Glucose transporter 1 (or GLUT1), also known as solute carrier family 2, facilitated glucose transporter member 1 (SLC2A1), is a uniporter protein that in humans is encoded by the …

Mar 30, 2025 · SLC2A1 (Solute Carrier Family 2 Member 1) is a Protein Coding gene. Diseases associated with SLC2A1 include Glut1 Deficiency Syndrome 2 and Dystonia 9. Among its …

GLUT1 deficiency is a rare genetic disorder. It is caused by variants in the SLC2A1 gene. SLC2A1 provides instructions for producing GLUT1. In the brain, the GLUT1 protein is …

The SLC2A1 gene provides instructions for producing a protein called the glucose transporter protein type 1 (GLUT1). The GLUT1 protein is embedded in the outer membrane surrounding …

GLUT1, encoded by the SLC2A1 gene, was one of the first membrane transporters to be purified (Baldwin and Lienhard, 1989; Kasahara and Hinkle, 1977) and cloned (Birnbaum et al., 1986; …

A de novo 5'-UTR variant in SLC2A1, generating a novel translation initiation codon, severely compromising SLC2A1 function was identified in a GLUT1 deficiency syndrome patient. High …

Apr 8, 2025 · miR-455-3p ameliorates pancreatic acinar cell injury by targeting Slc2a1. Systemic Reduction of Glut1 Normalizes Retinal Dysfunction, Inflammation, and Oxidative Stress in the …

The SLC2A1 gene encodes the major glucose transporter in brain, placenta, and erythrocytes (Baroni et al., 1992). SLC2A1 also transports dehydroascorbic acid (the oxidized form of …

Mar 24, 2016 · Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration.

Apr 5, 2017 · Using whole-genome sequencing, we identified a de novo 5′-UTR variant in SLC2A1, generating a novel translation initiation codon, severely compromising SLC2A1 …