WNT9A Wnt family member 9A

Information
Symbol
WNT9A
Type
protein-coding
Description
Wnt family member 9A
Entrez Gene ID
7483
Genome
hg19
Position
chr1:228,106,357-228,135,633
Genome
hg38
Position
chr1:227,918,656-227,947,932
MIM
602863 OMIM
HGNC
HGNC:12778 HGNC
Ensembl
ENSG00000143816 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
48
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 :
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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 WNT14
MIM 602863 OMIM
HGNC HGNC:12778 HGNC
Ensembl ENSG00000143816 Ensembl
AllianceGenome HGNC:12778
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000272164.6 hg38 chr1 227,918,656 227,947,932 29,277
ENST00000272164.6 hg19 chr1 228,106,357 228,135,633 29,277
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