CTSW cathepsin W

Information
Symbol
CTSW
Type
protein-coding
Description
cathepsin W
Entrez Gene ID
1521
Genome
hg19
Position
chr11:65,647,308-65,651,212
Genome
hg38
Position
chr11:65,879,837-65,883,741
MIM
602364 OMIM
HGNC
HGNC:2546 HGNC
Ensembl
ENSG00000172543 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
64
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 :
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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 LYPN
MIM 602364 OMIM
HGNC HGNC:2546 HGNC
Ensembl ENSG00000172543 Ensembl
AllianceGenome HGNC:2546
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000680670.1 hg38 chr11 65,879,837 65,883,741 3,905
ENST00000679584.1 hg38 chr11 65,879,837 65,883,741 3,905
ENST00000526034.2 hg38 chr11 65,879,837 65,883,741 3,905
ENST00000528419.6 hg38 chr11 65,879,809 65,883,741 3,933
ENST00000307886.8 hg38 chr11 65,879,837 65,883,741 3,905
ENST00000680443.1 hg38 chr11 65,879,837 65,883,741 3,905
ENST00000528419.6 hg19 chr11 65,647,280 65,651,212 3,933
ENST00000307886.8 hg19 chr11 65,647,308 65,651,212 3,905
ENST00000526034.2 hg19 chr11 65,647,308 65,651,212 3,905
ENST00000679584.1 hg19 chr11 65,647,308 65,651,212 3,905
ENST00000680443.1 hg19 chr11 65,647,308 65,651,212 3,905
ENST00000680670.1 hg19 chr11 65,647,308 65,651,212 3,905
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