Name

SLC6A2 Gene

solute carrier family 6 (neurotransmitter transporter), member 2

This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]

SLC6A20 Gene

solute carrier family 6 (proline IMINO transporter), member 20

Transport of small hydrophilic substances across cell membranes is mediated by substrate-specific transporter proteins which have been classified into several families of related genes. The protein encoded by this gene is a member of the subgroup of transporter with unidentified substrates within the Na+ and Cl- coupled transporter family. This gene is expressed in kidney, and its alternative splicing generates 2 transcript variants. [provided by RefSeq, Jul 2008]

SLC6A21P Gene

solute carrier family 6, member 21, pseudogene

slc6a2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term slc6a2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

SLC6A2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for SLC6A2 from the Pathway Commons Protein-Protein Interactions dataset.

SLC6A20 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for SLC6A20 from the Pathway Commons Protein-Protein Interactions dataset.