WNT5A Wnt family member 5A

Information
Symbol
WNT5A
Type
protein-coding
Description
Wnt family member 5A
Entrez Gene ID
7474
Genome
hg19
Position
chr3:55,499,743-55,523,973
Genome
hg38
Position
chr3:55,465,715-55,489,945
MIM
164975 OMIM
HGNC
HGNC:12784 HGNC
Ensembl
ENSG00000114251 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 8
Benign 0 52
Likely benign 0 140
Conflicting classifications of pathogenicity 0 36
not provided 0 2
Uncertain significance 0 186
Ranking
ClinVar
0
0
58
316
8
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
SYNONYM hWNT5A
MIM 164975 OMIM
HGNC HGNC:12784 HGNC
Ensembl ENSG00000114251 Ensembl
AllianceGenome HGNC:12784
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000264634.9 hg38 chr3 55,465,715 55,487,306 21,592
ENST00000474267.5 hg38 chr3 55,465,715 55,489,945 24,231
ENST00000497027.5 hg38 chr3 55,469,993 55,481,393 11,401
ENST00000264634.9 hg19 chr3 55,499,743 55,521,334 21,592
ENST00000474267.5 hg19 chr3 55,499,743 55,523,973 24,231
ENST00000497027.5 hg19 chr3 55,504,021 55,515,421 11,401
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