WSB2 WD repeat and SOCS box containing 2

Information
Symbol
WSB2
Type
protein-coding
Description
WD repeat and SOCS box containing 2
Entrez Gene ID
55884
Genome
hg19
Position
chr12:118,471,926-118,499,979
Genome
hg38
Position
chr12:118,034,121-118,062,174
HGNC
HGNC:19222 HGNC
Ensembl
ENSG00000176871 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 6
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
42
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 :
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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 SBA2
HGNC HGNC:19222 HGNC
Ensembl ENSG00000176871 Ensembl
AllianceGenome HGNC:19222
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000315436.8 hg38 chr12 118,032,687 118,061,179 28,493
ENST00000544233.5 hg38 chr12 118,032,694 118,061,211 28,518
ENST00000535496.5 hg38 chr12 118,034,196 118,052,604 18,409
ENST00000441406.6 hg38 chr12 118,034,121 118,062,174 28,054
ENST00000315436.8 hg19 chr12 118,470,492 118,498,984 28,493
ENST00000544233.5 hg19 chr12 118,470,499 118,499,016 28,518
ENST00000441406.6 hg19 chr12 118,471,926 118,499,979 28,054
ENST00000535496.5 hg19 chr12 118,472,001 118,490,409 18,409
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