HOXC4 homeobox C4

Information
Symbol
HOXC4
Type
protein-coding
Description
homeobox C4
Entrez Gene ID
3221
Genome
hg19
Position
chr12:54,447,619-54,449,814
Genome
hg38
Position
chr12:54,053,835-54,056,030
MIM
142974 OMIM
HGNC
HGNC:5126 HGNC
Ensembl
ENSG00000198353 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
70
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 HOX3E
SYNONYM cp19
MIM 142974 OMIM
HGNC HGNC:5126 HGNC
Ensembl ENSG00000198353 Ensembl
AllianceGenome HGNC:5126
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000430889.3 hg38 chr12 54,053,835 54,056,030 2,196
ENST00000303406.4 hg38 chr12 54,016,931 54,055,327 38,397
ENST00000303406.4 hg19 chr12 54,410,715 54,449,111 38,397
ENST00000430889.3 hg19 chr12 54,447,619 54,449,814 2,196
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