WBP11 WW domain binding protein 11

Information
Symbol
WBP11
Type
protein-coding
Description
WW domain binding protein 11
Entrez Gene ID
51729
Genome
hg19
Position
chr12:14,937,516-14,956,412
Genome
hg38
Position
chr12:14,784,582-14,803,478
MIM
618083 OMIM
HGNC
HGNC:16461 HGNC
Ensembl
ENSG00000084463 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 8
Benign 0 2
Likely benign 0 4
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 74
Ranking
ClinVar
0
0
4
90
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
SYNONYM BUG13
SYNONYM CFAP90
SYNONYM FAP90
SYNONYM NPWBP
SYNONYM PPP1R165
SYNONYM SIPP1
SYNONYM VCTERL
SYNONYM VCTRL
SYNONYM WBP-11
MIM 618083 OMIM
HGNC HGNC:16461 HGNC
Ensembl ENSG00000084463 Ensembl
AllianceGenome HGNC:16461
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000261167.7 hg38 chr12 14,784,582 14,803,478 18,897
ENST00000261167.7 hg19 chr12 14,937,516 14,956,412 18,897
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