HOXD8 homeobox D8

Information
Symbol
HOXD8
Type
protein-coding
Description
homeobox D8
Entrez Gene ID
3234
Genome
hg19
Position
chr2:176,994,433-176,997,423
Genome
hg38
Position
chr2:176,129,705-176,132,695
MIM
142985 OMIM
HGNC
HGNC:5139 HGNC
Ensembl
ENSG00000175879 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
56
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 HOX4
SYNONYM HOX4E
SYNONYM HOX5.4
MIM 142985 OMIM
HGNC HGNC:5139 HGNC
Ensembl ENSG00000175879 Ensembl
AllianceGenome HGNC:5139
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000429017.2 hg38 chr2 176,129,694 176,132,695 3,002
ENST00000313173.6 hg38 chr2 176,129,705 176,132,695 2,991
ENST00000544999.2 hg38 chr2 176,130,022 176,132,100 2,079
ENST00000450510.2 hg38 chr2 176,130,357 176,132,000 1,644
ENST00000429017.2 hg19 chr2 176,994,422 176,997,423 3,002
ENST00000313173.6 hg19 chr2 176,994,433 176,997,423 2,991
ENST00000544999.2 hg19 chr2 176,994,750 176,996,828 2,079
ENST00000450510.2 hg19 chr2 176,995,085 176,996,728 1,644
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