BSX brain specific homeobox

Information
Symbol
BSX
Type
protein-coding
Description
brain specific homeobox
Entrez Gene ID
390259
Genome
hg19
Position
chr11:122,848,278-122,852,542
Genome
hg38
Position
chr11:122,977,570-122,981,834
MIM
611074 OMIM
HGNC
HGNC:20450 HGNC
Ensembl
ENSG00000188909 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
34
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 BSX1
MIM 611074 OMIM
HGNC HGNC:20450 HGNC
Ensembl ENSG00000188909 Ensembl
AllianceGenome HGNC:20450
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000343035.3 hg38 chr11 122,977,570 122,981,834 4,265
ENST00000343035.3 hg19 chr11 122,848,278 122,852,542 4,265
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