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LRRK2 Gene - GeneCards | LRRK2 Protein | LRRK2 Antibody LRRK2 (Leucine Rich Repeat Kinase 2) is a Protein Coding gene Diseases associated with LRRK2 include Parkinson Disease 8, Autosomal Dominant and Parkinson's Disease
FGG Gene - GeneCards | FIBG Protein | FIBG Antibody The protein encoded by this gene is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots
APOE Gene - GeneCards | APOE Protein | APOE Antibody The protein encoded by this gene is a major apoprotein of the chylomicron It binds to a specific liver and peripheral cell receptor, and is essential for the normal catabolism of triglyceride-rich lipoprotein constituents
BRCA1 Gene - GeneCards | BRCA1 Protein | BRCA1 Antibody This gene encodes a 190 kD nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor The BRCA1 gene contains 22 exons spanning about 110 kb of DNA
CYP1A2 Gene - GeneCards | CP1A2 Protein | CP1A2 Antibody This gene encodes a member of the cytochrome P450 superfamily of enzymes The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids
DHDH Gene - GeneCards | DHDH Protein | DHDH Antibody This gene encodes an enzyme that belongs to the family of dihydrodiol dehydrogenases, which exist in multiple forms in mammalian tissues and are involved in the metabolism of xenobiotics and sugars
SLC12A3 Gene - GeneCards | S12A3 Protein | S12A3 Antibody This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule
HK1 Gene - GeneCards | HXK1 Protein | HXK1 Antibody This gene encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency