SLC1A2 wt Allele

Human SLC1A2 wild-type allele is located within 11p13-p12 and is approximately 169 kb in length. This allele, which encodes excitatory amino acid transporter 2 protein, is involved in the regulation of both amino acid transport and synaptic transmission. Mutation and deletion of the gene are associated with amyotrophic lateral sclerosis. (NCI Thesaurus)

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SLC1A2 Gene

This gene plays a role in amino acid transport and synaptic transmission.

SLC19A1 wt Allele

Human SLC19A1 wild-type allele is located in the vicinity of 21q22.3 and is approximately 51 kb in length. This allele, which encodes…

SLC19A1 Gene

This gene plays a role in folate transport.

SLC18A2 wt Allele

Human SLC18A2 wild-type allele is located in the vicinity of 10q25 and is approximately 38 kb in length. This allele, which encodes…

SLC18A2 Gene

This gene plays a role in neurotransmitter transport.

SLC18A1 wt Allele

Human SLC18A1 wild-type allele is located in the vicinity of 8p21.3 and is approximately 38 kb in length. This allele, which encodes…