Incidental Mutation 'R4720:Crybg3'
ID |
354411 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Crybg3
|
Ensembl Gene |
ENSMUSG00000022723 |
Gene Name |
beta-gamma crystallin domain containing 3 |
Synonyms |
Gm9581 |
MMRRC Submission |
041958-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.138)
|
Stock # |
R4720 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
16 |
Chromosomal Location |
59312451-59421410 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 59360180 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 787
(V787A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000037682
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044604]
[ENSMUST00000139989]
[ENSMUST00000172910]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000044604
AA Change: V787A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000037682 Gene: ENSMUSG00000022723 AA Change: V787A
Domain | Start | End | E-Value | Type |
low complexity region
|
258 |
273 |
N/A |
INTRINSIC |
low complexity region
|
282 |
290 |
N/A |
INTRINSIC |
XTALbg
|
430 |
516 |
2.78e-4 |
SMART |
Pfam:Crystall
|
536 |
599 |
3.3e-7 |
PFAM |
XTALbg
|
614 |
699 |
1.2e-21 |
SMART |
XTALbg
|
707 |
790 |
5.73e-19 |
SMART |
XTALbg
|
803 |
881 |
6.87e-5 |
SMART |
XTALbg
|
889 |
969 |
1.28e-7 |
SMART |
RICIN
|
972 |
1104 |
8.16e-14 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000129350
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139989
|
SMART Domains |
Protein: ENSMUSP00000122663 Gene: ENSMUSG00000022723
Domain | Start | End | E-Value | Type |
XTALbg
|
1 |
86 |
2.15e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000172910
AA Change: V2501A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,018,248 (GRCm39) |
I1124T |
probably damaging |
Het |
Acacb |
A |
G |
5: 114,367,975 (GRCm39) |
T1658A |
possibly damaging |
Het |
Acvrl1 |
C |
A |
15: 101,033,654 (GRCm39) |
P112Q |
probably damaging |
Het |
Ankar |
A |
T |
1: 72,738,170 (GRCm39) |
I4K |
possibly damaging |
Het |
Ankfn1 |
G |
C |
11: 89,332,252 (GRCm39) |
D431E |
possibly damaging |
Het |
Apobec4 |
T |
C |
1: 152,632,425 (GRCm39) |
V151A |
possibly damaging |
Het |
Atp10b |
A |
G |
11: 43,093,949 (GRCm39) |
S498G |
probably benign |
Het |
Azin1 |
A |
G |
15: 38,493,744 (GRCm39) |
V293A |
probably benign |
Het |
Ccdc88b |
T |
C |
19: 6,835,083 (GRCm39) |
E46G |
probably damaging |
Het |
Ccdc96 |
T |
C |
5: 36,642,219 (GRCm39) |
|
probably benign |
Het |
Ccnyl1 |
A |
G |
1: 64,752,290 (GRCm39) |
D169G |
probably benign |
Het |
Cdca3 |
T |
A |
6: 124,809,127 (GRCm39) |
V89E |
probably damaging |
Het |
Cdh19 |
A |
T |
1: 110,823,111 (GRCm39) |
|
probably null |
Het |
Chka |
G |
A |
19: 3,936,375 (GRCm39) |
V238I |
probably damaging |
Het |
Cntn3 |
T |
C |
6: 102,218,983 (GRCm39) |
K546E |
possibly damaging |
Het |
Dlgap3 |
T |
C |
4: 127,089,508 (GRCm39) |
|
probably null |
Het |
Dnah8 |
C |
T |
17: 30,902,608 (GRCm39) |
L889F |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,967,184 (GRCm39) |
E1658G |
probably damaging |
Het |
Dnajc11 |
A |
G |
4: 152,052,996 (GRCm39) |
D102G |
probably damaging |
Het |
Dync1i2 |
T |
G |
2: 71,064,018 (GRCm39) |
S121A |
probably damaging |
Het |
Ece1 |
G |
A |
4: 137,684,486 (GRCm39) |
E591K |
probably damaging |
Het |
Enthd1 |
G |
A |
15: 80,444,510 (GRCm39) |
S15L |
probably damaging |
Het |
Epb41l2 |
T |
A |
10: 25,347,524 (GRCm39) |
H372Q |
probably damaging |
Het |
Errfi1 |
T |
A |
4: 150,951,204 (GRCm39) |
Y211N |
probably damaging |
Het |
Fam193b |
G |
A |
13: 55,691,250 (GRCm39) |
T208M |
probably benign |
Het |
Flacc1 |
T |
C |
1: 58,717,507 (GRCm39) |
I135V |
possibly damaging |
Het |
Fmnl2 |
C |
T |
2: 52,997,552 (GRCm39) |
T501M |
possibly damaging |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gm4841 |
G |
T |
18: 60,403,135 (GRCm39) |
D319E |
probably benign |
Het |
Gucd1 |
A |
G |
10: 75,345,494 (GRCm39) |
F187S |
probably damaging |
Het |
Hcar2 |
GCGGATGCGCAC |
GC |
5: 124,002,752 (GRCm39) |
|
probably null |
Het |
Helz2 |
T |
C |
2: 180,880,210 (GRCm39) |
D502G |
probably damaging |
Het |
Hspa2 |
A |
G |
12: 76,451,639 (GRCm39) |
E111G |
possibly damaging |
Het |
Htr2a |
T |
A |
14: 74,882,499 (GRCm39) |
S162T |
probably damaging |
Het |
Ift80 |
A |
G |
3: 68,869,623 (GRCm39) |
Y223H |
possibly damaging |
Het |
Il1rl1 |
A |
G |
1: 40,485,838 (GRCm39) |
K330E |
probably benign |
Het |
Il23r |
A |
T |
6: 67,400,645 (GRCm39) |
F562I |
probably damaging |
Het |
Isx |
T |
C |
8: 75,600,487 (GRCm39) |
|
probably null |
Het |
Jcad |
G |
A |
18: 4,674,055 (GRCm39) |
V606I |
probably benign |
Het |
Kcnn2 |
A |
T |
18: 45,816,187 (GRCm39) |
T333S |
possibly damaging |
Het |
Kcnq5 |
C |
T |
1: 21,473,274 (GRCm39) |
A630T |
probably damaging |
Het |
Kif2c |
T |
C |
4: 117,028,946 (GRCm39) |
M188V |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,903,086 (GRCm39) |
V321A |
possibly damaging |
Het |
Krtap4-8 |
A |
T |
11: 99,671,271 (GRCm39) |
|
probably benign |
Het |
Lcor |
G |
C |
19: 41,574,334 (GRCm39) |
A1030P |
probably benign |
Het |
Lgals3bp |
A |
C |
11: 118,289,295 (GRCm39) |
L52R |
probably damaging |
Het |
Lipk |
C |
A |
19: 33,999,099 (GRCm39) |
H126Q |
probably damaging |
Het |
Lpgat1 |
T |
C |
1: 191,495,779 (GRCm39) |
Y323H |
probably damaging |
Het |
Lrp2 |
T |
G |
2: 69,311,517 (GRCm39) |
N2654H |
probably damaging |
Het |
Lsm14b |
C |
T |
2: 179,669,774 (GRCm39) |
Q6* |
probably null |
Het |
Lysmd3 |
C |
T |
13: 81,817,584 (GRCm39) |
A187V |
possibly damaging |
Het |
Map2k5 |
A |
G |
9: 63,201,001 (GRCm39) |
S211P |
probably damaging |
Het |
Mlph |
A |
T |
1: 90,869,419 (GRCm39) |
I474F |
probably damaging |
Het |
Mpped2 |
T |
C |
2: 106,614,091 (GRCm39) |
S142P |
probably damaging |
Het |
Nemf |
A |
C |
12: 69,371,062 (GRCm39) |
M678R |
probably benign |
Het |
Nfe2l1 |
A |
T |
11: 96,718,515 (GRCm39) |
Y7N |
probably damaging |
Het |
Nfkbie |
T |
G |
17: 45,867,232 (GRCm39) |
D122E |
probably benign |
Het |
Noc3l |
C |
A |
19: 38,778,066 (GRCm39) |
A783S |
probably benign |
Het |
Nol8 |
T |
C |
13: 49,816,229 (GRCm39) |
V761A |
probably damaging |
Het |
Nvl |
A |
G |
1: 180,929,152 (GRCm39) |
L743P |
probably damaging |
Het |
Or1j1 |
T |
A |
2: 36,702,484 (GRCm39) |
I207F |
probably benign |
Het |
Plcb1 |
A |
G |
2: 135,093,667 (GRCm39) |
K160R |
possibly damaging |
Het |
Plekhg3 |
G |
T |
12: 76,625,096 (GRCm39) |
G1313C |
possibly damaging |
Het |
Plekhh1 |
GTCAAA |
G |
12: 79,122,194 (GRCm39) |
|
probably null |
Het |
Popdc3 |
G |
A |
10: 45,191,002 (GRCm39) |
V38I |
probably benign |
Het |
Prdx3 |
A |
T |
19: 60,858,551 (GRCm39) |
V114D |
possibly damaging |
Het |
Prkdc |
T |
A |
16: 15,485,579 (GRCm39) |
S469T |
probably benign |
Het |
Rbm22 |
G |
A |
18: 60,697,463 (GRCm39) |
R56H |
probably damaging |
Het |
Reln |
A |
T |
5: 22,491,894 (GRCm39) |
F113I |
possibly damaging |
Het |
Rims1 |
A |
G |
1: 22,497,731 (GRCm39) |
Y808H |
probably damaging |
Het |
Rsbn1 |
C |
A |
3: 103,836,336 (GRCm39) |
T458N |
possibly damaging |
Het |
Serpina3b |
A |
G |
12: 104,096,889 (GRCm39) |
S57G |
possibly damaging |
Het |
Skor2 |
G |
T |
18: 76,948,878 (GRCm39) |
|
probably null |
Het |
Slc22a4 |
A |
T |
11: 53,879,719 (GRCm39) |
Y447N |
probably damaging |
Het |
Slco1a7 |
C |
A |
6: 141,668,948 (GRCm39) |
A495S |
probably damaging |
Het |
Stx19 |
G |
T |
16: 62,642,682 (GRCm39) |
R166L |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,205,869 (GRCm39) |
T170A |
possibly damaging |
Het |
Sycp2 |
T |
G |
2: 178,016,225 (GRCm39) |
S746R |
probably benign |
Het |
Tchh |
G |
T |
3: 93,355,189 (GRCm39) |
R1543L |
unknown |
Het |
Tjp2 |
T |
C |
19: 24,078,169 (GRCm39) |
D908G |
probably damaging |
Het |
Ttc8 |
C |
A |
12: 98,946,068 (GRCm39) |
A452E |
possibly damaging |
Het |
Unc5a |
T |
A |
13: 55,151,696 (GRCm39) |
W709R |
probably null |
Het |
Unc80 |
T |
A |
1: 66,549,951 (GRCm39) |
S736R |
possibly damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,742,788 (GRCm39) |
H387Q |
probably benign |
Het |
Vmn2r39 |
C |
T |
7: 9,026,469 (GRCm39) |
|
probably null |
Het |
Vmn2r88 |
T |
A |
14: 51,650,702 (GRCm39) |
D138E |
probably benign |
Het |
Vwce |
T |
C |
19: 10,625,831 (GRCm39) |
F448L |
possibly damaging |
Het |
Wdr75 |
C |
T |
1: 45,861,645 (GRCm39) |
S695F |
probably benign |
Het |
Zfand4 |
T |
C |
6: 116,265,122 (GRCm39) |
|
probably null |
Het |
Zfp511 |
T |
A |
7: 139,617,424 (GRCm39) |
|
probably null |
Het |
Zfyve9 |
T |
C |
4: 108,501,565 (GRCm39) |
K584E |
possibly damaging |
Het |
|
Other mutations in Crybg3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Crybg3
|
APN |
16 |
59,350,803 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01305:Crybg3
|
APN |
16 |
59,349,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01809:Crybg3
|
APN |
16 |
59,345,216 (GRCm39) |
critical splice donor site |
probably benign |
0.00 |
IGL02247:Crybg3
|
APN |
16 |
59,323,513 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02252:Crybg3
|
APN |
16 |
59,372,887 (GRCm39) |
splice site |
probably benign |
|
IGL03036:Crybg3
|
APN |
16 |
59,375,542 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03202:Crybg3
|
APN |
16 |
59,315,072 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03232:Crybg3
|
APN |
16 |
59,350,731 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU22:Crybg3
|
UTSW |
16 |
59,349,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Crybg3
|
UTSW |
16 |
59,386,019 (GRCm39) |
splice site |
probably benign |
|
R0335:Crybg3
|
UTSW |
16 |
59,364,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Crybg3
|
UTSW |
16 |
59,385,574 (GRCm39) |
critical splice donor site |
probably null |
|
R1511:Crybg3
|
UTSW |
16 |
59,374,475 (GRCm39) |
missense |
probably benign |
0.01 |
R1579:Crybg3
|
UTSW |
16 |
59,350,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R1965:Crybg3
|
UTSW |
16 |
59,323,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Crybg3
|
UTSW |
16 |
59,364,488 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2225:Crybg3
|
UTSW |
16 |
59,375,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Crybg3
|
UTSW |
16 |
59,376,120 (GRCm39) |
unclassified |
probably benign |
|
R4210:Crybg3
|
UTSW |
16 |
59,364,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R4393:Crybg3
|
UTSW |
16 |
59,380,458 (GRCm39) |
unclassified |
probably benign |
|
R4394:Crybg3
|
UTSW |
16 |
59,380,458 (GRCm39) |
unclassified |
probably benign |
|
R4397:Crybg3
|
UTSW |
16 |
59,380,458 (GRCm39) |
unclassified |
probably benign |
|
R4427:Crybg3
|
UTSW |
16 |
59,363,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Crybg3
|
UTSW |
16 |
59,350,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Crybg3
|
UTSW |
16 |
59,350,782 (GRCm39) |
missense |
probably benign |
0.14 |
R5007:Crybg3
|
UTSW |
16 |
59,378,463 (GRCm39) |
unclassified |
probably benign |
|
R5020:Crybg3
|
UTSW |
16 |
59,375,159 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5155:Crybg3
|
UTSW |
16 |
59,345,264 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5306:Crybg3
|
UTSW |
16 |
59,380,356 (GRCm39) |
unclassified |
probably benign |
|
R5342:Crybg3
|
UTSW |
16 |
59,342,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Crybg3
|
UTSW |
16 |
59,379,529 (GRCm39) |
missense |
probably benign |
0.00 |
R5763:Crybg3
|
UTSW |
16 |
59,374,973 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5860:Crybg3
|
UTSW |
16 |
59,385,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Crybg3
|
UTSW |
16 |
59,313,934 (GRCm39) |
unclassified |
probably benign |
|
R6007:Crybg3
|
UTSW |
16 |
59,374,837 (GRCm39) |
nonsense |
probably null |
|
R6042:Crybg3
|
UTSW |
16 |
59,370,838 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6049:Crybg3
|
UTSW |
16 |
59,364,417 (GRCm39) |
missense |
probably benign |
0.00 |
R6242:Crybg3
|
UTSW |
16 |
59,376,053 (GRCm39) |
missense |
probably benign |
|
R6301:Crybg3
|
UTSW |
16 |
59,350,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R6408:Crybg3
|
UTSW |
16 |
59,316,053 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6724:Crybg3
|
UTSW |
16 |
59,364,501 (GRCm39) |
missense |
probably benign |
0.13 |
R6745:Crybg3
|
UTSW |
16 |
59,372,607 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6777:Crybg3
|
UTSW |
16 |
59,378,678 (GRCm39) |
unclassified |
probably benign |
|
R6843:Crybg3
|
UTSW |
16 |
59,380,159 (GRCm39) |
missense |
probably benign |
0.22 |
R6914:Crybg3
|
UTSW |
16 |
59,360,183 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6942:Crybg3
|
UTSW |
16 |
59,360,183 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7033:Crybg3
|
UTSW |
16 |
59,374,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R7091:Crybg3
|
UTSW |
16 |
59,377,531 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7133:Crybg3
|
UTSW |
16 |
59,357,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Crybg3
|
UTSW |
16 |
59,379,956 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7204:Crybg3
|
UTSW |
16 |
59,379,253 (GRCm39) |
missense |
probably benign |
0.00 |
R7398:Crybg3
|
UTSW |
16 |
59,377,688 (GRCm39) |
missense |
probably benign |
0.38 |
R7666:Crybg3
|
UTSW |
16 |
59,379,700 (GRCm39) |
nonsense |
probably null |
|
R7691:Crybg3
|
UTSW |
16 |
59,376,497 (GRCm39) |
missense |
not run |
|
R7714:Crybg3
|
UTSW |
16 |
59,379,236 (GRCm39) |
missense |
probably benign |
0.19 |
R7860:Crybg3
|
UTSW |
16 |
59,375,605 (GRCm39) |
missense |
probably benign |
0.04 |
R7901:Crybg3
|
UTSW |
16 |
59,377,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R8371:Crybg3
|
UTSW |
16 |
59,377,414 (GRCm39) |
missense |
probably benign |
0.00 |
R8394:Crybg3
|
UTSW |
16 |
59,378,651 (GRCm39) |
missense |
probably benign |
0.06 |
R8438:Crybg3
|
UTSW |
16 |
59,385,655 (GRCm39) |
missense |
probably benign |
0.02 |
R8529:Crybg3
|
UTSW |
16 |
59,376,984 (GRCm39) |
missense |
probably damaging |
0.98 |
R8699:Crybg3
|
UTSW |
16 |
59,375,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R8766:Crybg3
|
UTSW |
16 |
59,375,696 (GRCm39) |
missense |
probably benign |
0.05 |
R8767:Crybg3
|
UTSW |
16 |
59,376,500 (GRCm39) |
missense |
probably benign |
|
R8789:Crybg3
|
UTSW |
16 |
59,375,359 (GRCm39) |
missense |
probably benign |
0.00 |
R8871:Crybg3
|
UTSW |
16 |
59,378,519 (GRCm39) |
missense |
probably benign |
|
R8878:Crybg3
|
UTSW |
16 |
59,380,547 (GRCm39) |
missense |
probably benign |
0.09 |
R8894:Crybg3
|
UTSW |
16 |
59,342,552 (GRCm39) |
missense |
probably damaging |
0.97 |
R8928:Crybg3
|
UTSW |
16 |
59,376,715 (GRCm39) |
missense |
probably benign |
0.40 |
R8928:Crybg3
|
UTSW |
16 |
59,315,123 (GRCm39) |
missense |
probably benign |
0.31 |
R8939:Crybg3
|
UTSW |
16 |
59,376,512 (GRCm39) |
missense |
probably benign |
0.00 |
R9010:Crybg3
|
UTSW |
16 |
59,374,702 (GRCm39) |
missense |
probably damaging |
0.98 |
R9266:Crybg3
|
UTSW |
16 |
59,372,544 (GRCm39) |
missense |
probably damaging |
0.99 |
R9348:Crybg3
|
UTSW |
16 |
59,421,256 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
R9353:Crybg3
|
UTSW |
16 |
59,421,107 (GRCm39) |
critical splice donor site |
probably null |
|
R9406:Crybg3
|
UTSW |
16 |
59,378,839 (GRCm39) |
missense |
probably benign |
0.42 |
R9429:Crybg3
|
UTSW |
16 |
59,375,556 (GRCm39) |
missense |
probably benign |
0.08 |
R9464:Crybg3
|
UTSW |
16 |
59,376,120 (GRCm39) |
unclassified |
probably benign |
|
R9621:Crybg3
|
UTSW |
16 |
59,326,613 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9703:Crybg3
|
UTSW |
16 |
59,375,939 (GRCm39) |
missense |
probably damaging |
0.96 |
R9751:Crybg3
|
UTSW |
16 |
59,377,887 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9766:Crybg3
|
UTSW |
16 |
59,376,207 (GRCm39) |
missense |
probably benign |
0.03 |
RF007:Crybg3
|
UTSW |
16 |
59,377,067 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Crybg3
|
UTSW |
16 |
59,376,841 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:Crybg3
|
UTSW |
16 |
59,375,756 (GRCm39) |
nonsense |
probably null |
|
Z1187:Crybg3
|
UTSW |
16 |
59,326,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGACCTTGCAACTCTTCTGTAG -3'
(R):5'- ATCCGTGCTATACTGTGAGCATG -3'
Sequencing Primer
(F):5'- TGCAACTCTTCTGTAGTTTTTAAGG -3'
(R):5'- CCGTGCTATACTGTGAGCATGTTAAG -3'
|
Posted On |
2015-10-21 |