Incidental Mutation 'R2151:Gpr158'
| ID |
234233 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Gpr158
|
| Ensembl Gene |
ENSMUSG00000045967 |
| Gene Name |
G protein-coupled receptor 158 |
| Synonyms |
5330427M13Rik |
| MMRRC Submission |
040154-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R2151 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
21372378-21835355 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 21832325 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Methionine
at position 1142
(V1142M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049708
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055946]
|
| AlphaFold |
Q8C419 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000055946
AA Change: V1142M
PolyPhen 2
Score 0.822 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000049708
Gene: ENSMUSG00000045967
AA Change: V1142M
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
low complexity region
|
110 |
125 |
N/A |
INTRINSIC |
|
SCOP:d1edmb_
|
313 |
359 |
5e-4 |
SMART |
|
Blast:EGF
|
318 |
365 |
2e-27 |
BLAST |
|
Pfam:7tm_3
|
426 |
669 |
1.2e-35 |
PFAM |
|
low complexity region
|
840 |
863 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.5%
- 20x: 95.8%
|
| Validation Efficiency |
100% (91/91) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930447C04Rik |
T |
C |
12: 72,954,725 (GRCm39) |
|
probably null |
Het |
| 4930579F01Rik |
A |
G |
3: 137,882,217 (GRCm39) |
|
probably null |
Het |
| Abhd17c |
G |
T |
7: 83,800,663 (GRCm39) |
H130Q |
probably damaging |
Het |
| Actr10 |
T |
A |
12: 70,987,575 (GRCm39) |
C27* |
probably null |
Het |
| Als2 |
G |
A |
1: 59,246,948 (GRCm39) |
H564Y |
probably damaging |
Het |
| Anxa2r1 |
C |
T |
13: 120,496,335 (GRCm39) |
C178Y |
unknown |
Het |
| Art5 |
A |
G |
7: 101,747,407 (GRCm39) |
L124P |
possibly damaging |
Het |
| Asap2 |
A |
T |
12: 21,162,084 (GRCm39) |
T14S |
probably damaging |
Het |
| Atp2c2 |
A |
G |
8: 120,482,841 (GRCm39) |
N901S |
probably benign |
Het |
| Bicd2 |
G |
T |
13: 49,533,052 (GRCm39) |
C546F |
probably damaging |
Het |
| Ccn3 |
G |
A |
15: 54,615,854 (GRCm39) |
A340T |
probably benign |
Het |
| Cnbp |
C |
T |
6: 87,822,281 (GRCm39) |
G81D |
probably damaging |
Het |
| Dnah5 |
T |
C |
15: 28,444,237 (GRCm39) |
Y4012H |
probably damaging |
Het |
| Dok5 |
G |
A |
2: 170,642,816 (GRCm39) |
G38D |
probably damaging |
Het |
| Drc3 |
A |
T |
11: 60,265,983 (GRCm39) |
E224V |
probably benign |
Het |
| Ehd2 |
T |
C |
7: 15,686,128 (GRCm39) |
K315E |
probably damaging |
Het |
| Eif6 |
A |
T |
2: 155,664,810 (GRCm39) |
N225K |
probably benign |
Het |
| Epg5 |
T |
C |
18: 78,070,517 (GRCm39) |
V2264A |
probably benign |
Het |
| Faf2 |
T |
C |
13: 54,796,220 (GRCm39) |
F126L |
probably damaging |
Het |
| Fiz1 |
T |
C |
7: 5,015,880 (GRCm39) |
S37G |
possibly damaging |
Het |
| Frs3 |
T |
C |
17: 48,013,987 (GRCm39) |
S227P |
probably benign |
Het |
| Garin3 |
A |
T |
11: 46,296,158 (GRCm39) |
K177* |
probably null |
Het |
| Gm4787 |
T |
A |
12: 81,423,993 (GRCm39) |
I722F |
probably benign |
Het |
| Gm6370 |
T |
A |
5: 146,430,451 (GRCm39) |
L212Q |
probably damaging |
Het |
| Gmnc |
G |
A |
16: 26,779,456 (GRCm39) |
H142Y |
possibly damaging |
Het |
| Gna15 |
T |
C |
10: 81,338,738 (GRCm39) |
Y367C |
probably damaging |
Het |
| Gpx6 |
A |
G |
13: 21,503,141 (GRCm39) |
K185R |
probably damaging |
Het |
| Hc |
A |
C |
2: 34,881,115 (GRCm39) |
|
probably benign |
Het |
| Hdac9 |
A |
G |
12: 34,440,255 (GRCm39) |
S375P |
probably damaging |
Het |
| Kat6b |
A |
T |
14: 21,718,735 (GRCm39) |
H1138L |
probably benign |
Het |
| Klre1 |
G |
A |
6: 129,556,996 (GRCm39) |
E33K |
possibly damaging |
Het |
| Ldhb |
C |
A |
6: 142,444,396 (GRCm39) |
V86L |
possibly damaging |
Het |
| Maco1 |
A |
G |
4: 134,538,534 (GRCm39) |
V470A |
probably benign |
Het |
| Magi3 |
T |
A |
3: 103,954,198 (GRCm39) |
K713I |
probably damaging |
Het |
| Magi3 |
T |
C |
3: 103,992,554 (GRCm39) |
Y306C |
probably damaging |
Het |
| Minar1 |
T |
G |
9: 89,484,221 (GRCm39) |
K392T |
possibly damaging |
Het |
| Mmp17 |
T |
C |
5: 129,682,725 (GRCm39) |
Y455H |
probably benign |
Het |
| Mmp25 |
T |
A |
17: 23,850,048 (GRCm39) |
Y504F |
probably damaging |
Het |
| Myo1a |
T |
C |
10: 127,556,050 (GRCm39) |
I969T |
probably benign |
Het |
| Nedd4l |
T |
A |
18: 65,343,401 (GRCm39) |
H820Q |
probably damaging |
Het |
| Nf1 |
T |
A |
11: 79,338,396 (GRCm39) |
M1136K |
possibly damaging |
Het |
| Nmi |
T |
C |
2: 51,842,555 (GRCm39) |
E179G |
probably damaging |
Het |
| Nrros |
A |
T |
16: 31,962,076 (GRCm39) |
M611K |
probably benign |
Het |
| Nsd1 |
A |
T |
13: 55,439,049 (GRCm39) |
N1692I |
probably damaging |
Het |
| Nuak1 |
T |
C |
10: 84,245,509 (GRCm39) |
N112S |
probably benign |
Het |
| Odf2l |
T |
C |
3: 144,854,785 (GRCm39) |
Y488H |
possibly damaging |
Het |
| Or4c106 |
C |
A |
2: 88,683,128 (GRCm39) |
P278H |
probably damaging |
Het |
| Or8g21 |
T |
A |
9: 38,906,012 (GRCm39) |
T240S |
probably damaging |
Het |
| Or8g30 |
T |
A |
9: 39,230,413 (GRCm39) |
I166F |
probably damaging |
Het |
| Otop2 |
A |
G |
11: 115,220,237 (GRCm39) |
D359G |
possibly damaging |
Het |
| Pi4ka |
A |
T |
16: 17,185,371 (GRCm39) |
F243Y |
probably benign |
Het |
| Pnma8b |
T |
C |
7: 16,679,837 (GRCm39) |
C274R |
probably benign |
Het |
| Ppp1r42 |
A |
G |
1: 10,073,572 (GRCm39) |
V6A |
probably benign |
Het |
| Prrg4 |
A |
G |
2: 104,669,733 (GRCm39) |
L128S |
probably damaging |
Het |
| Prss33 |
C |
T |
17: 24,053,817 (GRCm39) |
V87M |
probably damaging |
Het |
| Psen2 |
A |
G |
1: 180,061,229 (GRCm39) |
V278A |
probably damaging |
Het |
| Ptpn13 |
C |
A |
5: 103,673,651 (GRCm39) |
T538K |
probably damaging |
Het |
| Pttg1ip2 |
C |
T |
5: 5,528,875 (GRCm39) |
V47I |
possibly damaging |
Het |
| Rad51ap2 |
A |
G |
12: 11,507,986 (GRCm39) |
H636R |
probably benign |
Het |
| Rbak |
A |
C |
5: 143,162,257 (GRCm39) |
D35E |
possibly damaging |
Het |
| Rbms1 |
C |
A |
2: 60,592,392 (GRCm39) |
|
probably null |
Het |
| Rgs7bp |
T |
A |
13: 105,100,597 (GRCm39) |
N226I |
probably damaging |
Het |
| Rnf182 |
T |
A |
13: 43,821,899 (GRCm39) |
V150E |
probably benign |
Het |
| Sacs |
A |
G |
14: 61,447,089 (GRCm39) |
Y3045C |
probably damaging |
Het |
| Scp2 |
G |
T |
4: 107,921,141 (GRCm39) |
A23E |
probably benign |
Het |
| Sec16a |
A |
T |
2: 26,303,757 (GRCm39) |
|
probably benign |
Het |
| Slc30a5 |
A |
T |
13: 100,940,457 (GRCm39) |
H619Q |
probably damaging |
Het |
| Slfn10-ps |
T |
A |
11: 82,926,511 (GRCm39) |
|
noncoding transcript |
Het |
| Slmap |
A |
G |
14: 26,139,402 (GRCm39) |
Y771H |
probably damaging |
Het |
| Slx |
T |
A |
X: 26,489,689 (GRCm39) |
|
probably benign |
Het |
| Spns3 |
C |
A |
11: 72,436,787 (GRCm39) |
|
probably benign |
Het |
| Stxbp1 |
T |
A |
2: 32,692,868 (GRCm39) |
I383F |
probably damaging |
Het |
| Taf3 |
C |
T |
2: 9,956,377 (GRCm39) |
E597K |
possibly damaging |
Het |
| Tbcd |
A |
G |
11: 121,494,457 (GRCm39) |
Q1006R |
possibly damaging |
Het |
| Tenm4 |
G |
T |
7: 96,552,054 (GRCm39) |
V2498F |
probably damaging |
Het |
| Tex2 |
T |
C |
11: 106,458,161 (GRCm39) |
|
probably benign |
Het |
| Tkfc |
A |
T |
19: 10,576,421 (GRCm39) |
L154Q |
probably damaging |
Het |
| Tmem62 |
A |
G |
2: 120,817,343 (GRCm39) |
H257R |
probably damaging |
Het |
| Trpm2 |
T |
C |
10: 77,768,013 (GRCm39) |
I829V |
probably benign |
Het |
| Ttc38 |
A |
G |
15: 85,735,802 (GRCm39) |
|
probably null |
Het |
| Ttn |
A |
T |
2: 76,548,757 (GRCm39) |
Y30135* |
probably null |
Het |
| Ttn |
A |
G |
2: 76,810,477 (GRCm39) |
V17A |
probably benign |
Het |
| Ubqlnl |
A |
T |
7: 103,797,890 (GRCm39) |
C536S |
probably benign |
Het |
| Vmn1r230 |
T |
A |
17: 21,067,063 (GRCm39) |
M84K |
probably damaging |
Het |
| Vmn1r235 |
G |
A |
17: 21,482,628 (GRCm39) |
V318I |
probably benign |
Het |
| Vmn2r76 |
T |
C |
7: 85,879,692 (GRCm39) |
I203V |
probably benign |
Het |
| Vmn2r97 |
A |
T |
17: 19,167,584 (GRCm39) |
R613* |
probably null |
Het |
| Zfp180 |
A |
G |
7: 23,804,685 (GRCm39) |
H368R |
probably damaging |
Het |
| Zfp407 |
T |
C |
18: 84,227,774 (GRCm39) |
D1945G |
possibly damaging |
Het |
| Zfyve27 |
G |
T |
19: 42,160,170 (GRCm39) |
R62L |
probably benign |
Het |
|
| Other mutations in Gpr158 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00340:Gpr158
|
APN |
2 |
21,373,494 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00469:Gpr158
|
APN |
2 |
21,751,606 (GRCm39) |
splice site |
probably benign |
|
|
IGL00706:Gpr158
|
APN |
2 |
21,751,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00780:Gpr158
|
APN |
2 |
21,831,629 (GRCm39) |
nonsense |
probably null |
|
|
IGL00885:Gpr158
|
APN |
2 |
21,653,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01339:Gpr158
|
APN |
2 |
21,373,842 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL01368:Gpr158
|
APN |
2 |
21,831,909 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02141:Gpr158
|
APN |
2 |
21,788,101 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02455:Gpr158
|
APN |
2 |
21,373,511 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02554:Gpr158
|
APN |
2 |
21,831,407 (GRCm39) |
missense |
probably benign |
|
|
IGL02681:Gpr158
|
APN |
2 |
21,820,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02752:Gpr158
|
APN |
2 |
21,831,638 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02756:Gpr158
|
APN |
2 |
21,831,890 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
IGL03181:Gpr158
|
APN |
2 |
21,787,972 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03258:Gpr158
|
APN |
2 |
21,830,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03386:Gpr158
|
APN |
2 |
21,831,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4810001:Gpr158
|
UTSW |
2 |
21,831,682 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0071:Gpr158
|
UTSW |
2 |
21,815,479 (GRCm39) |
missense |
probably benign |
0.08 |
|
R0081:Gpr158
|
UTSW |
2 |
21,831,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0528:Gpr158
|
UTSW |
2 |
21,830,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0560:Gpr158
|
UTSW |
2 |
21,830,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0603:Gpr158
|
UTSW |
2 |
21,820,480 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R1560:Gpr158
|
UTSW |
2 |
21,831,125 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1561:Gpr158
|
UTSW |
2 |
21,820,505 (GRCm39) |
splice site |
probably null |
|
|
R1609:Gpr158
|
UTSW |
2 |
21,788,104 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1741:Gpr158
|
UTSW |
2 |
21,832,359 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1827:Gpr158
|
UTSW |
2 |
21,832,129 (GRCm39) |
missense |
probably benign |
|
|
R1854:Gpr158
|
UTSW |
2 |
21,373,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1871:Gpr158
|
UTSW |
2 |
21,820,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2273:Gpr158
|
UTSW |
2 |
21,831,674 (GRCm39) |
missense |
probably benign |
|
|
R2275:Gpr158
|
UTSW |
2 |
21,831,674 (GRCm39) |
missense |
probably benign |
|
|
R3004:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3151:Gpr158
|
UTSW |
2 |
21,581,771 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R3943:Gpr158
|
UTSW |
2 |
21,373,370 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R4238:Gpr158
|
UTSW |
2 |
21,373,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4379:Gpr158
|
UTSW |
2 |
21,830,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4381:Gpr158
|
UTSW |
2 |
21,832,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4464:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4467:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4496:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4506:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4530:Gpr158
|
UTSW |
2 |
21,373,811 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4646:Gpr158
|
UTSW |
2 |
21,831,864 (GRCm39) |
missense |
probably benign |
|
|
R4798:Gpr158
|
UTSW |
2 |
21,787,993 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4882:Gpr158
|
UTSW |
2 |
21,830,059 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4943:Gpr158
|
UTSW |
2 |
21,831,968 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5334:Gpr158
|
UTSW |
2 |
21,832,316 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5560:Gpr158
|
UTSW |
2 |
21,831,101 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R5600:Gpr158
|
UTSW |
2 |
21,832,046 (GRCm39) |
missense |
probably benign |
|
|
R5637:Gpr158
|
UTSW |
2 |
21,788,083 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5701:Gpr158
|
UTSW |
2 |
21,751,520 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5744:Gpr158
|
UTSW |
2 |
21,373,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5911:Gpr158
|
UTSW |
2 |
21,373,932 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5991:Gpr158
|
UTSW |
2 |
21,373,319 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6200:Gpr158
|
UTSW |
2 |
21,404,227 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6306:Gpr158
|
UTSW |
2 |
21,820,422 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R6324:Gpr158
|
UTSW |
2 |
21,815,365 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6384:Gpr158
|
UTSW |
2 |
21,831,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6698:Gpr158
|
UTSW |
2 |
21,831,921 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6997:Gpr158
|
UTSW |
2 |
21,653,802 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7086:Gpr158
|
UTSW |
2 |
21,831,386 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7175:Gpr158
|
UTSW |
2 |
21,373,113 (GRCm39) |
missense |
probably benign |
0.13 |
|
R7197:Gpr158
|
UTSW |
2 |
21,815,412 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7293:Gpr158
|
UTSW |
2 |
21,581,750 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R7427:Gpr158
|
UTSW |
2 |
21,832,129 (GRCm39) |
missense |
probably benign |
|
|
R7515:Gpr158
|
UTSW |
2 |
21,373,092 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7730:Gpr158
|
UTSW |
2 |
21,831,158 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8122:Gpr158
|
UTSW |
2 |
21,831,674 (GRCm39) |
missense |
probably benign |
|
|
R8311:Gpr158
|
UTSW |
2 |
21,373,701 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8754:Gpr158
|
UTSW |
2 |
21,581,693 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8782:Gpr158
|
UTSW |
2 |
21,404,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8792:Gpr158
|
UTSW |
2 |
21,558,137 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8842:Gpr158
|
UTSW |
2 |
21,581,751 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9009:Gpr158
|
UTSW |
2 |
21,581,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9102:Gpr158
|
UTSW |
2 |
21,830,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9150:Gpr158
|
UTSW |
2 |
21,831,251 (GRCm39) |
missense |
probably benign |
0.17 |
|
R9254:Gpr158
|
UTSW |
2 |
21,373,042 (GRCm39) |
start gained |
probably benign |
|
|
R9317:Gpr158
|
UTSW |
2 |
21,832,037 (GRCm39) |
missense |
probably benign |
|
|
R9379:Gpr158
|
UTSW |
2 |
21,373,042 (GRCm39) |
start gained |
probably benign |
|
|
R9428:Gpr158
|
UTSW |
2 |
21,787,972 (GRCm39) |
missense |
probably benign |
|
|
R9497:Gpr158
|
UTSW |
2 |
21,831,825 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9667:Gpr158
|
UTSW |
2 |
21,830,054 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9681:Gpr158
|
UTSW |
2 |
21,831,315 (GRCm39) |
missense |
probably damaging |
0.99 |
|
X0062:Gpr158
|
UTSW |
2 |
21,831,180 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Gpr158
|
UTSW |
2 |
21,815,501 (GRCm39) |
critical splice donor site |
probably null |
|
|
Z1177:Gpr158
|
UTSW |
2 |
21,832,083 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCCACAGTCAGTCCCTTTTAGAAG -3'
(R):5'- AGACTTCCTATTTCTGAGGCCC -3'
Sequencing Primer
(F):5'- CAGTCAGTCCCTTTTAGAAGATGAG -3'
(R):5'- GAGGCCCTGGTATCTTATTTGCAC -3'
|
| Posted On |
2014-10-01 |
Incidental Mutation