HOXC5 homeobox C5

Information
Symbol
HOXC5
Type
protein-coding
Description
homeobox C5
Entrez Gene ID
3222
Genome
hg19
Position
chr12:54,426,834-54,429,145
Genome
hg38
Position
chr12:54,033,050-54,035,361
MIM
142973 OMIM
HGNC
HGNC:5127 HGNC
Ensembl
ENSG00000172789 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
24
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 CP11
SYNONYM HOX3
SYNONYM HOX3D
MIM 142973 OMIM
HGNC HGNC:5127 HGNC
Ensembl ENSG00000172789 Ensembl
AllianceGenome HGNC:5127
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000312492.3 hg38 chr12 54,033,050 54,035,361 2,312
ENST00000312492.3 hg19 chr12 54,426,834 54,429,145 2,312
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