CUX2 cut like homeobox 2

Information
Symbol
CUX2
Type
protein-coding
Description
cut like homeobox 2
Entrez Gene ID
23316
Genome
hg19
Position
chr12:111,471,969-111,788,358
Genome
hg38
Position
chr12:111,034,165-111,350,554
MIM
610648 OMIM
HGNC
HGNC:19347 HGNC
Ensembl
ENSG00000111249 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 4
Benign 0 56
Likely benign 0 194
Conflicting classifications of pathogenicity 0 4
not provided 2 0
Uncertain significance 0 286
Ranking
ClinVar
0
0
82
424
12
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 CDP2
SYNONYM CUTL2
SYNONYM DEE67
SYNONYM EIEE67
MIM 610648 OMIM
HGNC HGNC:19347 HGNC
Ensembl ENSG00000111249 Ensembl
AllianceGenome HGNC:19347
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000261726.11 hg38 chr12 111,034,165 111,350,554 316,390
ENST00000261726.11 hg19 chr12 111,471,969 111,788,358 316,390
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