KRT16 keratin 16

Information
Symbol
KRT16
Type
protein-coding
Description
keratin 16
Entrez Gene ID
3868
Genome
hg19
Position
chr17:39,766,030-39,769,019
Genome
hg38
Position
chr17:41,609,778-41,612,767
MIM
148067 OMIM
HGNC
HGNC:6423 HGNC
Ensembl
ENSG00000186832 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 30
Likely pathogenic 0 10
Benign 14 54
Likely benign 0 74
Conflicting classifications of pathogenicity 0 14
not provided 0 14
Uncertain significance 0 66
Ranking
ClinVar
0
0
48
148
14
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 CK16
SYNONYM FNEPPK
SYNONYM K16
SYNONYM K1CP
SYNONYM KRT16A
SYNONYM NEPPK
SYNONYM PC1
MIM 148067 OMIM
HGNC HGNC:6423 HGNC
Ensembl ENSG00000186832 Ensembl
AllianceGenome HGNC:6423
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000301653.9 hg38 chr17 41,609,778 41,612,767 2,990
ENST00000301653.9 hg19 chr17 39,766,030 39,769,019 2,990
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