HOXC9 homeobox C9

Information
Symbol
HOXC9
Type
protein-coding
Description
homeobox C9
Entrez Gene ID
3225
Genome
hg19
Position
chr12:54,389,293-54,397,082
Genome
hg38
Position
chr12:53,995,509-54,003,298
MIM
142971 OMIM
HGNC
HGNC:5130 HGNC
Ensembl
ENSG00000180806 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
28
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 HOX3
SYNONYM HOX3B
MIM 142971 OMIM
HGNC HGNC:5130 HGNC
Ensembl ENSG00000180806 Ensembl
AllianceGenome HGNC:5130
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000303450.5 hg38 chr12 54,000,161 54,003,337 3,177
ENST00000508190.1 hg38 chr12 53,995,509 54,003,298 7,790
ENST00000508190.1 hg19 chr12 54,389,293 54,397,082 7,790
ENST00000303450.5 hg19 chr12 54,393,945 54,397,121 3,177
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