Mutagenetix > Incidental Mutation

Incidental Mutation 'R0652:Slc17a3'

62327

Institutional Source

Beutler Lab

Gene Symbol

Slc17a3

Ensembl Gene

ENSMUSG00000036083

Gene Name

solute carrier family 17 (sodium phosphate), member 3

Synonyms

Npt4

MMRRC Submission

038837-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0652 (G1)

Quality Score

206

Status

Not validated

Chromosome

Chromosomal Location

24023417-24044699 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 24039841 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Phenylalanine at position 293 (S293F)

Ref Sequence

ENSEMBL: ENSMUSP00000131308 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039721] [ENSMUST00000091698] [ENSMUST00000110422] [ENSMUST00000166467]

AlphaFold

G3UWD9

Predicted Effect

probably damaging
Transcript: ENSMUST00000039721
AA Change: S293F

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

SMART Domains

Protein: ENSMUSP00000039062
Gene: ENSMUSG00000036083
AA Change: S293F

Domain	Start	End	E-Value	Type
Pfam:MFS_1	45	377	3.3e-46	PFAM
transmembrane domain	393	415	N/A	INTRINSIC
transmembrane domain	430	452	N/A	INTRINSIC
transmembrane domain	459	481	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000091698
AA Change: S215F

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

SMART Domains

Protein: ENSMUSP00000089290
Gene: ENSMUSG00000036083
AA Change: S215F

Domain	Start	End	E-Value	Type
transmembrane domain	33	55	N/A	INTRINSIC
Pfam:MFS_1	95	293	2.8e-25	PFAM
transmembrane domain	310	332	N/A	INTRINSIC
transmembrane domain	352	369	N/A	INTRINSIC
transmembrane domain	379	398	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000110422
AA Change: S257F

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

SMART Domains

Protein: ENSMUSP00000106052
Gene: ENSMUSG00000036083
AA Change: S257F

Domain	Start	End	E-Value	Type
Pfam:MFS_1	39	425	6.7e-47	PFAM
transmembrane domain	453	475	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000166467
AA Change: S293F

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

SMART Domains

Protein: ENSMUSP00000131308
Gene: ENSMUSG00000036083
AA Change: S293F

Domain	Start	End	E-Value	Type
Pfam:MFS_1	9	338	2.3e-46	PFAM
transmembrane domain	357	379	N/A	INTRINSIC
transmembrane domain	394	416	N/A	INTRINSIC
transmembrane domain	423	445	N/A	INTRINSIC

Meta Mutation Damage Score

0.8156

Coding Region Coverage

1x: 99.3%
3x: 98.5%
10x: 96.3%
20x: 90.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a voltage-driven transporter that excretes intracellular urate and organic anions from the blood into renal tubule cells. Two transcript variants encoding different isoforms have been found for this gene. The longer isoform is a plasma membrane protein with transporter activity while the shorter isoform localizes to the endoplasmic reticulum. [provided by RefSeq, Aug 2012]

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	T	C	11: 110,042,889 (GRCm39)	N387D	probably benign	Het
Adgrg5	T	A	8: 95,660,785 (GRCm39)		probably null	Het
Ahi1	C	A	10: 20,855,360 (GRCm39)	H556Q	probably damaging	Het
Amph	A	G	13: 19,270,791 (GRCm39)		probably null	Het
Apol7a	T	C	15: 77,274,055 (GRCm39)		probably benign	Het
Apoo-ps	A	T	13: 107,550,910 (GRCm39)		noncoding transcript	Het
Arpc1b	A	G	5: 145,063,670 (GRCm39)	D306G	probably damaging	Het
Astn2	T	C	4: 65,712,795 (GRCm39)	D615G	probably damaging	Het
Atm	A	G	9: 53,397,314 (GRCm39)	V1673A	probably damaging	Het
B3gnt3	A	T	8: 72,146,466 (GRCm39)	V21E	probably benign	Het
Bco1	A	G	8: 117,832,435 (GRCm39)	D77G	probably damaging	Het
Brinp2	A	T	1: 158,074,191 (GRCm39)	H643Q	probably damaging	Het
Bsn	A	G	9: 107,982,941 (GRCm39)	F3604S	unknown	Het
Cacna1c	A	G	6: 118,579,190 (GRCm39)	F1753L	probably damaging	Het
Cd74	T	C	18: 60,944,957 (GRCm39)	S201P	probably damaging	Het
Cep192	T	A	18: 67,940,336 (GRCm39)	L101Q	probably benign	Het
Cfap161	T	C	7: 83,442,484 (GRCm39)	I110V	probably null	Het
Cnksr3	T	C	10: 7,070,463 (GRCm39)	D257G	probably damaging	Het
Col14a1	A	C	15: 55,208,278 (GRCm39)	E121A	unknown	Het
Cpne3	T	C	4: 19,532,486 (GRCm39)	D309G	probably benign	Het
Ctnnd1	A	G	2: 84,433,240 (GRCm39)	I609T	probably benign	Het
Cyp2s1	A	G	7: 25,508,683 (GRCm39)	V253A	probably damaging	Het
Dock7	T	C	4: 98,943,586 (GRCm39)	D552G	possibly damaging	Het
Dpyd	A	G	3: 119,220,924 (GRCm39)	D965G	probably damaging	Het
Efcab2	T	A	1: 178,308,911 (GRCm39)	M138K	probably damaging	Het
Eml3	T	C	19: 8,910,649 (GRCm39)	S204P	probably damaging	Het
Fbxw16	T	A	9: 109,265,236 (GRCm39)	S432C	possibly damaging	Het
Fbxw20	T	G	9: 109,061,400 (GRCm39)	Q116H	probably damaging	Het
Fech	A	G	18: 64,591,240 (GRCm39)	S395P	probably damaging	Het
Fgf7	A	G	2: 125,877,875 (GRCm39)	K81E	probably benign	Het
Fras1	T	A	5: 96,929,199 (GRCm39)	Y3868N	possibly damaging	Het
Ganab	A	T	19: 8,892,766 (GRCm39)		probably null	Het
Gfra1	T	C	19: 58,288,986 (GRCm39)	N153S	possibly damaging	Het
Gja4	T	A	4: 127,205,920 (GRCm39)	Y281F	probably benign	Het
Gm5141	T	C	13: 62,921,946 (GRCm39)	T407A	probably damaging	Het
Gm5422	T	C	10: 31,125,277 (GRCm39)		noncoding transcript	Het
Greb1	T	C	12: 16,746,457 (GRCm39)	Y1271C	probably damaging	Het
Hp1bp3	C	A	4: 137,956,080 (GRCm39)	N50K	possibly damaging	Het
Hspg2	T	C	4: 137,242,033 (GRCm39)	F589S	probably damaging	Het
Ido1	A	G	8: 25,075,260 (GRCm39)	F183S	probably damaging	Het
Iqgap1	T	A	7: 80,386,143 (GRCm39)	K936I	probably damaging	Het
Kdm4a	T	C	4: 118,032,886 (GRCm39)	D60G	probably benign	Het
L3mbtl4	G	A	17: 69,081,286 (GRCm39)	C558Y	probably damaging	Het
Lrrc28	T	C	7: 67,267,833 (GRCm39)	N98S	probably damaging	Het
Lypd11	T	A	7: 24,423,622 (GRCm39)	N14I	possibly damaging	Het
Map1a	A	G	2: 121,133,264 (GRCm39)	D1360G	probably benign	Het
Megf10	C	T	18: 57,410,796 (GRCm39)	P702S	probably benign	Het
Met	A	G	6: 17,491,709 (GRCm39)	E157G	probably benign	Het
Mff	A	G	1: 82,728,285 (GRCm39)	D187G	possibly damaging	Het
Mlph	A	T	1: 90,870,630 (GRCm39)	I514F	possibly damaging	Het
Mroh2a	C	T	1: 88,158,402 (GRCm39)	R150*	probably null	Het
Myo15b	T	C	11: 115,755,468 (GRCm39)	V976A	probably benign	Het
Myo9a	A	G	9: 59,779,209 (GRCm39)	D1655G	probably benign	Het
Ncoa6	C	T	2: 155,233,131 (GRCm39)	G2059D	probably benign	Het
Ndst4	A	T	3: 125,405,188 (GRCm39)	H481L	possibly damaging	Het
Nipbl	A	G	15: 8,332,964 (GRCm39)	S2220P	probably benign	Het
Nom1	C	A	5: 29,640,309 (GRCm39)	P212T	probably damaging	Het
Nsd1	A	G	13: 55,395,399 (GRCm39)	D1000G	possibly damaging	Het
Nudt9	T	C	5: 104,198,467 (GRCm39)	F44S	possibly damaging	Het
Numb	C	T	12: 83,842,566 (GRCm39)	V537I	probably damaging	Het
Or10j3b	T	A	1: 173,043,524 (GRCm39)	I102N	possibly damaging	Het
Or13a27	A	T	7: 139,925,545 (GRCm39)	M119K	probably damaging	Het
Or51q1c	A	G	7: 103,652,446 (GRCm39)		probably null	Het
Or5b109	A	T	19: 13,211,899 (GRCm39)	Y95F	possibly damaging	Het
Or5h17	A	G	16: 58,820,063 (GRCm39)	N5S	probably damaging	Het
Or6c211	T	A	10: 129,506,248 (GRCm39)	T47S	probably benign	Het
Osgin1	A	T	8: 120,172,211 (GRCm39)	Y335F	probably damaging	Het
Pcdh10	T	A	3: 45,334,199 (GRCm39)	V171E	probably damaging	Het
Pira13	T	A	7: 3,825,762 (GRCm39)	Y369F	probably benign	Het
Plxna4	T	C	6: 32,162,436 (GRCm39)	N1359S	probably damaging	Het
Ppp1r16a	C	T	15: 76,574,999 (GRCm39)		probably benign	Het
Prr5l	T	C	2: 101,602,635 (GRCm39)	T2A	possibly damaging	Het
Rbp3	T	A	14: 33,680,605 (GRCm39)	I1069N	possibly damaging	Het
Rnf144b	A	G	13: 47,373,983 (GRCm39)	Y60C	probably damaging	Het
Sbno2	A	T	10: 79,903,128 (GRCm39)	V396E	probably damaging	Het
Sdk1	A	G	5: 141,940,713 (GRCm39)	T494A	probably benign	Het
Serac1	G	T	17: 6,102,031 (GRCm39)	D384E	probably damaging	Het
Sgk1	A	G	10: 21,758,556 (GRCm39)	N7D	probably damaging	Het
Sigirr	A	T	7: 140,672,980 (GRCm39)	V69D	possibly damaging	Het
St6gal2	T	C	17: 55,805,290 (GRCm39)	Y396H	probably benign	Het
Ttn	A	T	2: 76,598,956 (GRCm39)	F19319Y	probably damaging	Het
Ubr4	T	A	4: 139,128,637 (GRCm39)	I599N	probably damaging	Het
Vmn1r213	A	G	13: 23,195,564 (GRCm39)		probably benign	Het
Vmn2r96	T	A	17: 18,817,830 (GRCm39)	M469K	probably benign	Het
Wasf1	T	A	10: 40,807,902 (GRCm39)		probably null	Het
Wdr20rt	T	C	12: 65,272,689 (GRCm39)	S51P	probably damaging	Het

Other mutations in Slc17a3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00920:Slc17a3	APN	13	24,040,464 (GRCm39)	missense	probably benign	0.20
IGL02569:Slc17a3	APN	13	24,030,285 (GRCm39)	missense	probably damaging	1.00
IGL02628:Slc17a3	APN	13	24,026,434 (GRCm39)	start codon destroyed	probably null	1.00
IGL02745:Slc17a3	APN	13	24,026,469 (GRCm39)	missense	probably benign	0.01
IGL03001:Slc17a3	APN	13	24,040,767 (GRCm39)	missense	probably damaging	1.00
IGL03143:Slc17a3	APN	13	24,039,962 (GRCm39)	splice site	probably null
IGL03144:Slc17a3	APN	13	24,030,423 (GRCm39)	missense	probably benign	0.00
R0052:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0054:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0131:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0131:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0152:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0153:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0233:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0234:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0257:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0294:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0295:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0318:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0319:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0352:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0462:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0610:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0627:Slc17a3	UTSW	13	24,039,841 (GRCm39)	missense	probably damaging	1.00
R0765:Slc17a3	UTSW	13	24,030,879 (GRCm39)	nonsense	probably null
R1529:Slc17a3	UTSW	13	24,029,428 (GRCm39)	missense	probably damaging	1.00
R1532:Slc17a3	UTSW	13	24,040,483 (GRCm39)	missense	probably damaging	1.00
R1569:Slc17a3	UTSW	13	24,039,591 (GRCm39)	missense	probably benign	0.09
R1640:Slc17a3	UTSW	13	24,036,340 (GRCm39)	nonsense	probably null
R1643:Slc17a3	UTSW	13	24,041,181 (GRCm39)	splice site	probably benign
R1715:Slc17a3	UTSW	13	24,040,724 (GRCm39)	missense	probably benign	0.19
R2407:Slc17a3	UTSW	13	24,036,418 (GRCm39)	critical splice donor site	probably null
R2512:Slc17a3	UTSW	13	24,030,230 (GRCm39)	missense	probably benign	0.13
R3923:Slc17a3	UTSW	13	24,042,037 (GRCm39)	missense	possibly damaging	0.89
R4449:Slc17a3	UTSW	13	24,040,715 (GRCm39)	missense	probably damaging	0.99
R5166:Slc17a3	UTSW	13	24,026,525 (GRCm39)	critical splice donor site	probably null
R5748:Slc17a3	UTSW	13	24,040,449 (GRCm39)	missense	probably damaging	1.00
R5989:Slc17a3	UTSW	13	24,026,411 (GRCm39)	start gained	probably benign
R6281:Slc17a3	UTSW	13	24,040,782 (GRCm39)	missense	probably benign	0.17
R6811:Slc17a3	UTSW	13	24,039,924 (GRCm39)	missense	possibly damaging	0.61
R7283:Slc17a3	UTSW	13	24,039,831 (GRCm39)	missense
R7341:Slc17a3	UTSW	13	24,030,867 (GRCm39)	nonsense	probably null
R7467:Slc17a3	UTSW	13	24,030,950 (GRCm39)	critical splice donor site	probably null
R7485:Slc17a3	UTSW	13	24,039,832 (GRCm39)	missense
R8065:Slc17a3	UTSW	13	24,042,070 (GRCm39)	missense	unknown
R8770:Slc17a3	UTSW	13	24,039,607 (GRCm39)	missense
R8809:Slc17a3	UTSW	13	24,039,575 (GRCm39)	nonsense	probably null
R8867:Slc17a3	UTSW	13	24,039,943 (GRCm39)	missense

Predicted Primers

PCR Primer
(F):5'- TGATTTATGATGACCCTGTCTCTCACCC -3'
(R):5'- ACTGTGACAGATGATGCAAACATGAAGA -3'

Sequencing Primer
(F):5'- TCTCTGAACCAACAGGTACATATAAG -3'
(R):5'- TGATGCAAACATGAAGAAGGAATG -3'

Posted On

2013-07-30