CLDN10 claudin 10

Information
Symbol
CLDN10
Type
protein-coding
Description
claudin 10
Entrez Gene ID
9071
Genome
hg19
Position
chr13:96,204,974-96,232,013
Genome
hg38
Position
chr13:95,552,720-95,579,759
MIM
617579 OMIM
HGNC
HGNC:2033 HGNC
Ensembl
ENSG00000134873 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 4
Benign 0 20
Uncertain significance 0 36
Ranking
ClinVar
0
0
4
50
12
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
SYNONYM CPETRL3
SYNONYM HELIX
SYNONYM OSP-L
SYNONYM OSPL
MIM 617579 OMIM
HGNC HGNC:2033 HGNC
Ensembl ENSG00000134873 Ensembl
AllianceGenome HGNC:2033
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376873.7 hg38 chr13 95,433,604 95,579,759 146,156
ENST00000299339.3 hg38 chr13 95,552,720 95,579,759 27,040
ENST00000376855.1 hg38 chr13 95,560,150 95,560,938 789
ENST00000376873.7 hg19 chr13 96,085,858 96,232,013 146,156
ENST00000299339.3 hg19 chr13 96,204,974 96,232,013 27,040
ENST00000376855.1 hg19 chr13 96,212,404 96,213,192 789
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