PROZ protein Z, vitamin K dependent plasma glycoprotein [ Homo sapiens (human) ]
Source: NCBI Gene (ID 8858)
Source: NCBI Gene (ID 8858)
Symbol: PROZ
Full name: protein Z, vitamin K dependent plasma glycoprotein
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: PZ
Summary: 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]
Expression: Biased expression in liver (RPKM 5.4), kidney (RPKM 4.0) and 1 other tissue
Orthologs: mouse
Gene size: 13739bp
Exon count: 10