Mutagenetix > Incidental Mutations

Incidental Mutation 'R4732:St7'

359058

Institutional Source

Beutler Lab

Gene Symbol

St7

Ensembl Gene

ENSMUSG00000029534

Gene Name

suppression of tumorigenicity 7

Synonyms

RAY1, SEN4, Fam4a2, TSG7, 9430001H04Rik, HELG

MMRRC Submission

042022-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.164) question?

Stock #

R4732 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

17692933-17943025 bp(+) (GRCm38)

Type of Mutation

splice site (6 bp from exon)

DNA Base Change (assembly)

T to A at 17906516 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000111080 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000000674] [ENSMUST00000052113] [ENSMUST00000053148] [ENSMUST00000077080] [ENSMUST00000081635] [ENSMUST00000115417] [ENSMUST00000115418] [ENSMUST00000115418] [ENSMUST00000115419] [ENSMUST00000115420] [ENSMUST00000115420] [ENSMUST00000144488] [ENSMUST00000150281]

Predicted Effect

probably null
Transcript: ENSMUST00000000674

SMART Domains

Protein: ENSMUSP00000000674
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	2	507	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000052113

SMART Domains

Protein: ENSMUSP00000062886
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	554	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000053148

SMART Domains

Protein: ENSMUSP00000057326
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	3	534	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000077080

SMART Domains

Protein: ENSMUSP00000076334
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	2	531	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000081635

SMART Domains

Protein: ENSMUSP00000080341
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	17	576	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000115417

SMART Domains

Protein: ENSMUSP00000111077
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	3	511	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000115418

SMART Domains

Protein: ENSMUSP00000111078
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	480	5e-278	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000115418

SMART Domains

Protein: ENSMUSP00000111078
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	480	5e-278	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000115419

SMART Domains

Protein: ENSMUSP00000111079
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	572	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000115420

SMART Domains

Protein: ENSMUSP00000111080
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	448	2.5e-278	PFAM
Pfam:ST7	445	523	2e-31	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000115420

SMART Domains

Protein: ENSMUSP00000111080
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	448	2.5e-278	PFAM
Pfam:ST7	445	523	2e-31	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127322

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138726

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140358

Predicted Effect

probably benign
Transcript: ENSMUST00000144488

SMART Domains

Protein: ENSMUSP00000115215
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	82	6.3e-33	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000150281

SMART Domains

Protein: ENSMUSP00000116304
Gene: ENSMUSG00000029534

Domain	Start	End	E-Value	Type
Pfam:ST7	16	58	1.9e-15	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154059

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183890

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000184157

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154497

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144743

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.2%
20x: 95.1%

Validation Efficiency

99% (110/111)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 192 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700128F08Rik	T	A	9: 8,222,173		noncoding transcript	Het
3110035E14Rik	T	C	1: 9,606,976	S24P	probably benign	Het
4933409G03Rik	A	G	2: 68,614,721		probably benign	Het
Acan	T	C	7: 79,098,609	S1043P	probably damaging	Het
Ackr2	A	G	9: 121,909,183	Y208C	probably damaging	Het
Actg1	C	T	11: 120,347,479		probably benign	Het
Adam1a	T	A	5: 121,519,434	T599S	probably benign	Het
Adamts12	A	T	15: 11,270,662	S668C	probably damaging	Het
Adcy8	A	G	15: 64,754,862	V709A	possibly damaging	Het
Adgrf2	A	C	17: 42,710,754	I393S	probably damaging	Het
Ahnak	G	T	19: 9,007,301	G1983V	probably damaging	Het
AI413582	A	G	17: 27,565,270		probably benign	Het
Aim2	T	A	1: 173,463,876	D282E	possibly damaging	Het
Ak8	A	G	2: 28,760,071	Y370C	probably damaging	Het
Akap9	A	G	5: 4,013,901	D1750G	probably damaging	Het
Als2cl	T	A	9: 110,889,136	V315E	probably damaging	Het
Ankrd28	A	C	14: 31,755,741	C115G	probably benign	Het
Ap3b2	C	T	7: 81,471,932	A519T	probably damaging	Het
Apool	C	T	X: 112,372,200	T166I	probably damaging	Het
Arhgef2	A	T	3: 88,631,940	K65*	probably null	Het
Arhgef38	G	T	3: 133,132,269	Y633*	probably null	Het
Asah2	T	C	19: 31,995,358	N659S	probably benign	Het
Atf7ip2	A	G	16: 10,241,886	D430G	possibly damaging	Het
Atp8a1	G	A	5: 67,813,120	S92L	probably benign	Het
Bag4	C	T	8: 25,769,488	A228T	probably benign	Het
BC024978	T	A	7: 27,201,043	M149K	probably damaging	Het
C130073F10Rik	C	A	4: 101,890,710	S89I	probably benign	Het
Cacna1g	T	C	11: 94,443,215	T867A	probably damaging	Het
Ccdc88a	T	G	11: 29,485,906	N1276K	probably benign	Het
Cdc42bpg	T	A	19: 6,311,191	V282E	probably damaging	Het
Cdipt	T	A	7: 126,978,358	L92H	probably damaging	Het
Celsr2	T	A	3: 108,398,952	D2012V	probably damaging	Het
Cenpt	A	G	8: 105,847,136	V254A	probably benign	Het
Cep104	T	A	4: 153,988,426	D380E	probably damaging	Het
Cers5	C	T	15: 99,741,637	R123Q	probably benign	Het
Ces2h	A	G	8: 105,014,604	E76G	probably damaging	Het
Cfap77	T	A	2: 28,984,388	E143D	probably benign	Het
Chmp7	C	A	14: 69,732,296	R65L	probably damaging	Het
Cldnd2	T	A	7: 43,442,189	C65S	possibly damaging	Het
Clec2g	C	A	6: 128,981,879	Y142*	probably null	Het
Coch	A	T	12: 51,605,019	E549V	probably benign	Het
Cog7	T	C	7: 121,964,244	D215G	probably benign	Het
Col4a2	A	G	8: 11,446,197	H1606R	probably benign	Het
Col4a2	T	C	8: 11,414,779	V348A	probably benign	Het
Cpd	T	C	11: 76,811,794	N583D	probably damaging	Het
Cyp2d11	T	A	15: 82,389,227	Y481F	probably benign	Het
D130043K22Rik	T	C	13: 24,899,665	S1038P	probably damaging	Het
Deptor	C	A	15: 55,181,010	H191N	probably benign	Het
Dgkz	A	T	2: 91,938,339	I699N	probably damaging	Het
Dnah12	C	T	14: 26,781,784	T1653I	probably damaging	Het
Dnah7c	T	A	1: 46,770,173	N3550K	probably damaging	Het
Dnah8	A	G	17: 30,775,061	K3384R	probably null	Het
Dnajc11	A	G	4: 151,970,967		probably benign	Het
Dnajc13	CT	C	9: 104,186,805		probably benign	Het
Dnhd1	C	A	7: 105,673,849	N521K	probably benign	Het
Drg2	T	C	11: 60,461,396		probably null	Het
Dync1h1	C	T	12: 110,649,507	Q3030*	probably null	Het
Efhb	G	A	17: 53,426,244	T533I	probably damaging	Het
Eif2d	T	C	1: 131,164,727	V374A	probably damaging	Het
Etfb	T	C	7: 43,444,200	V17A	probably damaging	Het
F5	C	T	1: 164,181,657	T332M	probably damaging	Het
Fcho1	T	C	8: 71,716,795	T156A	probably benign	Het
Fn1	A	T	1: 71,602,512		probably null	Het
Fnip2	A	T	3: 79,481,652	S561T	probably damaging	Het
Frs2	T	A	10: 117,074,093	T455S	probably benign	Het
Fry	G	A	5: 150,386,007	E639K	possibly damaging	Het
Fto	T	A	8: 91,409,714	D205E	probably damaging	Het
Galntl6	G	A	8: 58,427,813	P147L	probably damaging	Het
Gigyf1	T	A	5: 137,524,770	D844E	probably benign	Het
Gle1	T	C	2: 29,940,232	S267P	probably damaging	Het
Glg1	G	A	8: 111,187,755	R466W	probably damaging	Het
Gm10277	T	C	11: 77,786,097		probably benign	Het
Gm20388	A	G	8: 122,270,274		probably benign	Het
Gm5724	A	T	6: 141,723,179	M509K	probably benign	Het
Gm6871	T	C	7: 41,546,749	I39V	probably benign	Het
Gm9970	A	G	5: 31,241,066		probably benign	Het
Gpr35	T	G	1: 92,983,385	I57S	probably damaging	Het
Gprin1	C	T	13: 54,739,957	G168E	possibly damaging	Het
Gtdc1	A	G	2: 44,789,055		probably benign	Het
Gtf3c2	G	T	5: 31,160,057	P586T	probably damaging	Het
Gucy1a2	A	T	9: 3,759,424	H410L	probably benign	Het
Gucy2c	A	G	6: 136,767,152	S150P	probably damaging	Het
Ifi214	T	C	1: 173,526,591	Q171R	probably benign	Het
Ifit1bl1	T	C	19: 34,594,321	I245M	probably benign	Het
Igkv4-50	T	C	6: 69,701,000	K40R	probably benign	Het
Igkv8-18	T	A	6: 70,356,296	I74N	probably damaging	Het
Il2ra	T	A	2: 11,676,920	M112K	probably benign	Het
Itpr2	A	G	6: 146,373,173	F837S	probably damaging	Het
Kbtbd7	T	C	14: 79,428,800	*691Q	probably null	Het
Kcnn2	T	A	18: 45,560,349	S331T	possibly damaging	Het
Khnyn	T	A	14: 55,886,489		probably null	Het
Kif26a	G	A	12: 112,175,573	A754T	probably benign	Het
Klra3	T	A	6: 130,327,132	Y199F	possibly damaging	Het
Lhx2	A	G	2: 38,359,991	K274R	probably damaging	Het
Lrp2	T	C	2: 69,533,555	I313V	probably benign	Het
Lrrfip1	A	T	1: 91,115,647	E591D	probably benign	Het
Lrrk2	A	C	15: 91,688,849	E200A	probably damaging	Het
Lrrk2	G	A	15: 91,765,747	E1696K	probably damaging	Het
Mast4	A	T	13: 102,772,572	M465K	probably damaging	Het
Moxd2	T	G	6: 40,878,859	I599L	probably benign	Het
Mug2	T	C	6: 122,071,872	S866P	probably damaging	Het
Ncam2	A	G	16: 81,434,884	T79A	possibly damaging	Het
Ncoa6	C	A	2: 155,421,301	Q404H	probably damaging	Het
Neb	A	G	2: 52,279,079	Y1815H	probably damaging	Het
Nell1	A	G	7: 50,856,217	D724G	probably damaging	Het
Nkx3-2	A	G	5: 41,762,144	V167A	probably benign	Het
Nsun3	C	A	16: 62,735,119	C348F	possibly damaging	Het
Obox6	A	T	7: 15,834,772	S60T	possibly damaging	Het
Olfr1	T	C	11: 73,395,695	D109G	probably benign	Het
Olfr1378	G	A	11: 50,969,266	V83M	possibly damaging	Het
Olfr138	T	A	17: 38,275,547	Y259N	probably damaging	Het
Olfr466	T	C	13: 65,152,653	V143A	possibly damaging	Het
Olfr744	T	A	14: 50,618,569	C116S	probably benign	Het
Olfr94	T	C	17: 37,197,024	T315A	probably damaging	Het
Olfr980	A	T	9: 40,006,268	I227N	probably damaging	Het
Oog2	T	A	4: 144,193,941		probably benign	Het
Pabpc1	A	T	15: 36,599,284	V389E	probably benign	Het
Pank4	A	T	4: 154,971,390	M291L	probably benign	Het
Pcf11	T	C	7: 92,658,833	D709G	probably benign	Het
Pcgf1	T	A	6: 83,079,957		probably benign	Het
Pcnx	A	G	12: 81,995,751	I2256V	probably benign	Het
Pex6	A	G	17: 46,722,288	D579G	probably benign	Het
Pex6	A	G	17: 46,724,707		probably null	Het
Piezo2	C	T	18: 63,030,401	A2149T	probably damaging	Het
Pik3c2g	A	G	6: 139,935,985	E781G	probably benign	Het
Pik3r4	G	A	9: 105,678,176	V1111I	possibly damaging	Het
Pkd1l2	T	A	8: 116,995,842		probably null	Het
Plekhg1	T	A	10: 3,957,506	S808T	probably benign	Het
Pnkp	T	A	7: 44,860,454		probably benign	Het
Polr3c	A	T	3: 96,723,661	F148I	probably damaging	Het
Ppard	A	T	17: 28,286,443	T35S	probably benign	Het
Ptov1	T	C	7: 44,867,109	D134G	probably benign	Het
Ptprz1	T	A	6: 23,002,610	S1566R	probably benign	Het
Pum1	T	C	4: 130,718,193	S158P	probably benign	Het
Qk	T	C	17: 10,216,288	H269R	probably damaging	Het
Qrsl1	T	C	10: 43,876,663	Y388C	probably damaging	Het
Rapgef1	T	G	2: 29,689,160	I182S	probably damaging	Het
Ret	T	C	6: 118,163,193	S1013G	possibly damaging	Het
Rimbp3	A	G	16: 17,210,601	R630G	possibly damaging	Het
Rnmt	A	T	18: 68,317,960		probably benign	Het
Ryr2	A	T	13: 11,577,909	M4653K	possibly damaging	Het
Sacm1l	G	A	9: 123,590,830	V553I	probably benign	Het
Sec31b	A	T	19: 44,532,677	S110T	probably damaging	Het
Serpina3k	G	A	12: 104,340,860	G117D	probably damaging	Het
Sesn2	T	C	4: 132,494,591	Y410C	probably damaging	Het
Slc24a1	G	A	9: 64,949,554	R24C	probably benign	Het
Slc35g2	A	C	9: 100,552,502	V372G	probably benign	Het
Slc7a7	T	C	14: 54,408,733	Y91C	probably damaging	Het
Slc7a9	T	A	7: 35,453,563	Y135*	probably null	Het
Slco4a1	A	G	2: 180,473,615	N662D	probably damaging	Het
Slfn4	T	A	11: 83,189,282		probably benign	Het
Slmap	T	C	14: 26,468,535	N156S	probably damaging	Het
Snx18	A	G	13: 113,617,774	S208P	probably benign	Het
Sorbs1	T	A	19: 40,314,689	R485S	probably benign	Het
Spib	A	G	7: 44,528,885	S154P	probably damaging	Het
Spty2d1	T	C	7: 46,996,110	D595G	probably damaging	Het
Susd1	T	C	4: 59,428,029	T52A	possibly damaging	Het
Svs2	T	A	2: 164,237,123	D288V	possibly damaging	Het
Syt7	T	A	19: 10,442,924	I355N	probably damaging	Het
Tarm1	G	A	7: 3,496,900	Q145*	probably null	Het
Teddm2	T	A	1: 153,850,741	E76V	probably damaging	Het
Thsd7b	T	C	1: 129,613,186	S343P	probably damaging	Het
Tigd2	T	A	6: 59,211,415	H422Q	probably benign	Het
Tle1	T	C	4: 72,125,019	N538D	possibly damaging	Het
Tmc2	A	G	2: 130,261,397		probably null	Het
Tmtc1	A	C	6: 148,284,980		probably null	Het
Tns3	C	T	11: 8,450,986	R1104H	probably benign	Het
Trim6	T	C	7: 104,232,648	Y369H	probably damaging	Het
Triobp	G	A	15: 78,967,113	R489K	probably damaging	Het
Trpv4	T	C	5: 114,622,753	D732G	possibly damaging	Het
Trrap	G	A	5: 144,816,570	V1883I	probably damaging	Het
Tsc2	C	A	17: 24,603,275	V1141F	possibly damaging	Het
Ttn	A	T	2: 76,943,011	M2395K	unknown	Het
Ttn	A	G	2: 76,899,827		probably benign	Het
Tyrp1	A	T	4: 80,844,935	D353V	possibly damaging	Het
Ubd	A	C	17: 37,195,702	T160P	probably benign	Het
Ugt2b36	G	T	5: 87,081,538	Y156*	probably null	Het
Ulk4	G	A	9: 121,263,638	R178*	probably null	Het
Unc13d	A	G	11: 116,073,582	V312A	possibly damaging	Het
Urb2	G	T	8: 124,028,897	A448S	probably damaging	Het
Urod	G	A	4: 116,991,673	A92V	possibly damaging	Het
Vmn1r33	T	A	6: 66,611,819	R250S	probably benign	Het
Vmn1r87	A	T	7: 13,132,327	M11K	possibly damaging	Het
Vmn2r77	C	T	7: 86,800,987	T147I	probably benign	Het
Vstm4	A	G	14: 32,917,902	K96E	possibly damaging	Het
Washc4	A	T	10: 83,574,479	M644L	probably benign	Het
Wwp1	T	C	4: 19,661,990	D172G	probably benign	Het
Zbtb38	A	T	9: 96,687,684	V449E	probably damaging	Het
Zfhx4	T	C	3: 5,214,807		probably benign	Het
Zfp229	C	T	17: 21,745,286	H166Y	possibly damaging	Het
Zfp512b	A	G	2: 181,588,739	S453P	probably benign	Het
Zp2	C	A	7: 120,138,120	V282L	probably damaging	Het

Other mutations in St7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00572:St7	APN	6	17855006	missense	probably damaging	1.00
IGL01312:St7	APN	6	17922014	missense	probably damaging	1.00
IGL01562:St7	APN	6	17922035	missense	probably damaging	0.99
IGL01935:St7	APN	6	17930823	missense	probably damaging	0.99
IGL02127:St7	APN	6	17844969	intron	probably benign
IGL02954:St7	APN	6	17848031	missense	probably damaging	1.00
IGL02980:St7	UTSW	6	17749546	intron	probably benign
R0457:St7	UTSW	6	17819282	missense	probably damaging	1.00
R0666:St7	UTSW	6	17934239	missense	probably damaging	1.00
R0680:St7	UTSW	6	17942733	missense	probably damaging	0.99
R1575:St7	UTSW	6	17886111	missense	probably damaging	1.00
R2039:St7	UTSW	6	17886112	missense	probably damaging	1.00
R2144:St7	UTSW	6	17886007	missense	possibly damaging	0.58
R2194:St7	UTSW	6	17942719	missense	probably damaging	1.00
R2869:St7	UTSW	6	17819277	missense	probably damaging	1.00
R2869:St7	UTSW	6	17819277	missense	probably damaging	1.00
R2873:St7	UTSW	6	17819277	missense	probably damaging	1.00
R2874:St7	UTSW	6	17819277	missense	probably damaging	1.00
R2970:St7	UTSW	6	17844909	missense	probably damaging	1.00
R3076:St7	UTSW	6	17846238	nonsense	probably null
R3921:St7	UTSW	6	17846245	missense	probably benign	0.31
R4326:St7	UTSW	6	17819288	missense	probably damaging	1.00
R4327:St7	UTSW	6	17819288	missense	probably damaging	1.00
R4410:St7	UTSW	6	17854933	nonsense	probably null
R4733:St7	UTSW	6	17906516	splice site	probably null
R4868:St7	UTSW	6	17819266	missense	probably damaging	1.00
R4988:St7	UTSW	6	17934226	missense	probably damaging	0.99
R5132:St7	UTSW	6	17854957	missense	probably damaging	0.97
R5182:St7	UTSW	6	17846237	missense	probably damaging	0.99
R5195:St7	UTSW	6	17743637	intron	probably benign
R5358:St7	UTSW	6	17819318	missense	probably damaging	1.00
R5502:St7	UTSW	6	17834674	missense	possibly damaging	0.94
R5882:St7	UTSW	6	17846249	missense	probably damaging	1.00
R5976:St7	UTSW	6	17694222	missense	possibly damaging	0.93
R6049:St7	UTSW	6	17694348	missense	possibly damaging	0.92
R6139:St7	UTSW	6	17694354	missense	probably damaging	1.00
R6177:St7	UTSW	6	17819334	critical splice donor site	probably null
R6181:St7	UTSW	6	17694364	critical splice donor site	probably null
R6401:St7	UTSW	6	17855318	splice site	probably null
R6546:St7	UTSW	6	17852314	missense	probably damaging	1.00
R6711:St7	UTSW	6	17848070	missense	possibly damaging	0.82
R6898:St7	UTSW	6	17854946	missense	probably damaging	1.00
R7536:St7	UTSW	6	17886020	missense	probably damaging	0.99
R7583:St7	UTSW	6	17942754	missense	possibly damaging	0.54
R7626:St7	UTSW	6	17934217	missense	probably damaging	1.00
R7718:St7	UTSW	6	17854999	missense	probably damaging	0.99
R7943:St7	UTSW	6	17844912	missense	probably damaging	1.00
R8334:St7	UTSW	6	17934221	missense	probably damaging	1.00
R8415:St7	UTSW	6	17848081	critical splice donor site	probably null
Z1176:St7	UTSW	6	17848045	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AAGTTTGGAGAGCTTGTGCCC -3'
(R):5'- CCCTTGAGTGTAGGATTTCCC -3'

Sequencing Primer
(F):5'- AAGGGCCCTTCATGTATACTTG -3'
(R):5'- CACAGGTCCCAACTTTTG -3'

Posted On

2015-11-11