CLDN23 claudin 23

Information
Symbol
CLDN23
Type
protein-coding
Description
claudin 23
Entrez Gene ID
137075
Genome
hg19
Position
chr8:8,559,447-8,561,606
Genome
hg38
Position
chr8:8,701,937-8,704,096
MIM
609203 OMIM
HGNC
HGNC:17591 HGNC
Ensembl
ENSG00000253958 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
44
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 :
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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 CLDNL
SYNONYM hCG1646163
MIM 609203 OMIM
HGNC HGNC:17591 HGNC
Ensembl ENSG00000253958 Ensembl
AllianceGenome HGNC:17591
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000519106.2 hg38 chr8 8,701,937 8,704,096 2,160
ENST00000519106.2 hg19 chr8 8,559,447 8,561,606 2,160
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