SLCO1B1 wt Allele

Human SLCO1B1 wild-type allele is located in the vicinity of 12p12 and is approximately 109 kb in length. This allele, which encodes solute carrier organic anion transporter family member 1B1 protein, plays a role in both endogenous factor uptake in the liver and the removal of drug compounds. Mutations in this gene are associated with hyperbilirubinemia, Rotor type, digenic. (NCI Thesaurus)

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SLCO1B1 Gene

This gene is involved in sodium-independent uptake of numerous endogenous compounds in the liver.

SLC7A9 wt Allele

Human SLC7A9 wild-type allele is located in the vicinity of 19q13.1 and is approximately 39 kb in length. This allele, which encodes…

SLC7A9 Gene

This gene plays a role in amino acid transport.

SLC7A5 wt Allele

Human SLC7A5 wild-type allele is located in the vicinity of 16q24.3 and is approximately 39 kb in length. This allele, which encodes…

SLC7A5 Gene

This gene plays a role in high-affinity transport of large neutral amino acids.

SLC7A11 wt Allele

Human SLC7A11 wild-type allele is located within 4q28-q32 and is approximately 78 kb in length. This allele, which encodes cystine/glutamate transporter protein,…