CLDN8 claudin 8

Information
Symbol
CLDN8
Type
protein-coding
Description
claudin 8
Entrez Gene ID
9073
Genome
hg19
Position
chr21:31,586,324-31,588,415
Genome
hg38
Position
chr21:30,214,006-30,216,097
MIM
611231 OMIM
HGNC
HGNC:2050 HGNC
Ensembl
ENSG00000156284 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
32
4
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 HEL-S-79
MIM 611231 OMIM
HGNC HGNC:2050 HGNC
Ensembl ENSG00000156284 Ensembl
AllianceGenome HGNC:2050
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000399899.2 hg38 chr21 30,214,006 30,216,097 2,092
ENST00000399899.2 hg19 chr21 31,586,324 31,588,415 2,092
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