WNT11 Wnt family member 11

Information
Symbol
WNT11
Type
protein-coding
Description
Wnt family member 11
Entrez Gene ID
7481
Genome
hg19
Position
chr11:75,897,369-75,917,546
Genome
hg38
Position
chr11:76,186,325-76,206,502
MIM
603699 OMIM
HGNC
HGNC:12776 HGNC
Ensembl
ENSG00000085741 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 4
Uncertain significance 0 34
Ranking
ClinVar
0
0
2
44
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 :
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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 HWNT11
MIM 603699 OMIM
HGNC HGNC:12776 HGNC
Ensembl ENSG00000085741 Ensembl
AllianceGenome HGNC:12776
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000322563.8 hg38 chr11 76,186,325 76,206,502 20,178
ENST00000322563.8 hg19 chr11 75,897,369 75,917,546 20,178
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