KRT13 keratin 13

Information
Symbol
KRT13
Type
protein-coding
Description
keratin 13
Entrez Gene ID
3860
Genome
hg19
Position
chr17:39,657,233-39,661,864
Genome
hg38
Position
chr17:41,500,981-41,505,612
MIM
148065 OMIM
HGNC
HGNC:6415 HGNC
Ensembl
ENSG00000171401 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Benign 10 88
Likely benign 0 32
Conflicting classifications of pathogenicity 0 6
not provided 0 8
Uncertain significance 0 86
Ranking
ClinVar
0
0
42
150
6
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 CK13
SYNONYM K13
SYNONYM WSN2
MIM 148065 OMIM
HGNC HGNC:6415 HGNC
Ensembl ENSG00000171401 Ensembl
AllianceGenome HGNC:6415
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000246635.8 hg38 chr17 41,500,981 41,505,612 4,632
ENST00000587544.5 hg38 chr17 41,502,225 41,505,613 3,389
ENST00000336861.7 hg38 chr17 41,500,981 41,505,597 4,617
ENST00000336861.7 hg19 chr17 39,657,233 39,661,849 4,617
ENST00000246635.8 hg19 chr17 39,657,233 39,661,864 4,632
ENST00000587544.5 hg19 chr17 39,658,477 39,661,865 3,389
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