Incidental Mutation 'R3772:Lrig1'
ID |
273351 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Lrig1
|
Ensembl Gene |
ENSMUSG00000030029 |
Gene Name |
leucine-rich repeats and immunoglobulin-like domains 1 |
Synonyms |
LIG-1, Img |
MMRRC Submission |
040748-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R3772 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
94581510-94677139 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 94582798 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Proline
at position 1073
(L1073P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144963
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000032105]
[ENSMUST00000061118]
[ENSMUST00000101126]
[ENSMUST00000204645]
[ENSMUST00000204235]
[ENSMUST00000204764]
|
AlphaFold |
P70193 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000032105
AA Change: L1073P
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000032105 Gene: ENSMUSG00000030029 AA Change: L1073P
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
34 |
N/A |
INTRINSIC |
LRRNT
|
42 |
74 |
5.82e-6 |
SMART |
LRR
|
68 |
92 |
4.83e0 |
SMART |
LRR
|
93 |
115 |
9.96e-1 |
SMART |
LRR
|
142 |
163 |
6.22e0 |
SMART |
LRR
|
166 |
187 |
1.81e1 |
SMART |
LRR
|
190 |
212 |
5.72e0 |
SMART |
LRR
|
213 |
235 |
1.06e1 |
SMART |
LRR_TYP
|
236 |
259 |
2.79e-4 |
SMART |
LRR
|
260 |
283 |
2.54e1 |
SMART |
LRR
|
284 |
307 |
9.96e-1 |
SMART |
LRR
|
308 |
331 |
4.21e1 |
SMART |
LRR_TYP
|
332 |
355 |
8.6e-5 |
SMART |
LRR
|
356 |
382 |
1.06e1 |
SMART |
LRR
|
383 |
406 |
9.96e-1 |
SMART |
LRR_TYP
|
407 |
430 |
3.34e-2 |
SMART |
LRRCT
|
442 |
492 |
3.5e-15 |
SMART |
IGc2
|
509 |
586 |
1.34e-4 |
SMART |
IGc2
|
613 |
681 |
2.87e-13 |
SMART |
IGc2
|
707 |
772 |
6.44e-16 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000061118
|
SMART Domains |
Protein: ENSMUSP00000058028 Gene: ENSMUSG00000045100
Domain | Start | End | E-Value | Type |
Pfam:Mito_carr
|
2 |
82 |
7e-14 |
PFAM |
Pfam:Mito_carr
|
84 |
173 |
4e-16 |
PFAM |
Pfam:Mito_carr
|
176 |
269 |
2.8e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000101126
AA Change: L1073P
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000098686 Gene: ENSMUSG00000030029 AA Change: L1073P
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
34 |
N/A |
INTRINSIC |
LRRNT
|
42 |
74 |
5.82e-6 |
SMART |
LRR
|
68 |
92 |
4.83e0 |
SMART |
LRR
|
93 |
115 |
9.96e-1 |
SMART |
LRR
|
142 |
163 |
6.22e0 |
SMART |
LRR
|
166 |
187 |
1.81e1 |
SMART |
LRR
|
190 |
212 |
5.72e0 |
SMART |
LRR
|
213 |
235 |
1.06e1 |
SMART |
LRR_TYP
|
236 |
259 |
2.79e-4 |
SMART |
LRR
|
260 |
283 |
2.54e1 |
SMART |
LRR
|
284 |
307 |
9.96e-1 |
SMART |
LRR
|
308 |
331 |
4.21e1 |
SMART |
LRR_TYP
|
332 |
355 |
8.6e-5 |
SMART |
LRR
|
356 |
382 |
1.06e1 |
SMART |
LRR
|
383 |
406 |
9.96e-1 |
SMART |
LRR_TYP
|
407 |
430 |
3.34e-2 |
SMART |
LRRCT
|
442 |
492 |
3.5e-15 |
SMART |
IGc2
|
509 |
586 |
1.34e-4 |
SMART |
IGc2
|
613 |
681 |
2.87e-13 |
SMART |
IGc2
|
707 |
772 |
6.44e-16 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183891
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203484
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203876
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000204645
AA Change: L1073P
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000144963 Gene: ENSMUSG00000030029 AA Change: L1073P
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
34 |
N/A |
INTRINSIC |
LRRNT
|
42 |
74 |
5.82e-6 |
SMART |
LRR
|
68 |
92 |
4.83e0 |
SMART |
LRR
|
93 |
115 |
9.96e-1 |
SMART |
LRR
|
142 |
163 |
6.22e0 |
SMART |
LRR
|
166 |
187 |
1.81e1 |
SMART |
LRR
|
190 |
212 |
5.72e0 |
SMART |
LRR
|
213 |
235 |
1.06e1 |
SMART |
LRR_TYP
|
236 |
259 |
2.79e-4 |
SMART |
LRR
|
260 |
283 |
2.54e1 |
SMART |
LRR
|
284 |
307 |
9.96e-1 |
SMART |
LRR
|
308 |
331 |
4.21e1 |
SMART |
LRR_TYP
|
332 |
355 |
8.6e-5 |
SMART |
LRR
|
356 |
382 |
1.06e1 |
SMART |
LRR
|
383 |
406 |
9.96e-1 |
SMART |
LRR_TYP
|
407 |
430 |
3.34e-2 |
SMART |
LRRCT
|
442 |
492 |
3.5e-15 |
SMART |
IGc2
|
509 |
586 |
1.34e-4 |
SMART |
IGc2
|
613 |
681 |
2.87e-13 |
SMART |
IGc2
|
707 |
772 |
6.44e-16 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000204235
|
SMART Domains |
Protein: ENSMUSP00000145328 Gene: ENSMUSG00000045100
Domain | Start | End | E-Value | Type |
Pfam:Mito_carr
|
2 |
43 |
2.7e-7 |
PFAM |
Pfam:Mito_carr
|
38 |
82 |
8.2e-6 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000204764
|
SMART Domains |
Protein: ENSMUSP00000144816 Gene: ENSMUSG00000045100
Domain | Start | End | E-Value | Type |
Pfam:Mito_carr
|
2 |
44 |
1e-7 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205173
|
Meta Mutation Damage Score |
0.0614 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.5%
|
Validation Efficiency |
100% (77/77) |
MGI Phenotype |
PHENOTYPE: Homozygous null mice developed psoriasiform epidermal hyperplasia. Homozygotes exhibit hair follicle, epidermis, vertebral, eye and hearing abnormalities, decreased body size and fat amount, and increased susceptibility to bacterial infection. [provided by MGI curators]
|
Allele List at MGI |
All alleles(5) : Targeted(4) Gene trapped(1)
|
Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
A |
2: 69,159,720 (GRCm39) |
|
probably benign |
Het |
Adgrl1 |
A |
G |
8: 84,649,633 (GRCm39) |
N97S |
possibly damaging |
Het |
Aldh1a2 |
A |
G |
9: 71,160,202 (GRCm39) |
D76G |
probably damaging |
Het |
Aldh3a1 |
A |
G |
11: 61,105,431 (GRCm39) |
E179G |
possibly damaging |
Het |
Ap1g1 |
A |
G |
8: 110,564,418 (GRCm39) |
D324G |
probably damaging |
Het |
Arfgap2 |
A |
G |
2: 91,095,711 (GRCm39) |
T12A |
probably benign |
Het |
Aurka |
A |
G |
2: 172,208,880 (GRCm39) |
L85P |
probably benign |
Het |
Birc6 |
T |
A |
17: 74,925,424 (GRCm39) |
|
probably benign |
Het |
Bmp7 |
A |
T |
2: 172,712,015 (GRCm39) |
I403N |
probably damaging |
Het |
Carns1 |
A |
G |
19: 4,220,915 (GRCm39) |
|
probably benign |
Het |
Ccdc88c |
G |
A |
12: 100,932,359 (GRCm39) |
|
probably benign |
Het |
Ccl2 |
C |
T |
11: 81,927,784 (GRCm39) |
A76V |
probably damaging |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Clstn2 |
A |
G |
9: 97,464,615 (GRCm39) |
I180T |
probably damaging |
Het |
Col24a1 |
T |
C |
3: 145,251,041 (GRCm39) |
L1680P |
probably damaging |
Het |
Col4a6 |
C |
A |
X: 139,955,196 (GRCm39) |
G1416C |
probably damaging |
Het |
Ctnna2 |
T |
G |
6: 76,950,752 (GRCm39) |
N573T |
probably damaging |
Het |
Cts8 |
G |
A |
13: 61,398,715 (GRCm39) |
|
probably benign |
Het |
Cxcl17 |
A |
G |
7: 25,099,754 (GRCm39) |
|
probably benign |
Het |
Defb18 |
T |
C |
1: 18,306,845 (GRCm39) |
H37R |
possibly damaging |
Het |
Dis3l2 |
T |
C |
1: 86,782,130 (GRCm39) |
I229T |
probably benign |
Het |
Dysf |
G |
A |
6: 84,129,333 (GRCm39) |
S1474N |
possibly damaging |
Het |
Elf1 |
T |
C |
14: 79,804,650 (GRCm39) |
V105A |
possibly damaging |
Het |
F13a1 |
T |
C |
13: 37,082,108 (GRCm39) |
K532R |
probably benign |
Het |
Fmn1 |
T |
G |
2: 113,412,463 (GRCm39) |
S996A |
probably damaging |
Het |
Focad |
A |
C |
4: 88,254,398 (GRCm39) |
|
probably benign |
Het |
Frmd4a |
A |
T |
2: 4,595,433 (GRCm39) |
E109D |
probably damaging |
Het |
Frrs1 |
T |
G |
3: 116,672,036 (GRCm39) |
S45A |
possibly damaging |
Het |
Gm5422 |
T |
A |
10: 31,124,510 (GRCm39) |
|
noncoding transcript |
Het |
Gm5866 |
T |
C |
5: 52,740,088 (GRCm39) |
|
noncoding transcript |
Het |
Hmcn2 |
C |
T |
2: 31,250,908 (GRCm39) |
T790M |
probably damaging |
Het |
Iglon5 |
A |
T |
7: 43,130,037 (GRCm39) |
Y42* |
probably null |
Het |
Khdrbs2 |
C |
T |
1: 32,283,157 (GRCm39) |
Q90* |
probably null |
Het |
Krt74 |
T |
C |
15: 101,670,630 (GRCm39) |
|
noncoding transcript |
Het |
Lamc2 |
T |
A |
1: 152,999,997 (GRCm39) |
M1121L |
probably benign |
Het |
Lrp5 |
G |
A |
19: 3,662,330 (GRCm39) |
R173C |
probably damaging |
Het |
Man2c1 |
C |
A |
9: 57,047,661 (GRCm39) |
|
probably benign |
Het |
Megf10 |
G |
A |
18: 57,416,934 (GRCm39) |
D768N |
probably benign |
Het |
Mycbp2 |
T |
C |
14: 103,371,224 (GRCm39) |
N4108S |
possibly damaging |
Het |
Nid1 |
A |
G |
13: 13,651,003 (GRCm39) |
|
probably benign |
Het |
Nnt |
A |
G |
13: 119,533,488 (GRCm39) |
V59A |
probably damaging |
Het |
Nsd1 |
G |
A |
13: 55,394,486 (GRCm39) |
V696I |
probably benign |
Het |
Or1o4 |
T |
C |
17: 37,590,745 (GRCm39) |
T189A |
probably benign |
Het |
Pag1 |
G |
A |
3: 9,764,688 (GRCm39) |
T155M |
probably benign |
Het |
Pgam5 |
T |
C |
5: 110,413,459 (GRCm39) |
H176R |
probably damaging |
Het |
Pid1 |
T |
C |
1: 84,015,918 (GRCm39) |
D149G |
probably damaging |
Het |
Pkp3 |
G |
A |
7: 140,662,259 (GRCm39) |
M1I |
probably null |
Het |
Pld2 |
C |
T |
11: 70,434,949 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ptprs |
T |
C |
17: 56,735,978 (GRCm39) |
T152A |
possibly damaging |
Het |
Rab9b |
T |
A |
X: 135,762,198 (GRCm39) |
E67D |
probably damaging |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
Rnf214 |
T |
C |
9: 45,777,932 (GRCm39) |
M625V |
possibly damaging |
Het |
Rwdd2a |
A |
C |
9: 86,456,214 (GRCm39) |
N130T |
possibly damaging |
Het |
Scn9a |
T |
C |
2: 66,313,992 (GRCm39) |
N1909D |
probably benign |
Het |
Septin10 |
A |
T |
10: 59,012,709 (GRCm39) |
M303K |
probably damaging |
Het |
Sez6l2 |
A |
G |
7: 126,558,375 (GRCm39) |
E339G |
probably damaging |
Het |
Sf3b1 |
C |
A |
1: 55,039,150 (GRCm39) |
|
probably benign |
Het |
Shisal1 |
A |
T |
15: 84,290,886 (GRCm39) |
Y120* |
probably null |
Het |
Ska3 |
C |
T |
14: 58,047,534 (GRCm39) |
V334I |
probably benign |
Het |
Srebf2 |
A |
G |
15: 82,066,309 (GRCm39) |
K579R |
probably benign |
Het |
St18 |
A |
T |
1: 6,914,553 (GRCm39) |
K799I |
probably damaging |
Het |
Strada |
C |
T |
11: 106,055,648 (GRCm39) |
R333Q |
probably damaging |
Het |
Stradb |
A |
T |
1: 59,024,544 (GRCm39) |
I64L |
probably benign |
Het |
Sun1 |
A |
G |
5: 139,224,575 (GRCm39) |
|
probably benign |
Het |
Tecta |
T |
C |
9: 42,242,292 (GRCm39) |
T2094A |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,344,087 (GRCm39) |
R227W |
probably damaging |
Het |
Tnk2 |
A |
G |
16: 32,498,640 (GRCm39) |
D651G |
probably damaging |
Het |
Trim43c |
A |
T |
9: 88,729,810 (GRCm39) |
D417V |
probably damaging |
Het |
Tsc22d4 |
T |
C |
5: 137,757,495 (GRCm39) |
L374P |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,601,711 (GRCm39) |
T16872A |
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,180,011 (GRCm39) |
V262A |
possibly damaging |
Het |
Vmn2r60 |
A |
T |
7: 41,765,980 (GRCm39) |
N29I |
probably benign |
Het |
Xrn2 |
T |
C |
2: 146,903,207 (GRCm39) |
V765A |
probably benign |
Het |
Zbed4 |
C |
T |
15: 88,664,990 (GRCm39) |
P353S |
probably benign |
Het |
Zfp251 |
A |
G |
15: 76,737,836 (GRCm39) |
I414T |
possibly damaging |
Het |
Zfp426 |
A |
T |
9: 20,384,413 (GRCm39) |
|
probably null |
Het |
Zwilch |
A |
T |
9: 64,063,316 (GRCm39) |
F286I |
probably benign |
Het |
|
Other mutations in Lrig1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00474:Lrig1
|
APN |
6 |
94,588,385 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01356:Lrig1
|
APN |
6 |
94,586,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01356:Lrig1
|
APN |
6 |
94,631,901 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02001:Lrig1
|
APN |
6 |
94,584,305 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02019:Lrig1
|
APN |
6 |
94,593,410 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02177:Lrig1
|
APN |
6 |
94,640,977 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02274:Lrig1
|
APN |
6 |
94,640,919 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03197:Lrig1
|
APN |
6 |
94,583,099 (GRCm39) |
missense |
probably benign |
|
IGL03263:Lrig1
|
APN |
6 |
94,588,628 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03327:Lrig1
|
APN |
6 |
94,583,104 (GRCm39) |
missense |
probably benign |
0.10 |
N/A - 293:Lrig1
|
UTSW |
6 |
94,586,068 (GRCm39) |
missense |
probably benign |
|
R0019:Lrig1
|
UTSW |
6 |
94,584,330 (GRCm39) |
nonsense |
probably null |
|
R0019:Lrig1
|
UTSW |
6 |
94,584,330 (GRCm39) |
nonsense |
probably null |
|
R0961:Lrig1
|
UTSW |
6 |
94,640,895 (GRCm39) |
splice site |
probably benign |
|
R1018:Lrig1
|
UTSW |
6 |
94,599,583 (GRCm39) |
splice site |
probably benign |
|
R1381:Lrig1
|
UTSW |
6 |
94,583,111 (GRCm39) |
missense |
probably benign |
0.04 |
R1473:Lrig1
|
UTSW |
6 |
94,584,294 (GRCm39) |
missense |
probably benign |
0.16 |
R1498:Lrig1
|
UTSW |
6 |
94,604,968 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1888:Lrig1
|
UTSW |
6 |
94,631,859 (GRCm39) |
missense |
probably benign |
0.03 |
R1888:Lrig1
|
UTSW |
6 |
94,631,859 (GRCm39) |
missense |
probably benign |
0.03 |
R2273:Lrig1
|
UTSW |
6 |
94,585,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R2513:Lrig1
|
UTSW |
6 |
94,594,347 (GRCm39) |
splice site |
probably null |
|
R3001:Lrig1
|
UTSW |
6 |
94,585,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R3002:Lrig1
|
UTSW |
6 |
94,585,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Lrig1
|
UTSW |
6 |
94,588,557 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3732:Lrig1
|
UTSW |
6 |
94,588,557 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3733:Lrig1
|
UTSW |
6 |
94,588,557 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4089:Lrig1
|
UTSW |
6 |
94,586,840 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4093:Lrig1
|
UTSW |
6 |
94,590,559 (GRCm39) |
missense |
probably benign |
0.10 |
R4095:Lrig1
|
UTSW |
6 |
94,590,559 (GRCm39) |
missense |
probably benign |
0.10 |
R4225:Lrig1
|
UTSW |
6 |
94,599,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Lrig1
|
UTSW |
6 |
94,586,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R4951:Lrig1
|
UTSW |
6 |
94,640,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Lrig1
|
UTSW |
6 |
94,602,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Lrig1
|
UTSW |
6 |
94,588,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R5149:Lrig1
|
UTSW |
6 |
94,605,025 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5732:Lrig1
|
UTSW |
6 |
94,676,520 (GRCm39) |
nonsense |
probably null |
|
R5988:Lrig1
|
UTSW |
6 |
94,605,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R6064:Lrig1
|
UTSW |
6 |
94,603,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Lrig1
|
UTSW |
6 |
94,593,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6723:Lrig1
|
UTSW |
6 |
94,603,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R6815:Lrig1
|
UTSW |
6 |
94,602,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Lrig1
|
UTSW |
6 |
94,602,044 (GRCm39) |
missense |
probably benign |
0.07 |
R6995:Lrig1
|
UTSW |
6 |
94,588,610 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7404:Lrig1
|
UTSW |
6 |
94,603,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R7487:Lrig1
|
UTSW |
6 |
94,583,099 (GRCm39) |
missense |
probably benign |
|
R7732:Lrig1
|
UTSW |
6 |
94,603,358 (GRCm39) |
missense |
probably benign |
0.05 |
R7915:Lrig1
|
UTSW |
6 |
94,607,082 (GRCm39) |
critical splice donor site |
probably null |
|
R8133:Lrig1
|
UTSW |
6 |
94,588,610 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8768:Lrig1
|
UTSW |
6 |
94,631,840 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9045:Lrig1
|
UTSW |
6 |
94,585,688 (GRCm39) |
critical splice donor site |
probably null |
|
R9227:Lrig1
|
UTSW |
6 |
94,607,113 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lrig1
|
UTSW |
6 |
94,586,007 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
Predicted Primers |
PCR Primer
(F):5'- CTCACGTTTCTGAGCTCCAG -3'
(R):5'- GAGATTCCTCTTGGACTTTAGCAAAG -3'
Sequencing Primer
(F):5'- TAGCCGACTGACTGACATTC -3'
(R):5'- GTTACATGAAGCAGACTGCATAGACC -3'
|
Posted On |
2015-03-25 |