WNT5B Wnt family member 5B

Information
Symbol
WNT5B
Type
protein-coding
Description
Wnt family member 5B
Entrez Gene ID
81029
Genome
hg19
Position
chr12:1,738,397-1,756,378
Genome
hg38
Position
chr12:1,629,231-1,647,212
MIM
606361 OMIM
HGNC
HGNC:16265 HGNC
Ensembl
ENSG00000111186 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
78
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 :
Search word :
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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
MIM 606361 OMIM
HGNC HGNC:16265 HGNC
Ensembl ENSG00000111186 Ensembl
AllianceGenome HGNC:16265
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537031.5 hg38 chr12 1,574,657 1,646,367 71,711
ENST00000310594.7 hg38 chr12 1,617,056 1,647,211 30,156
ENST00000397196.7 hg38 chr12 1,629,231 1,647,212 17,982
ENST00000542408.1 hg38 chr12 1,631,315 1,645,933 14,619
ENST00000537031.5 hg19 chr12 1,683,823 1,755,533 71,711
ENST00000310594.7 hg19 chr12 1,726,222 1,756,377 30,156
ENST00000397196.7 hg19 chr12 1,738,397 1,756,378 17,982
ENST00000542408.1 hg19 chr12 1,740,481 1,755,099 14,619
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