CLDN20 claudin 20

Information
Symbol
CLDN20
Type
protein-coding
Description
claudin 20
Entrez Gene ID
49861
Genome
hg19
Position
chr6:155,585,147-155,597,682
Genome
hg38
Position
chr6:155,264,013-155,276,548
HGNC
HGNC:2042 HGNC
Ensembl
ENSG00000171217 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
20
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
HGNC HGNC:2042 HGNC
Ensembl ENSG00000171217 Ensembl
AllianceGenome HGNC:2042
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000367165.3 hg38 chr6 155,264,013 155,276,548 12,536
ENST00000367165.3 hg19 chr6 155,585,147 155,597,682 12,536
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