KRT38 keratin 38

Information
Symbol
KRT38
Type
protein-coding
Description
keratin 38
Entrez Gene ID
8687
Genome
hg19
Position
chr17:39,592,406-39,597,235
Genome
hg38
Position
chr17:41,436,154-41,440,983
MIM
604542 OMIM
HGNC
HGNC:6456 HGNC
Ensembl
ENSG00000171360 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
72
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 :
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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 HA8
SYNONYM KRTHA8
SYNONYM hHa8
MIM 604542 OMIM
HGNC HGNC:6456 HGNC
Ensembl ENSG00000171360 Ensembl
AllianceGenome HGNC:6456
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000246646.4 hg38 chr17 41,436,154 41,440,983 4,830
ENST00000246646.4 hg19 chr17 39,592,406 39,597,235 4,830
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