KRT5 Chromosome 12

Keratin 5
91 variants 91 Health Risk

Upload your DNA to see your personal genotypes for variants in KRT5.

What This Gene Does
The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the basal layer of the epidermis with family member KRT14. Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Keratins, type II
Locus Type
gene with protein product
Location
12q13.13
Ensembl
ENSG00000186081
Associated Conditions (26)
Epidermolysis bullosa simplex
Inborn genetic diseases
KRT5-related disorder
Koebner type
Epidermolysis bullosa simplex 1C
localized
Epidermolysis bullosa simplex 2A
generalized severe
Epidermolysis bullosa simplex 2B
generalized intermediate
Epidermolysis bullosa simplex 2C
EPIDERMOLYSIS BULLOSA SIMPLEX 2D
GENERALIZED SEVERE
AUTOSOMAL RECESSIVE
Epidermolysis bullosa simplex 1A
Epidermolysis bullosa simplex 2d
generalized
intermediate or severe
autosomal recessive
Epidermolysis bullosa simplex with migratory circinate erythema
+6 more conditions
Key Variants
RS1264710617
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
Health Risk
RS140352947
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex, Inborn genetic diseases, Epidermolysis bullosa simplex
Health Risk
RS143566042
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS146022149
Conflicting classifications of pathogenicity
KRT5-related disorder, KRT5-related disorder
Health Risk
RS146136560
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex, Inborn genetic diseases, Epidermolysis bullosa simplex
Health Risk
RS202104381
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
Health Risk
RS2498409143
Conflicting classifications of pathogenicity
KRT5-related disorder, KRT5-related disorder
Health Risk
RS267607448
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 1C
Health Risk
RS543574061
Conflicting classifications of pathogenicity
Health Risk
RS552561992
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS59184265
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
Health Risk
RS62642056
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex, Epidermolysis bullosa simplex 2A, generalized severe
Health Risk
All Variants (91)
RSID Category Clinical Significance Conditions
RS1264710617 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
RS140352947 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex, Inborn genetic diseases, Epidermolysis bullosa simplex
RS143566042 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS146022149 Health Risk Conflicting classifications of pathogenicity KRT5-related disorder, KRT5-related disorder
RS146136560 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex, Inborn genetic diseases, Epidermolysis bullosa simplex
RS202104381 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
RS2498409143 Health Risk Conflicting classifications of pathogenicity KRT5-related disorder, KRT5-related disorder
RS267607448 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 1C
RS543574061 Health Risk Conflicting classifications of pathogenicity
RS552561992 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS59184265 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
RS62642056 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex, Epidermolysis bullosa simplex 2A, generalized severe
RS753029185 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS754242209 Health Risk Conflicting classifications of pathogenicity KRT5-related disorder, KRT5-related disorder
RS776667863 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS777631293 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS111448623 Health Risk Likely pathogenic
RS1131691471 Health Risk Likely pathogenic
RS1555156076 Health Risk Likely pathogenic Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex
RS1555156100 Health Risk Likely pathogenic
RS1555156480 Health Risk Likely pathogenic KRT5-related disorder, KRT5-related disorder
RS1565593355 Health Risk Likely pathogenic Epidermolysis bullosa simplex, EPIDERMOLYSIS BULLOSA SIMPLEX 2D, GENERALIZED SEVERE
RS1938679596 Health Risk Likely pathogenic Epidermolysis bullosa simplex 1A, generalized severe, Epidermolysis bullosa simplex 1A
RS2498409261 Health Risk Likely pathogenic
RS2498409394 Health Risk Likely pathogenic
RS2498519756 Health Risk Likely pathogenic Epidermolysis bullosa simplex 2B, generalized intermediate, Epidermolysis bullosa simplex 2B
RS267607661 Health Risk Likely pathogenic
RS531299414 Health Risk Likely pathogenic
RS56790237 Health Risk Likely pathogenic
RS57845028 Health Risk Likely pathogenic
RS58107458 Health Risk Likely pathogenic KRT5-related disorder, KRT5-related disorder
RS59115483 Health Risk Likely pathogenic Epidermolysis bullosa simplex, Epidermolysis bullosa simplex 2C, localized
RS60617604 Health Risk Likely pathogenic
RS60720877 Health Risk Likely pathogenic KRT5-related disorder, KRT5-related disorder
RS748836260 Health Risk Likely pathogenic
RS1064793977 Health Risk Pathogenic
RS121912474 Health Risk Pathogenic Epidermolysis bullosa simplex 2B, generalized intermediate, Epidermolysis bullosa simplex 2B
RS121912475 Health Risk Pathogenic Epidermolysis bullosa simplex, Epidermolysis bullosa simplex 2B, generalized intermediate
RS1294665232 Health Risk Pathogenic
RS1592193619 Health Risk Pathogenic
RS1938635857 Health Risk Pathogenic Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
RS1938645889 Health Risk Pathogenic Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
RS1938667202 Health Risk Pathogenic Epidermolysis bullosa simplex, Epidermolysis bullosa simplex
RS2120468268 Health Risk Pathogenic Epidermolysis bullosa simplex with migratory circinate erythema, Epidermolysis bullosa simplex with migratory circinate erythema
RS2120468389 Health Risk Pathogenic Epidermolysis bullosa simplex with migratory circinate erythema, Epidermolysis bullosa simplex with migratory circinate erythema
RS2120471876 Health Risk Pathogenic EPIDERMOLYSIS BULLOSA SIMPLEX 2D, GENERALIZED SEVERE, AUTOSOMAL RECESSIVE
RS2120475630 Health Risk Pathogenic Epidermolysis bullosa simplex with migratory circinate erythema, Epidermolysis bullosa simplex with migratory circinate erythema
RS2498409200 Health Risk Pathogenic
RS2498517138 Health Risk Pathogenic
RS267607443 Health Risk Pathogenic
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