{{Rsnum
|rsid=57499817
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KRT5
|position=52520223
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT5
}}{{omim
|id=148040
|rsnum=57499817
|variant=0009
}}

{{ClinVar
|rsid=57499817
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=52914007
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=KRT5:3852
|GENE_NAME=KRT5
|GENE_ID=3852
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.52914007G>A
|CLNSRC=Epithelial Biology; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=KRT5:c.74C>T; NBK1369; 148040.0009
|CLNSIG=5
|CLNCUI=C0432316; C0432316
|CLNDBN=Epidermolysis bullosa simplex with mottled pigmentation; not provided
|Disease=Epidermolysis bullosa simplex with mottled pigmentation; not provided
|CLNACC=RCV000015754.21; RCV000056643.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1369:C0432316:131960:79397:254180002
}}

{{PMID Auto
|PMID=1049409
|Title=The adult learner in nursing: a program of continuing education in a hospital based school of nursing.
}}

{{PMID Auto
|PMID=2476664
|Title=Isolation, sequence, and expression of a human keratin K5 gene: transcriptional regulation of keratins and insights into pairwise control.
|OA=1
}}

{{PMID Auto
|PMID=8799157
|Title=The genetic basis of epidermolysis bullosa simplex with mottled pigmentation.
|OA=1
}}

{{PMID Auto
|PMID=9129237
|Title=A mutation in the V1 domain of keratin 5 causes epidermolysis bullosa simplex with mottled pigmentation.
}}

{{PMID Auto
|PMID=11167681
|Title=Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}