HOXC12 homeobox C12

Information
Symbol
HOXC12
Type
protein-coding
Description
homeobox C12
Entrez Gene ID
3228
Genome
hg19
Position
chr12:54,348,687-54,352,740
Genome
hg38
Position
chr12:53,954,903-53,958,956
MIM
142975 OMIM
HGNC
HGNC:5124 HGNC
Ensembl
ENSG00000123407 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 HOC3F
SYNONYM HOX3
SYNONYM HOX3F
MIM 142975 OMIM
HGNC HGNC:5124 HGNC
Ensembl ENSG00000123407 Ensembl
AllianceGenome HGNC:5124
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000243103.4 hg38 chr12 53,954,903 53,958,956 4,054
ENST00000243103.4 hg19 chr12 54,348,687 54,352,740 4,054
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