Mutagenetix > Incidental Mutation

Incidental Mutation 'R5719:Slc22a3'

451385

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

043339-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5719 (G1)

Quality Score

213

Status

Validated

Chromosome

Chromosomal Location

12638859-12726591 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 12642691 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 509 (V509M)

Ref Sequence

ENSEMBL: ENSMUSP00000024595 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000014578] [ENSMUST00000024595]

AlphaFold

Q9WTW5

Predicted Effect

probably benign
Transcript: ENSMUST00000014578

SMART Domains

Protein: ENSMUSP00000014578
Gene: ENSMUSG00000059481

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
PAN_AP	20	97	8.67e-14	SMART
KR	101	183	1.31e-41	SMART
KR	184	264	5.4e-43	SMART
KR	273	354	3.45e-50	SMART
KR	375	456	3.9e-49	SMART
KR	479	562	5.53e-40	SMART
Tryp_SPc	581	805	4.11e-94	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000024595
AA Change: V509M

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000024595
Gene: ENSMUSG00000023828
AA Change: V509M

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

Meta Mutation Damage Score

0.3806

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.3%

Validation Efficiency

98% (79/81)

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: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A130051J06Rik	C	T	15: 95,688,641 (GRCm39)		probably benign	Het
A630001G21Rik	T	A	1: 85,651,106 (GRCm39)	R110W	probably benign	Het
Abca4	T	C	3: 121,928,915 (GRCm39)		probably null	Het
Abcc3	T	C	11: 94,241,894 (GRCm39)	N1379S	probably damaging	Het
Actrt3	A	C	3: 30,652,276 (GRCm39)	F273V	probably benign	Het
Adam22	T	C	5: 8,417,217 (GRCm39)	D75G	probably benign	Het
Ash1l	C	A	3: 88,961,805 (GRCm39)	D2392E	possibly damaging	Het
Ash1l	T	C	3: 88,965,933 (GRCm39)	I2445T	probably damaging	Het
Bltp2	T	A	11: 78,164,071 (GRCm39)	H1137Q	probably damaging	Het
Cacna2d2	A	G	9: 107,401,851 (GRCm39)	I762V	probably benign	Het
Ccdc127	T	A	13: 74,505,187 (GRCm39)		probably benign	Het
Ccdc91	C	G	6: 147,477,001 (GRCm39)	L230V	unknown	Het
Cdk13	A	G	13: 17,894,240 (GRCm39)	I1129T	probably damaging	Het
Cnot1	C	T	8: 96,470,924 (GRCm39)	R1308H	possibly damaging	Het
Crhr2	T	C	6: 55,080,207 (GRCm39)	H144R	probably damaging	Het
Dnmt1	T	C	9: 20,823,891 (GRCm39)	N993S	possibly damaging	Het
Eif4g1	T	A	16: 20,507,761 (GRCm39)	V1182D	probably damaging	Het
Eml2	G	A	7: 18,935,088 (GRCm39)	V432I	probably damaging	Het
Fam234a	T	A	17: 26,433,627 (GRCm39)	Q399L	possibly damaging	Het
Fyb1	A	T	15: 6,610,350 (GRCm39)	K308*	probably null	Het
Gfral	C	T	9: 76,104,328 (GRCm39)	R228Q	probably benign	Het
Gm10309	A	T	17: 86,806,421 (GRCm39)		probably benign	Het
Gm11595	G	A	11: 99,663,381 (GRCm39)	R100C	unknown	Het
Gm5501	G	A	18: 9,917,417 (GRCm39)		noncoding transcript	Het
Gm6309	A	T	5: 146,104,992 (GRCm39)	V307D	probably benign	Het
Gm9871	T	A	6: 101,773,148 (GRCm39)		noncoding transcript	Het
Greb1l	G	A	18: 10,542,427 (GRCm39)	E1341K	probably damaging	Het
Herc3	T	A	6: 58,871,528 (GRCm39)	V70E	possibly damaging	Het
Hes7	A	G	11: 69,012,415 (GRCm39)	E41G	probably damaging	Het
Ifi27l2b	T	C	12: 103,422,046 (GRCm39)	D106G	unknown	Het
Igfbp6	A	T	15: 102,056,616 (GRCm39)	Y184F	probably damaging	Het
Isyna1	A	G	8: 71,047,352 (GRCm39)	Y25C	probably damaging	Het
Kcng3	G	T	17: 83,938,563 (GRCm39)	T162K	possibly damaging	Het
Krt36	T	C	11: 99,994,987 (GRCm39)	D195G	possibly damaging	Het
Lrwd1	A	T	5: 136,161,093 (GRCm39)		probably null	Het
Lsg1	C	T	16: 30,380,593 (GRCm39)	A615T	probably benign	Het
Myo5a	A	T	9: 75,059,213 (GRCm39)	E480D	probably damaging	Het
Myrf	T	A	19: 10,194,087 (GRCm39)	D690V	probably damaging	Het
N4bp1	T	C	8: 87,578,312 (GRCm39)	I684M	probably damaging	Het
Nlrc3	C	T	16: 3,781,589 (GRCm39)	A607T	probably damaging	Het
Nuak1	A	T	10: 84,245,584 (GRCm39)	I87N	probably damaging	Het
Odad2	G	T	18: 7,211,496 (GRCm39)	Q793K	probably benign	Het
Or5p66	T	G	7: 107,885,599 (GRCm39)	T245P	probably damaging	Het
Or5w11	T	C	2: 87,459,475 (GRCm39)		probably null	Het
Or8b4	A	T	9: 37,830,647 (GRCm39)	E236D	probably damaging	Het
Osbpl9	T	A	4: 108,919,763 (GRCm39)	R689*	probably null	Het
Ppargc1b	T	A	18: 61,440,639 (GRCm39)	M744L	probably benign	Het
Prss40	A	T	1: 34,591,598 (GRCm39)		probably benign	Het
Ptprd	T	A	4: 75,972,839 (GRCm39)		probably null	Het
Rft1	T	C	14: 30,385,183 (GRCm39)		probably benign	Het
Rftn2	C	T	1: 55,253,445 (GRCm39)	V53I	probably damaging	Het
Rnaset2a	T	C	17: 8,350,879 (GRCm39)	Y167C	probably damaging	Het
Schip1	T	C	3: 68,315,560 (GRCm39)		probably benign	Het
Scn5a	A	C	9: 119,359,118 (GRCm39)	L643R	possibly damaging	Het
Shroom3	T	A	5: 93,090,877 (GRCm39)	M1128K	probably benign	Het
Skint8	C	A	4: 111,807,390 (GRCm39)	L359M	probably damaging	Het
Slc14a2	A	G	18: 78,252,257 (GRCm39)	L18P	probably benign	Het
Slc7a5	A	C	8: 122,610,381 (GRCm39)	F478V	probably benign	Het
Smc1b	T	A	15: 84,980,859 (GRCm39)	N803I	probably benign	Het
Snf8	T	A	11: 95,932,551 (GRCm39)	N115K	probably damaging	Het
Stox2	T	A	8: 47,866,172 (GRCm39)	K57*	probably null	Het
Tmem248	T	A	5: 130,258,429 (GRCm39)	F41I	probably damaging	Het
Tmprss7	T	C	16: 45,506,793 (GRCm39)	S90G	probably damaging	Het
Top3b	T	C	16: 16,703,700 (GRCm39)	V285A	probably damaging	Het
Tsen15	T	C	1: 152,247,534 (GRCm39)	T153A	probably damaging	Het
Usp34	T	G	11: 23,304,846 (GRCm39)	S360A	probably benign	Het
Wdr24	T	C	17: 26,047,314 (GRCm39)		probably null	Het
Zbtb2	G	A	10: 4,319,456 (GRCm39)	T190I	probably benign	Het
Zranb3	T	C	1: 127,891,613 (GRCm39)	S788G	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
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
R6197:Slc22a3	UTSW	17	12,677,438 (GRCm39)	missense	probably benign	0.00
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'- TACTAGGGAACACTCCTCAGCC -3'
(R):5'- ATGAGCTGTGCAGAACTGAG -3'

Sequencing Primer
(F):5'- TCCTCAGCCACATTTTAAAAATAGC -3'
(R):5'- CTGTGCAGAACTGAGGAAGATG -3'

Posted On

2017-01-03