CLDN15 claudin 15

Information
Symbol
CLDN15
Type
protein-coding
Description
claudin 15
Entrez Gene ID
24146
Genome
hg19
Position
chr7:100,875,373-100,882,101
Genome
hg38
Position
chr7:101,232,092-101,238,820
MIM
615778 OMIM
HGNC
HGNC:2036 HGNC
Ensembl
ENSG00000106404 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
MIM 615778 OMIM
HGNC HGNC:2036 HGNC
Ensembl ENSG00000106404 Ensembl
AllianceGenome HGNC:2036
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000401528.5 hg38 chr7 101,232,092 101,238,820 6,729
ENST00000611078.4 hg38 chr7 101,232,093 101,237,946 5,854
ENST00000308344.10 hg38 chr7 101,232,094 101,237,802 5,709
ENST00000401528.5 hg19 chr7 100,875,373 100,882,101 6,729
ENST00000611078.4 hg19 chr7 100,875,374 100,881,227 5,854
ENST00000308344.10 hg19 chr7 100,875,375 100,881,083 5,709
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