|Institutional Source||Beutler Lab|
|Gene Name||solute carrier family 22 (organic cation transporter), member 3|
|Synonyms||Oct3, EMT, Orct3|
|Is this an essential gene?||Non essential (E-score: 0.000)|
|Stock #||R4865 (G1)|
|Chromosomal Location||12419972-12507704 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||A to T at 12464532 bp|
|Amino Acid Change||Methionine to Lysine at position 148 (M148K)|
|Ref Sequence||ENSEMBL: ENSMUSP00000024595 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000024595]|
|Predicted Effect||probably benign
AA Change: M148K
PolyPhen 2 Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
AA Change: M148K
|Meta Mutation Damage Score||0.1489|
|Coding Region Coverage||
|Validation Efficiency||98% (86/88)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to paraquat-induced dopamine neuron neurotoxicity. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Slc22a3||
(F):5'- CCAAACAAGTGTGAATGTTGTGG -3'
(R):5'- ACTAGGAATCCGATCCCCTG -3'
(F):5'- TGTGGGTGGTGGAATAAGAAATTG -3'
(R):5'- GATCCCCTGCAAGCATTTAAACTG -3'