WNT10B Wnt family member 10B

Information
Symbol
WNT10B
Type
protein-coding
Description
Wnt family member 10B
Entrez Gene ID
7480
Genome
hg19
Position
chr12:49,359,123-49,365,518
Genome
hg38
Position
chr12:48,965,340-48,971,735
MIM
601906 OMIM
HGNC
HGNC:12775 HGNC
Ensembl
ENSG00000169884 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 22
Likely pathogenic 0 14
Benign 0 18
Likely benign 0 28
Conflicting classifications of pathogenicity 0 6
Uncertain significance 0 78
Ranking
ClinVar
0
0
16
124
16
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 SHFM6
SYNONYM STHAG8
SYNONYM WNT-12
MIM 601906 OMIM
HGNC HGNC:12775 HGNC
Ensembl ENSG00000169884 Ensembl
AllianceGenome HGNC:12775
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000403957.5 hg38 chr12 48,965,556 48,971,718 6,163
ENST00000407467.5 hg38 chr12 48,965,405 48,971,498 6,094
ENST00000301061.9 hg38 chr12 48,965,340 48,971,735 6,396
ENST00000301061.9 hg19 chr12 49,359,123 49,365,518 6,396
ENST00000407467.5 hg19 chr12 49,359,188 49,365,281 6,094
ENST00000403957.5 hg19 chr12 49,359,339 49,365,501 6,163
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