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. 2010 Mar;62(1):1–96. doi: 10.1124/pr.109.002014

TABLE 16.

In vitro characterization of genetic polymorphisms in OAT1 and -3

In vitro function was assessed using prototypical substrates for OAT1 (methotrexate, ochratoxin A) and OAT3 (estrone sulfate, cimetidine). Nucleotide position was confirmed by PharmGKB (Hewett et al., 2002). OAT1 data from Bleasby et al. (2005) and Fujita et al. (2005). OAT3 data from Erdman et al. (2006).

Nucleotide Change Amino Acid Change In Vitro Function Protein Expression/Localization
SLC22A6 OAT1
    G149A     R50H N.D.
    C311T     P104L N.D.
    T677C     I226T N.D.
    C767T     A256V N.D.
    C877T     R293W N.D.
    G1361A     R454Q N.D.
SLC22A8 OAT3
    C387A     F129L N.D.
    C445A     R149S N.D.
    C715T     Gln239STOP N.D.
    T779G     I260R N.D.
    C829T     R277W ↓↔ N.D.
    T842C     V281A N.D.
    A913T     I305F Normal
    C929T     A310V N.D.
    G1195T     A399S N.D.
    G1342A     V448I N.D.

↓, reduced function; ↔, no change in function; N.D. not determined.