HOXD10 homeobox D10

Information
Symbol
HOXD10
Type
protein-coding
Description
homeobox D10
Entrez Gene ID
3236
Genome
hg19
Position
chr2:176,981,506-176,984,665
Genome
hg38
Position
chr2:176,116,778-176,119,937
MIM
142984 OMIM
HGNC
HGNC:5133 HGNC
Ensembl
ENSG00000128710 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 30
Likely benign 0 12
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 82
Ranking
ClinVar
0
0
14
108
2
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 HOX4D
SYNONYM HOX4E
SYNONYM Hox-4.4
MIM 142984 OMIM
HGNC HGNC:5133 HGNC
Ensembl ENSG00000128710 Ensembl
AllianceGenome HGNC:5133
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000249501.5 hg38 chr2 176,116,778 176,119,937 3,160
ENST00000249501.5 hg19 chr2 176,981,506 176,984,665 3,160
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