HOXC6 homeobox C6

Information
Symbol
HOXC6
Type
protein-coding
Description
homeobox C6
Entrez Gene ID
3223
Genome
hg19
Position
chr12:54,422,224-54,424,607
Genome
hg38
Position
chr12:54,028,440-54,030,823
MIM
142972 OMIM
HGNC
HGNC:5128 HGNC
Ensembl
ENSG00000197757 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
20
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 CP25
SYNONYM HHO.C8
SYNONYM HOX3
SYNONYM HOX3C
MIM 142972 OMIM
HGNC HGNC:5128 HGNC
Ensembl ENSG00000197757 Ensembl
AllianceGenome HGNC:5128
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000243108.5 hg38 chr12 54,028,440 54,030,823 2,384
ENST00000394331.3 hg38 chr12 54,015,897 54,030,733 14,837
ENST00000394331.3 hg19 chr12 54,409,681 54,424,517 14,837
ENST00000243108.5 hg19 chr12 54,422,224 54,424,607 2,384
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