KLKB1 wt Allele

Human KLKB1 wild-type allele is located in the vicinity of 4q35 and is approximately 49 kb in length. This allele, which encodes plasma kallikrein protein, is involved in the regulation of proteolysis, blood coagulation, fibrinolysis and inflammation. Mutation of the gene is associated with a blood coagulation disorder arising from prekallikrein deficiency. (NCI Thesaurus)

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KLKB1 Gene

This gene plays a role in proteolytic processing.

KLK3 wt Allele

Human KLK3 wild-type allele is located in the vicinity of 19q13.41 and is approximately 6 kb in length. This allele, which encodes…

KLK3 Gene

This gene is involved in the hydrolysis of high molecular mass seminal vesicle protein, resulting in the liquefaction of seminal coagulum. …

KLK2 wt Allele

Human KLK2 wild-type allele is located in the vicinity of 19q13.41 and is approximately 7 kb in length. This allele, which encodes…

KLK2 Gene

This gene plays a role in proteolysis.

KLK15 wt Allele

Human KLK15 wild-type allele is located in the vicinity of 19q13.41 and is approximately 6 kb in length. This allele, which encodes…