Mutagenetix > Incidental Mutation

Incidental Mutation 'R6197:Slc22a3'

503003

Institutional Source

Beutler Lab

Gene Symbol

Slc22a3

Ensembl Gene

ENSMUSG00000023828

Gene Name

solute carrier family 22 (organic cation transporter), member 3

Synonyms

EMT, Oct3, Orct3

MMRRC Submission

044337-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6197 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

12638859-12726591 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 12677438 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Isoleucine at position 243 (M243I)

Ref Sequence

ENSEMBL: ENSMUSP00000024595 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024595]

AlphaFold

Q9WTW5

Predicted Effect

probably benign
Transcript: ENSMUST00000024595
AA Change: M243I

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000024595
Gene: ENSMUSG00000023828
AA Change: M243I

Domain	Start	End	E-Value	Type
transmembrane domain	21	43	N/A	INTRINSIC
Pfam:Sugar_tr	105	526	1.2e-28	PFAM
Pfam:MFS_1	144	395	3.3e-22	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.7%

Validation Efficiency

92% (49/53)

MGI Phenotype

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

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700109H08Rik	T	A	5: 3,630,442 (GRCm39)	Y119*	probably null	Het
Abcb9	C	A	5: 124,209,812 (GRCm39)	E664*	probably null	Het
Adgrl2	T	C	3: 148,564,578 (GRCm39)	D334G	probably damaging	Het
Ak9	T	G	10: 41,193,826 (GRCm39)	C57G	probably damaging	Het
Als2cl	A	G	9: 110,724,952 (GRCm39)	K809E	probably damaging	Het
Arsi	G	A	18: 61,049,723 (GRCm39)	G202E	probably benign	Het
Atp11a	A	G	8: 12,896,099 (GRCm39)	I223V	probably benign	Het
Cacna2d3	A	T	14: 28,630,278 (GRCm39)	V1022E	probably benign	Het
Cc2d1b	C	T	4: 108,490,422 (GRCm39)	R825W	probably damaging	Het
Cd37	A	G	7: 44,886,598 (GRCm39)	C85R	probably damaging	Het
Ces1g	T	C	8: 94,063,764 (GRCm39)	S7G	probably benign	Het
Cltc	T	C	11: 86,611,188 (GRCm39)	N561S	probably benign	Het
Cnbd2	A	G	2: 156,217,494 (GRCm39)	E661G	possibly damaging	Het
Col6a3	A	T	1: 90,750,063 (GRCm39)	F257Y	probably damaging	Het
Cpt1b	T	C	15: 89,309,037 (GRCm39)	Y55C	possibly damaging	Het
Csmd1	A	G	8: 15,976,611 (GRCm39)	V2869A	probably benign	Het
Dnah11	T	C	12: 118,143,482 (GRCm39)	E387G	probably benign	Het
Eny2	T	A	15: 44,292,949 (GRCm39)		probably null	Het
Fbxo10	G	T	4: 45,043,857 (GRCm39)	H655Q	probably benign	Het
Gm14403	AAACCCTA	AA	2: 177,201,448 (GRCm39)		probably benign	Het
Gpx2	C	T	12: 76,842,068 (GRCm39)	G28S	probably damaging	Het
H2-Q5	G	T	17: 35,613,918 (GRCm39)	A156S	probably benign	Het
Hoxd4	A	G	2: 74,558,807 (GRCm39)	D210G	possibly damaging	Het
Hoxd9	A	G	2: 74,529,166 (GRCm39)	Q256R	probably damaging	Het
Macf1	A	G	4: 123,346,085 (GRCm39)	V2571A	probably damaging	Het
Mtus1	A	G	8: 41,537,074 (GRCm39)	V214A	possibly damaging	Het
Myh1	C	T	11: 67,111,793 (GRCm39)	A1716V	probably benign	Het
Nbeal1	A	G	1: 60,261,287 (GRCm39)	D249G	probably damaging	Het
Nup54	TCTGCTGCTGCTGCTGCTGCTGCTG	TCTGCTGCTGCTGCTGCTGCTG	5: 92,578,663 (GRCm39)		probably benign	Het
Or10v9	G	T	19: 11,833,148 (GRCm39)	H56Q	probably damaging	Het
Or4c124	A	T	2: 89,155,677 (GRCm39)	N282K	probably damaging	Het
Or5w17	C	T	2: 87,583,696 (GRCm39)	V214I	probably benign	Het
Or7a37	T	G	10: 78,805,974 (GRCm39)	L164V	probably damaging	Het
Peg10	GC	GCTCC	6: 4,756,452 (GRCm39)		probably benign	Het
Pramel23	T	C	4: 143,423,886 (GRCm39)	Y301C	possibly damaging	Het
Prss59	A	G	6: 40,897,939 (GRCm39)	I248T	probably benign	Het
Pwwp2a	A	G	11: 43,595,423 (GRCm39)	D196G	probably benign	Het
Rarg	A	T	15: 102,150,327 (GRCm39)	C93S	possibly damaging	Het
Rcc1	T	C	4: 132,065,073 (GRCm39)	D150G	possibly damaging	Het
Ripk2	A	G	4: 16,163,330 (GRCm39)	Y23H	probably damaging	Het
Rragc	A	G	4: 123,811,340 (GRCm39)	Y5C	possibly damaging	Het
Rubcnl	G	A	14: 75,269,369 (GRCm39)	G9D	probably damaging	Het
Sephs2	A	T	7: 126,872,073 (GRCm39)	V340E	probably damaging	Het
Slco6c1	A	G	1: 97,000,518 (GRCm39)		probably null	Het
Sncaip	T	G	18: 53,039,966 (GRCm39)	I308R	probably damaging	Het
Supt16	G	A	14: 52,408,338 (GRCm39)	T869M	probably damaging	Het
Tanc1	G	A	2: 59,674,366 (GRCm39)	E1817K	possibly damaging	Het
Usp4	C	A	9: 108,248,154 (GRCm39)	Q395K	probably damaging	Het
Usp49	T	A	17: 47,984,272 (GRCm39)	S210T	possibly damaging	Het
Virma	A	G	4: 11,505,498 (GRCm39)	I124M	probably damaging	Het
Vmn1r234	G	A	17: 21,449,589 (GRCm39)	V168I	probably benign	Het
Vnn3	T	A	10: 23,732,187 (GRCm39)	C146S	probably damaging	Het
Ylpm1	A	G	12: 85,088,953 (GRCm39)	D1234G	probably damaging	Het
Zfp617	T	A	8: 72,687,098 (GRCm39)	V476E	probably benign	Het

Other mutations in Slc22a3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00960:Slc22a3	APN	17	12,644,497 (GRCm39)	missense	probably damaging	1.00
IGL01343:Slc22a3	APN	17	12,644,516 (GRCm39)	missense	probably damaging	1.00
IGL01621:Slc22a3	APN	17	12,677,379 (GRCm39)	missense	probably benign	0.02
IGL02228:Slc22a3	APN	17	12,678,697 (GRCm39)	missense	probably damaging	1.00
R0466:Slc22a3	UTSW	17	12,677,380 (GRCm39)	nonsense	probably null
R1501:Slc22a3	UTSW	17	12,725,991 (GRCm39)	missense	probably benign	0.12
R1688:Slc22a3	UTSW	17	12,652,694 (GRCm39)	missense	probably damaging	1.00
R3030:Slc22a3	UTSW	17	12,676,521 (GRCm39)	missense	probably benign	0.00
R4604:Slc22a3	UTSW	17	12,678,658 (GRCm39)	missense	probably benign	0.38
R4754:Slc22a3	UTSW	17	12,726,082 (GRCm39)	missense	probably benign	0.03
R4796:Slc22a3	UTSW	17	12,642,675 (GRCm39)	missense	probably damaging	1.00
R4865:Slc22a3	UTSW	17	12,683,419 (GRCm39)	missense	probably benign	0.03
R5433:Slc22a3	UTSW	17	12,677,377 (GRCm39)	missense	probably damaging	1.00
R5483:Slc22a3	UTSW	17	12,683,354 (GRCm39)	missense	probably damaging	0.99
R5719:Slc22a3	UTSW	17	12,642,691 (GRCm39)	missense	probably damaging	1.00
R5750:Slc22a3	UTSW	17	12,652,395 (GRCm39)	missense	probably benign	0.01
R5872:Slc22a3	UTSW	17	12,652,355 (GRCm39)	missense	probably damaging	1.00
R5988:Slc22a3	UTSW	17	12,652,782 (GRCm39)	missense	possibly damaging	0.92
R7155:Slc22a3	UTSW	17	12,652,518 (GRCm39)	missense	possibly damaging	0.83
R7764:Slc22a3	UTSW	17	12,677,383 (GRCm39)	missense	probably damaging	1.00
R7775:Slc22a3	UTSW	17	12,683,350 (GRCm39)	missense	probably damaging	1.00
R7824:Slc22a3	UTSW	17	12,683,350 (GRCm39)	missense	probably damaging	1.00
R8098:Slc22a3	UTSW	17	12,642,619 (GRCm39)	critical splice donor site	probably null
R8407:Slc22a3	UTSW	17	12,640,368 (GRCm39)	missense	probably benign	0.08
R9135:Slc22a3	UTSW	17	12,645,619 (GRCm39)	missense	possibly damaging	0.92
R9251:Slc22a3	UTSW	17	12,726,093 (GRCm39)	missense	probably damaging	1.00
R9515:Slc22a3	UTSW	17	12,726,057 (GRCm39)	missense	probably damaging	0.99
X0027:Slc22a3	UTSW	17	12,677,358 (GRCm39)	missense	possibly damaging	0.91
Z1088:Slc22a3	UTSW	17	12,644,568 (GRCm39)	nonsense	probably null
Z1177:Slc22a3	UTSW	17	12,726,062 (GRCm39)	missense	probably damaging	1.00
Z1177:Slc22a3	UTSW	17	12,726,058 (GRCm39)	missense	probably damaging	1.00
Z1177:Slc22a3	UTSW	17	12,725,945 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TAGGAAATCCCCTGCATTGCC -3'
(R):5'- TCTCCAGCACTTCTGCACAG -3'

Sequencing Primer
(F):5'- TGCACGCTGCTTTGGGC -3'
(R):5'- GAAGCCTCCATGTCCTCATGTTCTAG -3'

Posted On

2018-02-27