SLC2A1 wt Allele

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. (NCI Thesaurus)

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SLC2A1 Gene

This gene is involved in glucose transport.

SLC29A2 wt Allele

Human SLC29A2 wild-type allele is located in the vicinity of 11q13 and is approximately 10 kb in length. This allele, which encodes…

SLC29A2 Gene

This gene plays a role in nucleoside transport.

SLC29A1 wt Allele

Human SLC29A1 wild-type allele is located in the vicinity of 6p21.1 and is approximately 15 kb in length. This allele, which encodes…

SLC29A1 Gene

This gene is involved in mediating the cellular uptake of nucleosides.

SLC28A3 wt Allele

Human SLC28A3 wild-type allele is located in the vicinity of 9q22.2 and is approximately 93 kb in length. This allele, which encodes…