SLC2A1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLC2A1 wild-type allele is located within 1p35-p31.3 and is approximately 33 kb in length. This allele, which encodes solute carrier family 2, facilitated glucose transporter member 1 protein, is involved in the regulation of glucose transport. Mutations that exhibit a premature stop codon in the gene are associated with GLUT1 deficiency syndrome.

**Synonyms:** - GLUT - GLUT1 - GTR1 - Glucose Transporter Type 1 Gene - SLC2A1 - Solute Carrier Family 2 (Facilitated Glucose Transporter), Member 1 wt Allele