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Protein Coding Gene : Slc22a30 solute carrier family 22, member 30
Primary Identifier  MGI:2442750 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  319800
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable short-chain fatty acid transmembrane transporter activity and sodium-independent organic anion transmembrane transporter activity. Predicted to be involved in organic anion transport. Predicted to be located in basolateral plasma membrane. Is expressed in several structures, including genitourinary system; heart; liver; lung; and spleen. Human ortholog(s) of this gene implicated in Lynch syndrome and mismatch repair cancer syndrome. Orthologous to several human genes including SLC22A25 (solute carrier family 22 member 25).
  • synonyms:
  • C730048C13Rik,
  • solute carrier family 22, member 30,
  • Slc22a30,
  • AA986766,
  • expressed sequence AA986766,
  • RIKEN cDNA C730048C13 gene,
  • MGI:2147468
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