WDR88 WD repeat domain 88

Information
Symbol
WDR88
Type
protein-coding
Description
WD repeat domain 88
Entrez Gene ID
126248
Genome
hg19
Position
chr19:33,623,020-33,666,705
Genome
hg38
Position
chr19:33,132,114-33,175,799
HGNC
HGNC:26999 HGNC
Ensembl
ENSG00000166359 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
44
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
SYNONYM PQWD
HGNC HGNC:26999 HGNC
Ensembl ENSG00000166359 Ensembl
AllianceGenome HGNC:26999
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000592765.5 hg38 chr19 33,132,090 33,148,804 16,715
ENST00000361680.6 hg38 chr19 33,132,092 33,175,795 43,704
ENST00000355868.4 hg38 chr19 33,132,114 33,175,799 43,686
ENST00000592765.5 hg19 chr19 33,622,996 33,639,710 16,715
ENST00000361680.6 hg19 chr19 33,622,998 33,666,701 43,704
ENST00000355868.4 hg19 chr19 33,623,020 33,666,705 43,686
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