CLDN12 claudin 12

Information
Symbol
CLDN12
Type
protein-coding
Description
claudin 12
Entrez Gene ID
9069
Genome
hg19
Position
chr7:90,032,700-90,045,268
Genome
hg38
Position
chr7:90,403,386-90,415,954
MIM
611232 OMIM
HGNC
HGNC:2034 HGNC
Ensembl
ENSG00000157224 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
10
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 611232 OMIM
HGNC HGNC:2034 HGNC
Ensembl ENSG00000157224 Ensembl
AllianceGenome HGNC:2034
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000496677.6 hg38 chr7 90,403,461 90,415,954 12,494
ENST00000287916.8 hg38 chr7 90,403,386 90,415,954 12,569
ENST00000394605.2 hg38 chr7 90,403,467 90,415,954 12,488
ENST00000287916.8 hg19 chr7 90,032,700 90,045,268 12,569
ENST00000496677.6 hg19 chr7 90,032,775 90,045,268 12,494
ENST00000394605.2 hg19 chr7 90,032,781 90,045,268 12,488
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