CBX3 chromobox 3

Information
Symbol
CBX3
Type
protein-coding
Description
chromobox 3
Entrez Gene ID
11335
Genome
hg19
Position
chr7:26,240,782-26,252,976
Genome
hg38
Position
chr7:26,201,162-26,213,356
MIM
604477 OMIM
HGNC
HGNC:1553 HGNC
Ensembl
ENSG00000122565 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
4
2
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 HECH
SYNONYM HP1-GAMMA
SYNONYM HP1Hs-gamma
SYNONYM HP1gamma
MIM 604477 OMIM
HGNC HGNC:1553 HGNC
Ensembl ENSG00000122565 Ensembl
AllianceGenome HGNC:1553
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000337620.8 hg38 chr7 26,201,162 26,213,356 12,195
ENST00000409747.5 hg38 chr7 26,201,765 26,213,356 11,592
ENST00000396386.7 hg38 chr7 26,201,745 26,213,607 11,863
ENST00000337620.8 hg19 chr7 26,240,782 26,252,976 12,195
ENST00000396386.7 hg19 chr7 26,241,365 26,253,227 11,863
ENST00000409747.5 hg19 chr7 26,241,385 26,252,976 11,592
KeyValue
strand+
start26,240,830
Gene SymbolCBX3
Entrez GeneId11,335
Chr Band7p15.2
end26,253,226
chrchr7
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