{{Rsnum
|rsid=59190510
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KRT5
|position=52516647
|Gene_s=KRT5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=59190510
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=52910431
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KRT5:3852
|GENE_NAME=KRT5
|GENE_ID=3852
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000012.11:g.52910431C>A; NC_000012.11:g.52910431C>T
|CLNSRC=Epithelial Biology; OMIM Allelic Variant; GeneReviews
|CLNORIGIN=1; 0
|CLNSRCID=KRT5:c.1429G>T; 148040.0015; KRT5:c.1429G>A; NBK1369
|CLNSIG=5
|CLNCUI=C0079295
|CLNDBN=Epidermolysis bullosa simplex, Dowling-Meara type, with severe palmoplantar keratoderma; not provided; Epidermolysis bullosa herpetiformis, Dowling-Meara
|Disease=Epidermolysis bullosa simplex; not provided; Epidermolysis bullosa herpetiformis
|CLNACC=RCV000015759.24; RCV000056566.1; RCV000020296.2; RCV000056565.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1369:C0079295:131760:79396
}}{{PMID Auto
|PMID=9036937
|Title=Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patients.
}}

{{PMID Auto
|PMID=16098032
|Title=Epidermolysis bullosa simplex: recurrent and de novo mutations in the KRT5 and KRT14 genes, phenotype/genotype correlations, and implications for genetic counseling and prenatal diagnosis.
}}

{{PMID Auto
|PMID=16601668
|Title=Epidermolysis bullosa simplex with mottled pigmentation resulting from a recurrent mutation in KRT14.
}}