HOXD12 homeobox D12

Information
Symbol
HOXD12
Type
protein-coding
Description
homeobox D12
Entrez Gene ID
3238
Genome
hg19
Position
chr2:176,964,523-176,967,217
Genome
hg38
Position
chr2:176,099,795-176,102,489
MIM
142988 OMIM
HGNC
HGNC:5135 HGNC
Ensembl
ENSG00000170178 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
48
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 HOX4H
MIM 142988 OMIM
HGNC HGNC:5135 HGNC
Ensembl ENSG00000170178 Ensembl
AllianceGenome HGNC:5135
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000406506.4 hg38 chr2 176,099,795 176,102,489 2,695
ENST00000404162.2 hg38 chr2 176,099,802 176,100,760 959
ENST00000406506.4 hg19 chr2 176,964,523 176,967,217 2,695
ENST00000404162.2 hg19 chr2 176,964,530 176,965,488 959
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