SEBOX SEBOX homeobox

Information
Symbol
SEBOX
Type
protein-coding
Description
SEBOX homeobox
Entrez Gene ID
645832
Genome
hg19
Position
chr17:26,690,528-26,692,221
Genome
hg38
Position
chr17:28,363,506-28,365,199
MIM
610975 OMIM
HGNC
HGNC:32942 HGNC
Ensembl
ENSG00000274529 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
18
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 OG-9
SYNONYM OG9
SYNONYM OG9X
MIM 610975 OMIM
HGNC HGNC:32942 HGNC
Ensembl ENSG00000274529 Ensembl
AllianceGenome HGNC:32942
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000536498.6 hg38 chr17 28,363,506 28,365,199 1,694
ENST00000536498.6 hg19 chr17 26,690,528 26,692,221 1,694
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