Incidental Mutation 'R6041:Pax6'
ID |
483531 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pax6
|
Ensembl Gene |
ENSMUSG00000027168 |
Gene Name |
paired box 6 |
Synonyms |
Pax-6, Dickie's small eye, Gsfaey11, 1500038E17Rik, Dey, AEY11 |
MMRRC Submission |
044209-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R6041 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
105499245-105527709 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 105514247 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Valine
at position 29
(I29V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129344
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090391]
[ENSMUST00000090397]
[ENSMUST00000111082]
[ENSMUST00000111083]
[ENSMUST00000111085]
[ENSMUST00000111086]
[ENSMUST00000111087]
[ENSMUST00000156216]
[ENSMUST00000111088]
[ENSMUST00000142772]
[ENSMUST00000167211]
|
AlphaFold |
P63015 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000090391
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000087870 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
142 |
7.36e-86 |
SMART |
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
HOX
|
224 |
286 |
4.93e-26 |
SMART |
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000090397
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000087878 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
128 |
6.11e-92 |
SMART |
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
HOX
|
210 |
272 |
4.93e-26 |
SMART |
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111082
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106711 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
128 |
6.11e-92 |
SMART |
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
HOX
|
210 |
272 |
4.93e-26 |
SMART |
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111083
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106712 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
128 |
6.11e-92 |
SMART |
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
HOX
|
210 |
272 |
4.93e-26 |
SMART |
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111085
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106714 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
142 |
7.36e-86 |
SMART |
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
HOX
|
224 |
286 |
4.93e-26 |
SMART |
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111086
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106715 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
142 |
7.36e-86 |
SMART |
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
HOX
|
224 |
286 |
4.93e-26 |
SMART |
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111087
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106716 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
128 |
6.11e-92 |
SMART |
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
HOX
|
210 |
272 |
4.93e-26 |
SMART |
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000156216
AA Change: I29V
PolyPhen 2
Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000119375 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
139 |
1.46e-80 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153011
|
SMART Domains |
Protein: ENSMUSP00000118457 Gene: ENSMUSG00000027168
Domain | Start | End | E-Value | Type |
PAX
|
2 |
109 |
4.98e-42 |
SMART |
low complexity region
|
155 |
166 |
N/A |
INTRINSIC |
Pfam:Homeobox
|
192 |
218 |
7.7e-9 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146803
|
SMART Domains |
Protein: ENSMUSP00000133346 Gene: ENSMUSG00000027168
Domain | Start | End | E-Value | Type |
Blast:PAX
|
1 |
62 |
1e-26 |
BLAST |
HOX
|
74 |
136 |
4.93e-26 |
SMART |
low complexity region
|
145 |
158 |
N/A |
INTRINSIC |
Blast:PAX
|
186 |
234 |
3e-23 |
BLAST |
low complexity region
|
251 |
259 |
N/A |
INTRINSIC |
low complexity region
|
262 |
276 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154643
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138365
|
SMART Domains |
Protein: ENSMUSP00000117154 Gene: ENSMUSG00000027168
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
15 |
N/A |
INTRINSIC |
PAX
|
33 |
192 |
4.87e-77 |
SMART |
low complexity region
|
238 |
249 |
N/A |
INTRINSIC |
SCOP:d1b72a_
|
254 |
291 |
2e-4 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145744
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155081
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135412
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140173
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154302
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123063
|
SMART Domains |
Protein: ENSMUSP00000121345 Gene: ENSMUSG00000027168
Domain | Start | End | E-Value | Type |
HOX
|
9 |
71 |
2.5e-28 |
SMART |
low complexity region
|
80 |
93 |
N/A |
INTRINSIC |
Blast:PAX
|
121 |
169 |
6e-24 |
BLAST |
low complexity region
|
186 |
194 |
N/A |
INTRINSIC |
low complexity region
|
197 |
211 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123000
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000111088
|
SMART Domains |
Protein: ENSMUSP00000106717 Gene: ENSMUSG00000027168
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
17 |
N/A |
INTRINSIC |
HOX
|
39 |
101 |
4.93e-26 |
SMART |
low complexity region
|
110 |
123 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000142772
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000167211
AA Change: I29V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000129344 Gene: ENSMUSG00000027168 AA Change: I29V
Domain | Start | End | E-Value | Type |
PAX
|
4 |
142 |
7.36e-86 |
SMART |
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
HOX
|
224 |
286 |
4.93e-26 |
SMART |
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.9229 |
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.5%
- 10x: 97.7%
- 20x: 93.1%
|
Validation Efficiency |
100% (62/62) |
MGI Phenotype |
FUNCTION: This gene encodes a homeobox-containing protein that functions as a regulator of transcription. It plays a key role in the development of neural tissues, particularly the eye. Activity of this protein is also required for expression of glucagon in the pancreas. This gene is regulated by multiple enhancers located up to tens or hundreds of kilobases upstream and downstream of the transcription start sites. Mutations in this gene or deletion of these regulatory elements results in severe defects in eye development. Alternative splicing and the use of alternative promoters results in multiple transcript variants, some of which encode proteins that lack the N-terminal paired domain. [provided by RefSeq, Jul 2015] PHENOTYPE: Null and hypomorphic mutants show a range of phenotypes from viable with small eyes and lens/cornea fusion to microphthalmia and cataract to embryonic or perinatal lethality with anophthalmia and severe craniofacial and forebrain defects. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
A |
17: 24,595,354 (GRCm39) |
M297K |
probably damaging |
Het |
Ace |
A |
C |
11: 105,866,134 (GRCm39) |
H34P |
probably benign |
Het |
Agbl2 |
A |
T |
2: 90,638,371 (GRCm39) |
N652I |
probably benign |
Het |
Auh |
T |
A |
13: 53,073,122 (GRCm39) |
L86F |
possibly damaging |
Het |
Bmp10 |
A |
G |
6: 87,411,302 (GRCm39) |
K365R |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,764,314 (GRCm39) |
S2086T |
probably damaging |
Het |
Calcoco1 |
C |
A |
15: 102,626,374 (GRCm39) |
R105L |
possibly damaging |
Het |
Casc3 |
T |
G |
11: 98,719,385 (GRCm39) |
V509G |
probably damaging |
Het |
Clmn |
A |
G |
12: 104,748,131 (GRCm39) |
V472A |
probably benign |
Het |
Cyp2b19 |
A |
T |
7: 26,458,852 (GRCm39) |
S142C |
probably damaging |
Het |
Derl3 |
T |
C |
10: 75,729,335 (GRCm39) |
L26P |
probably damaging |
Het |
Dgkh |
C |
T |
14: 78,825,067 (GRCm39) |
A863T |
probably damaging |
Het |
Dhx30 |
C |
T |
9: 109,913,666 (GRCm39) |
R1127Q |
probably benign |
Het |
Dmxl2 |
A |
G |
9: 54,324,037 (GRCm39) |
S1116P |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,328,805 (GRCm39) |
V3179A |
probably benign |
Het |
Dnajb11 |
A |
T |
16: 22,687,471 (GRCm39) |
N156I |
probably benign |
Het |
Dpep1 |
A |
T |
8: 123,927,394 (GRCm39) |
E316V |
probably damaging |
Het |
Entrep1 |
A |
T |
19: 23,962,193 (GRCm39) |
M270K |
probably benign |
Het |
F2rl2 |
T |
A |
13: 95,837,617 (GRCm39) |
F221I |
probably benign |
Het |
Flg2 |
T |
A |
3: 93,127,668 (GRCm39) |
D173E |
probably benign |
Het |
Fshr |
A |
T |
17: 89,293,414 (GRCm39) |
D421E |
probably damaging |
Het |
Gfm2 |
T |
A |
13: 97,309,131 (GRCm39) |
V612E |
probably benign |
Het |
Gm17655 |
T |
G |
5: 110,195,439 (GRCm39) |
K114N |
possibly damaging |
Het |
Gm45844 |
C |
A |
7: 7,281,183 (GRCm39) |
|
probably benign |
Het |
Gpr142 |
A |
T |
11: 114,697,203 (GRCm39) |
I250F |
probably damaging |
Het |
Hexa |
A |
G |
9: 59,470,519 (GRCm39) |
Q447R |
probably damaging |
Het |
Leng8 |
T |
C |
7: 4,148,568 (GRCm39) |
L780P |
probably benign |
Het |
Lrrk1 |
T |
C |
7: 65,911,881 (GRCm39) |
D1893G |
probably benign |
Het |
Macf1 |
T |
A |
4: 123,407,641 (GRCm39) |
I139F |
probably damaging |
Het |
Megf10 |
A |
T |
18: 57,313,621 (GRCm39) |
T22S |
probably benign |
Het |
Mup-ps1 |
C |
A |
4: 60,088,549 (GRCm39) |
|
noncoding transcript |
Het |
Myh13 |
A |
T |
11: 67,255,556 (GRCm39) |
E1642V |
probably damaging |
Het |
Myof |
A |
G |
19: 37,913,068 (GRCm39) |
Y1462H |
probably damaging |
Het |
Nipbl |
T |
A |
15: 8,353,748 (GRCm39) |
D1765V |
probably damaging |
Het |
Npy5r |
A |
T |
8: 67,134,675 (GRCm39) |
N39K |
possibly damaging |
Het |
Or5m13b |
G |
A |
2: 85,753,735 (GRCm39) |
G41D |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,178,436 (GRCm39) |
Y307H |
probably benign |
Het |
Pmf1 |
A |
C |
3: 88,303,358 (GRCm39) |
Y68D |
probably damaging |
Het |
Psen2 |
C |
A |
1: 180,073,292 (GRCm39) |
E10* |
probably null |
Het |
Ptprs |
T |
A |
17: 56,726,080 (GRCm39) |
M991L |
probably benign |
Het |
R3hdm4 |
A |
G |
10: 79,749,495 (GRCm39) |
V20A |
possibly damaging |
Het |
Rad17 |
T |
C |
13: 100,754,274 (GRCm39) |
N649D |
probably benign |
Het |
Rad9b |
A |
T |
5: 122,489,415 (GRCm39) |
C38S |
probably damaging |
Het |
Rapgef2 |
T |
C |
3: 78,976,469 (GRCm39) |
M1296V |
probably benign |
Het |
Rbp3 |
T |
C |
14: 33,678,439 (GRCm39) |
S796P |
probably damaging |
Het |
Rpl10-ps3 |
A |
G |
9: 50,256,082 (GRCm39) |
S54P |
probably benign |
Het |
Sclt1 |
T |
A |
3: 41,581,612 (GRCm39) |
I688F |
probably damaging |
Het |
Scn10a |
A |
G |
9: 119,438,535 (GRCm39) |
I1778T |
probably damaging |
Het |
Scrib |
C |
T |
15: 75,939,021 (GRCm39) |
R159Q |
possibly damaging |
Het |
Senp1 |
C |
T |
15: 97,956,097 (GRCm39) |
E441K |
probably damaging |
Het |
Sipa1l1 |
T |
A |
12: 82,389,024 (GRCm39) |
F417I |
probably damaging |
Het |
Slco1a7 |
A |
C |
6: 141,684,764 (GRCm39) |
D230E |
probably benign |
Het |
Smcr8 |
A |
G |
11: 60,670,394 (GRCm39) |
D514G |
probably damaging |
Het |
Tbc1d23 |
T |
G |
16: 56,993,513 (GRCm39) |
D551A |
probably benign |
Het |
Tet1 |
G |
T |
10: 62,649,152 (GRCm39) |
T149N |
probably damaging |
Het |
Them4 |
A |
T |
3: 94,224,806 (GRCm39) |
D61V |
possibly damaging |
Het |
Trak1 |
A |
T |
9: 121,289,478 (GRCm39) |
I597F |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,206,864 (GRCm39) |
I1666V |
possibly damaging |
Het |
Vipr2 |
A |
C |
12: 116,106,604 (GRCm39) |
N378T |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,821,231 (GRCm39) |
R575G |
probably benign |
Het |
Zfp941 |
A |
T |
7: 140,392,158 (GRCm39) |
C400* |
probably null |
Het |
Zswim5 |
A |
C |
4: 116,819,818 (GRCm39) |
S408R |
probably benign |
Het |
|
Other mutations in Pax6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02008:Pax6
|
APN |
2 |
105,522,623 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02256:Pax6
|
APN |
2 |
105,515,115 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02500:Pax6
|
APN |
2 |
105,523,115 (GRCm39) |
missense |
probably benign |
0.13 |
beady
|
UTSW |
2 |
105,522,036 (GRCm39) |
missense |
probably damaging |
1.00 |
red_hots
|
UTSW |
2 |
105,525,705 (GRCm39) |
missense |
probably benign |
0.00 |
G1citation:Pax6
|
UTSW |
2 |
105,516,268 (GRCm39) |
missense |
probably benign |
0.04 |
R1067:Pax6
|
UTSW |
2 |
105,510,646 (GRCm39) |
missense |
probably benign |
0.01 |
R1213:Pax6
|
UTSW |
2 |
105,516,258 (GRCm39) |
missense |
probably benign |
0.13 |
R1494:Pax6
|
UTSW |
2 |
105,521,955 (GRCm39) |
missense |
probably benign |
0.16 |
R1633:Pax6
|
UTSW |
2 |
105,522,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Pax6
|
UTSW |
2 |
105,516,228 (GRCm39) |
missense |
probably benign |
0.09 |
R3834:Pax6
|
UTSW |
2 |
105,526,795 (GRCm39) |
missense |
probably benign |
0.00 |
R3835:Pax6
|
UTSW |
2 |
105,526,795 (GRCm39) |
missense |
probably benign |
0.00 |
R4665:Pax6
|
UTSW |
2 |
105,514,343 (GRCm39) |
intron |
probably benign |
|
R4714:Pax6
|
UTSW |
2 |
105,525,745 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4747:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
R4764:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
R4767:Pax6
|
UTSW |
2 |
105,525,705 (GRCm39) |
missense |
probably benign |
0.00 |
R4771:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
R4772:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
R4816:Pax6
|
UTSW |
2 |
105,514,129 (GRCm39) |
intron |
probably benign |
|
R4819:Pax6
|
UTSW |
2 |
105,522,622 (GRCm39) |
critical splice donor site |
probably null |
|
R5418:Pax6
|
UTSW |
2 |
105,521,910 (GRCm39) |
missense |
probably benign |
0.00 |
R5683:Pax6
|
UTSW |
2 |
105,516,252 (GRCm39) |
missense |
probably benign |
0.06 |
R6263:Pax6
|
UTSW |
2 |
105,523,199 (GRCm39) |
critical splice donor site |
probably null |
|
R6651:Pax6
|
UTSW |
2 |
105,516,175 (GRCm39) |
missense |
probably benign |
0.00 |
R6822:Pax6
|
UTSW |
2 |
105,516,268 (GRCm39) |
missense |
probably benign |
0.04 |
R7042:Pax6
|
UTSW |
2 |
105,526,718 (GRCm39) |
missense |
probably benign |
|
R7088:Pax6
|
UTSW |
2 |
105,526,753 (GRCm39) |
missense |
probably benign |
0.00 |
R7102:Pax6
|
UTSW |
2 |
105,522,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R7294:Pax6
|
UTSW |
2 |
105,515,246 (GRCm39) |
nonsense |
probably null |
|
R7761:Pax6
|
UTSW |
2 |
105,522,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R7948:Pax6
|
UTSW |
2 |
105,516,222 (GRCm39) |
missense |
probably benign |
|
R8882:Pax6
|
UTSW |
2 |
105,521,963 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9151:Pax6
|
UTSW |
2 |
105,523,097 (GRCm39) |
missense |
probably benign |
0.10 |
R9796:Pax6
|
UTSW |
2 |
105,522,541 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pax6
|
UTSW |
2 |
105,516,161 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
Predicted Primers |
PCR Primer
(F):5'- AGGGAGCTGAGGTTGCATTG -3'
(R):5'- GACAGGGACCTTGGTGGAAG -3'
Sequencing Primer
(F):5'- AGCTGAGGTTGCATTGTGGTC -3'
(R):5'- TGGTGTAGTCAGTAATTAGTAGCG -3'
|
Posted On |
2017-07-14 |