SIX2 SIX homeobox 2

Information
Symbol
SIX2
Type
protein-coding
Description
SIX homeobox 2
Entrez Gene ID
10736
Genome
hg19
Position
chr2:45,232,321-45,236,591
Genome
hg38
Position
chr2:45,005,182-45,009,452
MIM
604994 OMIM
HGNC
HGNC:10888 HGNC
Ensembl
ENSG00000170577 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 16
Likely benign 0 56
Uncertain significance 0 46
Ranking
ClinVar
0
0
14
102
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
MIM 604994 OMIM
HGNC HGNC:10888 HGNC
Ensembl ENSG00000170577 Ensembl
AllianceGenome HGNC:10888
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000303077.7 hg38 chr2 45,005,182 45,009,452 4,271
ENST00000303077.7 hg19 chr2 45,232,321 45,236,591 4,271
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