WNT7B Wnt family member 7B

Information
Symbol
WNT7B
Type
protein-coding
Description
Wnt family member 7B
Entrez Gene ID
7477
Genome
hg19
Position
chr22:46,317,991-46,368,595
Genome
hg38
Position
chr22:45,922,111-45,972,715
MIM
601967 OMIM
HGNC
HGNC:12787 HGNC
Ensembl
ENSG00000188064 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 2
Benign 0 4
Likely benign 0 8
not provided 1 0
Uncertain significance 0 32
Ranking
ClinVar
0
0
2
46
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
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 601967 OMIM
HGNC HGNC:12787 HGNC
Ensembl ENSG00000188064 Ensembl
AllianceGenome HGNC:12787
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000410058.1 hg38 chr22 45,927,482 45,976,805 49,324
ENST00000339464.9 hg38 chr22 45,920,366 45,977,162 56,797
ENST00000409496.7 hg38 chr22 45,922,111 45,972,715 50,605
ENST00000410089.5 hg38 chr22 45,922,111 45,976,022 53,912
ENST00000339464.9 hg19 chr22 46,316,246 46,373,042 56,797
ENST00000409496.7 hg19 chr22 46,317,991 46,368,595 50,605
ENST00000410089.5 hg19 chr22 46,317,991 46,371,902 53,912
ENST00000410058.1 hg19 chr22 46,323,362 46,372,685 49,324
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