WBP2NL WBP2 N-terminal like

Information
Symbol
WBP2NL
Type
protein-coding
Description
WBP2 N-terminal like
Entrez Gene ID
164684
Genome
hg19
Position
chr22:42,394,792-42,424,479
Genome
hg38
Position
chr22:41,998,788-42,028,475
MIM
610981 OMIM
HGNC
HGNC:28389 HGNC
Ensembl
ENSG00000183066 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
46
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 GRAMD7
SYNONYM PAWP
MIM 610981 OMIM
HGNC HGNC:28389 HGNC
Ensembl ENSG00000183066 Ensembl
AllianceGenome HGNC:28389
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000328823.13 hg38 chr22 41,998,788 42,028,475 29,688
ENST00000328823.13 hg19 chr22 42,394,792 42,424,479 29,688
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