Incidental Mutation 'R6156:Ltbp4'
ID 489581
Institutional Source Beutler Lab
Gene Symbol Ltbp4
Ensembl Gene ENSMUSG00000040488
Gene Name latent transforming growth factor beta binding protein 4
Synonyms 2310046A13Rik
MMRRC Submission 044303-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6156 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 27004561-27037117 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 27029587 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 136 (T136K)
Ref Sequence ENSEMBL: ENSMUSP00000113674 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038618] [ENSMUST00000108369] [ENSMUST00000118583] [ENSMUST00000118961] [ENSMUST00000121175]
AlphaFold Q8K4G1
Predicted Effect unknown
Transcript: ENSMUST00000038618
AA Change: T202K
SMART Domains Protein: ENSMUSP00000037536
Gene: ENSMUSG00000040488
AA Change: T202K

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
low complexity region 87 100 N/A INTRINSIC
low complexity region 112 125 N/A INTRINSIC
EGF 151 180 2.74e-3 SMART
low complexity region 244 265 N/A INTRINSIC
EGF_CA 356 396 3.51e-10 SMART
Pfam:TB 416 457 4.8e-15 PFAM
low complexity region 490 501 N/A INTRINSIC
low complexity region 507 568 N/A INTRINSIC
low complexity region 579 590 N/A INTRINSIC
EGF 591 629 6.06e-5 SMART
EGF_CA 630 671 8.3e-12 SMART
EGF_CA 672 713 7.34e-13 SMART
EGF_CA 714 751 8.43e-13 SMART
EGF_CA 753 794 1.66e-11 SMART
EGF_CA 795 836 3.61e-12 SMART
EGF_CA 837 876 5.61e-9 SMART
EGF_CA 877 919 1.73e-9 SMART
EGF_CA 920 961 7.12e-11 SMART
EGF_CA 962 1002 3.56e-11 SMART
EGF_CA 1003 1046 1.61e-9 SMART
EGF_CA 1047 1090 2.13e-9 SMART
EGF_CA 1091 1132 1.02e-11 SMART
EGF 1136 1175 1.69e1 SMART
low complexity region 1185 1223 N/A INTRINSIC
Pfam:TB 1234 1276 1.7e-13 PFAM
EGF_CA 1295 1337 2.72e-7 SMART
EGF_CA 1338 1379 1.36e-7 SMART
Pfam:TB 1402 1443 4.3e-14 PFAM
low complexity region 1449 1461 N/A INTRINSIC
low complexity region 1478 1500 N/A INTRINSIC
EGF 1578 1615 6.06e-5 SMART
EGF_CA 1616 1660 9.54e-12 SMART
Predicted Effect unknown
Transcript: ENSMUST00000108369
AA Change: T201K
SMART Domains Protein: ENSMUSP00000104006
Gene: ENSMUSG00000040488
AA Change: T201K

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
low complexity region 116 145 N/A INTRINSIC
EGF 150 179 2.74e-3 SMART
low complexity region 243 264 N/A INTRINSIC
EGF_CA 355 395 3.51e-10 SMART
Pfam:TB 414 456 2.5e-14 PFAM
low complexity region 489 500 N/A INTRINSIC
low complexity region 506 567 N/A INTRINSIC
low complexity region 578 589 N/A INTRINSIC
EGF 590 628 6.06e-5 SMART
EGF_CA 629 670 8.3e-12 SMART
EGF_CA 671 712 7.34e-13 SMART
EGF_CA 713 750 8.43e-13 SMART
EGF_CA 752 793 1.66e-11 SMART
EGF_CA 794 835 3.61e-12 SMART
EGF_CA 836 875 5.61e-9 SMART
EGF_CA 876 918 1.73e-9 SMART
EGF_CA 919 960 7.12e-11 SMART
EGF_CA 961 1001 3.56e-11 SMART
EGF_CA 1002 1045 1.61e-9 SMART
EGF_CA 1046 1089 2.13e-9 SMART
EGF_CA 1090 1131 1.02e-11 SMART
EGF 1135 1174 1.69e1 SMART
low complexity region 1184 1222 N/A INTRINSIC
Pfam:TB 1232 1275 2.4e-13 PFAM
EGF_CA 1294 1336 2.72e-7 SMART
EGF_CA 1337 1378 1.36e-7 SMART
Pfam:TB 1400 1442 7.6e-15 PFAM
low complexity region 1448 1460 N/A INTRINSIC
low complexity region 1477 1499 N/A INTRINSIC
EGF 1577 1614 6.06e-5 SMART
EGF_CA 1615 1659 9.54e-12 SMART
Predicted Effect unknown
Transcript: ENSMUST00000118583
AA Change: T136K
SMART Domains Protein: ENSMUSP00000113523
Gene: ENSMUSG00000040488
AA Change: T136K

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 69 80 N/A INTRINSIC
EGF 85 114 2.74e-3 SMART
low complexity region 178 199 N/A INTRINSIC
EGF_CA 290 330 3.51e-10 SMART
Pfam:TB 349 391 2.3e-14 PFAM
low complexity region 424 435 N/A INTRINSIC
low complexity region 441 502 N/A INTRINSIC
low complexity region 513 524 N/A INTRINSIC
EGF 525 563 6.06e-5 SMART
EGF_CA 564 605 8.3e-12 SMART
EGF_CA 606 647 7.34e-13 SMART
EGF_CA 648 685 8.43e-13 SMART
EGF_CA 687 728 1.66e-11 SMART
EGF_CA 729 770 3.61e-12 SMART
EGF_CA 771 810 5.61e-9 SMART
EGF_CA 811 853 1.73e-9 SMART
EGF_CA 854 895 7.12e-11 SMART
EGF_CA 896 936 3.56e-11 SMART
EGF_CA 937 980 1.61e-9 SMART
EGF_CA 981 1024 2.13e-9 SMART
EGF_CA 1025 1066 1.02e-11 SMART
EGF 1070 1109 1.69e1 SMART
low complexity region 1119 1157 N/A INTRINSIC
Pfam:TB 1167 1210 2.2e-13 PFAM
EGF_CA 1229 1271 2.72e-7 SMART
EGF_CA 1272 1313 1.36e-7 SMART
Pfam:TB 1335 1377 7.1e-15 PFAM
low complexity region 1383 1395 N/A INTRINSIC
low complexity region 1412 1434 N/A INTRINSIC
EGF 1512 1549 6.06e-5 SMART
Predicted Effect unknown
Transcript: ENSMUST00000118961
AA Change: T136K
SMART Domains Protein: ENSMUSP00000113746
Gene: ENSMUSG00000040488
AA Change: T136K

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 69 80 N/A INTRINSIC
EGF 85 114 2.74e-3 SMART
low complexity region 178 199 N/A INTRINSIC
EGF_CA 290 330 3.51e-10 SMART
Pfam:TB 349 391 1.6e-14 PFAM
low complexity region 424 435 N/A INTRINSIC
low complexity region 441 502 N/A INTRINSIC
low complexity region 513 524 N/A INTRINSIC
EGF 525 563 6.06e-5 SMART
EGF_CA 564 605 8.3e-12 SMART
EGF_CA 606 647 7.34e-13 SMART
EGF_CA 648 685 8.43e-13 SMART
EGF_CA 687 728 1.66e-11 SMART
EGF_CA 729 770 3.61e-12 SMART
EGF_CA 771 810 5.61e-9 SMART
EGF_CA 811 853 1.73e-9 SMART
EGF_CA 854 895 7.12e-11 SMART
EGF_CA 896 936 3.56e-11 SMART
EGF_CA 937 980 1.61e-9 SMART
EGF_CA 981 1024 2.13e-9 SMART
EGF_CA 1025 1066 1.02e-11 SMART
EGF 1070 1109 1.69e1 SMART
Predicted Effect unknown
Transcript: ENSMUST00000121175
AA Change: T136K
SMART Domains Protein: ENSMUSP00000113674
Gene: ENSMUSG00000040488
AA Change: T136K

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 69 80 N/A INTRINSIC
EGF 85 114 2.74e-3 SMART
low complexity region 178 199 N/A INTRINSIC
EGF_CA 290 330 3.51e-10 SMART
Pfam:TB 349 391 3.4e-14 PFAM
low complexity region 424 435 N/A INTRINSIC
low complexity region 441 502 N/A INTRINSIC
low complexity region 513 524 N/A INTRINSIC
EGF 525 563 6.06e-5 SMART
EGF_CA 564 605 8.3e-12 SMART
EGF_CA 606 647 7.34e-13 SMART
EGF_CA 648 685 8.43e-13 SMART
EGF_CA 687 728 1.66e-11 SMART
EGF_CA 729 770 3.61e-12 SMART
EGF_CA 771 810 5.61e-9 SMART
EGF_CA 811 853 1.73e-9 SMART
EGF_CA 854 895 7.12e-11 SMART
EGF_CA 896 936 3.56e-11 SMART
EGF_CA 937 980 1.61e-9 SMART
EGF_CA 981 1024 2.13e-9 SMART
EGF_CA 1025 1066 1.02e-11 SMART
EGF 1070 1109 1.69e1 SMART
low complexity region 1119 1157 N/A INTRINSIC
Pfam:TB 1167 1210 3.3e-13 PFAM
EGF_CA 1229 1271 2.72e-7 SMART
EGF_CA 1272 1313 1.36e-7 SMART
Pfam:TB 1335 1377 1e-14 PFAM
low complexity region 1383 1395 N/A INTRINSIC
low complexity region 1412 1434 N/A INTRINSIC
EGF 1512 1549 6.06e-5 SMART
EGF_CA 1550 1594 9.54e-12 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206413
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.9%
Validation Efficiency 97% (68/70)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene binds transforming growth factor beta (TGFB) as it is secreted and targeted to the extracellular matrix. TGFB is biologically latent after secretion and insertion into the extracellular matrix, and sheds TGFB and other proteins upon activation. Defects in this gene may be a cause of cutis laxa and severe pulmonary, gastrointestinal, and urinary abnormalities. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]
PHENOTYPE: Homozygous disruption of this locus results in pulmonary emphysema, cardiomyopathy, and colon cancer. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy8 T G 15: 64,689,488 (GRCm39) probably null Het
Ank2 T C 3: 126,737,886 (GRCm39) D2579G probably damaging Het
Atp6v1b1 G C 6: 83,735,115 (GRCm39) G423R probably damaging Het
B4galnt3 T C 6: 120,191,801 (GRCm39) N644S probably benign Het
Bhmt1b C A 18: 87,775,231 (GRCm39) Y251* probably null Het
Capsl T G 15: 9,465,920 (GRCm39) M132R probably damaging Het
Cep120 A G 18: 53,836,295 (GRCm39) Y797H probably benign Het
Cimip4 T C 15: 78,263,013 (GRCm39) T214A probably damaging Het
Clec2e T A 6: 129,072,061 (GRCm39) D106V possibly damaging Het
Col6a2 C T 10: 76,440,004 (GRCm39) V634I possibly damaging Het
Dis3 T C 14: 99,336,215 (GRCm39) E97G probably benign Het
Dlec1 T C 9: 118,939,281 (GRCm39) probably null Het
Dock2 C A 11: 34,197,789 (GRCm39) V1484F possibly damaging Het
Ephb2 T A 4: 136,388,816 (GRCm39) M593L probably benign Het
Fcgrt T C 7: 44,751,484 (GRCm39) T125A probably benign Het
Gabbr1 T C 17: 37,359,319 (GRCm39) I98T probably benign Het
Gbp10 G A 5: 105,384,015 (GRCm39) probably benign Het
Gfod1 T C 13: 43,354,514 (GRCm39) S154G possibly damaging Het
Ggt5 C T 10: 75,445,160 (GRCm39) T389I probably damaging Het
Got2 A G 8: 96,598,896 (GRCm39) F169L probably benign Het
Gse1 A G 8: 121,215,866 (GRCm39) K5E possibly damaging Het
Hyal5 T C 6: 24,891,437 (GRCm39) I417T possibly damaging Het
Igkv4-91 G T 6: 68,745,607 (GRCm39) T97K probably damaging Het
Il4i1 T C 7: 44,489,608 (GRCm39) Y458H possibly damaging Het
Impg1 A T 9: 80,230,106 (GRCm39) C740S probably damaging Het
Itgb1 C G 8: 129,458,535 (GRCm39) T788R possibly damaging Het
Lman2l A G 1: 36,477,907 (GRCm39) V143A probably damaging Het
Macf1 A G 4: 123,366,073 (GRCm39) I1331T probably benign Het
Mmp11 G A 10: 75,762,325 (GRCm39) A336V probably damaging Het
Myh2 A T 11: 67,071,879 (GRCm39) I536F probably damaging Het
Myh4 A G 11: 67,141,618 (GRCm39) M826V probably benign Het
Naca T C 10: 127,875,160 (GRCm39) probably benign Het
Nr4a2 A G 2: 57,002,364 (GRCm39) Y30H probably damaging Het
Or12j4 A G 7: 140,046,758 (GRCm39) T215A probably benign Het
Or1e35 A T 11: 73,797,447 (GRCm39) Y290* probably null Het
Or2n1d T A 17: 38,646,064 (GRCm39) N5K probably damaging Het
Or4a67 T A 2: 88,597,934 (GRCm39) I242L probably benign Het
Or4f14d A T 2: 111,960,445 (GRCm39) L237Q probably damaging Het
Or4k42 A T 2: 111,320,095 (GRCm39) M136K probably damaging Het
Or4z4 A G 19: 12,076,484 (GRCm39) V173A possibly damaging Het
Or8g22 T A 9: 38,958,671 (GRCm39) M15L possibly damaging Het
Paqr3 A C 5: 97,256,128 (GRCm39) L82R probably damaging Het
Pex6 C T 17: 47,031,567 (GRCm39) P456S probably benign Het
Pih1d2 A T 9: 50,532,452 (GRCm39) K186I possibly damaging Het
Plekhh3 A G 11: 101,061,013 (GRCm39) probably benign Het
Ptpn23 C A 9: 110,216,849 (GRCm39) probably benign Het
Rcor3 T A 1: 191,812,142 (GRCm39) probably benign Het
Rgs11 T A 17: 26,429,439 (GRCm39) Y403* probably null Het
Scn10a T C 9: 119,464,649 (GRCm39) N984D probably benign Het
Snx14 C T 9: 88,289,392 (GRCm39) A287T possibly damaging Het
Stx3 T C 19: 11,780,874 (GRCm39) D33G probably damaging Het
Tacc2 A G 7: 130,227,494 (GRCm39) K1393R probably damaging Het
Tas2r129 T C 6: 132,928,455 (GRCm39) S131P probably benign Het
Tbx15 G T 3: 99,220,431 (GRCm39) probably null Het
Thada A G 17: 84,700,795 (GRCm39) V1237A probably damaging Het
Tnc A G 4: 63,888,589 (GRCm39) Y1735H probably damaging Het
Ttc22 A G 4: 106,495,780 (GRCm39) K378R probably benign Het
Tubg2 A G 11: 101,051,635 (GRCm39) K287E possibly damaging Het
Ugt3a1 T C 15: 9,310,762 (GRCm39) I348T possibly damaging Het
Unc79 A G 12: 103,027,717 (GRCm39) N436S probably damaging Het
Unc80 A T 1: 66,651,409 (GRCm39) I1585F probably benign Het
Vmn2r104 T C 17: 20,261,909 (GRCm39) Y407C probably damaging Het
Vmn2r108 T A 17: 20,692,447 (GRCm39) L136F probably benign Het
Vmn2r38 A G 7: 9,097,611 (GRCm39) S161P probably damaging Het
Vmn2r90 T C 17: 17,953,606 (GRCm39) I590T probably benign Het
Washc5 T C 15: 59,217,248 (GRCm39) E323G probably damaging Het
Wdhd1 C T 14: 47,505,653 (GRCm39) G273D probably damaging Het
Xpo6 G T 7: 125,708,016 (GRCm39) Q851K probably damaging Het
Zfp386 T C 12: 116,023,526 (GRCm39) S380P probably damaging Het
Zfp536 A G 7: 37,173,281 (GRCm39) C274R unknown Het
Zfp64 A G 2: 168,768,088 (GRCm39) I508T probably benign Het
Other mutations in Ltbp4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00434:Ltbp4 APN 7 27,028,230 (GRCm39) missense probably damaging 0.96
IGL00585:Ltbp4 APN 7 27,026,158 (GRCm39) missense probably damaging 0.98
IGL01320:Ltbp4 APN 7 27,027,784 (GRCm39) splice site probably benign
IGL01860:Ltbp4 APN 7 27,019,071 (GRCm39) missense probably damaging 1.00
IGL02026:Ltbp4 APN 7 27,026,842 (GRCm39) nonsense probably null
IGL02226:Ltbp4 APN 7 27,006,359 (GRCm39) missense probably damaging 1.00
IGL02422:Ltbp4 APN 7 27,019,097 (GRCm39) missense probably damaging 1.00
IGL02611:Ltbp4 APN 7 27,010,080 (GRCm39) missense probably damaging 1.00
IGL02892:Ltbp4 APN 7 27,010,074 (GRCm39) missense probably damaging 1.00
IGL02926:Ltbp4 APN 7 27,028,297 (GRCm39) splice site probably null
IGL02950:Ltbp4 APN 7 27,006,143 (GRCm39) missense probably damaging 0.99
IGL03008:Ltbp4 APN 7 27,023,789 (GRCm39) missense probably damaging 0.99
IGL03271:Ltbp4 APN 7 27,029,240 (GRCm39) missense unknown
IGL02837:Ltbp4 UTSW 7 27,013,806 (GRCm39) missense probably damaging 1.00
R0792:Ltbp4 UTSW 7 27,024,485 (GRCm39) missense probably damaging 1.00
R0980:Ltbp4 UTSW 7 27,023,587 (GRCm39) missense probably damaging 1.00
R1017:Ltbp4 UTSW 7 27,005,501 (GRCm39) missense possibly damaging 0.95
R1185:Ltbp4 UTSW 7 27,009,960 (GRCm39) missense probably damaging 1.00
R1185:Ltbp4 UTSW 7 27,009,960 (GRCm39) missense probably damaging 1.00
R1185:Ltbp4 UTSW 7 27,009,960 (GRCm39) missense probably damaging 1.00
R1403:Ltbp4 UTSW 7 27,028,464 (GRCm39) missense unknown
R1403:Ltbp4 UTSW 7 27,028,464 (GRCm39) missense unknown
R1448:Ltbp4 UTSW 7 27,006,002 (GRCm39) missense possibly damaging 0.86
R1575:Ltbp4 UTSW 7 27,022,245 (GRCm39) missense probably damaging 1.00
R1918:Ltbp4 UTSW 7 27,036,994 (GRCm39) unclassified probably benign
R1932:Ltbp4 UTSW 7 27,007,191 (GRCm39) critical splice donor site probably null
R1959:Ltbp4 UTSW 7 27,028,443 (GRCm39) missense unknown
R1960:Ltbp4 UTSW 7 27,028,443 (GRCm39) missense unknown
R1976:Ltbp4 UTSW 7 27,026,195 (GRCm39) missense probably damaging 1.00
R2060:Ltbp4 UTSW 7 27,008,378 (GRCm39) missense probably damaging 1.00
R2333:Ltbp4 UTSW 7 27,027,203 (GRCm39) missense possibly damaging 0.82
R2431:Ltbp4 UTSW 7 27,019,101 (GRCm39) missense possibly damaging 0.91
R3125:Ltbp4 UTSW 7 27,027,203 (GRCm39) missense possibly damaging 0.82
R4093:Ltbp4 UTSW 7 27,024,641 (GRCm39) missense possibly damaging 0.93
R4095:Ltbp4 UTSW 7 27,024,641 (GRCm39) missense possibly damaging 0.93
R4592:Ltbp4 UTSW 7 27,024,608 (GRCm39) missense probably damaging 0.96
R4610:Ltbp4 UTSW 7 27,006,125 (GRCm39) missense probably damaging 1.00
R4650:Ltbp4 UTSW 7 27,013,734 (GRCm39) missense probably damaging 1.00
R4912:Ltbp4 UTSW 7 27,005,541 (GRCm39) nonsense probably null
R5002:Ltbp4 UTSW 7 27,027,110 (GRCm39) frame shift probably null
R5016:Ltbp4 UTSW 7 27,027,110 (GRCm39) frame shift probably null
R5216:Ltbp4 UTSW 7 27,026,736 (GRCm39) small deletion probably benign
R5218:Ltbp4 UTSW 7 27,026,736 (GRCm39) small deletion probably benign
R5219:Ltbp4 UTSW 7 27,026,746 (GRCm39) missense probably benign 0.01
R5219:Ltbp4 UTSW 7 27,026,736 (GRCm39) small deletion probably benign
R5539:Ltbp4 UTSW 7 27,027,149 (GRCm39) missense probably damaging 0.97
R5991:Ltbp4 UTSW 7 27,008,741 (GRCm39) missense probably damaging 1.00
R6082:Ltbp4 UTSW 7 27,035,105 (GRCm39) unclassified probably benign
R6125:Ltbp4 UTSW 7 27,027,180 (GRCm39) missense probably damaging 1.00
R6146:Ltbp4 UTSW 7 27,019,149 (GRCm39) missense probably damaging 0.99
R6414:Ltbp4 UTSW 7 27,010,140 (GRCm39) missense probably damaging 1.00
R6563:Ltbp4 UTSW 7 27,008,488 (GRCm39) missense probably damaging 1.00
R6719:Ltbp4 UTSW 7 27,028,188 (GRCm39) missense probably damaging 0.99
R6940:Ltbp4 UTSW 7 27,008,369 (GRCm39) missense probably damaging 1.00
R7054:Ltbp4 UTSW 7 27,007,191 (GRCm39) critical splice donor site probably null
R7116:Ltbp4 UTSW 7 27,004,852 (GRCm39) missense probably damaging 0.99
R7326:Ltbp4 UTSW 7 27,029,180 (GRCm39) missense unknown
R7419:Ltbp4 UTSW 7 27,029,192 (GRCm39) missense unknown
R8068:Ltbp4 UTSW 7 27,023,593 (GRCm39) missense probably damaging 0.99
R8435:Ltbp4 UTSW 7 27,034,870 (GRCm39) missense unknown
R8543:Ltbp4 UTSW 7 27,024,666 (GRCm39) missense possibly damaging 0.84
R8897:Ltbp4 UTSW 7 27,026,119 (GRCm39) missense probably benign 0.09
R9103:Ltbp4 UTSW 7 27,028,186 (GRCm39) missense unknown
R9131:Ltbp4 UTSW 7 27,036,976 (GRCm39) missense unknown
R9206:Ltbp4 UTSW 7 27,022,350 (GRCm39) missense probably damaging 1.00
R9301:Ltbp4 UTSW 7 27,021,578 (GRCm39) missense probably damaging 0.98
R9302:Ltbp4 UTSW 7 27,008,481 (GRCm39) missense possibly damaging 0.80
X0025:Ltbp4 UTSW 7 27,025,227 (GRCm39) missense probably damaging 1.00
X0066:Ltbp4 UTSW 7 27,005,490 (GRCm39) critical splice donor site probably null
Z1088:Ltbp4 UTSW 7 27,007,217 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGCTCTGACTTGCTAGGAGTAG -3'
(R):5'- TGAGTTAGCTGTCTGCCAGG -3'

Sequencing Primer
(F):5'- ATGGCCTGCAATTTTCAGTGATC -3'
(R):5'- CTGCCAGGCACAGTACTGATATTTTG -3'
Posted On 2017-10-10