CLDN19 claudin 19

Information
Symbol
CLDN19
Type
protein-coding
Description
claudin 19
Entrez Gene ID
149461
Genome
hg19
Position
chr1:43,198,764-43,205,907
Genome
hg38
Position
chr1:42,733,093-42,740,236
MIM
610036 OMIM
HGNC
HGNC:2040 HGNC
Ensembl
ENSG00000164007 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 22
Likely pathogenic 0 12
Benign 0 30
Likely benign 0 84
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 166
Ranking
ClinVar
0
0
54
234
18
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 HOMG5
MIM 610036 OMIM
HGNC HGNC:2040 HGNC
Ensembl ENSG00000164007 Ensembl
AllianceGenome HGNC:2040
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000296387.6 hg38 chr1 42,733,093 42,740,236 7,144
ENST00000539749.5 hg38 chr1 42,733,093 42,740,254 7,162
ENST00000372539.3 hg38 chr1 42,734,995 42,740,140 5,146
ENST00000296387.6 hg19 chr1 43,198,764 43,205,907 7,144
ENST00000539749.5 hg19 chr1 43,198,764 43,205,925 7,162
ENST00000372539.3 hg19 chr1 43,200,666 43,205,811 5,146
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