Incidental Mutation 'R8110:Nav2'
ID 630808
Institutional Source Beutler Lab
Gene Symbol Nav2
Ensembl Gene ENSMUSG00000052512
Gene Name neuron navigator 2
Synonyms Rainb1, HELAD1, Unc53H2, RAINB2, 5330421F07Rik, POMFIL2
MMRRC Submission 067539-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.483) question?
Stock # R8110 (G1)
Quality Score 146.008
Status Validated
Chromosome 7
Chromosomal Location 48908716-49610090 bp(+) (GRCm38)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 49551950 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Leucine to Stop codon at position 235 (L235*)
Ref Sequence ENSEMBL: ENSMUSP00000138846 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000064395] [ENSMUST00000183659] [ENSMUST00000184109] [ENSMUST00000184945]
AlphaFold E9Q842
Predicted Effect probably null
Transcript: ENSMUST00000064395
AA Change: L1424*
SMART Domains Protein: ENSMUSP00000067448
Gene: ENSMUSG00000052512
AA Change: L1424*

DomainStartEndE-ValueType
CH 84 187 1.58e-13 SMART
low complexity region 202 210 N/A INTRINSIC
low complexity region 297 310 N/A INTRINSIC
low complexity region 337 348 N/A INTRINSIC
low complexity region 412 424 N/A INTRINSIC
coiled coil region 486 516 N/A INTRINSIC
low complexity region 580 591 N/A INTRINSIC
low complexity region 613 625 N/A INTRINSIC
low complexity region 640 662 N/A INTRINSIC
low complexity region 846 857 N/A INTRINSIC
low complexity region 920 944 N/A INTRINSIC
low complexity region 947 967 N/A INTRINSIC
low complexity region 990 1004 N/A INTRINSIC
low complexity region 1062 1074 N/A INTRINSIC
low complexity region 1343 1360 N/A INTRINSIC
low complexity region 1368 1385 N/A INTRINSIC
low complexity region 1417 1432 N/A INTRINSIC
low complexity region 1454 1466 N/A INTRINSIC
low complexity region 1526 1540 N/A INTRINSIC
low complexity region 1614 1628 N/A INTRINSIC
coiled coil region 1630 1717 N/A INTRINSIC
low complexity region 1789 1800 N/A INTRINSIC
coiled coil region 1841 1909 N/A INTRINSIC
AAA 2093 2247 1.69e-5 SMART
low complexity region 2404 2430 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000183659
AA Change: L1363*
SMART Domains Protein: ENSMUSP00000139309
Gene: ENSMUSG00000052512
AA Change: L1363*

DomainStartEndE-ValueType
low complexity region 2 11 N/A INTRINSIC
CH 23 126 6.19e-16 SMART
low complexity region 141 149 N/A INTRINSIC
low complexity region 236 249 N/A INTRINSIC
low complexity region 276 287 N/A INTRINSIC
low complexity region 351 363 N/A INTRINSIC
coiled coil region 425 455 N/A INTRINSIC
low complexity region 519 530 N/A INTRINSIC
low complexity region 552 564 N/A INTRINSIC
low complexity region 579 601 N/A INTRINSIC
low complexity region 785 796 N/A INTRINSIC
low complexity region 859 883 N/A INTRINSIC
low complexity region 886 906 N/A INTRINSIC
low complexity region 929 943 N/A INTRINSIC
low complexity region 1001 1013 N/A INTRINSIC
low complexity region 1282 1299 N/A INTRINSIC
low complexity region 1307 1324 N/A INTRINSIC
low complexity region 1356 1371 N/A INTRINSIC
low complexity region 1393 1405 N/A INTRINSIC
low complexity region 1465 1479 N/A INTRINSIC
low complexity region 1553 1567 N/A INTRINSIC
coiled coil region 1569 1656 N/A INTRINSIC
low complexity region 1728 1739 N/A INTRINSIC
coiled coil region 1780 1848 N/A INTRINSIC
AAA 2032 2186 1.69e-5 SMART
low complexity region 2343 2369 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000184109
AA Change: L235*
SMART Domains Protein: ENSMUSP00000138846
Gene: ENSMUSG00000052512
AA Change: L235*

DomainStartEndE-ValueType
low complexity region 154 171 N/A INTRINSIC
low complexity region 179 196 N/A INTRINSIC
low complexity region 228 243 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000184945
AA Change: L1424*
SMART Domains Protein: ENSMUSP00000139045
Gene: ENSMUSG00000052512
AA Change: L1424*

DomainStartEndE-ValueType
CH 84 187 1.58e-13 SMART
low complexity region 202 210 N/A INTRINSIC
low complexity region 297 310 N/A INTRINSIC
low complexity region 337 348 N/A INTRINSIC
low complexity region 412 424 N/A INTRINSIC
coiled coil region 486 516 N/A INTRINSIC
low complexity region 580 591 N/A INTRINSIC
low complexity region 613 625 N/A INTRINSIC
low complexity region 640 662 N/A INTRINSIC
low complexity region 846 857 N/A INTRINSIC
low complexity region 920 944 N/A INTRINSIC
low complexity region 947 967 N/A INTRINSIC
low complexity region 990 1004 N/A INTRINSIC
low complexity region 1062 1074 N/A INTRINSIC
low complexity region 1343 1360 N/A INTRINSIC
low complexity region 1368 1385 N/A INTRINSIC
low complexity region 1417 1432 N/A INTRINSIC
low complexity region 1454 1466 N/A INTRINSIC
low complexity region 1526 1540 N/A INTRINSIC
low complexity region 1614 1628 N/A INTRINSIC
coiled coil region 1630 1717 N/A INTRINSIC
low complexity region 1789 1800 N/A INTRINSIC
coiled coil region 1841 1909 N/A INTRINSIC
AAA 2093 2247 1.69e-5 SMART
low complexity region 2404 2430 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 93.1%
Validation Efficiency 99% (73/74)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the neuron navigator gene family, which may play a role in cellular growth and migration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
PHENOTYPE: Homozygous null mice display impaired olfaction and hearing, increased latency in a hot plate test, degeneration of the optic nerve, decreased exploration in new environments, and weight loss. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610010F05Rik G T 11: 23,576,764 (GRCm38) T696N probably benign Het
Ankrd45 T C 1: 161,151,319 (GRCm38) probably null Het
Appl1 C A 14: 26,927,794 (GRCm38) G592* probably null Het
Arfgef2 T A 2: 166,878,544 (GRCm38) M1501K probably benign Het
Calcrl C T 2: 84,339,339 (GRCm38) A333T probably damaging Het
Cd200r3 T A 16: 44,951,472 (GRCm38) I33N probably benign Het
Ceacam15 A G 7: 16,673,409 (GRCm38) L61P probably benign Het
Cfap69 T A 5: 5,582,515 (GRCm38) H827L possibly damaging Het
Csmd3 T A 15: 47,644,270 (GRCm38) E2780V probably damaging Het
Cyp2u1 G A 3: 131,293,654 (GRCm38) T426I probably damaging Het
Eefsec A C 6: 88,376,330 (GRCm38) I119S probably damaging Het
Fem1b T C 9: 62,796,268 (GRCm38) N570S probably damaging Het
Fmo9 A G 1: 166,663,526 (GRCm38) M461T probably benign Het
Fryl A G 5: 73,133,277 (GRCm38) Y95H probably benign Het
Fsip2 T C 2: 82,958,673 (GRCm38) I346T probably benign Het
Fto T C 8: 91,485,190 (GRCm38) F381S probably damaging Het
Gabbr1 G C 17: 37,048,583 (GRCm38) S150T probably benign Het
Galnt9 G T 5: 110,615,473 (GRCm38) W448L probably damaging Het
Gcnt2 G T 13: 40,917,722 (GRCm38) probably benign Het
Gm10800 CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA CAAGAAAACTGAAAATCA 2: 98,667,016 (GRCm38) probably null Het
Gm17727 T C 9: 35,778,033 (GRCm38) *84W probably null Het
Gm8882 C T 6: 132,361,568 (GRCm38) G229D unknown Het
Gmcl1 G T 6: 86,721,426 (GRCm38) A163E probably damaging Het
Hectd4 A G 5: 121,332,949 (GRCm38) Y2633C possibly damaging Het
Hsd11b2 A G 8: 105,522,634 (GRCm38) I214V probably damaging Het
Hspa12a T A 19: 58,821,013 (GRCm38) E217V possibly damaging Het
Itih2 A G 2: 10,097,137 (GRCm38) F845L probably damaging Het
Kcnn3 T A 3: 89,661,233 (GRCm38) L606H probably damaging Het
Krt6b G A 15: 101,680,142 (GRCm38) R28C probably damaging Het
Lama2 T A 10: 26,990,870 (GRCm38) D2876V probably damaging Het
Lmbrd2 T C 15: 9,175,192 (GRCm38) S397P probably damaging Het
Lmf2 C T 15: 89,352,358 (GRCm38) probably null Het
Lrp2 A G 2: 69,506,453 (GRCm38) I1325T probably benign Het
Ltbp2 A T 12: 84,803,902 (GRCm38) C879* probably null Het
Map3k1 A G 13: 111,755,313 (GRCm38) V1136A probably damaging Het
Mettl3 G T 14: 52,300,252 (GRCm38) H84N probably benign Het
Mia2 A G 12: 59,109,087 (GRCm38) probably null Het
Mlip G T 9: 77,239,579 (GRCm38) T92K probably damaging Het
Nalcn T A 14: 123,464,701 (GRCm38) Y466F probably benign Het
Nbn T C 4: 15,981,588 (GRCm38) V560A probably benign Het
Ncln A T 10: 81,493,153 (GRCm38) Y144N possibly damaging Het
Nfe2l2 A C 2: 75,679,421 (GRCm38) D18E probably benign Het
Olfr102 A G 17: 37,313,713 (GRCm38) F224L probably benign Het
Olfr1131 T C 2: 87,628,607 (GRCm38) I48T possibly damaging Het
Olfr356 T C 2: 36,937,709 (GRCm38) C197R possibly damaging Het
Olfr432 G A 1: 174,050,525 (GRCm38) A51T probably benign Het
Otop3 A T 11: 115,339,395 (GRCm38) M33L probably benign Het
Pdzd2 G A 15: 12,373,506 (GRCm38) S2181L probably benign Het
Phf14 T C 6: 11,953,423 (GRCm38) I387T possibly damaging Het
Prdm9 T A 17: 15,554,698 (GRCm38) N318Y probably damaging Het
Proca1 A G 11: 78,204,911 (GRCm38) D123G probably damaging Het
Prune2 G A 19: 17,120,719 (GRCm38) G1196S probably benign Het
Psd3 T A 8: 68,121,056 (GRCm38) S158C probably damaging Het
Rps18 A G 17: 33,955,136 (GRCm38) V15A probably benign Het
Sharpin C A 15: 76,347,765 (GRCm38) R271L possibly damaging Het
Smad5 C A 13: 56,723,888 (GRCm38) Q99K probably damaging Het
Sox5 T C 6: 144,116,474 (GRCm38) M151V possibly damaging Het
Sphkap A T 1: 83,278,771 (GRCm38) F419Y possibly damaging Het
Tbx20 T A 9: 24,725,525 (GRCm38) Y422F probably damaging Het
Tcirg1 A C 19: 3,899,099 (GRCm38) F397V probably damaging Het
Tex36 G A 7: 133,595,283 (GRCm38) S35F possibly damaging Het
Tsen54 G T 11: 115,814,934 (GRCm38) A26S unknown Het
Usp50 T A 2: 126,780,330 (GRCm38) probably null Het
Vmn2r5 A T 3: 64,491,288 (GRCm38) F757I probably benign Het
Zbbx T C 3: 75,155,442 (GRCm38) T3A possibly damaging Het
Zfp28 T A 7: 6,389,829 (GRCm38) M168K probably benign Het
Zfp568 G T 7: 30,023,126 (GRCm38) G499W probably damaging Het
Zfp7 C G 15: 76,890,931 (GRCm38) P391R possibly damaging Het
Other mutations in Nav2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01097:Nav2 APN 7 49,571,194 (GRCm38) missense probably damaging 1.00
IGL01150:Nav2 APN 7 49,452,521 (GRCm38) missense probably benign 0.17
IGL01649:Nav2 APN 7 49,575,729 (GRCm38) missense probably damaging 1.00
IGL01662:Nav2 APN 7 49,571,209 (GRCm38) missense probably damaging 1.00
IGL02297:Nav2 APN 7 49,594,229 (GRCm38) missense probably damaging 0.98
IGL02313:Nav2 APN 7 49,558,773 (GRCm38) missense probably damaging 0.99
IGL02441:Nav2 APN 7 49,452,512 (GRCm38) missense probably damaging 1.00
IGL02472:Nav2 APN 7 49,546,041 (GRCm38) missense probably damaging 1.00
IGL02477:Nav2 APN 7 49,582,875 (GRCm38) missense probably damaging 0.99
IGL02725:Nav2 APN 7 49,565,095 (GRCm38) missense probably damaging 1.00
IGL02944:Nav2 APN 7 49,420,256 (GRCm38) missense probably damaging 0.99
IGL02953:Nav2 APN 7 49,548,423 (GRCm38) missense probably damaging 1.00
IGL03105:Nav2 APN 7 49,464,879 (GRCm38) missense probably damaging 1.00
IGL03234:Nav2 APN 7 49,462,008 (GRCm38) missense possibly damaging 0.94
IGL03274:Nav2 APN 7 49,362,099 (GRCm38) missense probably damaging 1.00
IGL03294:Nav2 APN 7 49,491,457 (GRCm38) nonsense probably null
R0006:Nav2 UTSW 7 49,453,230 (GRCm38) missense possibly damaging 0.50
R0070:Nav2 UTSW 7 49,570,714 (GRCm38) missense probably damaging 1.00
R0113:Nav2 UTSW 7 49,535,953 (GRCm38) missense probably damaging 1.00
R0306:Nav2 UTSW 7 49,545,903 (GRCm38) missense probably benign 0.01
R0346:Nav2 UTSW 7 49,604,585 (GRCm38) missense probably benign 0.11
R0539:Nav2 UTSW 7 49,461,938 (GRCm38) missense probably damaging 1.00
R0669:Nav2 UTSW 7 49,408,683 (GRCm38) missense probably damaging 1.00
R0785:Nav2 UTSW 7 49,420,333 (GRCm38) missense probably benign 0.06
R0970:Nav2 UTSW 7 49,584,153 (GRCm38) missense probably damaging 1.00
R1162:Nav2 UTSW 7 49,536,040 (GRCm38) splice site probably benign
R1274:Nav2 UTSW 7 49,604,430 (GRCm38) nonsense probably null
R1463:Nav2 UTSW 7 49,535,962 (GRCm38) missense probably damaging 1.00
R1464:Nav2 UTSW 7 49,362,204 (GRCm38) missense probably damaging 1.00
R1464:Nav2 UTSW 7 49,362,204 (GRCm38) missense probably damaging 1.00
R1536:Nav2 UTSW 7 49,545,934 (GRCm38) missense probably damaging 1.00
R1612:Nav2 UTSW 7 49,571,211 (GRCm38) missense probably damaging 1.00
R1638:Nav2 UTSW 7 49,452,465 (GRCm38) missense probably benign
R1731:Nav2 UTSW 7 49,548,174 (GRCm38) missense probably damaging 1.00
R1734:Nav2 UTSW 7 49,575,720 (GRCm38) missense probably damaging 1.00
R1865:Nav2 UTSW 7 49,548,195 (GRCm38) missense possibly damaging 0.95
R1945:Nav2 UTSW 7 49,464,872 (GRCm38) missense probably damaging 1.00
R1997:Nav2 UTSW 7 49,548,471 (GRCm38) missense probably benign 0.16
R2061:Nav2 UTSW 7 49,598,897 (GRCm38) splice site probably benign
R2117:Nav2 UTSW 7 49,464,580 (GRCm38) missense probably benign 0.00
R2174:Nav2 UTSW 7 49,452,663 (GRCm38) missense probably damaging 0.99
R2182:Nav2 UTSW 7 49,597,254 (GRCm38) missense probably benign 0.38
R2251:Nav2 UTSW 7 49,453,277 (GRCm38) missense probably damaging 1.00
R2283:Nav2 UTSW 7 49,491,404 (GRCm38) missense probably damaging 1.00
R2343:Nav2 UTSW 7 49,598,817 (GRCm38) missense possibly damaging 0.82
R2472:Nav2 UTSW 7 49,408,884 (GRCm38) missense probably benign
R2568:Nav2 UTSW 7 49,597,564 (GRCm38) missense probably damaging 1.00
R2656:Nav2 UTSW 7 49,545,942 (GRCm38) missense probably damaging 1.00
R2964:Nav2 UTSW 7 49,557,032 (GRCm38) missense probably damaging 1.00
R2966:Nav2 UTSW 7 49,557,032 (GRCm38) missense probably damaging 1.00
R3817:Nav2 UTSW 7 49,464,562 (GRCm38) missense probably benign 0.00
R3834:Nav2 UTSW 7 49,545,858 (GRCm38) missense possibly damaging 0.91
R4207:Nav2 UTSW 7 49,597,231 (GRCm38) missense probably damaging 1.00
R4207:Nav2 UTSW 7 49,572,298 (GRCm38) splice site probably null
R4411:Nav2 UTSW 7 49,398,109 (GRCm38) missense probably benign 0.37
R4413:Nav2 UTSW 7 49,398,109 (GRCm38) missense probably benign 0.37
R4440:Nav2 UTSW 7 49,575,263 (GRCm38) splice site probably benign
R4440:Nav2 UTSW 7 49,552,037 (GRCm38) missense possibly damaging 0.86
R4454:Nav2 UTSW 7 49,548,544 (GRCm38) splice site probably null
R4729:Nav2 UTSW 7 49,452,819 (GRCm38) missense probably benign 0.17
R4801:Nav2 UTSW 7 49,545,852 (GRCm38) missense possibly damaging 0.94
R4802:Nav2 UTSW 7 49,545,852 (GRCm38) missense possibly damaging 0.94
R4824:Nav2 UTSW 7 49,409,001 (GRCm38) intron probably benign
R4887:Nav2 UTSW 7 49,548,434 (GRCm38) nonsense probably null
R4908:Nav2 UTSW 7 49,604,510 (GRCm38) missense probably damaging 1.00
R4952:Nav2 UTSW 7 49,304,540 (GRCm38) intron probably benign
R4965:Nav2 UTSW 7 49,552,877 (GRCm38) nonsense probably null
R5169:Nav2 UTSW 7 49,548,483 (GRCm38) nonsense probably null
R5224:Nav2 UTSW 7 49,551,725 (GRCm38) missense probably benign 0.00
R5249:Nav2 UTSW 7 49,535,913 (GRCm38) missense probably damaging 1.00
R5285:Nav2 UTSW 7 49,548,234 (GRCm38) missense probably damaging 1.00
R5314:Nav2 UTSW 7 49,408,692 (GRCm38) small deletion probably benign
R5320:Nav2 UTSW 7 49,491,373 (GRCm38) missense probably benign 0.00
R5377:Nav2 UTSW 7 49,589,160 (GRCm38) missense probably benign 0.02
R5471:Nav2 UTSW 7 49,548,169 (GRCm38) missense probably damaging 1.00
R5754:Nav2 UTSW 7 49,557,046 (GRCm38) missense probably damaging 1.00
R5832:Nav2 UTSW 7 49,548,069 (GRCm38) splice site probably null
R5884:Nav2 UTSW 7 49,597,169 (GRCm38) nonsense probably null
R5921:Nav2 UTSW 7 49,304,576 (GRCm38) intron probably benign
R6180:Nav2 UTSW 7 49,458,167 (GRCm38) missense probably benign 0.39
R6208:Nav2 UTSW 7 49,564,103 (GRCm38) missense probably damaging 0.99
R6373:Nav2 UTSW 7 49,453,175 (GRCm38) missense probably damaging 1.00
R6450:Nav2 UTSW 7 49,594,366 (GRCm38) missense probably damaging 1.00
R6522:Nav2 UTSW 7 49,597,533 (GRCm38) missense probably damaging 1.00
R6626:Nav2 UTSW 7 49,594,352 (GRCm38) missense probably damaging 1.00
R6695:Nav2 UTSW 7 49,464,904 (GRCm38) missense probably benign 0.04
R6705:Nav2 UTSW 7 49,551,916 (GRCm38) missense probably damaging 1.00
R6842:Nav2 UTSW 7 49,458,169 (GRCm38) missense possibly damaging 0.91
R6847:Nav2 UTSW 7 49,491,456 (GRCm38) missense probably benign 0.14
R7287:Nav2 UTSW 7 49,420,328 (GRCm38) missense probably benign 0.01
R7312:Nav2 UTSW 7 49,461,924 (GRCm38) missense possibly damaging 0.55
R7315:Nav2 UTSW 7 49,548,289 (GRCm38) missense possibly damaging 0.61
R7337:Nav2 UTSW 7 49,551,773 (GRCm38) missense possibly damaging 0.56
R7366:Nav2 UTSW 7 49,554,203 (GRCm38) splice site probably null
R7451:Nav2 UTSW 7 49,552,829 (GRCm38) splice site probably null
R7545:Nav2 UTSW 7 49,582,857 (GRCm38) missense probably damaging 1.00
R7706:Nav2 UTSW 7 49,594,319 (GRCm38) missense probably benign 0.35
R7730:Nav2 UTSW 7 49,572,397 (GRCm38) missense probably damaging 1.00
R7812:Nav2 UTSW 7 49,597,173 (GRCm38) missense probably benign 0.13
R8097:Nav2 UTSW 7 49,587,777 (GRCm38) missense probably damaging 1.00
R8119:Nav2 UTSW 7 49,453,484 (GRCm38) missense probably damaging 0.99
R8298:Nav2 UTSW 7 49,554,261 (GRCm38) critical splice donor site probably null
R8306:Nav2 UTSW 7 49,546,017 (GRCm38) missense probably benign 0.33
R8331:Nav2 UTSW 7 49,452,623 (GRCm38) missense probably benign
R8402:Nav2 UTSW 7 49,453,437 (GRCm38) missense probably benign 0.43
R8421:Nav2 UTSW 7 49,452,521 (GRCm38) missense probably benign
R8478:Nav2 UTSW 7 49,461,985 (GRCm38) missense probably damaging 0.99
R8724:Nav2 UTSW 7 49,491,436 (GRCm38) missense possibly damaging 0.82
R8753:Nav2 UTSW 7 49,452,572 (GRCm38) missense probably benign
R8835:Nav2 UTSW 7 49,598,803 (GRCm38) missense possibly damaging 0.83
R8933:Nav2 UTSW 7 49,461,957 (GRCm38) missense probably damaging 1.00
R8957:Nav2 UTSW 7 49,571,216 (GRCm38) missense probably damaging 1.00
R9069:Nav2 UTSW 7 49,558,813 (GRCm38) missense probably damaging 0.99
R9095:Nav2 UTSW 7 49,604,545 (GRCm38) missense probably damaging 1.00
R9223:Nav2 UTSW 7 49,552,851 (GRCm38) missense probably damaging 1.00
R9261:Nav2 UTSW 7 49,597,156 (GRCm38) missense probably damaging 1.00
X0023:Nav2 UTSW 7 49,547,899 (GRCm38) missense possibly damaging 0.47
Z1177:Nav2 UTSW 7 49,594,223 (GRCm38) missense probably benign 0.01
Z1177:Nav2 UTSW 7 49,452,761 (GRCm38) missense possibly damaging 0.47
Predicted Primers PCR Primer
(F):5'- CCCAGCAAGGTAACCTAGAGTC -3'
(R):5'- CTGCCAGGTAACAGCGAAGTAG -3'

Sequencing Primer
(F):5'- GCCCTCTCTACAGTAAGAACGTGG -3'
(R):5'- CAGCGAAGTAGTTTTTAGATCCC -3'
Posted On 2020-06-30