Incidental Mutation 'R9564:Tek'
ID 721323
Institutional Source Beutler Lab
Gene Symbol Tek
Ensembl Gene ENSMUSG00000006386
Gene Name TEK receptor tyrosine kinase
Synonyms Cd202b, Tie2, tie-2, Hyk
MMRRC Submission
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R9564 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 94627526-94763213 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 94762172 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 1103 (N1103K)
Ref Sequence ENSEMBL: ENSMUSP00000099862 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071168] [ENSMUST00000073939] [ENSMUST00000102798]
AlphaFold Q02858
Predicted Effect probably damaging
Transcript: ENSMUST00000071168
AA Change: N1102K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000071162
Gene: ENSMUSG00000006386
AA Change: N1102K

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:Ig_Tie2_1 23 118 1.2e-57 PFAM
IG_like 128 209 6.52e0 SMART
EGF_Lam 227 264 1.26e-2 SMART
EGF 267 299 2.2e1 SMART
internal_repeat_1 302 346 4.35e-7 PROSPERO
IG_like 356 442 3.29e1 SMART
FN3 445 526 2.11e0 SMART
FN3 541 624 9.77e-5 SMART
FN3 638 720 1.18e-12 SMART
transmembrane domain 747 769 N/A INTRINSIC
TyrKc 822 1090 1.9e-138 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000073939
AA Change: N1052K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000073595
Gene: ENSMUSG00000006386
AA Change: N1052K

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:Ig_Tie2_1 23 118 7.1e-58 PFAM
EGF_Lam 176 213 1.26e-2 SMART
EGF 216 248 2.2e1 SMART
internal_repeat_1 251 295 4.22e-7 PROSPERO
FN3 394 475 2.11e0 SMART
FN3 490 573 9.77e-5 SMART
FN3 587 669 1.18e-12 SMART
transmembrane domain 696 718 N/A INTRINSIC
TyrKc 772 1040 1.9e-138 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000102798
AA Change: N1103K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000099862
Gene: ENSMUSG00000006386
AA Change: N1103K

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:Ig_Tie2_1 24 118 5e-44 PFAM
IG_like 128 209 6.52e0 SMART
EGF_Lam 227 264 1.26e-2 SMART
EGF 267 299 2.2e1 SMART
internal_repeat_1 302 346 4.36e-7 PROSPERO
IG_like 356 442 3.29e1 SMART
FN3 445 526 2.11e0 SMART
FN3 541 624 9.77e-5 SMART
FN3 638 720 1.18e-12 SMART
transmembrane domain 747 769 N/A INTRINSIC
TyrKc 823 1091 1.9e-138 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a receptor that belongs to the protein tyrosine kinase Tie2 family. The encoded protein possesses a unique extracellular region that contains two immunoglobulin-like domains, three epidermal growth factor (EGF)-like domains and three fibronectin type III repeats. The ligand angiopoietin-1 binds to this receptor and mediates a signaling pathway that functions in embryonic vascular development. Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Feb 2014]
PHENOTYPE: Homozygous mutation of this gene results in embryonic lethality during organogenesis, impaired vascular branching in the embryo and yolk sac, abnormal cardiac development, and in some cases hemorrhages. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 135 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700097O09Rik A T 12: 55,104,090 (GRCm39) N176K possibly damaging Het
3110009E18Rik T A 1: 120,097,006 (GRCm39) V134E Het
Abca8a T A 11: 109,965,010 (GRCm39) H429L probably benign Het
Acsf2 T A 11: 94,463,891 (GRCm39) I98F possibly damaging Het
Actr5 A G 2: 158,470,135 (GRCm39) D255G probably damaging Het
Adam21 C T 12: 81,605,833 (GRCm39) C643Y probably damaging Het
Adcy7 TGG TG 8: 89,053,053 (GRCm39) probably null Het
AI429214 A G 8: 37,461,067 (GRCm39) S72G possibly damaging Het
Akap13 T C 7: 75,259,161 (GRCm39) V595A probably benign Het
Akt3 T C 1: 176,907,769 (GRCm39) T209A possibly damaging Het
Alpk2 C T 18: 65,439,014 (GRCm39) G793D probably damaging Het
Amotl1 T C 9: 14,473,513 (GRCm39) K562R possibly damaging Het
Ankib1 T A 5: 3,805,733 (GRCm39) N178I possibly damaging Het
Arfgef1 A T 1: 10,217,758 (GRCm39) D1560E probably benign Het
Arhgap20 AAGAGAG AAGAG 9: 51,761,413 (GRCm39) probably null Het
Arpc5l A G 2: 38,905,124 (GRCm39) T152A probably benign Het
Asic3 C G 5: 24,620,875 (GRCm39) D252E possibly damaging Het
Atf7 T A 15: 102,442,712 (GRCm39) M466L probably benign Het
Bcl9l A G 9: 44,420,554 (GRCm39) D1320G probably damaging Het
Bdkrb1 G A 12: 105,571,078 (GRCm39) V215I probably benign Het
Brpf3 T G 17: 29,026,152 (GRCm39) D408E probably benign Het
Btn2a2 C A 13: 23,662,848 (GRCm39) K367N possibly damaging Het
Btnl10 T A 11: 58,813,189 (GRCm39) F273I probably benign Het
C1qtnf12 C T 4: 156,049,473 (GRCm39) T145I probably benign Het
Cacna1s T C 1: 136,046,516 (GRCm39) C1763R probably benign Het
Ccdc154 C A 17: 25,387,381 (GRCm39) Q372K possibly damaging Het
Cd300ld2 CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG 11: 114,903,257 (GRCm39) probably benign Het
Celsr2 T C 3: 108,321,834 (GRCm39) Y326C probably damaging Het
Cfap46 A T 7: 139,231,471 (GRCm39) V914E Het
Coil T A 11: 88,872,626 (GRCm39) V329E possibly damaging Het
Copb1 A G 7: 113,836,034 (GRCm39) I449T possibly damaging Het
Copg1 T G 6: 87,869,683 (GRCm39) S187R probably damaging Het
Cps1 T A 1: 67,198,048 (GRCm39) F371Y probably benign Het
Cpt1b A T 15: 89,303,472 (GRCm39) F554L probably damaging Het
Ctdsp2 A G 10: 126,832,040 (GRCm39) D216G probably damaging Het
Ctla2b A T 13: 61,043,856 (GRCm39) Y104* probably null Het
Cyp2j6 A G 4: 96,414,245 (GRCm39) I340T probably damaging Het
Ddi1 T A 9: 6,265,730 (GRCm39) D213V probably damaging Het
Degs1l G T 1: 180,882,810 (GRCm39) V191F possibly damaging Het
Dennd2b G T 7: 109,125,536 (GRCm39) D980E probably damaging Het
Dlgap1 T G 17: 70,964,458 (GRCm39) N400K probably benign Het
Dnah5 G A 15: 28,290,422 (GRCm39) V1271M probably benign Het
Dnah8 T A 17: 30,932,021 (GRCm39) V1463E probably benign Het
Dstyk G A 1: 132,362,023 (GRCm39) R151H probably damaging Het
Ehd3 T G 17: 74,137,361 (GRCm39) V510G probably benign Het
Enthd1 G T 15: 80,444,235 (GRCm39) Q107K probably damaging Het
Entpd7 A G 19: 43,705,889 (GRCm39) E237G probably benign Het
Fadd A T 7: 144,136,048 (GRCm39) C27S probably damaging Het
Fan1 A G 7: 63,999,240 (GRCm39) L874P possibly damaging Het
Fbxw17 T C 13: 50,579,605 (GRCm39) W141R probably damaging Het
Fig4 A G 10: 41,161,387 (GRCm39) V63A probably benign Het
Fmo3 T C 1: 162,786,021 (GRCm39) D323G probably damaging Het
Gas8 T A 8: 124,263,179 (GRCm39) V452E possibly damaging Het
Gdf9 T A 11: 53,327,511 (GRCm39) S156T probably damaging Het
Hlcs T C 16: 93,935,580 (GRCm39) S571G probably benign Het
Hmox2 A G 16: 4,582,870 (GRCm39) Y201C probably damaging Het
Ikzf3 T A 11: 98,358,032 (GRCm39) D435V probably damaging Het
Kank2 T C 9: 21,705,852 (GRCm39) T389A possibly damaging Het
Kank2 A G 9: 21,706,631 (GRCm39) L129P probably damaging Het
Kdr T A 5: 76,125,565 (GRCm39) K339N probably benign Het
Lmntd2 A G 7: 140,790,701 (GRCm39) S516P Het
Lrrc37 T C 11: 103,503,822 (GRCm39) I2715M unknown Het
Lrrc40 T A 3: 157,746,078 (GRCm39) V51D probably benign Het
Lrrtm1 A G 6: 77,221,536 (GRCm39) N331S probably benign Het
Lvrn T G 18: 47,017,506 (GRCm39) I612S probably damaging Het
Map3k3 T A 11: 106,041,860 (GRCm39) I413N probably damaging Het
Mcm9 C T 10: 53,506,104 (GRCm39) A57T possibly damaging Het
Met T A 6: 17,531,425 (GRCm39) F568I probably benign Het
Mkx A G 18: 7,002,457 (GRCm39) F30L probably benign Het
Mrc1 A G 2: 14,266,117 (GRCm39) N345S probably benign Het
Mstn T A 1: 53,103,367 (GRCm39) N234K probably benign Het
Mtmr3 A T 11: 4,440,992 (GRCm39) S554T possibly damaging Het
Mug1 G A 6: 121,861,587 (GRCm39) V1350I probably benign Het
Myh8 T C 11: 67,177,215 (GRCm39) V427A probably benign Het
Nr4a2 A T 2: 57,000,190 (GRCm39) I365N probably damaging Het
Nrxn2 A G 19: 6,559,887 (GRCm39) D1215G probably damaging Het
Or2d3c A G 7: 106,525,847 (GRCm39) M273T probably benign Het
Or6c33 T C 10: 129,853,287 (GRCm39) I19T probably benign Het
Or7g18 G A 9: 18,786,640 (GRCm39) V3I probably benign Het
Osbpl6 T A 2: 76,426,321 (GRCm39) W967R probably damaging Het
Pcdhb21 T C 18: 37,646,972 (GRCm39) S34P possibly damaging Het
Pibf1 G T 14: 99,374,610 (GRCm39) D350Y possibly damaging Het
Pira1 C T 7: 3,742,646 (GRCm39) V21M possibly damaging Het
Plekhs1 A T 19: 56,461,628 (GRCm39) I123F probably damaging Het
Pold2 C T 11: 5,824,163 (GRCm39) G214D probably benign Het
Pomc A G 12: 4,009,971 (GRCm39) T71A probably benign Het
Pot1b A G 17: 55,969,465 (GRCm39) S568P possibly damaging Het
Prkd2 C A 7: 16,591,744 (GRCm39) Q592K possibly damaging Het
Prss28 C T 17: 25,528,911 (GRCm39) A84V probably damaging Het
Prtg T A 9: 72,766,153 (GRCm39) Y649N probably damaging Het
Psip1 T C 4: 83,386,888 (GRCm39) E161G possibly damaging Het
Rab3gap2 A G 1: 185,014,691 (GRCm39) D1280G probably damaging Het
Rab3ip A T 10: 116,751,780 (GRCm39) I329N probably damaging Het
Rarres2 C T 6: 48,549,164 (GRCm39) G13D possibly damaging Het
Rbp3 A G 14: 33,677,477 (GRCm39) D475G probably damaging Het
Ric3 A G 7: 108,638,018 (GRCm39) V246A probably damaging Het
Robo3 A G 9: 37,340,900 (GRCm39) F124S probably damaging Het
Rpl27a C A 7: 109,118,837 (GRCm39) H17N probably benign Het
Rptn A G 3: 93,304,536 (GRCm39) D623G probably benign Het
Rtl1 G T 12: 109,556,713 (GRCm39) Q1709K probably benign Het
Sacs T A 14: 61,449,046 (GRCm39) D3697E probably damaging Het
Sec61b A G 4: 47,483,049 (GRCm39) Y93C probably damaging Het
Serpina3a A T 12: 104,084,886 (GRCm39) I94L probably benign Het
Skic2 C T 17: 35,063,758 (GRCm39) A562T probably benign Het
Skor2 C T 18: 76,946,376 (GRCm39) H33Y unknown Het
Slc12a3 G A 8: 95,082,983 (GRCm39) V874I probably benign Het
Slit1 T A 19: 41,591,861 (GRCm39) M1254L probably benign Het
Smg1 A G 7: 117,812,208 (GRCm39) S52P unknown Het
Sorl1 A G 9: 41,957,893 (GRCm39) Y584H probably damaging Het
Spata32 T A 11: 103,099,779 (GRCm39) Q242L possibly damaging Het
Sptbn4 T G 7: 27,117,504 (GRCm39) E415A probably damaging Het
St6galnac5 T C 3: 152,545,782 (GRCm39) R259G probably damaging Het
Stat3 T C 11: 100,784,614 (GRCm39) I589V probably benign Het
Tecta T A 9: 42,249,123 (GRCm39) K1913M probably damaging Het
Telo2 A G 17: 25,334,199 (GRCm39) I16T probably benign Het
Tmem207 G T 16: 26,335,499 (GRCm39) C79* probably null Het
Topaz1 C T 9: 122,579,219 (GRCm39) H710Y probably benign Het
Trim33 T A 3: 103,238,965 (GRCm39) S648T probably benign Het
Trpm6 A G 19: 18,851,240 (GRCm39) T1734A possibly damaging Het
Trpm8 A G 1: 88,254,158 (GRCm39) E127G possibly damaging Het
Ttc3 T A 16: 94,248,918 (GRCm39) C1139S probably benign Het
Ttn T C 2: 76,580,330 (GRCm39) E23521G probably damaging Het
Ush2a T C 1: 188,268,551 (GRCm39) I1669T possibly damaging Het
Vcpip1 C A 1: 9,817,456 (GRCm39) S309I possibly damaging Het
Vmn1r208 A G 13: 22,956,789 (GRCm39) V236A probably damaging Het
Vmn1r74 T C 7: 11,581,534 (GRCm39) F278S probably damaging Het
Vmn2r33 T C 7: 7,557,081 (GRCm39) S540G probably benign Het
Vmn2r52 T C 7: 9,905,182 (GRCm39) D219G probably benign Het
Wiz G T 17: 32,575,939 (GRCm39) D812E probably benign Het
Ylpm1 C T 12: 85,091,176 (GRCm39) P1787S probably benign Het
Zan T C 5: 137,404,688 (GRCm39) E3858G unknown Het
Zfp760 T G 17: 21,942,272 (GRCm39) H482Q possibly damaging Het
Zfp78 A G 7: 6,381,390 (GRCm39) T147A probably benign Het
Zfp808 T A 13: 62,320,661 (GRCm39) I630K possibly damaging Het
Zpld1 T A 16: 55,061,701 (GRCm39) R227* probably null Het
Other mutations in Tek
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00654:Tek APN 4 94,715,538 (GRCm39) missense probably benign 0.03
IGL00805:Tek APN 4 94,686,956 (GRCm39) missense probably damaging 1.00
IGL00806:Tek APN 4 94,686,956 (GRCm39) missense probably damaging 1.00
IGL00807:Tek APN 4 94,686,956 (GRCm39) missense probably damaging 1.00
IGL00870:Tek APN 4 94,761,318 (GRCm39) nonsense probably null
IGL01348:Tek APN 4 94,747,895 (GRCm39) missense probably damaging 1.00
IGL01398:Tek APN 4 94,738,014 (GRCm39) missense probably damaging 1.00
IGL01683:Tek APN 4 94,747,148 (GRCm39) missense probably damaging 1.00
IGL01827:Tek APN 4 94,627,882 (GRCm39) missense probably benign 0.24
IGL02063:Tek APN 4 94,627,882 (GRCm39) missense probably benign 0.24
IGL02218:Tek APN 4 94,743,574 (GRCm39) missense probably damaging 1.00
IGL02502:Tek APN 4 94,741,818 (GRCm39) critical splice donor site probably null
IGL02852:Tek APN 4 94,743,561 (GRCm39) missense probably damaging 1.00
IGL02995:Tek APN 4 94,627,877 (GRCm39) utr 5 prime probably benign
IGL03182:Tek APN 4 94,740,002 (GRCm39) missense probably damaging 1.00
IGL03247:Tek APN 4 94,753,680 (GRCm39) missense possibly damaging 0.85
IGL03014:Tek UTSW 4 94,715,500 (GRCm39) missense probably benign 0.05
R0022:Tek UTSW 4 94,725,509 (GRCm39) missense probably damaging 0.98
R0373:Tek UTSW 4 94,692,578 (GRCm39) missense probably damaging 1.00
R0479:Tek UTSW 4 94,692,549 (GRCm39) missense probably benign 0.01
R1178:Tek UTSW 4 94,692,524 (GRCm39) missense probably damaging 1.00
R1289:Tek UTSW 4 94,693,067 (GRCm39) missense probably damaging 1.00
R1331:Tek UTSW 4 94,627,943 (GRCm39) splice site probably benign
R1502:Tek UTSW 4 94,669,339 (GRCm39) missense probably damaging 1.00
R1606:Tek UTSW 4 94,738,004 (GRCm39) missense probably damaging 0.99
R2073:Tek UTSW 4 94,715,966 (GRCm39) missense probably benign 0.01
R2075:Tek UTSW 4 94,715,966 (GRCm39) missense probably benign 0.01
R2230:Tek UTSW 4 94,699,573 (GRCm39) missense probably damaging 1.00
R2851:Tek UTSW 4 94,708,461 (GRCm39) missense probably benign 0.30
R2852:Tek UTSW 4 94,708,461 (GRCm39) missense probably benign 0.30
R3775:Tek UTSW 4 94,692,549 (GRCm39) missense probably benign 0.01
R3845:Tek UTSW 4 94,693,109 (GRCm39) missense probably damaging 1.00
R4114:Tek UTSW 4 94,737,920 (GRCm39) missense probably damaging 0.99
R4115:Tek UTSW 4 94,737,920 (GRCm39) missense probably damaging 0.99
R4273:Tek UTSW 4 94,718,207 (GRCm39) missense probably damaging 1.00
R4425:Tek UTSW 4 94,751,904 (GRCm39) missense probably damaging 1.00
R4488:Tek UTSW 4 94,737,993 (GRCm39) missense possibly damaging 0.72
R4579:Tek UTSW 4 94,751,903 (GRCm39) nonsense probably null
R4623:Tek UTSW 4 94,751,898 (GRCm39) missense probably damaging 1.00
R4651:Tek UTSW 4 94,669,121 (GRCm39) missense probably damaging 1.00
R4652:Tek UTSW 4 94,669,121 (GRCm39) missense probably damaging 1.00
R4723:Tek UTSW 4 94,687,397 (GRCm39) missense possibly damaging 0.71
R5059:Tek UTSW 4 94,692,551 (GRCm39) missense probably benign 0.10
R5652:Tek UTSW 4 94,743,561 (GRCm39) missense probably damaging 1.00
R5793:Tek UTSW 4 94,708,333 (GRCm39) missense probably benign 0.01
R5855:Tek UTSW 4 94,741,790 (GRCm39) missense probably damaging 1.00
R5912:Tek UTSW 4 94,686,877 (GRCm39) missense probably damaging 1.00
R6537:Tek UTSW 4 94,725,561 (GRCm39) missense probably benign 0.19
R6727:Tek UTSW 4 94,741,732 (GRCm39) nonsense probably null
R6835:Tek UTSW 4 94,741,671 (GRCm39) missense possibly damaging 0.94
R6883:Tek UTSW 4 94,725,426 (GRCm39) missense possibly damaging 0.89
R6887:Tek UTSW 4 94,693,181 (GRCm39) missense probably damaging 1.00
R7027:Tek UTSW 4 94,753,747 (GRCm39) missense probably damaging 1.00
R7108:Tek UTSW 4 94,741,724 (GRCm39) missense probably damaging 1.00
R7121:Tek UTSW 4 94,699,647 (GRCm39) missense probably benign 0.19
R7220:Tek UTSW 4 94,692,541 (GRCm39) missense probably damaging 1.00
R7346:Tek UTSW 4 94,715,533 (GRCm39) missense probably benign
R7417:Tek UTSW 4 94,699,582 (GRCm39) missense probably benign
R7465:Tek UTSW 4 94,716,063 (GRCm39) critical splice donor site probably null
R7818:Tek UTSW 4 94,715,953 (GRCm39) missense possibly damaging 0.67
R7917:Tek UTSW 4 94,708,372 (GRCm39) missense possibly damaging 0.89
R7942:Tek UTSW 4 94,740,111 (GRCm39) splice site probably null
R7956:Tek UTSW 4 94,687,580 (GRCm39) splice site probably null
R8098:Tek UTSW 4 94,715,907 (GRCm39) missense probably benign 0.19
R8442:Tek UTSW 4 94,715,922 (GRCm39) missense probably benign 0.04
R8523:Tek UTSW 4 94,687,403 (GRCm39) missense probably benign 0.12
R8676:Tek UTSW 4 94,738,074 (GRCm39) missense probably benign
R8787:Tek UTSW 4 94,738,037 (GRCm39) missense probably damaging 1.00
R9020:Tek UTSW 4 94,708,339 (GRCm39) missense probably benign 0.40
R9172:Tek UTSW 4 94,692,583 (GRCm39) missense probably benign 0.02
R9429:Tek UTSW 4 94,715,515 (GRCm39) missense probably benign
R9602:Tek UTSW 4 94,715,968 (GRCm39) missense possibly damaging 0.91
R9643:Tek UTSW 4 94,692,523 (GRCm39) missense possibly damaging 0.51
R9721:Tek UTSW 4 94,692,539 (GRCm39) missense possibly damaging 0.94
R9722:Tek UTSW 4 94,692,539 (GRCm39) missense possibly damaging 0.94
R9723:Tek UTSW 4 94,692,539 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- GTCAATGGACGCAATTCAGAAG -3'
(R):5'- AGATCCGCACGAGCTGTATG -3'

Sequencing Primer
(F):5'- TCAATGGACGCAATTCAGAAGTAAAC -3'
(R):5'- CTGTATGAGGAGGGTCCCAAACAC -3'
Posted On 2022-08-09