CLDN7 claudin 7

Information
Symbol
CLDN7
Type
protein-coding
Description
claudin 7
Entrez Gene ID
1366
Genome
hg19
Position
chr17:7,163,222-7,165,797
Genome
hg38
Position
chr17:7,259,903-7,262,478
MIM
609131 OMIM
HGNC
HGNC:2049 HGNC
Ensembl
ENSG00000181885 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 20
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
[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 CEPTRL2
SYNONYM CLDN-7
SYNONYM CPETRL2
SYNONYM Hs.84359
SYNONYM claudin-1
MIM 609131 OMIM
HGNC HGNC:2049 HGNC
Ensembl ENSG00000181885 Ensembl
AllianceGenome HGNC:2049
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397317.8 hg38 chr17 7,260,137 7,263,213 3,077
ENST00000360325.11 hg38 chr17 7,259,903 7,262,478 2,576
ENST00000538261.7 hg38 chr17 7,259,904 7,262,945 3,042
ENST00000571881.2 hg38 chr17 7,260,654 7,262,343 1,690
ENST00000360325.11 hg19 chr17 7,163,222 7,165,797 2,576
ENST00000538261.7 hg19 chr17 7,163,223 7,166,264 3,042
ENST00000397317.8 hg19 chr17 7,163,456 7,166,532 3,077
ENST00000571881.2 hg19 chr17 7,163,973 7,165,662 1,690
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