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Slc22a21

Official Full Name
solute carrier family 22 (organic cation transporter), member 21
Organism
Mus musculus
GeneID
56517
Background
Enables carnitine transmembrane transporter activity. Acts upstream of or within carnitine transport. Located in peroxisomal membrane. Is expressed in several structures, including genitourinary system; liver; lung; nasal cavity mucosa; and spleen. Human ortholog(s) of this gene implicated in Crohn's disease; cardiomyopathy; inherited metabolic disorder; and systemic primary carnitine deficiency disease. Orthologous to human SLC22A5 (solute carrier family 22 member 5). [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
Slc22a21; Octn3; Slc22a9;

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