SERPINE1 wt Allele

Human SERPINE1 wild-type allele is located within 7q21.3-q22 and is approximately 12 kb in length. This allele, which encodes plasminogen activator inhibitor 1 protein, plays a role in preventing the generation of plasmin. Defects in the SERPINE1 gene cause PAI-1 deficiency. Overexpression of this gene is associated with thrombophilia. (NCI Thesaurus)

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SERPINE1 Gene

This gene is involved in the control of blood coagulation.

SERPINC1 wt Allele

Human SERPINC1 wild-type allele is located in the vicinity of 1q25.1 and is approximately 14 kb in length. This allele, which encodes…

SERPINC1 Gene

This gene is involved in the regulation of the coagulation cascade.

SERPINB9 wt Allele

Human SERPINB9 wild-type allele is located in the vicinity of 6p25 and is approximately 16 kb in length. This allele, which encodes…

SERPINB9 Gene

This gene plays a role in the regulation of granzyme B-mediated proteolysis.

SERPINB5 wt Allele

Human SERPINB5 wild-type allele is located within 18q21.3 and is approximately 28 kb in length. This allele, which encodes serpin B5 protein,…