Mutagenetix > Incidental Mutation

Incidental Mutation 'R0047:Slc47a2'

32979

Institutional Source

Beutler Lab

Gene Symbol

Slc47a2

Ensembl Gene

ENSMUSG00000069855

Gene Name

solute carrier family 47, member 2

Synonyms

4933429E10Rik

MMRRC Submission

038341-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0047 (G1)

Quality Score

215

Status

Validated (trace)

Chromosome

Chromosomal Location

61301631-61342860 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 61336242 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 167 (V167M)

Ref Sequence

ENSEMBL: ENSMUSP00000120907 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000093029] [ENSMUST00000134423]

AlphaFold

Q3V050

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000082784

Predicted Effect

possibly damaging
Transcript: ENSMUST00000093029
AA Change: V167M

PolyPhen 2 Score 0.886 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000090710
Gene: ENSMUSG00000069855
AA Change: V167M

Domain	Start	End	E-Value	Type
low complexity region	22	34	N/A	INTRINSIC
Pfam:MatE	53	213	1.7e-35	PFAM
transmembrane domain	227	246	N/A	INTRINSIC
Pfam:MatE	274	435	4e-34	PFAM
transmembrane domain	444	466	N/A	INTRINSIC
transmembrane domain	545	567	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000134423
AA Change: V167M

PolyPhen 2 Score 0.899 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000120907
Gene: ENSMUSG00000069855
AA Change: V167M

Domain	Start	End	E-Value	Type
low complexity region	22	34	N/A	INTRINSIC
Pfam:MatE	53	213	3.5e-32	PFAM
transmembrane domain	227	246	N/A	INTRINSIC
Pfam:MatE	274	435	1.7e-36	PFAM
transmembrane domain	444	466	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147450

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.0%
20x: 94.8%

Validation Efficiency

100% (98/98)

Allele List at MGI

Other mutations in this stock

Total: 99 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	A	G	3: 138,066,264	T405A	probably damaging	Het
4932438A13Rik	T	A	3: 36,908,192	L481M	possibly damaging	Het
Acer1	A	T	17: 56,955,624	D175E	possibly damaging	Het
Acsf2	T	C	11: 94,569,342	I395V	probably benign	Het
Adamts9	G	A	6: 92,905,306		probably benign	Het
Amigo3	T	C	9: 108,054,658	S427P	probably benign	Het
Ankrd35	A	G	3: 96,684,063	K555R	probably benign	Het
Arhgap35	A	T	7: 16,561,992	H1049Q	probably benign	Het
Arhgef5	G	A	6: 43,265,621		probably null	Het
Arid4a	T	G	12: 71,075,419	L858W	probably damaging	Het
Bbox1	A	G	2: 110,268,302	F310S	probably damaging	Het
Bhlhe22	T	C	3: 18,055,569	L261P	probably damaging	Het
Bmper	T	A	9: 23,406,686	C534S	probably damaging	Het
Cacna1d	T	G	14: 30,346,790		probably benign	Het
Camk2g	G	A	14: 20,771,068		probably benign	Het
Capn12	G	A	7: 28,890,387		probably null	Het
Cdkl4	T	G	17: 80,550,845	N115T	probably benign	Het
Chchd1	T	C	14: 20,704,163	S48P	possibly damaging	Het
Chia1	G	T	3: 106,115,257	C49F	probably damaging	Het
Cnot7	A	G	8: 40,495,921		probably benign	Het
Crh	T	C	3: 19,694,037	E147G	probably damaging	Het
Cux1	T	C	5: 136,363,253		probably benign	Het
Cyp2b19	T	A	7: 26,766,826	D351E	probably benign	Het
Dctn1	G	T	6: 83,182,632	G31*	probably null	Het
Duox1	T	A	2: 122,346,641		probably benign	Het
Egflam	T	G	15: 7,253,430	E382A	possibly damaging	Het
Ext1	T	C	15: 53,345,146	N73S	probably benign	Het
Ffar4	A	G	19: 38,114,004		probably benign	Het
Glg1	A	T	8: 111,165,582	M866K	probably damaging	Het
Golm1	T	A	13: 59,645,100	H197L	probably benign	Het
Gtse1	A	G	15: 85,862,378	K132E	probably damaging	Het
Gxylt2	A	T	6: 100,733,378		probably benign	Het
Hrc	T	A	7: 45,336,689	S421R	probably benign	Het
Ighg2c	T	A	12: 113,288,168		probably benign	Het
Ihh	A	G	1: 74,946,591	I245T	probably benign	Het
Ilf3	T	A	9: 21,388,714	M65K	possibly damaging	Het
Insr	A	G	8: 3,202,947	V404A	probably damaging	Het
Irak2	G	T	6: 113,672,953		probably benign	Het
Irak2	G	A	6: 113,678,738	V367I	probably benign	Het
Kat7	A	C	11: 95,300,208	N119K	probably benign	Het
Kif9	A	G	9: 110,485,038	I33V	probably benign	Het
Klf17	A	G	4: 117,761,032	Y43H	probably benign	Het
Kng2	T	A	16: 22,987,563	T629S	possibly damaging	Het
Lama1	A	T	17: 67,795,186		probably benign	Het
Lamb1	T	C	12: 31,278,601	I188T	possibly damaging	Het
Lpp	T	A	16: 24,661,800		probably benign	Het
Lrp12	T	C	15: 39,878,239	E360G	probably damaging	Het
Mark2	A	C	19: 7,283,577		probably benign	Het
Mmp3	T	C	9: 7,451,910		probably benign	Het
Mthfd1l	T	A	10: 3,978,727		probably benign	Het
Mtr	A	T	13: 12,222,226	S569T	probably damaging	Het
Myh13	T	A	11: 67,367,237	S1752T	probably benign	Het
Myo5a	T	A	9: 75,156,207	L565H	probably damaging	Het
Nanos3	C	T	8: 84,176,134	R133Q	probably damaging	Het
Nfkb1	A	T	3: 135,595,053	L72*	probably null	Het
Numa1	A	G	7: 102,009,453	K296E	probably damaging	Het
Olfr1477	A	G	19: 13,502,589	E82G	probably benign	Het
Olfr186	T	A	16: 59,027,224	M228L	probably benign	Het
Olfr201	C	T	16: 59,269,211	G152D	probably damaging	Het
Olfr508	A	G	7: 108,630,552	I187V	probably benign	Het
Olfr613	A	T	7: 103,552,322	Y179F	probably damaging	Het
Pcdhb5	A	T	18: 37,321,268	I234F	possibly damaging	Het
Pgm5	T	A	19: 24,684,556	I545F	probably damaging	Het
Pla2g2c	T	C	4: 138,743,590		probably benign	Het
Pnpla7	A	T	2: 25,011,606	E548V	probably damaging	Het
Ppm1m	C	A	9: 106,196,696	E273*	probably null	Het
Ppp2r1b	C	T	9: 50,861,573	R117*	probably null	Het
Rabgap1l	G	A	1: 160,231,789		probably benign	Het
Rapgef6	T	A	11: 54,546,378	M49K	possibly damaging	Het
Rhox4f	A	C	X: 37,607,469	V15G	probably benign	Het
Rnf219	T	A	14: 104,503,344		probably null	Het
Rtel1	T	G	2: 181,323,405	I146M	probably damaging	Het
Sdr9c7	A	T	10: 127,903,672	M219L	probably benign	Het
Serpina3g	T	A	12: 104,240,284	S115T	possibly damaging	Het
Serpinb1a	A	T	13: 32,850,276	L44Q	probably damaging	Het
Slc13a4	A	G	6: 35,287,362	I190T	possibly damaging	Het
Slc46a2	A	G	4: 59,914,392	L177P	probably damaging	Het
Snrnp200	C	T	2: 127,234,954		probably benign	Het
Snx13	C	A	12: 35,101,124		probably benign	Het
Snx25	C	T	8: 46,041,365	A828T	probably damaging	Het
Spic	A	G	10: 88,675,941	L151P	probably damaging	Het
Ssu2	G	A	6: 112,374,820	H315Y	probably damaging	Het
Stk32a	T	C	18: 43,313,378		probably benign	Het
Tbx3	A	T	5: 119,680,446	E382V	probably damaging	Het
Tcaf2	A	G	6: 42,629,613	I469T	probably benign	Het
Tln2	A	G	9: 67,240,672		probably benign	Het
Top2a	T	A	11: 98,997,856	I1260L	probably benign	Het
Treml1	C	A	17: 48,364,980	S91*	probably null	Het
Trim26	T	C	17: 36,857,864		probably benign	Het
Trmt11	T	C	10: 30,535,243	N418S	probably benign	Het
Ttf1	A	G	2: 29,084,655	Y801C	probably damaging	Het
Usp34	C	T	11: 23,464,403	A2782V	probably benign	Het
Vmn2r77	T	C	7: 86,811,650	V728A	probably benign	Het
Vps4a	T	C	8: 107,036,701	L29P	probably damaging	Het
Wdfy3	A	G	5: 101,944,033	I480T	probably damaging	Het
Wdr41	A	G	13: 95,010,287	I197V	probably damaging	Het
Ywhag	A	T	5: 135,911,299	V147E	probably damaging	Het
Zan	A	G	5: 137,403,656	M4058T	unknown	Het
Zfp236	C	T	18: 82,680,692	C88Y	probably damaging	Het

Other mutations in Slc47a2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00848:Slc47a2	APN	11	61302233	missense	probably benign	0.16
IGL01367:Slc47a2	APN	11	61329781	missense	probably benign	0.03
IGL01681:Slc47a2	APN	11	61338040	missense	probably damaging	1.00
IGL01874:Slc47a2	APN	11	61312859	critical splice acceptor site	probably null
IGL02049:Slc47a2	APN	11	61342539	missense	probably damaging	0.98
IGL02399:Slc47a2	APN	11	61302194	unclassified	probably benign
IGL02481:Slc47a2	APN	11	61336241	missense	possibly damaging	0.58
IGL02880:Slc47a2	APN	11	61307540	missense	probably damaging	0.97
IGL03068:Slc47a2	APN	11	61303943	missense	probably damaging	1.00
IGL03136:Slc47a2	APN	11	61310765	missense	probably benign	0.00
IGL03236:Slc47a2	APN	11	61313679	missense	probably damaging	1.00
IGL03286:Slc47a2	APN	11	61342467	missense	possibly damaging	0.57
R0047:Slc47a2	UTSW	11	61336242	missense	possibly damaging	0.90
R0597:Slc47a2	UTSW	11	61309976	missense	probably damaging	0.98
R0690:Slc47a2	UTSW	11	61342504	missense	possibly damaging	0.62
R2042:Slc47a2	UTSW	11	61338082	missense	probably benign	0.05
R2217:Slc47a2	UTSW	11	61313671	missense	probably benign	0.00
R2218:Slc47a2	UTSW	11	61313671	missense	probably benign	0.00
R2271:Slc47a2	UTSW	11	61328526	critical splice donor site	probably null
R2272:Slc47a2	UTSW	11	61328526	critical splice donor site	probably null
R4067:Slc47a2	UTSW	11	61303947	missense	probably benign	0.00
R4861:Slc47a2	UTSW	11	61336233	missense	probably benign	0.00
R4861:Slc47a2	UTSW	11	61336233	missense	probably benign	0.00
R4862:Slc47a2	UTSW	11	61313694	missense	possibly damaging	0.69
R4985:Slc47a2	UTSW	11	61302233	missense	probably benign
R5419:Slc47a2	UTSW	11	61307586	missense	probably benign
R5593:Slc47a2	UTSW	11	61342660	missense	probably benign	0.00
R7105:Slc47a2	UTSW	11	61342443	missense	probably benign	0.07
R7358:Slc47a2	UTSW	11	61308873	missense	possibly damaging	0.78
R7522:Slc47a2	UTSW	11	61302250	missense	probably benign	0.14
R8743:Slc47a2	UTSW	11	61342762	missense	probably benign	0.03
R8916:Slc47a2	UTSW	11	61302292	missense	probably damaging	1.00
R9060:Slc47a2	UTSW	11	61336873	missense	probably benign	0.00
R9383:Slc47a2	UTSW	11	61336923	missense	probably damaging	1.00
R9484:Slc47a2	UTSW	11	61336234	missense	possibly damaging	0.46
Z1176:Slc47a2	UTSW	11	61325889	missense	probably benign	0.28
Z1177:Slc47a2	UTSW	11	61328575	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- gggaaACTGAGTATGATCCAACGGC -3'
(R):5'- TGTATTGGCTCAGCTTGTAGCACG -3'

Sequencing Primer
(F):5'- GATCCAACGGCATTATATACAGG -3'
(R):5'- CTACACTGAAAAGTCTCTGCTG -3'

Posted On

2013-05-09