Incidental Mutation 'R4876:Ncam2'
ID |
376916 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ncam2
|
Ensembl Gene |
ENSMUSG00000022762 |
Gene Name |
neural cell adhesion molecule 2 |
Synonyms |
Ncam-2, RNCAM, R4B12 antigen, Ocam |
MMRRC Submission |
042485-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4876 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
80997585-81423716 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 81287234 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Threonine
at position 383
(A383T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000063468
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037785]
[ENSMUST00000067602]
|
AlphaFold |
O35136 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000037785
AA Change: A383T
PolyPhen 2
Score 0.268 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000049390 Gene: ENSMUSG00000022762 AA Change: A383T
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
13 |
N/A |
INTRINSIC |
IGc2
|
33 |
100 |
3.18e-6 |
SMART |
IGc2
|
127 |
193 |
1.13e-11 |
SMART |
IGc2
|
223 |
288 |
2.03e-13 |
SMART |
IGc2
|
313 |
387 |
1.12e-15 |
SMART |
IGc2
|
413 |
482 |
9.93e-8 |
SMART |
FN3
|
496 |
578 |
5.91e-13 |
SMART |
FN3
|
594 |
675 |
2.87e-2 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000067602
AA Change: A383T
PolyPhen 2
Score 0.268 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000063468 Gene: ENSMUSG00000022762 AA Change: A383T
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
13 |
N/A |
INTRINSIC |
IGc2
|
33 |
100 |
3.18e-6 |
SMART |
IGc2
|
127 |
193 |
1.13e-11 |
SMART |
IGc2
|
223 |
288 |
2.03e-13 |
SMART |
IGc2
|
313 |
387 |
1.12e-15 |
SMART |
IGc2
|
413 |
482 |
9.93e-8 |
SMART |
FN3
|
496 |
578 |
5.91e-13 |
SMART |
FN3
|
594 |
675 |
2.87e-2 |
SMART |
transmembrane domain
|
696 |
718 |
N/A |
INTRINSIC |
low complexity region
|
741 |
757 |
N/A |
INTRINSIC |
low complexity region
|
789 |
812 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000231687
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232550
|
Meta Mutation Damage Score |
0.0737 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.4%
- 20x: 92.5%
|
Validation Efficiency |
99% (97/98) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein and may function in selective fasciculation and zone-to-zone projection of the primary olfactory axons. [provided by RefSeq, Jul 2008] PHENOTYPE: A gene trap insertion into an intron of this gene results in no obvious phenotype. Mice homozygous for a knock-out allele exhibit exhibit increased proliferation rate and clonogenic frequency in spinal cord-derived neurospheres. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
C |
16: 4,667,536 (GRCm39) |
F309S |
unknown |
Het |
A630001G21Rik |
C |
T |
1: 85,646,761 (GRCm39) |
V167M |
probably damaging |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Ano4 |
A |
G |
10: 88,948,697 (GRCm39) |
F138L |
probably damaging |
Het |
Aoc1 |
T |
C |
6: 48,883,681 (GRCm39) |
V519A |
possibly damaging |
Het |
Arhgef37 |
A |
T |
18: 61,631,310 (GRCm39) |
Y558* |
probably null |
Het |
Atxn3 |
T |
A |
12: 101,914,638 (GRCm39) |
S29C |
probably damaging |
Het |
Bbs2 |
T |
C |
8: 94,796,788 (GRCm39) |
|
probably benign |
Het |
Bicral |
A |
T |
17: 47,136,502 (GRCm39) |
I236N |
probably damaging |
Het |
Cabcoco1 |
A |
G |
10: 68,377,599 (GRCm39) |
V30A |
probably benign |
Het |
Cap2 |
A |
G |
13: 46,684,497 (GRCm39) |
M1V |
probably null |
Het |
Ccdc153 |
T |
C |
9: 44,152,305 (GRCm39) |
M1T |
probably null |
Het |
Ccnf |
A |
T |
17: 24,449,311 (GRCm39) |
V489D |
probably damaging |
Het |
Cdin1 |
A |
C |
2: 115,500,539 (GRCm39) |
H159P |
probably damaging |
Het |
Cntnap3 |
T |
C |
13: 64,935,520 (GRCm39) |
T448A |
probably benign |
Het |
Cpa4 |
G |
A |
6: 30,590,814 (GRCm39) |
D371N |
probably benign |
Het |
Csl |
T |
A |
10: 99,594,402 (GRCm39) |
Y221F |
possibly damaging |
Het |
Dalrd3 |
T |
C |
9: 108,448,635 (GRCm39) |
|
probably benign |
Het |
Dennd4a |
T |
A |
9: 64,803,872 (GRCm39) |
N1070K |
probably benign |
Het |
Dipk2a |
C |
T |
9: 94,419,630 (GRCm39) |
R100H |
probably damaging |
Het |
Dmwd |
A |
T |
7: 18,814,472 (GRCm39) |
D374V |
probably damaging |
Het |
Eea1 |
G |
T |
10: 95,831,475 (GRCm39) |
A189S |
probably benign |
Het |
Fasn |
A |
G |
11: 120,703,138 (GRCm39) |
V1629A |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,842,225 (GRCm39) |
|
probably benign |
Het |
Fndc1 |
T |
C |
17: 7,990,471 (GRCm39) |
D1075G |
unknown |
Het |
Fsip2 |
A |
G |
2: 82,805,202 (GRCm39) |
N507S |
possibly damaging |
Het |
Gabra5 |
T |
G |
7: 57,063,413 (GRCm39) |
E337A |
probably damaging |
Het |
Gsg1l |
A |
G |
7: 125,490,841 (GRCm39) |
Y288H |
probably benign |
Het |
H2-M11 |
A |
T |
17: 36,858,401 (GRCm39) |
D65V |
probably benign |
Het |
Hmgxb3 |
A |
T |
18: 61,279,606 (GRCm39) |
C736S |
possibly damaging |
Het |
Hsd3b3 |
A |
T |
3: 98,649,960 (GRCm39) |
I121N |
probably damaging |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Il16 |
A |
C |
7: 83,322,302 (GRCm39) |
S338A |
probably benign |
Het |
Itpr1 |
G |
A |
6: 108,459,867 (GRCm39) |
A2054T |
probably damaging |
Het |
Lamp3 |
T |
A |
16: 19,474,220 (GRCm39) |
I385F |
probably damaging |
Het |
Limch1 |
G |
A |
5: 67,039,270 (GRCm39) |
V66I |
possibly damaging |
Het |
Lmod2 |
A |
G |
6: 24,604,278 (GRCm39) |
R418G |
probably benign |
Het |
Ly6g6c |
A |
T |
17: 35,288,416 (GRCm39) |
D96V |
probably damaging |
Het |
Map2k2 |
G |
A |
10: 80,950,947 (GRCm39) |
V131M |
probably damaging |
Het |
Mapk9 |
T |
C |
11: 49,745,152 (GRCm39) |
V22A |
probably damaging |
Het |
Mettl2 |
T |
C |
11: 105,019,894 (GRCm39) |
I177T |
probably damaging |
Het |
Mob4 |
C |
T |
1: 55,191,995 (GRCm39) |
|
probably benign |
Het |
Mybpc1 |
A |
T |
10: 88,372,286 (GRCm39) |
N781K |
probably benign |
Het |
Mybpc1 |
T |
C |
10: 88,358,853 (GRCm39) |
I1113V |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,384,405 (GRCm39) |
T707A |
probably damaging |
Het |
Nomo1 |
T |
C |
7: 45,715,915 (GRCm39) |
S761P |
probably damaging |
Het |
Nsd3 |
T |
A |
8: 26,181,161 (GRCm39) |
S921T |
possibly damaging |
Het |
Omp |
A |
T |
7: 97,794,233 (GRCm39) |
D131E |
probably benign |
Het |
Or10d1c |
A |
T |
9: 38,893,922 (GRCm39) |
C139* |
probably null |
Het |
Or4f7d-ps1 |
C |
G |
2: 111,675,040 (GRCm39) |
|
noncoding transcript |
Het |
Or8d4 |
C |
T |
9: 40,038,514 (GRCm39) |
V248I |
probably damaging |
Het |
Pard3 |
T |
C |
8: 128,287,950 (GRCm39) |
|
probably benign |
Het |
Parg |
A |
G |
14: 31,993,625 (GRCm39) |
T286A |
probably damaging |
Het |
Parp1 |
T |
A |
1: 180,396,600 (GRCm39) |
M1K |
probably null |
Het |
Pclo |
T |
A |
5: 14,861,694 (GRCm39) |
S4882R |
unknown |
Het |
Pcnx2 |
C |
T |
8: 126,498,847 (GRCm39) |
E1551K |
probably damaging |
Het |
Pcyox1l |
A |
G |
18: 61,832,565 (GRCm39) |
Y161H |
probably damaging |
Het |
Pdzd8 |
A |
T |
19: 59,289,236 (GRCm39) |
C721* |
probably null |
Het |
Piwil4 |
T |
C |
9: 14,651,761 (GRCm39) |
D90G |
probably benign |
Het |
Plxdc2 |
T |
A |
2: 16,708,129 (GRCm39) |
C306S |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,326,083 (GRCm39) |
F6I |
probably benign |
Het |
Prkaa1 |
T |
C |
15: 5,203,886 (GRCm39) |
M265T |
probably benign |
Het |
Prrc2b |
T |
C |
2: 32,104,212 (GRCm39) |
V1230A |
probably benign |
Het |
Rfx2 |
T |
C |
17: 57,091,706 (GRCm39) |
E329G |
probably benign |
Het |
Scg2 |
T |
C |
1: 79,413,636 (GRCm39) |
I322M |
probably damaging |
Het |
Scly |
T |
A |
1: 91,247,850 (GRCm39) |
N399K |
probably damaging |
Het |
Sec23b |
T |
A |
2: 144,428,281 (GRCm39) |
|
probably null |
Het |
Sephs2 |
A |
T |
7: 126,872,219 (GRCm39) |
Y291* |
probably null |
Het |
Slc45a3 |
T |
C |
1: 131,909,285 (GRCm39) |
I494T |
possibly damaging |
Het |
Slc6a21 |
C |
A |
7: 44,929,535 (GRCm39) |
Y76* |
probably null |
Het |
Slfn14 |
T |
A |
11: 83,167,098 (GRCm39) |
I806L |
possibly damaging |
Het |
Slfn4 |
T |
A |
11: 83,077,844 (GRCm39) |
S211T |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,071,577 (GRCm39) |
V1624A |
probably damaging |
Het |
Sugp1 |
T |
A |
8: 70,523,834 (GRCm39) |
M567K |
probably damaging |
Het |
Tmem121 |
A |
T |
12: 113,152,348 (GRCm39) |
M189L |
probably benign |
Het |
Tmem201 |
A |
G |
4: 149,806,727 (GRCm39) |
S444P |
probably damaging |
Het |
Tmem63a |
T |
C |
1: 180,800,751 (GRCm39) |
V744A |
probably benign |
Het |
Tnrc18 |
G |
A |
5: 142,717,380 (GRCm39) |
S2358F |
unknown |
Het |
Ubash3b |
A |
G |
9: 40,929,405 (GRCm39) |
V404A |
probably benign |
Het |
Unc13c |
A |
T |
9: 73,656,821 (GRCm39) |
C1127S |
probably damaging |
Het |
Unc5a |
T |
C |
13: 55,145,042 (GRCm39) |
V253A |
probably benign |
Het |
Vmn1r-ps123 |
C |
T |
13: 23,180,535 (GRCm39) |
|
noncoding transcript |
Het |
Wdr74 |
A |
G |
19: 8,716,849 (GRCm39) |
E253G |
possibly damaging |
Het |
Wwox |
T |
C |
8: 115,174,988 (GRCm39) |
Y107H |
probably damaging |
Het |
Zdhhc22 |
A |
T |
12: 87,035,012 (GRCm39) |
Y147N |
probably damaging |
Het |
Zfp131 |
T |
C |
13: 120,250,491 (GRCm39) |
H44R |
possibly damaging |
Het |
Zfp235 |
A |
G |
7: 23,840,384 (GRCm39) |
T268A |
probably benign |
Het |
Zfp280d |
T |
C |
9: 72,206,140 (GRCm39) |
|
probably benign |
Het |
Zfp358 |
T |
C |
8: 3,546,170 (GRCm39) |
S251P |
probably damaging |
Het |
|
Other mutations in Ncam2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01138:Ncam2
|
APN |
16 |
81,314,467 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01369:Ncam2
|
APN |
16 |
81,258,459 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01554:Ncam2
|
APN |
16 |
81,309,823 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01892:Ncam2
|
APN |
16 |
81,386,587 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02320:Ncam2
|
APN |
16 |
81,231,725 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02669:Ncam2
|
APN |
16 |
81,314,429 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03073:Ncam2
|
APN |
16 |
81,418,235 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03353:Ncam2
|
APN |
16 |
81,231,788 (GRCm39) |
missense |
probably benign |
0.04 |
BB009:Ncam2
|
UTSW |
16 |
81,412,708 (GRCm39) |
missense |
probably damaging |
0.99 |
BB019:Ncam2
|
UTSW |
16 |
81,412,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R0087:Ncam2
|
UTSW |
16 |
81,231,789 (GRCm39) |
missense |
probably benign |
0.11 |
R0097:Ncam2
|
UTSW |
16 |
81,314,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Ncam2
|
UTSW |
16 |
81,314,517 (GRCm39) |
splice site |
probably benign |
|
R0279:Ncam2
|
UTSW |
16 |
81,420,225 (GRCm39) |
splice site |
probably benign |
|
R0471:Ncam2
|
UTSW |
16 |
80,997,772 (GRCm39) |
start gained |
probably benign |
|
R0523:Ncam2
|
UTSW |
16 |
81,258,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R1353:Ncam2
|
UTSW |
16 |
80,997,803 (GRCm39) |
start codon destroyed |
probably null |
|
R1646:Ncam2
|
UTSW |
16 |
81,262,594 (GRCm39) |
critical splice donor site |
probably benign |
|
R1884:Ncam2
|
UTSW |
16 |
81,234,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Ncam2
|
UTSW |
16 |
81,386,586 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2157:Ncam2
|
UTSW |
16 |
81,287,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R2330:Ncam2
|
UTSW |
16 |
81,309,809 (GRCm39) |
missense |
probably benign |
0.17 |
R2404:Ncam2
|
UTSW |
16 |
81,287,128 (GRCm39) |
splice site |
probably benign |
|
R2434:Ncam2
|
UTSW |
16 |
81,392,113 (GRCm39) |
missense |
probably benign |
0.01 |
R3104:Ncam2
|
UTSW |
16 |
81,262,598 (GRCm39) |
splice site |
probably benign |
|
R3842:Ncam2
|
UTSW |
16 |
81,231,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R3954:Ncam2
|
UTSW |
16 |
81,386,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4039:Ncam2
|
UTSW |
16 |
81,287,211 (GRCm39) |
missense |
probably benign |
0.02 |
R4210:Ncam2
|
UTSW |
16 |
81,323,991 (GRCm39) |
missense |
probably benign |
0.02 |
R4514:Ncam2
|
UTSW |
16 |
81,309,884 (GRCm39) |
missense |
probably benign |
0.13 |
R4583:Ncam2
|
UTSW |
16 |
81,314,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Ncam2
|
UTSW |
16 |
81,262,457 (GRCm39) |
missense |
probably benign |
0.06 |
R4710:Ncam2
|
UTSW |
16 |
81,262,594 (GRCm39) |
critical splice donor site |
probably null |
|
R4732:Ncam2
|
UTSW |
16 |
81,231,772 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4733:Ncam2
|
UTSW |
16 |
81,231,772 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4923:Ncam2
|
UTSW |
16 |
81,386,679 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5131:Ncam2
|
UTSW |
16 |
81,234,550 (GRCm39) |
missense |
probably benign |
0.44 |
R5329:Ncam2
|
UTSW |
16 |
81,231,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R5478:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5479:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5481:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5519:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5522:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5523:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5524:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5526:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5718:Ncam2
|
UTSW |
16 |
81,386,702 (GRCm39) |
splice site |
probably null |
|
R5793:Ncam2
|
UTSW |
16 |
81,372,991 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6050:Ncam2
|
UTSW |
16 |
81,240,054 (GRCm39) |
nonsense |
probably null |
|
R6212:Ncam2
|
UTSW |
16 |
81,229,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R6847:Ncam2
|
UTSW |
16 |
81,229,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R6935:Ncam2
|
UTSW |
16 |
81,323,879 (GRCm39) |
missense |
probably benign |
0.24 |
R7159:Ncam2
|
UTSW |
16 |
81,287,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Ncam2
|
UTSW |
16 |
81,386,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Ncam2
|
UTSW |
16 |
81,309,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Ncam2
|
UTSW |
16 |
81,420,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R7568:Ncam2
|
UTSW |
16 |
81,386,689 (GRCm39) |
missense |
probably benign |
0.19 |
R7686:Ncam2
|
UTSW |
16 |
81,418,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R7759:Ncam2
|
UTSW |
16 |
81,412,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:Ncam2
|
UTSW |
16 |
81,287,267 (GRCm39) |
missense |
probably benign |
|
R7932:Ncam2
|
UTSW |
16 |
81,412,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R8078:Ncam2
|
UTSW |
16 |
81,240,136 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8287:Ncam2
|
UTSW |
16 |
81,323,883 (GRCm39) |
missense |
probably benign |
0.07 |
R8354:Ncam2
|
UTSW |
16 |
81,309,847 (GRCm39) |
missense |
probably benign |
0.00 |
R8429:Ncam2
|
UTSW |
16 |
81,386,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Ncam2
|
UTSW |
16 |
81,309,867 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8546:Ncam2
|
UTSW |
16 |
81,314,419 (GRCm39) |
missense |
probably benign |
0.21 |
R8775:Ncam2
|
UTSW |
16 |
81,314,429 (GRCm39) |
missense |
probably benign |
0.18 |
R8775-TAIL:Ncam2
|
UTSW |
16 |
81,314,429 (GRCm39) |
missense |
probably benign |
0.18 |
R9082:Ncam2
|
UTSW |
16 |
81,412,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Ncam2
|
UTSW |
16 |
81,252,204 (GRCm39) |
missense |
probably benign |
0.07 |
R9386:Ncam2
|
UTSW |
16 |
81,252,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Ncam2
|
UTSW |
16 |
81,309,887 (GRCm39) |
missense |
probably benign |
0.03 |
R9510:Ncam2
|
UTSW |
16 |
81,420,341 (GRCm39) |
makesense |
probably null |
|
R9587:Ncam2
|
UTSW |
16 |
81,262,501 (GRCm39) |
missense |
probably benign |
0.00 |
R9616:Ncam2
|
UTSW |
16 |
81,240,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Ncam2
|
UTSW |
16 |
81,418,251 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TAACACGATGAATTTGGGGACTG -3'
(R):5'- AGGAACTCTGGGAATTGACTGAATTG -3'
Sequencing Primer
(F):5'- TTAAAGGGCAGCATGGAC -3'
(R):5'- GAATTGACTGAATTGTTGCCTTCTC -3'
|
Posted On |
2016-03-17 |