HOXD13 homeobox D13

Information
Symbol
HOXD13
Type
protein-coding
Description
homeobox D13
Entrez Gene ID
3239
Genome
hg19
Position
chr2:176,957,449-176,960,672
Genome
hg38
Position
chr2:176,092,721-176,095,944
MIM
142989 OMIM
HGNC
HGNC:5136 HGNC
Ensembl
ENSG00000128714 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 52
Likely pathogenic 0 8
Benign 6 28
Likely benign 0 28
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 96
Ranking
ClinVar
0
0
44
122
36
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 BDE
SYNONYM BDSD
SYNONYM HOX4I
SYNONYM SPD
SYNONYM SPD1
MIM 142989 OMIM
HGNC HGNC:5136 HGNC
Ensembl ENSG00000128714 Ensembl
AllianceGenome HGNC:5136
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000392539.4 hg38 chr2 176,092,721 176,095,944 3,224
ENST00000392539.4 hg19 chr2 176,957,449 176,960,672 3,224
KeyValue
strand+
start176,957,531
Gene SymbolHOXD13
Entrez GeneId3,239
Chr Band2q31-q32
end176,960,665
chrchr2
Namehomeo box D13
Genome browser