OCT1 Monoclonal Antibody, 50ul Pasteur Pipets Mutations in this gene cause

Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP)

6-biphosphate levels through the activity of 6-phosphofructo-2-kinase/fructose-2

not all variants have been fully characterized

E2F2 and E2F3

HNRNPUL2 (Heterogeneous Nuclear Ribonucleoprotein U-Like 2) is a Protein Coding gene

OCT1 Monoclonal Antibody, 50ul Pasteur Pipets Mutations in this gene causePolyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants