Incidental Mutation 'R4989:Notch1'
ID 385989
Institutional Source Beutler Lab
Gene Symbol Notch1
Ensembl Gene ENSMUSG00000026923
Gene Name notch 1
Synonyms 9930111A19Rik, Motch A, Tan1, Mis6, lin-12, N1
MMRRC Submission 042583-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4989 (G1)
Quality Score 166
Status Validated
Chromosome 2
Chromosomal Location 26347914-26393834 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 26371193 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Lysine at position 298 (E298K)
Ref Sequence ENSEMBL: ENSMUSP00000028288 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028288] [ENSMUST00000132820]
AlphaFold Q01705
PDB Structure The Crystal Structure of a Partial Mouse Notch-1 Ankyrin Domain: Repeats 4 Through 7 Preserve an Ankyrin Fold [X-RAY DIFFRACTION]
Mouse Notch 1 Ankyrin Repeat Intracellular Domain [X-RAY DIFFRACTION]
Structure of sugar modified epidermal growth factor-like repeat 12 of mouse Notch-1 receptor [SOLUTION NMR]
Structure of epidermal growth factor-like repeat 12 of mouse Notch-1 receptor [SOLUTION NMR]
Structure of O-fucosylated epidermal growth factor-like repeat 12 of mouse Notch-1 receptor [SOLUTION NMR]
Factor inhibiting HIF-1 Alpha in complex with Notch 1 fragment mouse notch (1930-1949) peptide [X-RAY DIFFRACTION]
Factor inhibiting HIF-1 Alpha in complex with Notch 1 fragment mouse notch (1997-2016) peptide [X-RAY DIFFRACTION]
Predicted Effect probably damaging
Transcript: ENSMUST00000028288
AA Change: E298K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000028288
Gene: ENSMUSG00000026923
AA Change: E298K

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
EGF 23 58 1.63e1 SMART
EGF 62 99 4.29e-5 SMART
EGF 105 139 6.25e-7 SMART
EGF_CA 140 176 1.02e-6 SMART
EGF_CA 178 216 4.21e-13 SMART
EGF 221 255 6.7e-7 SMART
EGF_CA 257 293 6.8e-8 SMART
EGF_CA 295 333 1.16e-10 SMART
EGF_CA 335 371 3.17e-8 SMART
EGF 375 410 5.32e-1 SMART
EGF_CA 412 450 4.59e-14 SMART
EGF_CA 452 488 1.02e-11 SMART
EGF_CA 490 526 4.81e-8 SMART
EGF_CA 528 564 3.19e-13 SMART
EGF_CA 566 601 1.91e-11 SMART
EGF_CA 603 639 1.78e-11 SMART
EGF_CA 641 676 9.62e-8 SMART
EGF_CA 678 714 2.38e-12 SMART
EGF_CA 716 751 5.23e-9 SMART
EGF_CA 753 789 6.25e-7 SMART
EGF_CA 791 827 1.1e-11 SMART
EGF 832 867 2.03e-6 SMART
EGF_CA 869 905 5.73e-15 SMART
EGF_CA 907 943 4.56e-9 SMART
EGF_CA 945 981 1.64e-10 SMART
EGF_CA 983 1019 5.83e-7 SMART
EGF_CA 1021 1057 1.05e-13 SMART
EGF 1062 1095 8.12e-6 SMART
EGF 1100 1143 5.66e-5 SMART
EGF_CA 1145 1181 1.1e-11 SMART
EGF_CA 1183 1219 3.87e-12 SMART
EGF_CA 1221 1265 2.89e-11 SMART
EGF_CA 1267 1305 1.2e-8 SMART
EGF 1310 1346 5.74e-6 SMART
EGF 1351 1384 4.1e-2 SMART
EGF 1390 1426 2.66e-1 SMART
NL 1442 1480 4.08e-16 SMART
NL 1483 1522 1.08e-15 SMART
NL 1523 1562 7.39e-14 SMART
NOD 1566 1622 1.81e-32 SMART
NODP 1660 1722 3.27e-30 SMART
low complexity region 1729 1746 N/A INTRINSIC
ANK 1870 1912 1.07e2 SMART
ANK 1917 1946 4.82e-3 SMART
ANK 1950 1980 6.71e-2 SMART
ANK 1984 2013 1.23e0 SMART
ANK 2017 2046 9.13e-4 SMART
ANK 2050 2079 2.97e-3 SMART
low complexity region 2205 2222 N/A INTRINSIC
low complexity region 2364 2395 N/A INTRINSIC
DUF3454 2453 2517 2.01e-30 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000132820
Meta Mutation Damage Score 0.9309 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.4%
Validation Efficiency 100% (115/115)
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 NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma. [provided by RefSeq, Jan 2016]
PHENOTYPE: Homozygotes for null alleles exhibit defects in embryonic development resulting in lethality at some point in organogenesis. Lethal phenotype may be affected by genetic background. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 114 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik G T 12: 71,211,320 (GRCm39) E685* probably null Het
2700049A03Rik A T 12: 71,211,321 (GRCm39) E685V possibly damaging Het
Acot6 A G 12: 84,155,789 (GRCm39) K246E probably benign Het
Actl11 T A 9: 107,808,615 (GRCm39) H979Q probably damaging Het
Adal T A 2: 120,986,030 (GRCm39) probably benign Het
Add2 G A 6: 86,087,840 (GRCm39) V596I probably benign Het
Adrb3 A C 8: 27,717,798 (GRCm39) M217R probably damaging Het
Ank1 T C 8: 23,631,134 (GRCm39) probably benign Het
Ank2 A T 3: 126,757,094 (GRCm39) N1054K possibly damaging Het
Ankib1 T C 5: 3,763,217 (GRCm39) Y504C probably damaging Het
Ankrd29 T C 18: 12,395,242 (GRCm39) K217R probably damaging Het
Ankrd45 T C 1: 160,982,876 (GRCm39) V129A probably damaging Het
Aox4 A T 1: 58,275,835 (GRCm39) D389V probably benign Het
Aph1a G T 3: 95,802,843 (GRCm39) G148W probably damaging Het
Arhgef26 G A 3: 62,247,806 (GRCm39) D297N possibly damaging Het
Atxn7l3b C A 10: 112,764,649 (GRCm39) probably benign Het
Auh A G 13: 52,995,065 (GRCm39) S167P probably damaging Het
Bach1 A T 16: 87,515,888 (GRCm39) K143I possibly damaging Het
Bbx T A 16: 50,045,101 (GRCm39) T487S probably damaging Het
Bche T G 3: 73,609,177 (GRCm39) D83A probably benign Het
Bri3bp G T 5: 125,518,760 (GRCm39) probably benign Het
Cd3d A T 9: 44,896,296 (GRCm39) E28D probably damaging Het
Cdc42bpa A G 1: 179,965,366 (GRCm39) T1028A probably damaging Het
Ceacam23 A G 7: 17,639,143 (GRCm39) probably null Het
Celsr2 T C 3: 108,319,945 (GRCm39) I956V possibly damaging Het
Cep95 A T 11: 106,707,480 (GRCm39) probably null Het
Cic G T 7: 24,986,535 (GRCm39) G1289C probably damaging Het
Cndp1 A G 18: 84,650,025 (GRCm39) Y223H probably damaging Het
Cops8 A G 1: 90,538,724 (GRCm39) D51G probably damaging Het
Csgalnact1 T C 8: 68,913,623 (GRCm39) E194G probably benign Het
Ctsm A G 13: 61,686,776 (GRCm39) Y39H probably damaging Het
Dhrs2 T C 14: 55,474,722 (GRCm39) V119A probably damaging Het
Drosha T A 15: 12,935,093 (GRCm39) M1336K probably benign Het
Dsp G A 13: 38,381,678 (GRCm39) D2808N possibly damaging Het
Ehmt1 G T 2: 24,767,509 (GRCm39) P135T probably damaging Het
Epas1 A G 17: 87,116,882 (GRCm39) N184S probably damaging Het
Erich3 C T 3: 154,454,025 (GRCm39) T597I possibly damaging Het
F10 T C 8: 13,105,698 (GRCm39) V421A probably damaging Het
Fabp3 C T 4: 130,206,180 (GRCm39) T57I probably benign Het
Fam227b G A 2: 125,958,043 (GRCm39) P241S probably damaging Het
Fcgrt C T 7: 44,751,372 (GRCm39) G192D probably benign Het
Fras1 A G 5: 96,798,541 (GRCm39) E1184G possibly damaging Het
Garre1 A C 7: 33,945,225 (GRCm39) Y552D probably damaging Het
Grn C A 11: 102,321,380 (GRCm39) probably benign Het
Gvin-ps5 A T 7: 105,928,664 (GRCm39) noncoding transcript Het
Hadh A T 3: 131,029,197 (GRCm39) L274* probably null Het
Hus1 T C 11: 8,956,027 (GRCm39) S169G probably damaging Het
Hydin A T 8: 111,290,554 (GRCm39) I3338F possibly damaging Het
Ighv11-1 T G 12: 113,945,768 (GRCm39) E28D probably benign Het
Kctd9 C T 14: 67,966,805 (GRCm39) T106I probably damaging Het
Krit1 A T 5: 3,872,238 (GRCm39) N421I probably damaging Het
Lamb1 A G 12: 31,376,677 (GRCm39) D1619G probably damaging Het
Lpar6 G A 14: 73,476,147 (GRCm39) C36Y probably damaging Het
Lrrc37a G C 11: 103,347,565 (GRCm39) F3043L unknown Het
Lrrc46 A T 11: 96,931,765 (GRCm39) V19D probably damaging Het
Mapkap1 G T 2: 34,471,303 (GRCm39) S197I probably damaging Het
Mrps35 A C 6: 146,961,645 (GRCm39) K173N possibly damaging Het
Mtf2 A G 5: 108,220,894 (GRCm39) probably benign Het
Ncf1 A C 5: 134,252,267 (GRCm39) D261E probably damaging Het
Nrxn1 A T 17: 90,928,274 (GRCm39) probably benign Het
Or13a18 C A 7: 140,190,304 (GRCm39) A75E possibly damaging Het
Or4x13 T A 2: 90,231,107 (GRCm39) M34K probably benign Het
Or52a33 A G 7: 103,289,308 (GRCm39) F13S probably damaging Het
Or5k3 T C 16: 58,969,981 (GRCm39) L256P probably damaging Het
Or5v1 G T 17: 37,810,017 (GRCm39) L158F probably benign Het
Otud4 G A 8: 80,382,318 (GRCm39) V176I probably damaging Het
Pakap T A 4: 57,856,552 (GRCm39) V668E probably benign Het
Papolg T C 11: 23,823,919 (GRCm39) probably null Het
Pgk2 A G 17: 40,518,402 (GRCm39) V342A probably damaging Het
Phf2 G A 13: 48,961,320 (GRCm39) A790V unknown Het
Prkdc T C 16: 15,491,861 (GRCm39) I602T possibly damaging Het
Prl3d3 T C 13: 27,343,072 (GRCm39) I86T possibly damaging Het
Prss8 G T 7: 127,525,635 (GRCm39) Q295K probably benign Het
Ptpre C T 7: 135,270,861 (GRCm39) H346Y probably benign Het
Ptpro T A 6: 137,420,592 (GRCm39) V1007D probably damaging Het
Pwwp3a T C 10: 80,068,702 (GRCm39) L282P probably benign Het
Qrfpr A G 3: 36,276,285 (GRCm39) V35A probably damaging Het
Rpf1 A G 3: 146,212,293 (GRCm39) L349S probably damaging Het
Rpl41 G T 10: 128,384,652 (GRCm39) probably null Het
Rprd2 G C 3: 95,672,632 (GRCm39) R924G probably benign Het
Serpini1 T A 3: 75,521,795 (GRCm39) N95K probably benign Het
Sfxn1 A T 13: 54,242,933 (GRCm39) T64S probably benign Het
Siae T G 9: 37,557,816 (GRCm39) I541S possibly damaging Het
Slc25a4 T A 8: 46,660,509 (GRCm39) K296N probably benign Het
Slc37a1 A G 17: 31,541,120 (GRCm39) N204S probably damaging Het
Slc9c1 A G 16: 45,413,800 (GRCm39) N976S probably benign Het
Smarcal1 T C 1: 72,672,019 (GRCm39) S847P possibly damaging Het
Smg1 A T 7: 117,757,323 (GRCm39) probably benign Het
Smg1 C T 7: 117,807,274 (GRCm39) A168T probably benign Het
Sptlc1 A G 13: 53,505,692 (GRCm39) I242T probably damaging Het
St8sia2 T C 7: 73,616,709 (GRCm39) I89V possibly damaging Het
Supt20 A T 3: 54,602,555 (GRCm39) probably benign Het
Tep1 T C 14: 51,076,457 (GRCm39) D1659G probably benign Het
Tex10 C A 4: 48,458,525 (GRCm39) probably benign Het
Thbs3 CAGAAG CAG 3: 89,130,409 (GRCm39) probably benign Het
Tmbim6 C A 15: 99,299,950 (GRCm39) S22* probably null Het
Tmc2 A T 2: 130,043,961 (GRCm39) K65M possibly damaging Het
Tmod1 A G 4: 46,090,872 (GRCm39) S142G probably damaging Het
Tns2 C T 15: 102,017,369 (GRCm39) R281C probably damaging Het
Trmt6 T C 2: 132,650,191 (GRCm39) R349G possibly damaging Het
Ttn T A 2: 76,537,586 (GRCm39) T26454S possibly damaging Het
Ttn C T 2: 76,605,122 (GRCm39) V16555I probably benign Het
Tut4 T A 4: 108,384,042 (GRCm39) probably benign Het
Ubr3 T C 2: 69,850,790 (GRCm39) probably benign Het
Vmn1r17 A C 6: 57,337,460 (GRCm39) F253V possibly damaging Het
Vmn1r201 G T 13: 22,659,622 (GRCm39) A279S possibly damaging Het
Vmn2r17 A T 5: 109,575,739 (GRCm39) R203S probably benign Het
Vwa5a A G 9: 38,633,926 (GRCm39) E43G probably benign Het
Wdr86 C T 5: 24,917,843 (GRCm39) probably null Het
Wdsub1 A T 2: 59,700,758 (GRCm39) probably benign Het
Zcchc7 T C 4: 44,931,039 (GRCm39) L76P probably damaging Het
Zfp108 G T 7: 23,960,163 (GRCm39) K251N probably benign Het
Zfp263 T C 16: 3,566,992 (GRCm39) C148R probably damaging Het
Zfp687 A C 3: 94,917,697 (GRCm39) F692V probably damaging Het
Other mutations in Notch1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00164:Notch1 APN 2 26,350,058 (GRCm39) missense probably damaging 0.98
IGL01343:Notch1 APN 2 26,362,917 (GRCm39) missense probably benign 0.25
IGL02066:Notch1 APN 2 26,350,408 (GRCm39) missense possibly damaging 0.71
IGL02158:Notch1 APN 2 26,350,351 (GRCm39) missense probably damaging 1.00
IGL02541:Notch1 APN 2 26,358,515 (GRCm39) missense probably benign 0.12
IGL03280:Notch1 APN 2 26,367,886 (GRCm39) intron probably benign
IGL03338:Notch1 APN 2 26,349,971 (GRCm39) missense probably benign
Antero UTSW 2 26,366,126 (GRCm39) missense possibly damaging 0.96
march UTSW 2 26,359,911 (GRCm39) missense probably damaging 0.98
PIT4494001:Notch1 UTSW 2 26,356,485 (GRCm39) missense probably damaging 1.00
R0013:Notch1 UTSW 2 26,363,830 (GRCm39) missense possibly damaging 0.64
R0025:Notch1 UTSW 2 26,360,943 (GRCm39) missense probably damaging 1.00
R0129:Notch1 UTSW 2 26,350,470 (GRCm39) missense probably benign 0.06
R0285:Notch1 UTSW 2 26,350,873 (GRCm39) missense possibly damaging 0.88
R0531:Notch1 UTSW 2 26,356,584 (GRCm39) missense probably benign 0.00
R0747:Notch1 UTSW 2 26,362,152 (GRCm39) missense unknown
R1440:Notch1 UTSW 2 26,370,976 (GRCm39) intron probably benign
R1502:Notch1 UTSW 2 26,374,335 (GRCm39) missense possibly damaging 0.95
R1539:Notch1 UTSW 2 26,362,125 (GRCm39) nonsense probably null
R1623:Notch1 UTSW 2 26,368,624 (GRCm39) missense possibly damaging 0.88
R1844:Notch1 UTSW 2 26,350,446 (GRCm39) missense probably benign 0.12
R1863:Notch1 UTSW 2 26,359,962 (GRCm39) missense probably damaging 1.00
R1874:Notch1 UTSW 2 26,371,591 (GRCm39) missense possibly damaging 0.89
R1926:Notch1 UTSW 2 26,371,669 (GRCm39) missense probably damaging 1.00
R2156:Notch1 UTSW 2 26,350,873 (GRCm39) missense possibly damaging 0.91
R2196:Notch1 UTSW 2 26,353,816 (GRCm39) nonsense probably null
R2209:Notch1 UTSW 2 26,350,019 (GRCm39) missense probably benign
R2382:Notch1 UTSW 2 26,363,793 (GRCm39) missense probably benign 0.40
R2508:Notch1 UTSW 2 26,355,485 (GRCm39) missense possibly damaging 0.80
R2873:Notch1 UTSW 2 26,350,247 (GRCm39) missense possibly damaging 0.89
R2874:Notch1 UTSW 2 26,350,247 (GRCm39) missense possibly damaging 0.89
R3798:Notch1 UTSW 2 26,368,630 (GRCm39) missense probably benign 0.00
R4019:Notch1 UTSW 2 26,371,154 (GRCm39) missense probably benign 0.03
R4305:Notch1 UTSW 2 26,367,936 (GRCm39) missense probably damaging 1.00
R4334:Notch1 UTSW 2 26,350,048 (GRCm39) missense probably benign 0.22
R4504:Notch1 UTSW 2 26,362,189 (GRCm39) missense probably benign 0.16
R4624:Notch1 UTSW 2 26,368,093 (GRCm39) missense possibly damaging 0.94
R4659:Notch1 UTSW 2 26,360,901 (GRCm39) missense probably damaging 0.99
R4703:Notch1 UTSW 2 26,361,170 (GRCm39) missense probably benign
R4869:Notch1 UTSW 2 26,361,191 (GRCm39) missense probably benign 0.21
R4938:Notch1 UTSW 2 26,364,136 (GRCm39) nonsense probably null
R5010:Notch1 UTSW 2 26,366,126 (GRCm39) missense possibly damaging 0.96
R5283:Notch1 UTSW 2 26,358,638 (GRCm39) missense probably damaging 1.00
R5303:Notch1 UTSW 2 26,368,631 (GRCm39) missense probably benign 0.01
R5635:Notch1 UTSW 2 26,366,173 (GRCm39) missense probably damaging 1.00
R5755:Notch1 UTSW 2 26,363,704 (GRCm39) missense probably benign 0.12
R5926:Notch1 UTSW 2 26,366,116 (GRCm39) missense probably benign 0.35
R5947:Notch1 UTSW 2 26,352,540 (GRCm39) intron probably benign
R6053:Notch1 UTSW 2 26,362,924 (GRCm39) missense probably benign 0.06
R6161:Notch1 UTSW 2 26,358,743 (GRCm39) missense probably damaging 1.00
R6162:Notch1 UTSW 2 26,352,207 (GRCm39) missense probably benign
R6174:Notch1 UTSW 2 26,375,454 (GRCm39) missense possibly damaging 0.50
R6199:Notch1 UTSW 2 26,359,911 (GRCm39) missense probably damaging 0.98
R6209:Notch1 UTSW 2 26,362,817 (GRCm39) missense probably damaging 1.00
R6251:Notch1 UTSW 2 26,364,182 (GRCm39) missense possibly damaging 0.64
R6493:Notch1 UTSW 2 26,362,110 (GRCm39) missense unknown
R6723:Notch1 UTSW 2 26,368,118 (GRCm39) missense probably damaging 1.00
R6736:Notch1 UTSW 2 26,350,298 (GRCm39) missense probably benign 0.01
R7020:Notch1 UTSW 2 26,371,586 (GRCm39) missense possibly damaging 0.95
R7058:Notch1 UTSW 2 26,353,830 (GRCm39) missense probably benign 0.05
R7154:Notch1 UTSW 2 26,349,950 (GRCm39) missense probably benign
R7291:Notch1 UTSW 2 26,366,387 (GRCm39) missense probably benign 0.01
R7379:Notch1 UTSW 2 26,369,479 (GRCm39) missense probably damaging 1.00
R7560:Notch1 UTSW 2 26,350,177 (GRCm39) missense probably benign 0.43
R7610:Notch1 UTSW 2 26,368,191 (GRCm39) missense probably benign 0.13
R7833:Notch1 UTSW 2 26,349,545 (GRCm39) makesense probably null
R7988:Notch1 UTSW 2 26,361,013 (GRCm39) missense probably benign 0.00
R8493:Notch1 UTSW 2 26,362,251 (GRCm39) missense unknown
R8514:Notch1 UTSW 2 26,362,181 (GRCm39) missense probably damaging 1.00
R8523:Notch1 UTSW 2 26,354,917 (GRCm39) missense possibly damaging 0.82
R8677:Notch1 UTSW 2 26,359,936 (GRCm39) missense probably damaging 1.00
R8696:Notch1 UTSW 2 26,368,004 (GRCm39) critical splice acceptor site probably benign
R8833:Notch1 UTSW 2 26,371,615 (GRCm39) missense probably damaging 1.00
R8964:Notch1 UTSW 2 26,371,062 (GRCm39) missense possibly damaging 0.65
R9091:Notch1 UTSW 2 26,369,895 (GRCm39) missense probably damaging 0.99
R9144:Notch1 UTSW 2 26,349,587 (GRCm39) missense probably benign 0.00
R9145:Notch1 UTSW 2 26,349,587 (GRCm39) missense probably benign 0.00
R9151:Notch1 UTSW 2 26,367,939 (GRCm39) missense probably benign 0.01
R9270:Notch1 UTSW 2 26,369,895 (GRCm39) missense probably damaging 0.99
R9463:Notch1 UTSW 2 26,359,845 (GRCm39) missense probably benign 0.20
R9546:Notch1 UTSW 2 26,371,127 (GRCm39) missense probably damaging 0.97
R9674:Notch1 UTSW 2 26,361,308 (GRCm39) missense probably damaging 0.98
X0018:Notch1 UTSW 2 26,352,239 (GRCm39) nonsense probably null
X0066:Notch1 UTSW 2 26,360,347 (GRCm39) missense possibly damaging 0.90
Z1088:Notch1 UTSW 2 26,367,127 (GRCm39) missense probably damaging 0.99
Z1177:Notch1 UTSW 2 26,350,321 (GRCm39) missense possibly damaging 0.74
Predicted Primers PCR Primer
(F):5'- TTCGCAGTAGAAGGAAGCCAC -3'
(R):5'- GCATCAGATGGTTCTTGTGAGC -3'

Sequencing Primer
(F):5'- CACGGTCGTGGCAAGTG -3'
(R):5'- TTAGCAGCTAACATCCAGAGTCAGG -3'
Posted On 2016-05-10