Mutagenetix > Incidental Mutation

Incidental Mutation 'R9367:Slc22a2'

709086

Institutional Source

Beutler Lab

Gene Symbol

Slc22a2

Ensembl Gene

ENSMUSG00000040966

Gene Name

solute carrier family 22 (organic cation transporter), member 2

Synonyms

Oct2, Orct2

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9367 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

12803076-12847376 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 12824837 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Phenylalanine at position 233 (Y233F)

Ref Sequence

ENSEMBL: ENSMUSP00000041186 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046959]

AlphaFold

O70577

Predicted Effect

probably benign
Transcript: ENSMUST00000046959
AA Change: Y233F

PolyPhen 2 Score 0.190 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000041186
Gene: ENSMUSG00000040966
AA Change: Y233F

Domain	Start	End	E-Value	Type
transmembrane domain	21	43	N/A	INTRINSIC
Pfam:Sugar_tr	80	528	7.6e-37	PFAM
Pfam:MFS_1	134	398	3.5e-21	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

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. 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

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2200002D01Rik	CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC	CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC	7: 28,947,048 (GRCm39)		probably benign	Het
4930568D16Rik	A	T	2: 35,244,939 (GRCm39)	Y138N	probably benign	Het
Abca4	T	C	3: 121,838,197 (GRCm39)	M1T	probably null	Het
Acer3	A	G	7: 97,908,621 (GRCm39)	V104A	probably damaging	Het
Agpat4	A	G	17: 12,435,597 (GRCm39)	E287G	probably benign	Het
Akip1	C	T	7: 109,308,156 (GRCm39)	A146V	unknown	Het
Ank2	T	C	3: 126,738,678 (GRCm39)	N2402S	unknown	Het
Arhgdig	A	T	17: 26,418,451 (GRCm39)	Y177*	probably null	Het
Arhgef38	T	A	3: 132,847,998 (GRCm39)	T355S	unknown	Het
Atp8a2	C	A	14: 60,249,827 (GRCm39)		probably null	Het
Atp8b4	A	G	2: 126,216,430 (GRCm39)	I672T	probably damaging	Het
Baat	T	A	4: 49,503,008 (GRCm39)	D38V	probably damaging	Het
Bcl9	T	C	3: 97,117,861 (GRCm39)	S278G	probably benign	Het
Ccdc150	C	T	1: 54,324,760 (GRCm39)	L350F	probably damaging	Het
Ceacam20	T	G	7: 19,705,533 (GRCm39)	S175A	probably damaging	Het
Chd6	A	T	2: 160,871,784 (GRCm39)	I217K	possibly damaging	Het
Cnppd1	T	C	1: 75,117,617 (GRCm39)	I35V	probably benign	Het
Col15a1	T	C	4: 47,245,603 (GRCm39)	I118T	probably damaging	Het
Csmd3	A	T	15: 47,567,564 (GRCm39)	Y1289N		Het
Dio2	T	C	12: 90,696,587 (GRCm39)	T134A	probably benign	Het
Dnaaf9	A	T	2: 130,581,380 (GRCm39)	N678K	probably benign	Het
Dnah17	A	G	11: 117,987,464 (GRCm39)	V1282A	possibly damaging	Het
Dnah17	A	G	11: 118,012,212 (GRCm39)	S517P	possibly damaging	Het
Dync2h1	C	T	9: 7,125,730 (GRCm39)		probably null	Het
Echdc2	C	A	4: 108,036,111 (GRCm39)	P274Q	probably damaging	Het
Fam117a	T	A	11: 95,271,570 (GRCm39)	C381S	probably damaging	Het
Fbxl12	A	G	9: 20,550,130 (GRCm39)	F122S	probably damaging	Het
Gen1	G	A	12: 11,291,309 (GRCm39)	Q892*	probably null	Het
Gimap4	A	G	6: 48,667,746 (GRCm39)	Y167C	probably damaging	Het
Gle1	T	A	2: 29,839,014 (GRCm39)	F476L	probably damaging	Het
Gpr135	A	T	12: 72,117,473 (GRCm39)	V98E	possibly damaging	Het
Greb1l	A	T	18: 10,522,130 (GRCm39)	H742L	probably benign	Het
Habp2	G	T	19: 56,304,781 (GRCm39)	C392F	probably damaging	Het
Hapln3	G	T	7: 78,771,455 (GRCm39)	R145S	probably damaging	Het
Ikbkb	A	G	8: 23,171,711 (GRCm39)	C179R	probably damaging	Het
Kat6a	A	T	8: 23,400,156 (GRCm39)	I306L	possibly damaging	Het
Lmo3	A	T	6: 138,342,958 (GRCm39)	Y140*	probably null	Het
Lrrc32	T	A	7: 98,148,937 (GRCm39)	N572K	probably damaging	Het
Lrrn1	T	A	6: 107,545,093 (GRCm39)	M297K	probably damaging	Het
Magi2	G	A	5: 20,766,308 (GRCm39)	V676I	probably damaging	Het
Mdga1	T	C	17: 30,051,282 (GRCm39)	*957W	probably null	Het
Mip	G	T	10: 128,063,029 (GRCm39)	G158V	probably damaging	Het
Mmp14	T	C	14: 54,677,960 (GRCm39)	I527T	probably benign	Het
Mmp27	G	A	9: 7,573,550 (GRCm39)	G188D	probably damaging	Het
Mylk4	A	T	13: 32,960,236 (GRCm39)	C17S	possibly damaging	Het
Naa50	T	G	16: 43,977,554 (GRCm39)	I94R	probably damaging	Het
Nyap1	A	T	5: 137,734,248 (GRCm39)	Y262N	probably damaging	Het
Obsl1	A	G	1: 75,466,177 (GRCm39)	V1517A	probably benign	Het
P4htm	T	A	9: 108,459,147 (GRCm39)	M262L	probably benign	Het
Pappa2	T	C	1: 158,784,542 (GRCm39)	E156G	probably benign	Het
Pcdhb15	A	T	18: 37,607,971 (GRCm39)	Y401F	possibly damaging	Het
Pde2a	G	A	7: 101,160,361 (GRCm39)	R845H	probably damaging	Het
Peg10	CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG	CCACATCAGGATCCACATCAGGATGCACATCAG	6: 4,756,398 (GRCm39)		probably benign	Het
Penk	C	T	4: 4,134,097 (GRCm39)	M183I	probably benign	Het
Pole	T	C	5: 110,444,955 (GRCm39)	V437A	probably damaging	Het
Ppp1r7	T	C	1: 93,279,262 (GRCm39)	I114T	probably damaging	Het
Prr27	C	A	5: 87,990,994 (GRCm39)	P202Q	probably benign	Het
Pwp2	G	A	10: 78,014,827 (GRCm39)	Q386*	probably null	Het
Rad17	A	T	13: 100,769,720 (GRCm39)	S280T	possibly damaging	Het
Rhebl1	C	T	15: 98,776,414 (GRCm39)	E128K	possibly damaging	Het
Sema3e	G	T	5: 14,291,084 (GRCm39)	V615L	probably benign	Het
Ssu2	A	G	6: 112,357,975 (GRCm39)	S123P	probably damaging	Het
Stk10	A	G	11: 32,538,878 (GRCm39)	E239G		Het
Surf6	G	T	2: 26,782,380 (GRCm39)	Q316K	probably damaging	Het
Tcerg1	G	A	18: 42,685,573 (GRCm39)	D637N	possibly damaging	Het
Tm7sf3	C	T	6: 146,525,179 (GRCm39)	D89N	possibly damaging	Het
Tnxb	C	A	17: 34,931,993 (GRCm39)	F2175L	probably damaging	Het
Trp53i11	G	C	2: 93,029,273 (GRCm39)	V91L	probably benign	Het
Tspan9	A	G	6: 127,944,102 (GRCm39)	V66A	probably damaging	Het
Usp16	C	T	16: 87,261,669 (GRCm39)	T95M	probably benign	Het
Usp9y	A	T	Y: 1,324,982 (GRCm39)	F1691Y	probably damaging	Het
Uty	A	T	Y: 1,099,584 (GRCm39)	L1204I	possibly damaging	Het
Vmn1r192	A	T	13: 22,371,800 (GRCm39)	V140D	possibly damaging	Het
Vps54	T	C	11: 21,250,234 (GRCm39)	V552A	probably benign	Het
Vps8	T	C	16: 21,340,668 (GRCm39)	V804A	possibly damaging	Het
Zfp869	A	C	8: 70,161,057 (GRCm39)	L33R	probably damaging	Het

Other mutations in Slc22a2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00592:Slc22a2	APN	17	12,827,305 (GRCm39)	missense	possibly damaging	0.79
IGL00658:Slc22a2	APN	17	12,834,202 (GRCm39)	missense	probably benign	0.37
IGL01073:Slc22a2	APN	17	12,803,236 (GRCm39)	missense	probably benign	0.00
IGL01573:Slc22a2	APN	17	12,824,848 (GRCm39)	missense	probably damaging	0.99
IGL02000:Slc22a2	APN	17	12,803,270 (GRCm39)	missense	possibly damaging	0.77
IGL02943:Slc22a2	APN	17	12,828,948 (GRCm39)	missense	probably damaging	1.00
IGL03301:Slc22a2	APN	17	12,824,926 (GRCm39)	missense	probably damaging	1.00
R0492:Slc22a2	UTSW	17	12,834,159 (GRCm39)	missense	probably benign	0.00
R0835:Slc22a2	UTSW	17	12,831,318 (GRCm39)	missense	probably benign	0.01
R1330:Slc22a2	UTSW	17	12,805,699 (GRCm39)	missense	possibly damaging	0.94
R1432:Slc22a2	UTSW	17	12,803,195 (GRCm39)	missense	possibly damaging	0.89
R1559:Slc22a2	UTSW	17	12,803,298 (GRCm39)	missense	probably damaging	1.00
R1855:Slc22a2	UTSW	17	12,805,699 (GRCm39)	missense	probably damaging	0.99
R1884:Slc22a2	UTSW	17	12,833,713 (GRCm39)	splice site	probably benign
R2042:Slc22a2	UTSW	17	12,818,012 (GRCm39)	missense	probably benign	0.01
R2197:Slc22a2	UTSW	17	12,817,949 (GRCm39)	missense	probably damaging	1.00
R2255:Slc22a2	UTSW	17	12,818,062 (GRCm39)	missense	probably damaging	1.00
R2271:Slc22a2	UTSW	17	12,805,692 (GRCm39)	missense	probably benign
R4003:Slc22a2	UTSW	17	12,831,337 (GRCm39)	missense	probably benign	0.01
R4021:Slc22a2	UTSW	17	12,803,376 (GRCm39)	missense	probably damaging	1.00
R4093:Slc22a2	UTSW	17	12,831,281 (GRCm39)	missense	probably damaging	1.00
R4404:Slc22a2	UTSW	17	12,833,651 (GRCm39)	missense	probably damaging	1.00
R4419:Slc22a2	UTSW	17	12,831,473 (GRCm39)	nonsense	probably null
R4564:Slc22a2	UTSW	17	12,828,943 (GRCm39)	missense	probably benign	0.08
R4866:Slc22a2	UTSW	17	12,803,316 (GRCm39)	missense	probably damaging	1.00
R4877:Slc22a2	UTSW	17	12,833,702 (GRCm39)	missense	possibly damaging	0.53
R5224:Slc22a2	UTSW	17	12,805,719 (GRCm39)	missense	probably damaging	0.97
R5668:Slc22a2	UTSW	17	12,827,296 (GRCm39)	missense	probably benign
R6326:Slc22a2	UTSW	17	12,831,297 (GRCm39)	nonsense	probably null
R7137:Slc22a2	UTSW	17	12,803,228 (GRCm39)	missense	probably benign
R7211:Slc22a2	UTSW	17	12,805,770 (GRCm39)	critical splice donor site	probably null
R7378:Slc22a2	UTSW	17	12,831,278 (GRCm39)	missense	probably damaging	1.00
R7521:Slc22a2	UTSW	17	12,805,710 (GRCm39)	missense	probably benign	0.14
R7524:Slc22a2	UTSW	17	12,824,944 (GRCm39)	missense	possibly damaging	0.87
R7735:Slc22a2	UTSW	17	12,828,917 (GRCm39)	missense	probably damaging	0.99
R8136:Slc22a2	UTSW	17	12,824,917 (GRCm39)	missense	probably damaging	1.00
R8671:Slc22a2	UTSW	17	12,824,863 (GRCm39)	nonsense	probably null
R8799:Slc22a2	UTSW	17	12,831,425 (GRCm39)	missense	probably benign	0.14
R8874:Slc22a2	UTSW	17	12,828,866 (GRCm39)	missense	probably benign	0.37
R9046:Slc22a2	UTSW	17	12,834,234 (GRCm39)	missense	probably null	0.15
R9220:Slc22a2	UTSW	17	12,838,757 (GRCm39)	missense	probably benign	0.03
R9410:Slc22a2	UTSW	17	12,805,732 (GRCm39)	missense	probably damaging	0.99
R9511:Slc22a2	UTSW	17	12,828,916 (GRCm39)	missense	probably damaging	0.98
R9580:Slc22a2	UTSW	17	12,803,177 (GRCm39)	missense	probably benign	0.00
Z1088:Slc22a2	UTSW	17	12,833,663 (GRCm39)	missense	probably benign	0.36
Z1176:Slc22a2	UTSW	17	12,803,512 (GRCm39)	missense	possibly damaging	0.79
Z1177:Slc22a2	UTSW	17	12,824,897 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CTGCAACGAAATGCCCACTA -3'
(R):5'- TTCATGGGGAAGGAAGACTTG -3'

Sequencing Primer
(F):5'- CGAAATGCCCACTACTACTACTAC -3'
(R):5'- TGGGGAAGGAAGACTTGGATGAC -3'

Posted On

2022-04-18