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PROZ

This gene encodes a liver vitamin K-dependent glycoprotein that is synthesized in the liver and secreted into the plasma. The encoded protein plays a role in regulating blood coagulation by complexing with protein Z-dependent protease inhibitor to directly inhibit activated factor X at the phospholipid surface. Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss. Mutations in this gene are the cause of protein Z deficiency. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]
Protein class

Candidate cardiovascular disease genes, Enzymes, Plasma proteins

Predicted location

Secreted

Single cell type specificity

Group enriched (Hepatocytes, Proximal tubular cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enhanced (HaCaT, Hep G2)

Interaction

Interacts with SERPINA10.

Molecular function

Serine protease homolog

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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