WNT16 Wnt family member 16

Information
Symbol
WNT16
Type
protein-coding
Description
Wnt family member 16
Entrez Gene ID
51384
Genome
hg19
Position
chr7:120,969,054-120,981,158
Genome
hg38
Position
chr7:121,329,000-121,341,104
MIM
606267 OMIM
HGNC
HGNC:16267 HGNC
Ensembl
ENSG00000002745 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
40
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 :
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
MIM 606267 OMIM
HGNC HGNC:16267 HGNC
Ensembl ENSG00000002745 Ensembl
AllianceGenome HGNC:16267
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361301.6 hg38 chr7 121,325,367 121,339,458 14,092
ENST00000222462.3 hg38 chr7 121,329,000 121,341,104 12,105
ENST00000361301.6 hg19 chr7 120,965,421 120,979,512 14,092
ENST00000222462.3 hg19 chr7 120,969,054 120,981,158 12,105
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