CLDN17 claudin 17

Information
Symbol
CLDN17
Type
protein-coding
Description
claudin 17
Entrez Gene ID
26285
Genome
hg19
Position
chr21:31,537,883-31,539,123
Genome
hg38
Position
chr21:30,165,565-30,166,805
MIM
617005 OMIM
HGNC
HGNC:2038 HGNC
Ensembl
ENSG00000156282 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
32
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
MIM 617005 OMIM
HGNC HGNC:2038 HGNC
Ensembl ENSG00000156282 Ensembl
AllianceGenome HGNC:2038
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000286808.5 hg38 chr21 30,165,565 30,166,805 1,241
ENST00000286808.5 hg19 chr21 31,537,883 31,539,123 1,241
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