Incidental Mutation 'R1782:Gtf3c1'
ID |
195391 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Gtf3c1
|
Ensembl Gene |
ENSMUSG00000032777 |
Gene Name |
general transcription factor III C 1 |
Synonyms |
|
MMRRC Submission |
039813-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1782 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
125240126-125306860 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 125266246 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Glutamic Acid
at position 1030
(V1030E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000145939
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055506]
[ENSMUST00000205444]
[ENSMUST00000205659]
|
AlphaFold |
Q8K284 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000055506
AA Change: V1030E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000056719 Gene: ENSMUSG00000032777 AA Change: V1030E
Domain | Start | End | E-Value | Type |
Pfam:B-block_TFIIIC
|
174 |
250 |
5.1e-20 |
PFAM |
low complexity region
|
344 |
354 |
N/A |
INTRINSIC |
low complexity region
|
474 |
514 |
N/A |
INTRINSIC |
low complexity region
|
538 |
549 |
N/A |
INTRINSIC |
low complexity region
|
592 |
604 |
N/A |
INTRINSIC |
low complexity region
|
725 |
745 |
N/A |
INTRINSIC |
low complexity region
|
859 |
872 |
N/A |
INTRINSIC |
low complexity region
|
1158 |
1173 |
N/A |
INTRINSIC |
low complexity region
|
1359 |
1372 |
N/A |
INTRINSIC |
low complexity region
|
1423 |
1443 |
N/A |
INTRINSIC |
low complexity region
|
1585 |
1620 |
N/A |
INTRINSIC |
low complexity region
|
1895 |
1915 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000205444
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000205659
AA Change: V1030E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205697
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205827
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000206694
|
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.2%
- 20x: 92.3%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a transgenic gene disruption may exhibit preimplantation lethality. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,247,971 (GRCm39) |
T2573S |
probably benign |
Het |
Adgra3 |
G |
T |
5: 50,129,404 (GRCm39) |
T738K |
probably benign |
Het |
Adgrl4 |
C |
T |
3: 151,248,442 (GRCm39) |
Q705* |
probably null |
Het |
Atp2b1 |
T |
G |
10: 98,839,063 (GRCm39) |
D630E |
probably benign |
Het |
Atp2c1 |
G |
A |
9: 105,308,786 (GRCm39) |
R577C |
probably damaging |
Het |
Atp9b |
A |
G |
18: 80,809,137 (GRCm39) |
V211A |
probably damaging |
Het |
C8g |
T |
A |
2: 25,389,094 (GRCm39) |
D163V |
possibly damaging |
Het |
Catsper1 |
T |
C |
19: 5,385,937 (GRCm39) |
Y57H |
probably benign |
Het |
Ccdc25 |
C |
T |
14: 66,091,597 (GRCm39) |
A72V |
probably benign |
Het |
Cdca2 |
T |
G |
14: 67,915,260 (GRCm39) |
E666D |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,324,321 (GRCm39) |
T313I |
probably damaging |
Het |
Cfap57 |
C |
A |
4: 118,472,172 (GRCm39) |
R69L |
probably damaging |
Het |
Chat |
C |
A |
14: 32,130,944 (GRCm39) |
V566L |
probably damaging |
Het |
Cntn3 |
T |
C |
6: 102,250,772 (GRCm39) |
I259V |
probably damaging |
Het |
Cog1 |
A |
G |
11: 113,544,792 (GRCm39) |
T325A |
probably benign |
Het |
Cxcl10 |
A |
G |
5: 92,495,662 (GRCm39) |
*94Q |
probably null |
Het |
Cyp4a12b |
T |
C |
4: 115,291,178 (GRCm39) |
Y369H |
probably damaging |
Het |
Dhx33 |
T |
C |
11: 70,892,466 (GRCm39) |
Y101C |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,723,142 (GRCm39) |
M1593T |
probably damaging |
Het |
Dpy19l3 |
T |
C |
7: 35,407,580 (GRCm39) |
T488A |
possibly damaging |
Het |
Elapor2 |
A |
T |
5: 9,471,620 (GRCm39) |
K320N |
possibly damaging |
Het |
Fbxw14 |
A |
G |
9: 109,107,759 (GRCm39) |
I205T |
possibly damaging |
Het |
Fbxw7 |
T |
C |
3: 84,811,126 (GRCm39) |
F84L |
probably benign |
Het |
Flii |
T |
C |
11: 60,605,462 (GRCm39) |
T1212A |
probably benign |
Het |
Fosl1 |
T |
A |
19: 5,500,210 (GRCm39) |
I43N |
probably damaging |
Het |
Gabrr2 |
G |
A |
4: 33,085,593 (GRCm39) |
A338T |
probably damaging |
Het |
Gask1b |
T |
C |
3: 79,793,838 (GRCm39) |
L102S |
possibly damaging |
Het |
Gatad2b |
T |
C |
3: 90,249,178 (GRCm39) |
V72A |
probably benign |
Het |
Gorasp1 |
G |
T |
9: 119,761,888 (GRCm39) |
N48K |
probably damaging |
Het |
Gramd1b |
C |
A |
9: 40,324,633 (GRCm39) |
D139Y |
probably damaging |
Het |
Havcr2 |
C |
T |
11: 46,345,844 (GRCm39) |
T6I |
unknown |
Het |
Hgs |
A |
G |
11: 120,369,331 (GRCm39) |
E340G |
probably damaging |
Het |
Irx2 |
A |
G |
13: 72,779,585 (GRCm39) |
T290A |
probably benign |
Het |
Itgb8 |
T |
A |
12: 119,155,853 (GRCm39) |
I200F |
probably damaging |
Het |
Josd2 |
A |
G |
7: 44,120,577 (GRCm39) |
I105V |
probably damaging |
Het |
Kcnh7 |
T |
A |
2: 62,566,513 (GRCm39) |
D806V |
probably damaging |
Het |
Kctd8 |
A |
G |
5: 69,498,319 (GRCm39) |
V109A |
possibly damaging |
Het |
Kmt2d |
T |
A |
15: 98,755,429 (GRCm39) |
|
probably benign |
Het |
Krtap2-4 |
A |
T |
11: 99,505,353 (GRCm39) |
V86E |
probably damaging |
Het |
Lgr6 |
C |
G |
1: 134,915,717 (GRCm39) |
V344L |
probably damaging |
Het |
Lime1 |
A |
T |
2: 181,024,849 (GRCm39) |
R168W |
possibly damaging |
Het |
Macroh2a1 |
A |
T |
13: 56,222,134 (GRCm39) |
M339K |
probably damaging |
Het |
Magel2 |
C |
T |
7: 62,030,605 (GRCm39) |
Q1170* |
probably null |
Het |
Ndufaf3 |
A |
T |
9: 108,443,210 (GRCm39) |
I169N |
probably damaging |
Het |
Neb |
T |
A |
2: 52,174,357 (GRCm39) |
K1501* |
probably null |
Het |
Nim1k |
A |
T |
13: 120,173,687 (GRCm39) |
S402R |
probably benign |
Het |
Nt5dc2 |
T |
G |
14: 30,860,158 (GRCm39) |
S395R |
probably damaging |
Het |
Oaz2 |
G |
T |
9: 65,596,143 (GRCm39) |
V132L |
probably benign |
Het |
Or2t45 |
T |
A |
11: 58,669,631 (GRCm39) |
L226H |
probably damaging |
Het |
Or4l1 |
A |
T |
14: 50,166,096 (GRCm39) |
W302R |
probably benign |
Het |
Or5b104 |
T |
A |
19: 13,072,167 (GRCm39) |
I282F |
probably damaging |
Het |
Or7g25 |
C |
T |
9: 19,159,877 (GRCm39) |
V273I |
probably benign |
Het |
Or8k39 |
T |
C |
2: 86,563,026 (GRCm39) |
K310R |
probably benign |
Het |
Pfkl |
A |
G |
10: 77,824,554 (GRCm39) |
V717A |
probably benign |
Het |
Phf8-ps |
T |
C |
17: 33,286,662 (GRCm39) |
I47V |
probably benign |
Het |
Phgdh |
C |
T |
3: 98,228,063 (GRCm39) |
V231I |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,635,935 (GRCm39) |
M465K |
probably damaging |
Het |
Ppp3r1 |
A |
G |
11: 17,148,281 (GRCm39) |
H163R |
probably benign |
Het |
Prune2 |
T |
A |
19: 17,099,537 (GRCm39) |
N1680K |
probably benign |
Het |
Puf60 |
T |
A |
15: 75,943,724 (GRCm39) |
I216L |
probably benign |
Het |
Rev3l |
T |
A |
10: 39,675,881 (GRCm39) |
N190K |
probably benign |
Het |
Rp1 |
G |
A |
1: 4,419,312 (GRCm39) |
S600L |
probably benign |
Het |
Rpl3l |
A |
G |
17: 24,952,430 (GRCm39) |
I217V |
probably benign |
Het |
Scly |
T |
A |
1: 91,236,102 (GRCm39) |
V194D |
probably damaging |
Het |
Scnn1b |
A |
G |
7: 121,517,184 (GRCm39) |
T607A |
probably benign |
Het |
Slc13a3 |
G |
A |
2: 165,287,439 (GRCm39) |
L172F |
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,258,733 (GRCm39) |
Y1090C |
probably damaging |
Het |
Spag17 |
T |
A |
3: 99,918,070 (GRCm39) |
M351K |
probably benign |
Het |
St14 |
A |
G |
9: 31,011,460 (GRCm39) |
Y444H |
probably damaging |
Het |
Taf8 |
C |
A |
17: 47,809,136 (GRCm39) |
A109S |
probably benign |
Het |
Tbc1d30 |
T |
A |
10: 121,103,525 (GRCm39) |
K502N |
probably damaging |
Het |
Them5 |
T |
C |
3: 94,251,796 (GRCm39) |
S136P |
probably benign |
Het |
Tmem248 |
T |
A |
5: 130,260,769 (GRCm39) |
N111K |
probably damaging |
Het |
Tmem74 |
C |
A |
15: 43,730,348 (GRCm39) |
V232L |
probably damaging |
Het |
Tnip2 |
A |
T |
5: 34,657,012 (GRCm39) |
H264Q |
probably benign |
Het |
Trim5 |
A |
G |
7: 103,915,023 (GRCm39) |
|
probably null |
Het |
Trim63 |
A |
G |
4: 134,050,349 (GRCm39) |
Q211R |
probably benign |
Het |
Trrap |
T |
C |
5: 144,759,513 (GRCm39) |
V2231A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,565,831 (GRCm39) |
S28174G |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,229,440 (GRCm39) |
D341G |
possibly damaging |
Het |
Uroc1 |
G |
A |
6: 90,313,901 (GRCm39) |
E63K |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,643,382 (GRCm39) |
V4248A |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,822,435 (GRCm39) |
H583R |
probably damaging |
Het |
Usp8 |
T |
A |
2: 126,561,971 (GRCm39) |
F55Y |
probably damaging |
Het |
Vmn2r13 |
T |
A |
5: 109,306,040 (GRCm39) |
T513S |
probably benign |
Het |
Wdr73 |
T |
C |
7: 80,541,526 (GRCm39) |
T339A |
probably damaging |
Het |
Wnt2 |
T |
A |
6: 18,008,639 (GRCm39) |
N266I |
possibly damaging |
Het |
Wwp2 |
AGAACT |
A |
8: 108,233,031 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gtf3c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00480:Gtf3c1
|
APN |
7 |
125,243,430 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00535:Gtf3c1
|
APN |
7 |
125,243,325 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00778:Gtf3c1
|
APN |
7 |
125,266,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00832:Gtf3c1
|
APN |
7 |
125,253,632 (GRCm39) |
splice site |
probably benign |
|
IGL01383:Gtf3c1
|
APN |
7 |
125,298,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01472:Gtf3c1
|
APN |
7 |
125,250,226 (GRCm39) |
splice site |
probably benign |
|
IGL01743:Gtf3c1
|
APN |
7 |
125,262,587 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01867:Gtf3c1
|
APN |
7 |
125,261,548 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02016:Gtf3c1
|
APN |
7 |
125,267,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02096:Gtf3c1
|
APN |
7 |
125,258,284 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02121:Gtf3c1
|
APN |
7 |
125,245,903 (GRCm39) |
nonsense |
probably null |
|
IGL02226:Gtf3c1
|
APN |
7 |
125,267,162 (GRCm39) |
splice site |
probably null |
|
IGL02376:Gtf3c1
|
APN |
7 |
125,268,168 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02581:Gtf3c1
|
APN |
7 |
125,245,687 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02750:Gtf3c1
|
APN |
7 |
125,275,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03063:Gtf3c1
|
APN |
7 |
125,245,675 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03167:Gtf3c1
|
APN |
7 |
125,269,752 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0052:Gtf3c1
|
UTSW |
7 |
125,267,143 (GRCm39) |
splice site |
probably null |
|
R0266:Gtf3c1
|
UTSW |
7 |
125,243,306 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0378:Gtf3c1
|
UTSW |
7 |
125,246,786 (GRCm39) |
nonsense |
probably null |
|
R0387:Gtf3c1
|
UTSW |
7 |
125,280,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:Gtf3c1
|
UTSW |
7 |
125,262,188 (GRCm39) |
nonsense |
probably null |
|
R0458:Gtf3c1
|
UTSW |
7 |
125,243,306 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0613:Gtf3c1
|
UTSW |
7 |
125,243,306 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0634:Gtf3c1
|
UTSW |
7 |
125,256,649 (GRCm39) |
unclassified |
probably benign |
|
R0658:Gtf3c1
|
UTSW |
7 |
125,298,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R0904:Gtf3c1
|
UTSW |
7 |
125,268,014 (GRCm39) |
splice site |
probably benign |
|
R1051:Gtf3c1
|
UTSW |
7 |
125,306,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Gtf3c1
|
UTSW |
7 |
125,292,310 (GRCm39) |
critical splice donor site |
probably null |
|
R1590:Gtf3c1
|
UTSW |
7 |
125,275,833 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1981:Gtf3c1
|
UTSW |
7 |
125,243,444 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2513:Gtf3c1
|
UTSW |
7 |
125,280,345 (GRCm39) |
missense |
probably benign |
0.01 |
R2697:Gtf3c1
|
UTSW |
7 |
125,243,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R3963:Gtf3c1
|
UTSW |
7 |
125,292,397 (GRCm39) |
splice site |
probably null |
|
R4125:Gtf3c1
|
UTSW |
7 |
125,246,622 (GRCm39) |
nonsense |
probably null |
|
R4127:Gtf3c1
|
UTSW |
7 |
125,246,622 (GRCm39) |
nonsense |
probably null |
|
R4646:Gtf3c1
|
UTSW |
7 |
125,258,266 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4653:Gtf3c1
|
UTSW |
7 |
125,273,272 (GRCm39) |
missense |
probably benign |
0.23 |
R4668:Gtf3c1
|
UTSW |
7 |
125,266,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Gtf3c1
|
UTSW |
7 |
125,262,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R5138:Gtf3c1
|
UTSW |
7 |
125,246,664 (GRCm39) |
missense |
probably benign |
0.05 |
R5149:Gtf3c1
|
UTSW |
7 |
125,267,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R5286:Gtf3c1
|
UTSW |
7 |
125,262,580 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5437:Gtf3c1
|
UTSW |
7 |
125,266,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5493:Gtf3c1
|
UTSW |
7 |
125,269,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5610:Gtf3c1
|
UTSW |
7 |
125,303,117 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5656:Gtf3c1
|
UTSW |
7 |
125,261,826 (GRCm39) |
missense |
probably benign |
0.27 |
R5754:Gtf3c1
|
UTSW |
7 |
125,243,237 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5969:Gtf3c1
|
UTSW |
7 |
125,244,848 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6009:Gtf3c1
|
UTSW |
7 |
125,246,602 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6223:Gtf3c1
|
UTSW |
7 |
125,275,797 (GRCm39) |
missense |
probably benign |
0.01 |
R6580:Gtf3c1
|
UTSW |
7 |
125,243,519 (GRCm39) |
missense |
probably benign |
0.02 |
R6628:Gtf3c1
|
UTSW |
7 |
125,267,246 (GRCm39) |
missense |
probably benign |
0.04 |
R6774:Gtf3c1
|
UTSW |
7 |
125,240,793 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6781:Gtf3c1
|
UTSW |
7 |
125,258,369 (GRCm39) |
nonsense |
probably null |
|
R6978:Gtf3c1
|
UTSW |
7 |
125,244,706 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7078:Gtf3c1
|
UTSW |
7 |
125,244,914 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7096:Gtf3c1
|
UTSW |
7 |
125,295,731 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7146:Gtf3c1
|
UTSW |
7 |
125,271,993 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7246:Gtf3c1
|
UTSW |
7 |
125,268,266 (GRCm39) |
|
|
|
R7330:Gtf3c1
|
UTSW |
7 |
125,303,055 (GRCm39) |
missense |
probably benign |
0.36 |
R7345:Gtf3c1
|
UTSW |
7 |
125,244,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7480:Gtf3c1
|
UTSW |
7 |
125,241,713 (GRCm39) |
missense |
probably benign |
0.22 |
R7490:Gtf3c1
|
UTSW |
7 |
125,246,663 (GRCm39) |
missense |
probably damaging |
0.98 |
R7555:Gtf3c1
|
UTSW |
7 |
125,244,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7895:Gtf3c1
|
UTSW |
7 |
125,271,994 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7949:Gtf3c1
|
UTSW |
7 |
125,250,253 (GRCm39) |
missense |
probably benign |
|
R8123:Gtf3c1
|
UTSW |
7 |
125,303,196 (GRCm39) |
start gained |
probably benign |
|
R8295:Gtf3c1
|
UTSW |
7 |
125,262,234 (GRCm39) |
missense |
probably benign |
0.01 |
R8421:Gtf3c1
|
UTSW |
7 |
125,298,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R8438:Gtf3c1
|
UTSW |
7 |
125,241,701 (GRCm39) |
nonsense |
probably null |
|
R8517:Gtf3c1
|
UTSW |
7 |
125,253,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:Gtf3c1
|
UTSW |
7 |
125,272,227 (GRCm39) |
unclassified |
probably benign |
|
R9005:Gtf3c1
|
UTSW |
7 |
125,303,069 (GRCm39) |
missense |
probably benign |
0.25 |
R9156:Gtf3c1
|
UTSW |
7 |
125,244,949 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9292:Gtf3c1
|
UTSW |
7 |
125,273,563 (GRCm39) |
intron |
probably benign |
|
R9400:Gtf3c1
|
UTSW |
7 |
125,275,683 (GRCm39) |
missense |
probably damaging |
0.96 |
R9658:Gtf3c1
|
UTSW |
7 |
125,306,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Gtf3c1
|
UTSW |
7 |
125,262,199 (GRCm39) |
missense |
possibly damaging |
0.52 |
X0065:Gtf3c1
|
UTSW |
7 |
125,240,862 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Gtf3c1
|
UTSW |
7 |
125,303,136 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Gtf3c1
|
UTSW |
7 |
125,266,294 (GRCm39) |
missense |
probably benign |
0.15 |
|
Predicted Primers |
PCR Primer
(F):5'- TGAAAGACAATGGACTCTGCAACCC -3'
(R):5'- AGAGAAAGCTCCTGCCTTACCCTG -3'
Sequencing Primer
(F):5'- GCAACCCCCAGGCTCTC -3'
(R):5'- TAAAGACCAGGTAGTGCTTCC -3'
|
Posted On |
2014-05-23 |