CBX2 chromobox 2

Information
Symbol
CBX2
Type
protein-coding
Description
chromobox 2
Entrez Gene ID
84733
Genome
hg19
Position
chr17:77,751,947-77,761,782
Genome
hg38
Position
chr17:79,778,148-79,787,983
MIM
602770 OMIM
HGNC
HGNC:1552 HGNC
Ensembl
ENSG00000173894 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Benign 0 34
Likely benign 0 70
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 132
Ranking
ClinVar
0
0
26
200
8
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 CDCA6
SYNONYM M33
SYNONYM SRXY5
MIM 602770 OMIM
HGNC HGNC:1552 HGNC
Ensembl ENSG00000173894 Ensembl
AllianceGenome HGNC:1552
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000269399.5 hg38 chr17 79,778,194 79,782,532 4,339
ENST00000310942.9 hg38 chr17 79,778,148 79,787,983 9,836
ENST00000310942.9 hg19 chr17 77,751,947 77,761,782 9,836
ENST00000269399.5 hg19 chr17 77,751,993 77,756,331 4,339
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