WNT9B Wnt family member 9B

Information
Symbol
WNT9B
Type
protein-coding
Description
Wnt family member 9B
Entrez Gene ID
7484
Genome
hg19
Position
chr17:44,928,949-44,957,926
Genome
hg38
Position
chr17:46,851,583-46,880,560
MIM
602864 OMIM
HGNC
HGNC:12779 HGNC
Ensembl
ENSG00000158955 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 4
Benign 0 36
Likely benign 0 40
Uncertain significance 0 50
Ranking
ClinVar
0
0
20
98
4
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 WNT14B
SYNONYM WNT15
MIM 602864 OMIM
HGNC HGNC:12779 HGNC
Ensembl ENSG00000158955 Ensembl
AllianceGenome HGNC:12779
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000393461.2 hg38 chr17 46,851,586 46,886,730 35,145
ENST00000290015.7 hg38 chr17 46,851,583 46,880,560 28,978
ENST00000290015.7 hg19 chr17 44,928,949 44,957,926 28,978
ENST00000393461.2 hg19 chr17 44,928,952 44,964,096 35,145
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