Incidental Mutation 'R7134:Nlrc5'
ID |
552917 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nlrc5
|
Ensembl Gene |
ENSMUSG00000074151 |
Gene Name |
NLR family, CARD domain containing 5 |
Synonyms |
AI451557 |
MMRRC Submission |
045219-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7134 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
95160984-95253900 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 95206350 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 734
(I734F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138322
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053085]
[ENSMUST00000182409]
[ENSMUST00000211816]
|
AlphaFold |
C3VPR6 |
PDB Structure |
The solution NMR structure of the NLRC5 caspase recruitment domain (CARD) [SOLUTION NMR]
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000053085
AA Change: I734F
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000138322 Gene: ENSMUSG00000074151 AA Change: I734F
Domain | Start | End | E-Value | Type |
low complexity region
|
136 |
151 |
N/A |
INTRINSIC |
Pfam:NACHT
|
223 |
386 |
1.8e-32 |
PFAM |
LRR
|
716 |
743 |
6.89e1 |
SMART |
LRR
|
744 |
771 |
9.86e1 |
SMART |
LRR
|
772 |
796 |
1.22e2 |
SMART |
LRR
|
844 |
870 |
2.16e2 |
SMART |
LRR
|
871 |
898 |
1.76e-1 |
SMART |
LRR
|
1006 |
1033 |
1.9e0 |
SMART |
LRR
|
1034 |
1061 |
4.51e1 |
SMART |
low complexity region
|
1141 |
1169 |
N/A |
INTRINSIC |
LRR
|
1240 |
1267 |
2.67e1 |
SMART |
LRR
|
1273 |
1295 |
1.22e1 |
SMART |
low complexity region
|
1341 |
1351 |
N/A |
INTRINSIC |
LRR
|
1519 |
1546 |
5.48e1 |
SMART |
LRR
|
1547 |
1574 |
3.36e1 |
SMART |
LRR
|
1575 |
1602 |
1.69e1 |
SMART |
LRR
|
1603 |
1630 |
8.99e-1 |
SMART |
LRR
|
1631 |
1654 |
5.26e0 |
SMART |
LRR
|
1659 |
1686 |
2.81e0 |
SMART |
LRR
|
1687 |
1714 |
1.6e-4 |
SMART |
LRR
|
1715 |
1742 |
1.06e0 |
SMART |
LRR
|
1743 |
1768 |
8e0 |
SMART |
LRR
|
1793 |
1820 |
2.06e1 |
SMART |
LRR
|
1821 |
1848 |
5.42e-2 |
SMART |
LRR
|
1849 |
1876 |
3.54e0 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000182409
AA Change: I734F
PolyPhen 2
Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000183132
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000211816
AA Change: I734F
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
99% (84/85) |
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 caspase recruitment domain-containing NLR family. This gene plays a role in cytokine response and antiviral immunity through its inhibition of NF-kappa-B activation and negative regulation of type I interferon signaling pathways. [provided by RefSeq, Oct 2011] PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal cytokine production induced by virus and bacteria infection. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
A |
G |
17: 36,270,144 (GRCm39) |
F638S |
possibly damaging |
Het |
Actl6b |
T |
A |
5: 137,562,762 (GRCm39) |
N159K |
probably damaging |
Het |
Adam6a |
T |
G |
12: 113,508,655 (GRCm39) |
S343A |
probably benign |
Het |
Ankrd17 |
G |
A |
5: 90,380,173 (GRCm39) |
T2505I |
probably damaging |
Het |
Ankrd17 |
T |
C |
5: 90,433,382 (GRCm39) |
T728A |
probably benign |
Het |
Asap2 |
G |
T |
12: 21,315,964 (GRCm39) |
E919* |
probably null |
Het |
Atp10b |
A |
T |
11: 43,136,291 (GRCm39) |
I1140F |
probably damaging |
Het |
Cep126 |
A |
T |
9: 8,103,383 (GRCm39) |
V209E |
probably damaging |
Het |
Cfap65 |
C |
T |
1: 74,965,792 (GRCm39) |
R406Q |
probably benign |
Het |
Cldn1 |
T |
C |
16: 26,190,376 (GRCm39) |
M1V |
probably null |
Het |
Cryl1 |
C |
T |
14: 57,512,956 (GRCm39) |
D304N |
probably benign |
Het |
D3Ertd751e |
T |
C |
3: 41,708,212 (GRCm39) |
|
probably null |
Het |
D630044L22Rik |
A |
T |
17: 26,181,090 (GRCm39) |
M156L |
probably benign |
Het |
Ddx21 |
T |
C |
10: 62,427,634 (GRCm39) |
D423G |
possibly damaging |
Het |
Dock2 |
T |
A |
11: 34,260,363 (GRCm39) |
M993L |
probably benign |
Het |
Dusp29 |
A |
T |
14: 21,727,129 (GRCm39) |
I173N |
probably damaging |
Het |
Eif4g1 |
C |
T |
16: 20,500,252 (GRCm39) |
A675V |
probably damaging |
Het |
Eml1 |
C |
T |
12: 108,472,810 (GRCm39) |
S206L |
probably benign |
Het |
Farp2 |
A |
C |
1: 93,531,181 (GRCm39) |
I560L |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,223,969 (GRCm39) |
D593E |
probably benign |
Het |
Fetub |
A |
G |
16: 22,748,007 (GRCm39) |
D61G |
possibly damaging |
Het |
Fpgs |
T |
C |
2: 32,576,641 (GRCm39) |
K329E |
probably benign |
Het |
Fpgt |
T |
C |
3: 154,797,120 (GRCm39) |
Y45C |
probably damaging |
Het |
Gas2l1 |
A |
T |
11: 5,011,106 (GRCm39) |
C574* |
probably null |
Het |
Gm9747 |
G |
T |
1: 82,211,837 (GRCm39) |
C12F |
unknown |
Het |
H2-T23 |
T |
C |
17: 36,342,709 (GRCm39) |
Y143C |
probably damaging |
Het |
Hhip |
A |
T |
8: 80,719,142 (GRCm39) |
S462T |
probably benign |
Het |
Hnf1a |
C |
T |
5: 115,091,446 (GRCm39) |
G416R |
probably damaging |
Het |
Hoxa5 |
C |
T |
6: 52,181,023 (GRCm39) |
C103Y |
probably damaging |
Het |
Kansl3 |
G |
T |
1: 36,390,848 (GRCm39) |
D395E |
possibly damaging |
Het |
Marchf10 |
A |
G |
11: 105,299,502 (GRCm39) |
S116P |
probably benign |
Het |
Med12l |
C |
T |
3: 59,001,180 (GRCm39) |
Q748* |
probably null |
Het |
Mroh7 |
T |
A |
4: 106,577,791 (GRCm39) |
N296Y |
probably damaging |
Het |
Mtbp |
T |
G |
15: 55,421,961 (GRCm39) |
D61E |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,411,391 (GRCm39) |
I1446L |
unknown |
Het |
Myh15 |
T |
C |
16: 48,901,705 (GRCm39) |
V266A |
possibly damaging |
Het |
Nap1l1 |
G |
A |
10: 111,330,655 (GRCm39) |
|
probably null |
Het |
Napsa |
A |
G |
7: 44,235,159 (GRCm39) |
T315A |
probably benign |
Het |
Nnt |
A |
G |
13: 119,531,198 (GRCm39) |
V183A |
probably damaging |
Het |
Nploc4 |
A |
T |
11: 120,276,614 (GRCm39) |
D477E |
probably benign |
Het |
Nrip3 |
A |
G |
7: 109,364,695 (GRCm39) |
S144P |
probably damaging |
Het |
Ntng1 |
A |
T |
3: 109,842,445 (GRCm39) |
F109L |
probably benign |
Het |
Or5p61 |
A |
G |
7: 107,758,883 (GRCm39) |
Y66H |
probably damaging |
Het |
Or5v1 |
T |
A |
17: 37,809,776 (GRCm39) |
V78D |
probably damaging |
Het |
Or6aa1 |
G |
A |
7: 86,044,752 (GRCm39) |
|
probably benign |
Het |
Or8b36 |
A |
G |
9: 37,937,795 (GRCm39) |
E231G |
probably benign |
Het |
Pacsin1 |
G |
A |
17: 27,921,707 (GRCm39) |
D30N |
probably damaging |
Het |
Pbld2 |
A |
T |
10: 62,860,368 (GRCm39) |
|
probably benign |
Het |
Pcnx4 |
C |
T |
12: 72,613,750 (GRCm39) |
T565I |
probably damaging |
Het |
Pdzk1 |
A |
T |
3: 96,763,246 (GRCm39) |
T225S |
probably benign |
Het |
Phyhip |
T |
G |
14: 70,704,639 (GRCm39) |
I286S |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,813,086 (GRCm39) |
Y3903N |
probably damaging |
Het |
Plcb3 |
A |
T |
19: 6,942,698 (GRCm39) |
L222Q |
probably damaging |
Het |
Plcd4 |
T |
A |
1: 74,593,662 (GRCm39) |
H262Q |
probably benign |
Het |
Plekhh1 |
C |
T |
12: 79,109,390 (GRCm39) |
A474V |
probably benign |
Het |
Plppr3 |
T |
C |
10: 79,701,537 (GRCm39) |
E435G |
probably damaging |
Het |
Poln |
T |
A |
5: 34,276,340 (GRCm39) |
N305I |
possibly damaging |
Het |
Pou3f2 |
T |
C |
4: 22,486,874 (GRCm39) |
T420A |
probably benign |
Het |
Ppdpf |
T |
C |
2: 180,829,523 (GRCm39) |
Y17H |
probably damaging |
Het |
Prrx2 |
C |
A |
2: 30,768,485 (GRCm39) |
T104K |
probably damaging |
Het |
Ptprj |
A |
T |
2: 90,294,822 (GRCm39) |
L462H |
probably benign |
Het |
Radil |
T |
C |
5: 142,471,304 (GRCm39) |
T991A |
probably damaging |
Het |
Rbsn |
T |
C |
6: 92,178,608 (GRCm39) |
E147G |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,300,742 (GRCm39) |
V35M |
probably benign |
Het |
Rps6ka1 |
T |
C |
4: 133,599,373 (GRCm39) |
Q18R |
probably benign |
Het |
Setbp1 |
T |
A |
18: 78,902,734 (GRCm39) |
D311V |
possibly damaging |
Het |
Setd2 |
C |
T |
9: 110,377,865 (GRCm39) |
S560L |
possibly damaging |
Het |
Slc12a5 |
A |
T |
2: 164,816,878 (GRCm39) |
I134F |
probably damaging |
Het |
Speer1h |
C |
T |
5: 11,647,706 (GRCm39) |
T148I |
possibly damaging |
Het |
Svil |
A |
G |
18: 5,116,080 (GRCm39) |
D2035G |
probably damaging |
Het |
Syngap1 |
T |
C |
17: 27,178,985 (GRCm39) |
Y665H |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,043,519 (GRCm39) |
Y547H |
possibly damaging |
Het |
Tgm2 |
A |
G |
2: 157,980,812 (GRCm39) |
V83A |
probably benign |
Het |
Tmem233 |
T |
C |
5: 116,189,429 (GRCm39) |
I117V |
probably benign |
Het |
Tsen34 |
A |
G |
7: 3,703,640 (GRCm39) |
T293A |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,709,023 (GRCm39) |
V8752A |
unknown |
Het |
Ubac1 |
A |
G |
2: 25,904,974 (GRCm39) |
V88A |
probably benign |
Het |
Uchl4 |
T |
C |
9: 64,142,621 (GRCm39) |
V34A |
probably damaging |
Het |
Ugt2a2 |
C |
T |
5: 87,608,435 (GRCm39) |
R468H |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,897,749 (GRCm39) |
T255S |
probably benign |
Het |
Wdr6 |
T |
A |
9: 108,450,564 (GRCm39) |
N988I |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,903,389 (GRCm39) |
I2359N |
unknown |
Het |
Ybey |
A |
G |
10: 76,304,025 (GRCm39) |
V59A |
probably benign |
Het |
Zfp268 |
T |
A |
4: 145,349,375 (GRCm39) |
C271S |
possibly damaging |
Het |
Zfp397 |
A |
G |
18: 24,090,122 (GRCm39) |
N142S |
probably benign |
Het |
Zfy1 |
A |
T |
Y: 725,788 (GRCm39) |
V659E |
probably damaging |
Het |
|
Other mutations in Nlrc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Nlrc5
|
APN |
8 |
95,228,839 (GRCm39) |
splice site |
probably benign |
|
IGL00232:Nlrc5
|
APN |
8 |
95,211,251 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00324:Nlrc5
|
APN |
8 |
95,248,107 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02715:Nlrc5
|
APN |
8 |
95,201,296 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02992:Nlrc5
|
APN |
8 |
95,233,201 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03095:Nlrc5
|
APN |
8 |
95,248,536 (GRCm39) |
splice site |
probably benign |
|
IGL03389:Nlrc5
|
APN |
8 |
95,248,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03406:Nlrc5
|
APN |
8 |
95,203,483 (GRCm39) |
missense |
probably benign |
0.01 |
cassis
|
UTSW |
8 |
95,203,021 (GRCm39) |
nonsense |
probably null |
|
cowberry
|
UTSW |
8 |
95,218,153 (GRCm39) |
missense |
possibly damaging |
0.83 |
lingon
|
UTSW |
8 |
95,208,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R0037:Nlrc5
|
UTSW |
8 |
95,216,163 (GRCm39) |
missense |
probably benign |
0.00 |
R0048:Nlrc5
|
UTSW |
8 |
95,201,284 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0092:Nlrc5
|
UTSW |
8 |
95,216,222 (GRCm39) |
splice site |
probably benign |
|
R0506:Nlrc5
|
UTSW |
8 |
95,219,753 (GRCm39) |
splice site |
probably benign |
|
R0548:Nlrc5
|
UTSW |
8 |
95,248,411 (GRCm39) |
missense |
probably null |
0.09 |
R2014:Nlrc5
|
UTSW |
8 |
95,252,138 (GRCm39) |
splice site |
probably benign |
|
R3051:Nlrc5
|
UTSW |
8 |
95,203,343 (GRCm39) |
missense |
probably benign |
0.01 |
R3776:Nlrc5
|
UTSW |
8 |
95,199,467 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3837:Nlrc5
|
UTSW |
8 |
95,237,929 (GRCm39) |
splice site |
probably benign |
|
R4012:Nlrc5
|
UTSW |
8 |
95,202,620 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4367:Nlrc5
|
UTSW |
8 |
95,203,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4400:Nlrc5
|
UTSW |
8 |
95,220,981 (GRCm39) |
missense |
probably benign |
0.08 |
R4469:Nlrc5
|
UTSW |
8 |
95,247,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R4561:Nlrc5
|
UTSW |
8 |
95,203,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Nlrc5
|
UTSW |
8 |
95,203,903 (GRCm39) |
missense |
probably damaging |
0.96 |
R4758:Nlrc5
|
UTSW |
8 |
95,238,956 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4834:Nlrc5
|
UTSW |
8 |
95,232,113 (GRCm39) |
missense |
probably benign |
0.00 |
R4896:Nlrc5
|
UTSW |
8 |
95,247,844 (GRCm39) |
unclassified |
probably benign |
|
R5004:Nlrc5
|
UTSW |
8 |
95,247,844 (GRCm39) |
unclassified |
probably benign |
|
R5018:Nlrc5
|
UTSW |
8 |
95,252,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R5115:Nlrc5
|
UTSW |
8 |
95,203,447 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5116:Nlrc5
|
UTSW |
8 |
95,208,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R5126:Nlrc5
|
UTSW |
8 |
95,201,299 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5148:Nlrc5
|
UTSW |
8 |
95,203,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R5224:Nlrc5
|
UTSW |
8 |
95,220,944 (GRCm39) |
missense |
probably benign |
0.26 |
R5527:Nlrc5
|
UTSW |
8 |
95,217,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R5640:Nlrc5
|
UTSW |
8 |
95,202,421 (GRCm39) |
missense |
probably benign |
0.02 |
R5705:Nlrc5
|
UTSW |
8 |
95,202,385 (GRCm39) |
missense |
probably benign |
0.00 |
R5778:Nlrc5
|
UTSW |
8 |
95,206,154 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5830:Nlrc5
|
UTSW |
8 |
95,199,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R5850:Nlrc5
|
UTSW |
8 |
95,247,675 (GRCm39) |
missense |
probably benign |
0.00 |
R5978:Nlrc5
|
UTSW |
8 |
95,215,221 (GRCm39) |
missense |
probably damaging |
0.98 |
R6335:Nlrc5
|
UTSW |
8 |
95,228,902 (GRCm39) |
missense |
probably benign |
0.01 |
R6372:Nlrc5
|
UTSW |
8 |
95,206,378 (GRCm39) |
missense |
probably damaging |
0.98 |
R6486:Nlrc5
|
UTSW |
8 |
95,247,927 (GRCm39) |
splice site |
probably null |
|
R6765:Nlrc5
|
UTSW |
8 |
95,216,996 (GRCm39) |
missense |
probably benign |
0.20 |
R6861:Nlrc5
|
UTSW |
8 |
95,247,857 (GRCm39) |
unclassified |
probably benign |
|
R6869:Nlrc5
|
UTSW |
8 |
95,248,583 (GRCm39) |
missense |
probably benign |
0.00 |
R7204:Nlrc5
|
UTSW |
8 |
95,218,153 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7231:Nlrc5
|
UTSW |
8 |
95,248,433 (GRCm39) |
critical splice donor site |
probably null |
|
R7309:Nlrc5
|
UTSW |
8 |
95,200,670 (GRCm39) |
missense |
probably benign |
0.01 |
R7368:Nlrc5
|
UTSW |
8 |
95,203,021 (GRCm39) |
nonsense |
probably null |
|
R7497:Nlrc5
|
UTSW |
8 |
95,248,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R7606:Nlrc5
|
UTSW |
8 |
95,203,745 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7611:Nlrc5
|
UTSW |
8 |
95,239,276 (GRCm39) |
critical splice donor site |
probably null |
|
R7685:Nlrc5
|
UTSW |
8 |
95,248,028 (GRCm39) |
splice site |
probably null |
|
R7810:Nlrc5
|
UTSW |
8 |
95,231,772 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7829:Nlrc5
|
UTSW |
8 |
95,248,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R7910:Nlrc5
|
UTSW |
8 |
95,219,720 (GRCm39) |
missense |
probably benign |
0.00 |
R7921:Nlrc5
|
UTSW |
8 |
95,214,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R8131:Nlrc5
|
UTSW |
8 |
95,208,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Nlrc5
|
UTSW |
8 |
95,252,753 (GRCm39) |
missense |
unknown |
|
R8493:Nlrc5
|
UTSW |
8 |
95,249,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8888:Nlrc5
|
UTSW |
8 |
95,252,118 (GRCm39) |
missense |
probably benign |
0.04 |
R8964:Nlrc5
|
UTSW |
8 |
95,232,116 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9053:Nlrc5
|
UTSW |
8 |
95,217,013 (GRCm39) |
missense |
probably benign |
0.00 |
R9058:Nlrc5
|
UTSW |
8 |
95,238,938 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9161:Nlrc5
|
UTSW |
8 |
95,213,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R9278:Nlrc5
|
UTSW |
8 |
95,237,908 (GRCm39) |
missense |
probably benign |
0.00 |
R9285:Nlrc5
|
UTSW |
8 |
95,199,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9405:Nlrc5
|
UTSW |
8 |
95,199,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R9591:Nlrc5
|
UTSW |
8 |
95,249,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R9620:Nlrc5
|
UTSW |
8 |
95,203,034 (GRCm39) |
missense |
probably benign |
0.44 |
RF021:Nlrc5
|
UTSW |
8 |
95,203,516 (GRCm39) |
missense |
probably benign |
0.16 |
Z1088:Nlrc5
|
UTSW |
8 |
95,231,092 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1177:Nlrc5
|
UTSW |
8 |
95,233,208 (GRCm39) |
critical splice donor site |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- GCAGGAGTTTGCCTACTATGGG -3'
(R):5'- GGATTTGACCCACCTCAGTC -3'
Sequencing Primer
(F):5'- CCTACTATGGGGAGCCTGAAGAC -3'
(R):5'- AGTCTTGGACTGACATCCCC -3'
|
Posted On |
2019-05-15 |