WDR13 WD repeat domain 13

Information
Symbol
WDR13
Type
protein-coding
Description
WD repeat domain 13
Entrez Gene ID
64743
Genome
hg19
Position
chrX:48,455,880-48,467,257
Genome
hg38
Position
chrX:48,597,492-48,608,869
MIM
300512 OMIM
HGNC
HGNC:14352 HGNC
Ensembl
ENSG00000101940 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 10
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
40
2
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
SYNONYM MG21
MIM 300512 OMIM
HGNC HGNC:14352 HGNC
Ensembl ENSG00000101940 Ensembl
AllianceGenome HGNC:14352
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376729.10 hg38 chrX 48,597,492 48,608,869 11,378
ENST00000218056.9 hg38 chrX 48,597,492 48,605,193 7,702
ENST00000218056.9 hg19 chrX 48,455,880 48,463,581 7,702
ENST00000376729.10 hg19 chrX 48,455,880 48,467,257 11,378
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