Disease-gene associations mined from literature

Literature associating SLC1A2 and encephalomalacia

SLC1A2 [ENSP00000278379]

Solute carrier family 1 (glial high affinity glutamate transporter), member 2; Sodium-dependent, high-affinity amino acid transporter that mediates the uptake of L-glutamate and also L-aspartate and D-aspartate. Functions as a symporter that transports one amino acid molecule together with two or three Na(+) ions and one proton, in parallel with the counter-transport of one K(+) ion. Mediates Cl(-) flux that is not coupled to amino acid transport; this avoids the accumulation of negative charges due to aspartate and Na(+) symport. Essential for the rapid removal of released glutamate from the synaptic cleft, and for terminating the postsynaptic action of glutamate (By similarity); Belongs to the dicarboxylate/amino acid:cation symporter (DAACS) (TC 2.A.23) family. SLC1A2 subfamily.

Synonyms:  SLC1A2,  SLC1A2p,  hSLC1A2,  A2A2U1,  C9J9N5 ...

Linkouts:  STRING  Pharos  UniProt  OMIM