BCL9L BCL9 like

Information
Symbol
BCL9L
Type
protein-coding
Description
BCL9 like
Entrez Gene ID
283149
Genome
hg19
Position
chr11:118,764,584-118,781,613
Genome
hg38
Position
chr11:118,893,875-118,910,904
MIM
609004 OMIM
HGNC
HGNC:23688 HGNC
Ensembl
ENSG00000186174 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 30
Likely benign 0 10
Uncertain significance 0 242
Ranking
ClinVar
0
0
2
280
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 B9L
SYNONYM BCL9-2
SYNONYM DLNB11
MIM 609004 OMIM
HGNC HGNC:23688 HGNC
Ensembl ENSG00000186174 Ensembl
AllianceGenome HGNC:23688
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000334801.7 hg38 chr11 118,893,875 118,910,904 17,030
ENST00000683865.1 hg38 chr11 118,896,136 118,925,926 29,791
ENST00000526143.2 hg38 chr11 118,897,746 118,925,608 27,863
ENST00000334801.7 hg19 chr11 118,764,584 118,781,613 17,030
ENST00000683865.1 hg19 chr11 118,766,845 118,796,635 29,791
ENST00000526143.2 hg19 chr11 118,768,455 118,796,317 27,863
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