Pages
Products

SLC22A9


Official Full Name
solute carrier family 22 member 9
Organism
Homo sapiens
Gene ID
114571
Background
Enables short-chain fatty acid transmembrane transporter activity and sodium-independent organic anion transmembrane transporter activity. Involved in hormone transport; short-chain fatty acid transmembrane transport; and sodium-independent organic anion transport. Located in basolateral plasma membrane. Implicated in Lynch syndrome and mismatch repair cancer syndrome. [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
OAT4; OAT7; ust3; HOAT4; UST3H

Cat.No. Product Name Price
SHH409264 shRNA set against Human SLC22A9 (NM_080866.2) Inquiry
SHH409268 shRNA set against Rat SLC22A9 (NM_173302.1) Inquiry
Cat.No. Product Name Price
CDFG007527 Human SLC22A9 cDNA Clone(NM_080866.2) Inquiry
CDFR014817 Rat Slc22a9 cDNA Clone(NM_173302.1) Inquiry
MiUTR1H-09467 SLC22A9 miRNA 3'UTR clone Inquiry
CDCH081334 human SLC22A9 ORF clone (NM_080866.2) Inquiry
CDCR381880 Rat Slc22a9 ORF Clone(NM_173302.1) Inquiry
CDCS416690 Human SLC22A9 ORF Clone (BC022379) Inquiry
CDCS416691 Human SLC22A9 ORF Clone (BC126288) Inquiry
Quick Inquiry