KRT86 keratin 86

Information
Symbol
KRT86
Type
protein-coding
Description
keratin 86
Entrez Gene ID
3892
Genome
hg19
Position
chr12:52,668,429-52,702,947
Genome
hg38
Position
chr12:52,274,645-52,309,163
MIM
601928 OMIM
HGNC
HGNC:6463 HGNC
Ensembl
ENSG00000170442 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Benign 10 128
Likely benign 0 70
Conflicting classifications of pathogenicity 0 4
not provided 0 2
Uncertain significance 0 162
Ranking
ClinVar
0
0
14
336
16
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 HB6
SYNONYM Hb1
SYNONYM K86
SYNONYM KRTHB1
SYNONYM KRTHB6
SYNONYM MNX
MIM 601928 OMIM
HGNC HGNC:6463 HGNC
Ensembl ENSG00000170442 Ensembl
AllianceGenome HGNC:6463
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000293525.5 hg38 chr12 52,301,865 52,309,163 7,299
ENST00000423955.7 hg38 chr12 52,274,645 52,309,163 34,519
ENST00000423955.7 hg19 chr12 52,668,429 52,702,947 34,519
ENST00000293525.5 hg19 chr12 52,695,649 52,702,947 7,299
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