceGenome HGNC:5118
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000239165.9 hg38 chr17 48,607,232 48,611,017 3,786
ENST00000239165.9 hg19 chr17 46,684,594 46,688,379 3,786
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