Incidental Mutation 'R2219:Parp10'
ID 241370
Institutional Source Beutler Lab
Gene Symbol Parp10
Ensembl Gene ENSMUSG00000063268
Gene Name poly (ADP-ribose) polymerase family, member 10
Synonyms
MMRRC Submission 040221-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.097) question?
Stock # R2219 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 76117195-76127640 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 76117783 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 868 (Y868H)
Ref Sequence ENSEMBL: ENSMUSP00000129765 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074834] [ENSMUST00000075689] [ENSMUST00000089610] [ENSMUST00000165738] [ENSMUST00000166428] [ENSMUST00000167754]
AlphaFold Q8CIE4
Predicted Effect probably benign
Transcript: ENSMUST00000074834
SMART Domains Protein: ENSMUSP00000074383
Gene: ENSMUSG00000022565

DomainStartEndE-ValueType
CH 35 134 4.57e-28 SMART
CH 151 249 3.52e-20 SMART
internal_repeat_2 284 366 1.19e-5 PROSPERO
internal_repeat_2 360 442 1.19e-5 PROSPERO
SPEC 507 604 3.08e-5 SMART
SPEC 607 707 1.29e-7 SMART
SPEC 713 875 3.01e0 SMART
low complexity region 954 968 N/A INTRINSIC
SPEC 971 1077 3.48e0 SMART
SPEC 1080 1191 7.63e-1 SMART
SPEC 1198 1358 2.59e-1 SMART
low complexity region 1362 1402 N/A INTRINSIC
low complexity region 1429 1446 N/A INTRINSIC
low complexity region 1459 1490 N/A INTRINSIC
low complexity region 1501 1550 N/A INTRINSIC
low complexity region 1592 1621 N/A INTRINSIC
low complexity region 1646 1671 N/A INTRINSIC
low complexity region 1709 1730 N/A INTRINSIC
low complexity region 1757 1821 N/A INTRINSIC
low complexity region 1837 1862 N/A INTRINSIC
low complexity region 1923 1937 N/A INTRINSIC
low complexity region 1951 1977 N/A INTRINSIC
low complexity region 2007 2041 N/A INTRINSIC
low complexity region 2047 2061 N/A INTRINSIC
low complexity region 2068 2096 N/A INTRINSIC
low complexity region 2105 2154 N/A INTRINSIC
low complexity region 2171 2186 N/A INTRINSIC
low complexity region 2274 2290 N/A INTRINSIC
low complexity region 2313 2331 N/A INTRINSIC
low complexity region 2382 2395 N/A INTRINSIC
low complexity region 2433 2463 N/A INTRINSIC
low complexity region 2516 2537 N/A INTRINSIC
low complexity region 2541 2556 N/A INTRINSIC
low complexity region 2558 2599 N/A INTRINSIC
PLEC 2638 2675 2.99e1 SMART
PLEC 2676 2713 4.49e-7 SMART
PLEC 2714 2751 4.49e-7 SMART
PLEC 2752 2789 3.54e-5 SMART
PLEC 2790 2827 3.27e-9 SMART
PLEC 2831 2865 6.31e-2 SMART
low complexity region 2936 2954 N/A INTRINSIC
PLEC 2966 3003 3.84e0 SMART
PLEC 3004 3041 1.59e-7 SMART
PLEC 3042 3079 3.54e-5 SMART
PLEC 3080 3117 8.64e-9 SMART
PLEC 3118 3155 1.53e-9 SMART
PLEC 3158 3193 2.18e2 SMART
low complexity region 3265 3284 N/A INTRINSIC
PLEC 3335 3372 3.22e-8 SMART
PLEC 3373 3410 7.82e-7 SMART
PLEC 3411 3448 1.9e-5 SMART
PLEC 3449 3486 7.01e-9 SMART
PLEC 3490 3524 3.38e-2 SMART
low complexity region 3536 3557 N/A INTRINSIC
low complexity region 3563 3573 N/A INTRINSIC
low complexity region 3606 3619 N/A INTRINSIC
PLEC 3670 3707 1.22e-8 SMART
PLEC 3708 3745 1.26e-10 SMART
PLEC 3746 3783 2.24e-7 SMART
PLEC 3784 3821 1.82e-7 SMART
PLEC 3825 3858 5.49e1 SMART
PLEC 3862 3895 3.2e2 SMART
PLEC 3913 3950 8.77e-10 SMART
PLEC 3951 3988 4.13e-6 SMART
PLEC 3989 4026 3.03e-4 SMART
PLEC 4027 4064 4.77e-11 SMART
PLEC 4068 4102 1.28e-2 SMART
PLEC 4115 4155 1.05e-7 SMART
low complexity region 4157 4167 N/A INTRINSIC
PLEC 4169 4206 1.73e1 SMART
low complexity region 4232 4247 N/A INTRINSIC
PLEC 4258 4295 3.65e-7 SMART
PLEC 4296 4333 9.99e-14 SMART
PLEC 4334 4371 4.71e-1 SMART
PLEC 4372 4409 2.44e-8 SMART
PLEC 4410 4447 2.87e-5 SMART
low complexity region 4457 4492 N/A INTRINSIC
low complexity region 4495 4521 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000075689
AA Change: Y868H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000075110
Gene: ENSMUSG00000063268
AA Change: Y868H

DomainStartEndE-ValueType
Blast:RRM_2 9 72 1e-13 BLAST
PDB:2DHX|A 9 98 1e-30 PDB
low complexity region 183 193 N/A INTRINSIC
low complexity region 275 285 N/A INTRINSIC
low complexity region 566 575 N/A INTRINSIC
low complexity region 579 593 N/A INTRINSIC
UIM 605 624 9.27e1 SMART
UIM 628 647 1.88e1 SMART
low complexity region 728 738 N/A INTRINSIC
Pfam:PARP 766 954 8.1e-38 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000089610
SMART Domains Protein: ENSMUSP00000087037
Gene: ENSMUSG00000022565

DomainStartEndE-ValueType
low complexity region 16 28 N/A INTRINSIC
low complexity region 40 54 N/A INTRINSIC
CH 73 189 1.46e-26 SMART
CH 206 304 3.52e-20 SMART
internal_repeat_2 339 421 1.38e-5 PROSPERO
internal_repeat_2 415 497 1.38e-5 PROSPERO
SPEC 562 659 3.08e-5 SMART
SPEC 662 762 1.29e-7 SMART
SPEC 768 930 3.01e0 SMART
low complexity region 1009 1023 N/A INTRINSIC
SPEC 1026 1132 3.48e0 SMART
SPEC 1135 1246 7.63e-1 SMART
SPEC 1253 1413 2.59e-1 SMART
low complexity region 1417 1457 N/A INTRINSIC
low complexity region 1484 1501 N/A INTRINSIC
low complexity region 1514 1545 N/A INTRINSIC
low complexity region 1556 1605 N/A INTRINSIC
low complexity region 1647 1676 N/A INTRINSIC
low complexity region 1701 1726 N/A INTRINSIC
low complexity region 1764 1785 N/A INTRINSIC
low complexity region 1812 1876 N/A INTRINSIC
low complexity region 1892 1917 N/A INTRINSIC
low complexity region 1978 1992 N/A INTRINSIC
low complexity region 2006 2032 N/A INTRINSIC
low complexity region 2062 2096 N/A INTRINSIC
low complexity region 2102 2116 N/A INTRINSIC
low complexity region 2123 2151 N/A INTRINSIC
low complexity region 2160 2209 N/A INTRINSIC
low complexity region 2226 2241 N/A INTRINSIC
low complexity region 2329 2345 N/A INTRINSIC
low complexity region 2368 2386 N/A INTRINSIC
low complexity region 2437 2450 N/A INTRINSIC
low complexity region 2488 2518 N/A INTRINSIC
low complexity region 2571 2592 N/A INTRINSIC
low complexity region 2596 2611 N/A INTRINSIC
low complexity region 2613 2654 N/A INTRINSIC
PLEC 2693 2730 2.99e1 SMART
PLEC 2731 2768 4.49e-7 SMART
PLEC 2769 2806 4.49e-7 SMART
PLEC 2807 2844 3.54e-5 SMART
PLEC 2845 2882 3.27e-9 SMART
PLEC 2886 2920 6.31e-2 SMART
low complexity region 2991 3009 N/A INTRINSIC
PLEC 3021 3058 3.84e0 SMART
PLEC 3059 3096 1.59e-7 SMART
PLEC 3097 3134 3.54e-5 SMART
PLEC 3135 3172 8.64e-9 SMART
PLEC 3173 3210 1.53e-9 SMART
PLEC 3213 3248 2.18e2 SMART
low complexity region 3320 3339 N/A INTRINSIC
PLEC 3390 3427 3.22e-8 SMART
PLEC 3428 3465 7.82e-7 SMART
PLEC 3466 3503 1.9e-5 SMART
PLEC 3504 3541 7.01e-9 SMART
PLEC 3545 3579 3.38e-2 SMART
low complexity region 3591 3612 N/A INTRINSIC
low complexity region 3618 3628 N/A INTRINSIC
low complexity region 3661 3674 N/A INTRINSIC
PLEC 3725 3762 1.22e-8 SMART
PLEC 3763 3800 1.26e-10 SMART
PLEC 3801 3838 2.24e-7 SMART
PLEC 3839 3876 1.82e-7 SMART
PLEC 3880 3913 5.49e1 SMART
PLEC 3917 3950 3.2e2 SMART
PLEC 3968 4005 8.77e-10 SMART
PLEC 4006 4043 4.13e-6 SMART
PLEC 4044 4081 3.03e-4 SMART
PLEC 4082 4119 4.77e-11 SMART
PLEC 4123 4157 1.28e-2 SMART
PLEC 4170 4210 1.05e-7 SMART
low complexity region 4212 4222 N/A INTRINSIC
PLEC 4224 4261 1.73e1 SMART
low complexity region 4287 4302 N/A INTRINSIC
PLEC 4313 4350 3.65e-7 SMART
PLEC 4351 4388 9.99e-14 SMART
PLEC 4389 4426 4.71e-1 SMART
PLEC 4427 4464 2.44e-8 SMART
PLEC 4465 4502 2.87e-5 SMART
low complexity region 4512 4547 N/A INTRINSIC
low complexity region 4550 4576 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000165135
Predicted Effect probably damaging
Transcript: ENSMUST00000165738
AA Change: Y868H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129765
Gene: ENSMUSG00000063268
AA Change: Y868H

DomainStartEndE-ValueType
Blast:RRM_2 9 72 1e-13 BLAST
PDB:2DHX|A 9 98 1e-30 PDB
low complexity region 183 193 N/A INTRINSIC
low complexity region 275 285 N/A INTRINSIC
low complexity region 566 575 N/A INTRINSIC
low complexity region 579 593 N/A INTRINSIC
UIM 605 624 9.27e1 SMART
UIM 628 647 1.88e1 SMART
low complexity region 728 738 N/A INTRINSIC
Pfam:PARP 766 954 8.1e-38 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000166151
Predicted Effect unknown
Transcript: ENSMUST00000170226
AA Change: Y17H
SMART Domains Protein: ENSMUSP00000131370
Gene: ENSMUSG00000063268
AA Change: Y17H

DomainStartEndE-ValueType
Pfam:PARP 1 104 6.1e-17 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170851
Predicted Effect noncoding transcript
Transcript: ENSMUST00000169255
Predicted Effect probably benign
Transcript: ENSMUST00000166428
SMART Domains Protein: ENSMUSP00000130915
Gene: ENSMUSG00000022565

DomainStartEndE-ValueType
low complexity region 16 28 N/A INTRINSIC
low complexity region 40 54 N/A INTRINSIC
CH 73 189 1.46e-26 SMART
CH 206 304 3.52e-20 SMART
PDB:2ODU|A 318 549 1e-154 PDB
Blast:SPEC 328 431 3e-63 BLAST
SPEC 562 659 3.08e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000167754
SMART Domains Protein: ENSMUSP00000127867
Gene: ENSMUSG00000022565

DomainStartEndE-ValueType
low complexity region 16 28 N/A INTRINSIC
low complexity region 40 54 N/A INTRINSIC
CH 73 189 1.46e-26 SMART
CH 206 304 3.52e-20 SMART
PDB:2ODU|A 318 549 1e-154 PDB
Blast:SPEC 328 431 3e-63 BLAST
SPEC 562 659 3.08e-5 SMART
low complexity region 677 682 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.0%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Poly(ADP-ribose) polymerases (PARPs), such as PARP10, regulate gene transcription by altering chromatin organization by adding ADP-ribose to histones. PARPs can also function as transcriptional cofactors (Yu et al., 2005 [PubMed 15674325]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 87 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933421I07Rik A G 7: 42,095,769 (GRCm39) Y160H probably damaging Het
Adamts16 G A 13: 70,927,637 (GRCm39) probably benign Het
Adgre1 T A 17: 57,708,912 (GRCm39) N34K possibly damaging Het
Ago2 T A 15: 73,018,260 (GRCm39) E59D probably benign Het
Akap8l G T 17: 32,553,605 (GRCm39) Q372K probably benign Het
Aox1 A G 1: 58,388,289 (GRCm39) probably null Het
Apc2 T C 10: 80,144,943 (GRCm39) V618A probably benign Het
Cacna1d A T 14: 29,764,047 (GRCm39) C2140S probably damaging Het
Cadps2 A G 6: 23,410,831 (GRCm39) L671P probably damaging Het
Capn9 C T 8: 125,335,898 (GRCm39) R529* probably null Het
Ccdc180 T A 4: 45,944,949 (GRCm39) N1452K probably damaging Het
Cdh5 A T 8: 104,869,538 (GRCm39) I755F possibly damaging Het
Cdkal1 T A 13: 29,538,741 (GRCm39) M473L probably benign Het
Cfap65 T C 1: 74,943,184 (GRCm39) I1614V probably damaging Het
Champ1 A G 8: 13,930,017 (GRCm39) H725R probably damaging Het
Cntnap5a A T 1: 116,508,369 (GRCm39) T1294S possibly damaging Het
Cops8 A C 1: 90,534,341 (GRCm39) N94T probably benign Het
Cpne7 G T 8: 123,851,177 (GRCm39) V155L probably benign Het
Dhx29 T C 13: 113,089,338 (GRCm39) V703A probably damaging Het
Dhx30 A G 9: 109,916,703 (GRCm39) L575P probably damaging Het
Dmc1 T A 15: 79,469,327 (GRCm39) H156L possibly damaging Het
Dnmt3a A G 12: 3,899,654 (GRCm39) probably benign Het
Dst C G 1: 34,209,514 (GRCm39) L869V probably damaging Het
Eif3d A T 15: 77,849,142 (GRCm39) M180K probably benign Het
Erbb3 T C 10: 128,405,740 (GRCm39) T1173A probably damaging Het
Fat4 A T 3: 39,064,364 (GRCm39) K4773N probably damaging Het
Fbn2 G A 18: 58,186,035 (GRCm39) P1771L possibly damaging Het
Fer1l4 T G 2: 155,873,684 (GRCm39) Y1207S probably damaging Het
Fermt2 G A 14: 45,713,354 (GRCm39) T87I probably benign Het
Fpr3 T A 17: 18,191,644 (GRCm39) M305K possibly damaging Het
Fzd2 A G 11: 102,496,249 (GRCm39) E231G probably benign Het
Ggcx T C 6: 72,404,965 (GRCm39) Y458H probably benign Het
Ggt7 A G 2: 155,337,639 (GRCm39) S504P probably damaging Het
Gm4884 A G 7: 40,692,910 (GRCm39) H293R possibly damaging Het
Gm5475 A G 15: 100,322,094 (GRCm39) probably benign Het
Gm5930 A T 14: 44,573,993 (GRCm39) L115M probably damaging Het
Itln1 T A 1: 171,359,115 (GRCm39) T122S probably damaging Het
Itpr3 T A 17: 27,334,027 (GRCm39) L2033Q probably benign Het
Lama2 T C 10: 26,919,565 (GRCm39) D2222G probably damaging Het
Lars2 T C 9: 123,247,845 (GRCm39) L334P probably damaging Het
Ly9 T C 1: 171,425,249 (GRCm39) probably null Het
Man1a T C 10: 53,853,145 (GRCm39) I324M probably damaging Het
Mast3 T C 8: 71,233,607 (GRCm39) E994G probably damaging Het
Mettl21a A T 1: 64,655,442 (GRCm39) V46E probably damaging Het
Mmp15 A G 8: 96,096,801 (GRCm39) D398G probably benign Het
Mybpc1 T A 10: 88,391,540 (GRCm39) D319V probably damaging Het
Or10ad1c T A 15: 98,084,848 (GRCm39) K277* probably null Het
Or4a47 A T 2: 89,665,769 (GRCm39) D173E probably damaging Het
Or4a78 A T 2: 89,498,211 (GRCm39) N6K possibly damaging Het
Or4c35 G A 2: 89,808,256 (GRCm39) V45I possibly damaging Het
Or4f61 A T 2: 111,922,752 (GRCm39) I98N probably damaging Het
Or5b113 T A 19: 13,342,901 (GRCm39) I303N possibly damaging Het
Or5p5 G A 7: 107,414,429 (GRCm39) V213I probably benign Het
Or9m1 A C 2: 87,733,269 (GRCm39) Y250* probably null Het
Otogl C T 10: 107,692,838 (GRCm39) C882Y probably damaging Het
Pick1 T A 15: 79,123,899 (GRCm39) I90N probably damaging Het
Piezo1 C T 8: 123,218,227 (GRCm39) V1170I probably benign Het
Pim3 G A 15: 88,747,115 (GRCm39) V54I possibly damaging Het
Pinlyp T C 7: 24,245,433 (GRCm39) probably benign Het
Pira12 A T 7: 3,900,488 (GRCm39) N87K probably benign Het
Ppfia3 G A 7: 45,004,314 (GRCm39) Q473* probably null Het
Rab3gap2 G A 1: 185,008,113 (GRCm39) G1056E probably damaging Het
Ralgapa2 G A 2: 146,263,599 (GRCm39) T706I probably benign Het
Reln T C 5: 22,177,045 (GRCm39) T1874A possibly damaging Het
Rftn1 C A 17: 50,476,173 (GRCm39) M1I probably null Het
Ros1 T A 10: 52,042,175 (GRCm39) Q250L probably damaging Het
Slc11a1 T A 1: 74,419,824 (GRCm39) F166I probably damaging Het
Slc17a9 A G 2: 180,373,755 (GRCm39) T59A probably benign Het
Slc26a5 T C 5: 22,028,476 (GRCm39) K364R probably damaging Het
Slitrk2 T C X: 65,698,754 (GRCm39) I415T probably damaging Het
Stom A G 2: 35,211,613 (GRCm39) I136T possibly damaging Het
Strc G T 2: 121,195,004 (GRCm39) P1728T probably damaging Het
Telo2 C A 17: 25,322,673 (GRCm39) V640F probably benign Het
Tg T C 15: 66,553,782 (GRCm39) V399A probably benign Het
Tmem214 A G 5: 31,030,975 (GRCm39) K383E possibly damaging Het
Tomm40l A T 1: 171,049,550 (GRCm39) L13* probably null Het
Tonsl A T 15: 76,518,840 (GRCm39) N526K probably damaging Het
Top2b T G 14: 16,409,189 (GRCm38) I777M probably damaging Het
Tymp T A 15: 89,258,965 (GRCm39) M240L probably benign Het
Ubr2 A T 17: 47,296,968 (GRCm39) S271T possibly damaging Het
Uggt2 A T 14: 119,312,749 (GRCm39) N353K probably damaging Het
Ugt2b35 T A 5: 87,151,191 (GRCm39) F266I possibly damaging Het
Vmn2r103 C T 17: 20,013,909 (GRCm39) R234W probably damaging Het
Zfp109 C A 7: 23,927,886 (GRCm39) D508Y probably damaging Het
Zfp623 T C 15: 75,819,379 (GRCm39) S112P possibly damaging Het
Zfp735 A G 11: 73,601,851 (GRCm39) N265S possibly damaging Het
Zfp879 A G 11: 50,724,094 (GRCm39) C321R probably damaging Het
Other mutations in Parp10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01376:Parp10 APN 15 76,125,877 (GRCm39) missense probably benign 0.09
IGL01419:Parp10 APN 15 76,125,588 (GRCm39) missense probably damaging 1.00
PIT4687001:Parp10 UTSW 15 76,125,122 (GRCm39) missense probably benign 0.00
R0053:Parp10 UTSW 15 76,126,446 (GRCm39) missense probably damaging 1.00
R0053:Parp10 UTSW 15 76,126,446 (GRCm39) missense probably damaging 1.00
R0126:Parp10 UTSW 15 76,127,266 (GRCm39) missense probably damaging 0.98
R0207:Parp10 UTSW 15 76,126,833 (GRCm39) missense probably benign 0.00
R1300:Parp10 UTSW 15 76,126,190 (GRCm39) missense possibly damaging 0.93
R1412:Parp10 UTSW 15 76,127,284 (GRCm39) missense probably damaging 0.99
R1510:Parp10 UTSW 15 76,125,617 (GRCm39) missense probably damaging 1.00
R1670:Parp10 UTSW 15 76,126,270 (GRCm39) missense probably benign 0.01
R1875:Parp10 UTSW 15 76,127,051 (GRCm39) missense probably damaging 1.00
R2351:Parp10 UTSW 15 76,127,056 (GRCm39) missense probably benign
R4027:Parp10 UTSW 15 76,125,354 (GRCm39) critical splice donor site probably null
R4659:Parp10 UTSW 15 76,127,185 (GRCm39) missense probably damaging 1.00
R4763:Parp10 UTSW 15 76,117,627 (GRCm39) missense probably damaging 0.99
R4828:Parp10 UTSW 15 76,127,281 (GRCm39) missense probably benign 0.00
R5066:Parp10 UTSW 15 76,125,146 (GRCm39) splice site probably benign
R5090:Parp10 UTSW 15 76,125,925 (GRCm39) missense probably damaging 0.97
R5495:Parp10 UTSW 15 76,127,366 (GRCm39) missense probably benign
R6271:Parp10 UTSW 15 76,126,202 (GRCm39) missense probably benign
R6335:Parp10 UTSW 15 76,126,388 (GRCm39) missense probably benign 0.00
R6503:Parp10 UTSW 15 76,126,684 (GRCm39) missense probably damaging 1.00
R6606:Parp10 UTSW 15 76,124,308 (GRCm39) missense possibly damaging 0.66
R6868:Parp10 UTSW 15 76,127,306 (GRCm39) missense probably damaging 1.00
R7197:Parp10 UTSW 15 76,126,616 (GRCm39) missense probably damaging 1.00
R8496:Parp10 UTSW 15 76,117,749 (GRCm39) missense probably damaging 1.00
R8678:Parp10 UTSW 15 76,117,599 (GRCm39) missense probably damaging 1.00
R9053:Parp10 UTSW 15 76,125,964 (GRCm39) missense possibly damaging 0.95
X0027:Parp10 UTSW 15 76,125,704 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AAGATTCTGGGCTGCTGAAGG -3'
(R):5'- CCTCTACCATGGCACTTCAGAG -3'

Sequencing Primer
(F):5'- AGTCCACAGCGCTGTCGTAG -3'
(R):5'- ATGGCACTTCAGAGTCTGCAG -3'
Posted On 2014-10-15