Incidental Mutation 'R9036:Arfgef1'
ID 687351
Institutional Source Beutler Lab
Gene Symbol Arfgef1
Ensembl Gene ENSMUSG00000067851
Gene Name ADP ribosylation factor guanine nucleotide exchange factor 1
Synonyms D730028O18Rik, D130059B05Rik, BIG1, P200, ARFGEP1
MMRRC Submission 068865-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R9036 (G1)
Quality Score 225.009
Status Not validated
Chromosome 1
Chromosomal Location 10207796-10302895 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 10259055 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 681 (S681T)
Ref Sequence ENSEMBL: ENSMUSP00000085986 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088615] [ENSMUST00000131556]
AlphaFold G3X9K3
Predicted Effect probably benign
Transcript: ENSMUST00000088615
AA Change: S681T

PolyPhen 2 Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000085986
Gene: ENSMUSG00000067851
AA Change: S681T

DomainStartEndE-ValueType
Pfam:DCB 28 213 5.2e-45 PFAM
low complexity region 221 233 N/A INTRINSIC
low complexity region 291 306 N/A INTRINSIC
Pfam:Sec7_N 416 575 1.3e-52 PFAM
Blast:Sec7 588 637 6e-24 BLAST
low complexity region 661 681 N/A INTRINSIC
Sec7 692 879 1.15e-105 SMART
Blast:Sec7 897 933 6e-13 BLAST
Blast:Sec7 947 986 8e-18 BLAST
Pfam:DUF1981 1217 1300 3.6e-39 PFAM
low complexity region 1587 1602 N/A INTRINSIC
low complexity region 1777 1782 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000131556
AA Change: S681T

PolyPhen 2 Score 0.185 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000118805
Gene: ENSMUSG00000067851
AA Change: S681T

DomainStartEndE-ValueType
coiled coil region 207 234 N/A INTRINSIC
low complexity region 291 306 N/A INTRINSIC
Pfam:Sec7_N 413 576 3.1e-59 PFAM
Blast:Sec7 588 637 2e-24 BLAST
low complexity region 661 681 N/A INTRINSIC
Sec7 692 879 1.15e-105 SMART
Blast:Sec7 897 933 3e-13 BLAST
Blast:Sec7 947 986 2e-18 BLAST
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] ADP-ribosylation factors (ARFs) play an important role in intracellular vesicular trafficking. The protein encoded by this gene is involved in the activation of ARFs by accelerating replacement of bound GDP with GTP. It contains a Sec7 domain, which may be responsible for guanine-nucleotide exchange activity and also brefeldin A inhibition. [provided by RefSeq, Aug 2011]
PHENOTYPE: Mice homozygous for a null allele exhibit neonatal lethality, absent gastric milk and decreased brain size with increased neuron apoptosis, abnormal axon guidance and hypersensitivity to glutamate. [provided by MGI curators]
Allele List at MGI

All alleles(10) : Gene trapped(10)

Other mutations in this stock
Total: 93 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl6 G T 11: 54,227,840 (GRCm39) probably null Het
Anapc5 A G 5: 122,957,716 (GRCm39) L69P possibly damaging Het
Aoc1l3 CCTAAATTTCCTATCCCGATCAGCAAGGGTGGCCCTCGAGTGCCCCAGCCCCATGCTAAATTTCC CCTAAATTTCC 6: 48,965,074 (GRCm39) probably benign Het
Arhgef19 A G 4: 140,976,549 (GRCm39) D437G probably damaging Het
Arhgef25 A G 10: 127,019,089 (GRCm39) V576A probably benign Het
Arl5b T C 2: 15,073,012 (GRCm39) probably null Het
Atg10 T A 13: 91,189,071 (GRCm39) T80S probably benign Het
BC034090 A G 1: 155,117,419 (GRCm39) V233A possibly damaging Het
Bicdl2 C T 17: 23,887,158 (GRCm39) R482C probably damaging Het
Ccdc63 G A 5: 122,247,346 (GRCm39) P500S probably benign Het
Ccn2 A T 10: 24,472,647 (GRCm39) T186S probably benign Het
Ccng1 A T 11: 40,643,078 (GRCm39) I123K possibly damaging Het
Ccp110 C T 7: 118,324,680 (GRCm39) S734F probably damaging Het
Cds2 T C 2: 132,139,614 (GRCm39) probably null Het
Cenpw G A 10: 30,074,523 (GRCm39) T58I probably benign Het
Cfap61 T A 2: 145,850,839 (GRCm39) L326I probably benign Het
Cgn T A 3: 94,674,551 (GRCm39) Q862L possibly damaging Het
Cntrl T A 2: 35,016,071 (GRCm39) D362E probably damaging Het
Col22a1 C T 15: 71,762,431 (GRCm39) G76E probably damaging Het
Cplane1 C T 15: 8,252,622 (GRCm39) T1948I possibly damaging Het
Crip2 A G 12: 113,108,030 (GRCm39) T140A probably benign Het
Csde1 T C 3: 102,950,976 (GRCm39) V229A probably damaging Het
Cyp2d34 A G 15: 82,500,523 (GRCm39) F439L probably damaging Het
Dync1h1 A G 12: 110,606,186 (GRCm39) T2419A probably benign Het
Dync2h1 A T 9: 7,051,495 (GRCm39) F3147I probably damaging Het
Dynlt1f T C 17: 6,916,707 (GRCm39) T101A probably benign Het
Efcab3 A G 11: 104,927,601 (GRCm39) H4790R probably benign Het
Efcab8 G A 2: 153,622,888 (GRCm39) S19N Het
Eno2 A T 6: 124,740,091 (GRCm39) I315K possibly damaging Het
Erich3 A G 3: 154,468,886 (GRCm39) T1113A unknown Het
Fam217a A T 13: 35,095,007 (GRCm39) Y251N possibly damaging Het
Fcrlb A T 1: 170,734,938 (GRCm39) H396Q probably benign Het
Fcsk A G 8: 111,614,064 (GRCm39) V693A probably benign Het
Fgd5 A T 6: 92,046,447 (GRCm39) K1397* probably null Het
Frem1 C A 4: 82,831,785 (GRCm39) L2010F probably benign Het
Fzd8 A G 18: 9,214,661 (GRCm39) Y581C probably damaging Het
Gcc2 T C 10: 58,106,411 (GRCm39) V549A possibly damaging Het
Gcnt4 G A 13: 97,083,042 (GRCm39) V113I probably benign Het
Gldn A G 9: 54,245,747 (GRCm39) I433V probably benign Het
Gm3336 A G 8: 71,173,069 (GRCm39) D27G unknown Het
Gm6133 T A 18: 78,393,146 (GRCm39) Y47N probably damaging Het
Gm8257 A T 14: 44,893,877 (GRCm39) N62K probably benign Het
Gpr18 T G 14: 122,149,667 (GRCm39) R119S probably damaging Het
Grm5 A T 7: 87,685,397 (GRCm39) I505F possibly damaging Het
Hdgfl1 T C 13: 26,953,428 (GRCm39) E215G probably benign Het
Heg1 T A 16: 33,527,339 (GRCm39) C100S probably benign Het
Isg20l2 T C 3: 87,839,302 (GRCm39) V171A probably benign Het
Lrrc49 A T 9: 60,495,150 (GRCm39) C694S probably benign Het
Map7d1 A T 4: 126,133,911 (GRCm39) I217N probably damaging Het
Mbnl2 A T 14: 120,562,712 (GRCm39) Q21L probably benign Het
Mfsd10 A T 5: 34,792,751 (GRCm39) F220Y probably benign Het
Mmp1b A C 9: 7,387,909 (GRCm39) N28K probably null Het
Muc16 A T 9: 18,555,975 (GRCm39) N3439K unknown Het
Myef2l C A 3: 10,157,341 (GRCm39) Q495K unknown Het
Myo9a A T 9: 59,687,584 (GRCm39) K230* probably null Het
Mysm1 T C 4: 94,835,294 (GRCm39) T790A probably benign Het
Nell2 C T 15: 95,194,117 (GRCm39) C532Y probably damaging Het
Nmnat1 T A 4: 149,553,482 (GRCm39) N210I probably damaging Het
Or14j7 T G 17: 38,235,168 (GRCm39) V237G probably benign Het
Or2aj6 A T 16: 19,443,295 (GRCm39) L185* probably null Het
Or4k41 T C 2: 111,280,343 (GRCm39) I286T probably damaging Het
Or7g16 G A 9: 18,727,569 (GRCm39) T7I probably damaging Het
Pabpc6 T C 17: 9,888,281 (GRCm39) D90G probably damaging Het
Pacs2 A T 12: 113,026,104 (GRCm39) I554F possibly damaging Het
Padi3 C A 4: 140,523,004 (GRCm39) V323L probably benign Het
Piezo1 G A 8: 123,215,090 (GRCm39) P1484L Het
Pogk A G 1: 166,227,254 (GRCm39) I299T possibly damaging Het
Ptprk A G 10: 28,461,928 (GRCm39) I1164V probably benign Het
Raph1 A G 1: 60,542,124 (GRCm39) M278T unknown Het
Rasa3 T A 8: 13,645,851 (GRCm39) Q163L probably benign Het
Rbm6 T A 9: 107,660,911 (GRCm39) K884I probably damaging Het
Rtl1 A G 12: 109,559,691 (GRCm39) V716A probably benign Het
Sag A G 1: 87,749,054 (GRCm39) K151R probably damaging Het
Scara5 G A 14: 66,000,197 (GRCm39) V456M probably benign Het
Selplg GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT 5: 113,957,756 (GRCm39) probably benign Het
Slc4a1 A T 11: 102,243,279 (GRCm39) V784D probably damaging Het
Sstr1 T C 12: 58,259,569 (GRCm39) I64T possibly damaging Het
Steap1 A G 5: 5,790,708 (GRCm39) I80T probably benign Het
Tbc1d24 T A 17: 24,427,491 (GRCm39) D157V probably benign Het
Thsd7a T C 6: 12,418,249 (GRCm39) E660G Het
Trappc3l A G 10: 33,932,786 (GRCm39) probably benign Het
Tsc22d2 T C 3: 58,323,497 (GRCm39) S130P probably benign Het
Tti2 T A 8: 31,645,814 (GRCm39) I376N probably damaging Het
Ttll2 C A 17: 7,619,054 (GRCm39) W291L probably benign Het
Ttll3 G A 6: 113,376,657 (GRCm39) V345I possibly damaging Het
Ttn A G 2: 76,565,046 (GRCm39) Y28394H probably damaging Het
Usp45 A G 4: 21,832,201 (GRCm39) Y684C probably damaging Het
Vdr A G 15: 97,765,089 (GRCm39) S217P probably benign Het
Xpot A G 10: 121,447,580 (GRCm39) L105P probably damaging Het
Zan A G 5: 137,464,206 (GRCm39) I533T probably damaging Het
Zbtb8a T C 4: 129,248,059 (GRCm39) E404G probably benign Het
Zfp106 T A 2: 120,369,906 (GRCm39) I62F probably damaging Het
Zfp451 A T 1: 33,815,562 (GRCm39) F796Y probably damaging Het
Other mutations in Arfgef1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00766:Arfgef1 APN 1 10,270,012 (GRCm39) missense probably benign
IGL00919:Arfgef1 APN 1 10,243,462 (GRCm39) missense probably damaging 1.00
IGL01022:Arfgef1 APN 1 10,244,301 (GRCm39) missense probably damaging 1.00
IGL01155:Arfgef1 APN 1 10,269,207 (GRCm39) splice site probably benign
IGL01288:Arfgef1 APN 1 10,283,436 (GRCm39) missense possibly damaging 0.67
IGL01397:Arfgef1 APN 1 10,229,796 (GRCm39) missense probably benign 0.40
IGL01433:Arfgef1 APN 1 10,223,657 (GRCm39) missense probably damaging 1.00
IGL01653:Arfgef1 APN 1 10,230,133 (GRCm39) nonsense probably null
IGL01669:Arfgef1 APN 1 10,229,840 (GRCm39) missense probably damaging 1.00
IGL01795:Arfgef1 APN 1 10,217,753 (GRCm39) missense probably benign 0.01
IGL01860:Arfgef1 APN 1 10,224,621 (GRCm39) missense probably damaging 1.00
IGL02137:Arfgef1 APN 1 10,283,338 (GRCm39) missense probably damaging 1.00
IGL02365:Arfgef1 APN 1 10,270,108 (GRCm39) missense probably benign 0.00
IGL02519:Arfgef1 APN 1 10,279,893 (GRCm39) missense probably benign 0.13
IGL02542:Arfgef1 APN 1 10,243,067 (GRCm39) missense probably benign 0.24
IGL02604:Arfgef1 APN 1 10,251,275 (GRCm39) splice site probably benign
IGL02743:Arfgef1 APN 1 10,270,054 (GRCm39) missense probably benign 0.00
IGL03225:Arfgef1 APN 1 10,224,543 (GRCm39) missense probably damaging 1.00
Collected UTSW 1 10,251,163 (GRCm39) missense probably damaging 1.00
uncle_joe UTSW 1 10,231,060 (GRCm39) missense probably damaging 1.00
G1Funyon:Arfgef1 UTSW 1 10,250,058 (GRCm39) missense probably damaging 1.00
I2288:Arfgef1 UTSW 1 10,243,478 (GRCm39) missense probably damaging 1.00
I2289:Arfgef1 UTSW 1 10,243,478 (GRCm39) missense probably damaging 1.00
R0383:Arfgef1 UTSW 1 10,269,067 (GRCm39) critical splice donor site probably null
R0491:Arfgef1 UTSW 1 10,250,212 (GRCm39) splice site probably benign
R0636:Arfgef1 UTSW 1 10,270,076 (GRCm39) missense probably benign
R1006:Arfgef1 UTSW 1 10,210,706 (GRCm39) missense probably benign 0.00
R1212:Arfgef1 UTSW 1 10,286,784 (GRCm39) missense probably benign 0.05
R1233:Arfgef1 UTSW 1 10,254,315 (GRCm39) missense probably damaging 1.00
R1346:Arfgef1 UTSW 1 10,229,958 (GRCm39) missense probably benign 0.41
R1416:Arfgef1 UTSW 1 10,243,164 (GRCm39) missense probably damaging 1.00
R1477:Arfgef1 UTSW 1 10,259,509 (GRCm39) missense probably damaging 1.00
R1581:Arfgef1 UTSW 1 10,270,103 (GRCm39) missense probably benign 0.02
R1587:Arfgef1 UTSW 1 10,230,184 (GRCm39) missense probably damaging 0.99
R1602:Arfgef1 UTSW 1 10,275,115 (GRCm39) missense probably benign 0.01
R1745:Arfgef1 UTSW 1 10,243,480 (GRCm39) missense probably damaging 1.00
R1831:Arfgef1 UTSW 1 10,275,115 (GRCm39) missense probably benign 0.01
R1832:Arfgef1 UTSW 1 10,275,115 (GRCm39) missense probably benign 0.01
R1833:Arfgef1 UTSW 1 10,275,115 (GRCm39) missense probably benign 0.01
R1918:Arfgef1 UTSW 1 10,270,103 (GRCm39) missense probably benign 0.02
R1919:Arfgef1 UTSW 1 10,270,103 (GRCm39) missense probably benign 0.02
R2059:Arfgef1 UTSW 1 10,258,977 (GRCm39) splice site probably null
R2146:Arfgef1 UTSW 1 10,270,103 (GRCm39) missense probably benign 0.02
R2148:Arfgef1 UTSW 1 10,270,103 (GRCm39) missense probably benign 0.02
R2149:Arfgef1 UTSW 1 10,270,103 (GRCm39) missense probably benign 0.02
R2150:Arfgef1 UTSW 1 10,270,103 (GRCm39) missense probably benign 0.02
R2373:Arfgef1 UTSW 1 10,244,367 (GRCm39) missense probably damaging 1.00
R2516:Arfgef1 UTSW 1 10,223,879 (GRCm39) missense possibly damaging 0.89
R3863:Arfgef1 UTSW 1 10,212,811 (GRCm39) frame shift probably null
R3916:Arfgef1 UTSW 1 10,259,668 (GRCm39) missense probably benign 0.01
R3948:Arfgef1 UTSW 1 10,212,811 (GRCm39) frame shift probably null
R3949:Arfgef1 UTSW 1 10,212,811 (GRCm39) frame shift probably null
R3977:Arfgef1 UTSW 1 10,279,859 (GRCm39) missense probably benign 0.01
R3978:Arfgef1 UTSW 1 10,279,859 (GRCm39) missense probably benign 0.01
R3979:Arfgef1 UTSW 1 10,279,859 (GRCm39) missense probably benign 0.01
R4086:Arfgef1 UTSW 1 10,233,984 (GRCm39) missense probably benign 0.06
R4175:Arfgef1 UTSW 1 10,229,861 (GRCm39) missense probably damaging 1.00
R4257:Arfgef1 UTSW 1 10,229,771 (GRCm39) intron probably benign
R4572:Arfgef1 UTSW 1 10,283,366 (GRCm39) missense probably damaging 1.00
R4652:Arfgef1 UTSW 1 10,243,487 (GRCm39) missense probably damaging 0.98
R4678:Arfgef1 UTSW 1 10,212,891 (GRCm39) missense probably benign 0.03
R4737:Arfgef1 UTSW 1 10,259,836 (GRCm39) missense possibly damaging 0.85
R4779:Arfgef1 UTSW 1 10,223,958 (GRCm39) missense probably damaging 1.00
R4818:Arfgef1 UTSW 1 10,286,772 (GRCm39) missense probably benign
R4898:Arfgef1 UTSW 1 10,229,798 (GRCm39) missense possibly damaging 0.75
R4979:Arfgef1 UTSW 1 10,283,334 (GRCm39) missense probably damaging 1.00
R5039:Arfgef1 UTSW 1 10,269,961 (GRCm39) missense probably benign 0.37
R5194:Arfgef1 UTSW 1 10,275,132 (GRCm39) missense probably benign 0.09
R5428:Arfgef1 UTSW 1 10,231,060 (GRCm39) missense probably damaging 1.00
R5533:Arfgef1 UTSW 1 10,269,952 (GRCm39) critical splice donor site probably null
R5547:Arfgef1 UTSW 1 10,231,201 (GRCm39) missense probably damaging 1.00
R5562:Arfgef1 UTSW 1 10,214,971 (GRCm39) missense probably damaging 1.00
R5635:Arfgef1 UTSW 1 10,259,085 (GRCm39) missense possibly damaging 0.81
R5697:Arfgef1 UTSW 1 10,231,063 (GRCm39) missense probably benign 0.03
R5704:Arfgef1 UTSW 1 10,229,808 (GRCm39) missense probably damaging 0.98
R5722:Arfgef1 UTSW 1 10,209,109 (GRCm39) missense probably benign 0.04
R5793:Arfgef1 UTSW 1 10,279,753 (GRCm39) missense probably benign 0.01
R5835:Arfgef1 UTSW 1 10,230,964 (GRCm39) missense probably damaging 1.00
R5870:Arfgef1 UTSW 1 10,251,163 (GRCm39) missense probably damaging 1.00
R5990:Arfgef1 UTSW 1 10,243,146 (GRCm39) missense probably damaging 0.99
R6290:Arfgef1 UTSW 1 10,259,036 (GRCm39) missense possibly damaging 0.91
R6460:Arfgef1 UTSW 1 10,283,285 (GRCm39) missense probably damaging 1.00
R6613:Arfgef1 UTSW 1 10,264,621 (GRCm39) missense possibly damaging 0.95
R6802:Arfgef1 UTSW 1 10,259,677 (GRCm39) missense probably benign 0.35
R6967:Arfgef1 UTSW 1 10,223,904 (GRCm39) missense probably damaging 0.99
R6967:Arfgef1 UTSW 1 10,223,903 (GRCm39) missense probably damaging 1.00
R6968:Arfgef1 UTSW 1 10,223,904 (GRCm39) missense probably damaging 0.99
R6968:Arfgef1 UTSW 1 10,223,903 (GRCm39) missense probably damaging 1.00
R6969:Arfgef1 UTSW 1 10,223,904 (GRCm39) missense probably damaging 0.99
R6969:Arfgef1 UTSW 1 10,223,903 (GRCm39) missense probably damaging 1.00
R6970:Arfgef1 UTSW 1 10,223,904 (GRCm39) missense probably damaging 0.99
R6970:Arfgef1 UTSW 1 10,223,903 (GRCm39) missense probably damaging 1.00
R7092:Arfgef1 UTSW 1 10,223,901 (GRCm39) missense probably damaging 1.00
R7251:Arfgef1 UTSW 1 10,269,200 (GRCm39) missense possibly damaging 0.81
R7334:Arfgef1 UTSW 1 10,254,685 (GRCm39) missense probably damaging 1.00
R7399:Arfgef1 UTSW 1 10,251,122 (GRCm39) missense probably benign 0.00
R7631:Arfgef1 UTSW 1 10,302,694 (GRCm39) missense probably benign 0.00
R7699:Arfgef1 UTSW 1 10,264,636 (GRCm39) missense possibly damaging 0.78
R7700:Arfgef1 UTSW 1 10,264,636 (GRCm39) missense possibly damaging 0.78
R7772:Arfgef1 UTSW 1 10,227,235 (GRCm39) missense possibly damaging 0.96
R7968:Arfgef1 UTSW 1 10,243,145 (GRCm39) missense probably damaging 1.00
R8195:Arfgef1 UTSW 1 10,243,478 (GRCm39) missense probably damaging 1.00
R8292:Arfgef1 UTSW 1 10,227,194 (GRCm39) missense probably benign 0.06
R8301:Arfgef1 UTSW 1 10,250,058 (GRCm39) missense probably damaging 1.00
R8341:Arfgef1 UTSW 1 10,224,553 (GRCm39) missense probably benign 0.37
R8410:Arfgef1 UTSW 1 10,229,867 (GRCm39) missense possibly damaging 0.94
R8411:Arfgef1 UTSW 1 10,286,759 (GRCm39) missense probably benign 0.01
R8793:Arfgef1 UTSW 1 10,212,832 (GRCm39) missense possibly damaging 0.95
R8903:Arfgef1 UTSW 1 10,211,838 (GRCm39) missense probably damaging 1.00
R8955:Arfgef1 UTSW 1 10,270,062 (GRCm39) missense probably benign 0.25
R9185:Arfgef1 UTSW 1 10,215,004 (GRCm39) missense probably damaging 1.00
R9252:Arfgef1 UTSW 1 10,243,122 (GRCm39) nonsense probably null
R9333:Arfgef1 UTSW 1 10,222,037 (GRCm39) nonsense probably null
R9335:Arfgef1 UTSW 1 10,228,236 (GRCm39) missense probably damaging 1.00
R9348:Arfgef1 UTSW 1 10,283,419 (GRCm39) missense probably benign 0.03
R9355:Arfgef1 UTSW 1 10,270,000 (GRCm39) missense probably benign 0.00
R9564:Arfgef1 UTSW 1 10,217,758 (GRCm39) missense probably benign 0.00
R9600:Arfgef1 UTSW 1 10,233,977 (GRCm39) missense probably benign 0.01
R9789:Arfgef1 UTSW 1 10,243,427 (GRCm39) missense probably damaging 1.00
V1662:Arfgef1 UTSW 1 10,243,478 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGCTGGACATCTCATGGATC -3'
(R):5'- ACTCTCAAACTACCCTTGGTAAG -3'

Sequencing Primer
(F):5'- GGACATCTCATGGATCTGATTAAGAC -3'
(R):5'- GATGCCATTAAAGTAGTCTTGTGATG -3'
Posted On 2021-11-19