CLDN34 claudin 34

Information
Symbol
CLDN34
Type
protein-coding
Description
claudin 34
Entrez Gene ID
100288814
Genome
hg19
Position
chrX:9,935,398-9,936,392
Genome
hg38
Position
chrX:9,967,358-9,968,352
HGNC
HGNC:51259 HGNC
Ensembl
ENSG00000234469 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 7 0
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
24
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
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:51259 HGNC
Ensembl ENSG00000234469 Ensembl
AllianceGenome HGNC:51259
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000445307.4 hg38 chrX 9,967,358 9,968,352 995
ENST00000445307.4 hg19 chrX 9,935,398 9,936,392 995
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