|Institutional Source||Beutler Lab|
|Gene Name||solute carrier family 22 (organic cation transporter), member 2|
|Is this an essential gene?||Non essential (E-score: 0.000)|
|Stock #||R5668 (G1)|
|Chromosomal Location||12584189-12628465 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to C at 12608409 bp|
|Amino Acid Change||Valine to Alanine at position 316 (V316A)|
|Ref Sequence||ENSEMBL: ENSMUSP00000041186 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000046959]|
|Predicted Effect||probably benign
AA Change: V316A
PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
AA Change: V316A
|Meta Mutation Damage Score||0.132|
|Coding Region Coverage||
|Validation Efficiency||99% (84/85)|
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. It is found primarily in the kidney, where it may mediate the first step in cation reabsorption. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knockout allele are viable and fertile and display no obvious phenotypic abnormalities. No significant defects in the renal secretion of a model organic cation are observed. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Slc22a2||
(F):5'- GGCCTACTCAGAAGATCCAACTG -3'
(R):5'- TCTCAGGGAACATGAGTCTTGTG -3'
(F):5'- GTGCTCCCAGAAACTCAACTGTG -3'
(R):5'- TCACTAGTACACGTGGCA -3'