Ribosomal Protein L17 Polyclonal Antibody, 100ul Bottle-Top Dispenser Mutations in this gene cause

Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement

The encoded protein is likely associated with the late (trans) Golgi compartments| which are involved in the delivery of secretory and membrane proteins to the endosome| lysosome or the plasma membrane

Diseases associated with NEGR1 include podoconiosis

SSTR4 (somatostatin receptor 4) is a member of the superfamily of receptors having seven transmembrane segments and is expressed in highest levels in fetal and adult brain and lung

This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor

Ribosomal Protein L17 Polyclonal Antibody, 100ul Bottle-Top Dispenser Mutations in this gene causeRibosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. RPL17 encodes a ribosomal protein that is a component of the 60S subunit. 60S ribosomal protein L17 belongs to the L22P family of ribosomal proteins. It is located in the cytoplasm. This gene has been referred to as rpL23 because the