Incidental Mutation 'R6306:Gpr158'
| ID |
509637 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Gpr158
|
| Ensembl Gene |
ENSMUSG00000045967 |
| Gene Name |
G protein-coupled receptor 158 |
| Synonyms |
5330427M13Rik |
| MMRRC Submission |
044468-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R6306 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
21372378-21835355 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to G
at 21820422 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Alanine
at position 640
(P640A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049708
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055946]
|
| AlphaFold |
Q8C419 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000055946
AA Change: P640A
PolyPhen 2
Score 0.839 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000049708
Gene: ENSMUSG00000045967
AA Change: P640A
| 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 |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155760
|
| Meta Mutation Damage Score |
0.1712 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.4%
|
| Validation Efficiency |
100% (88/88) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts7 |
G |
A |
9: 90,060,331 (GRCm39) |
|
probably null |
Het |
| Adora2a |
T |
A |
10: 75,169,238 (GRCm39) |
V234E |
probably damaging |
Het |
| Alpk1 |
T |
C |
3: 127,479,965 (GRCm39) |
D188G |
probably damaging |
Het |
| Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
| Ankrd17 |
A |
G |
5: 90,392,013 (GRCm39) |
F1886L |
probably benign |
Het |
| Anks1 |
T |
G |
17: 28,269,613 (GRCm39) |
L769R |
probably damaging |
Het |
| Apol10a |
A |
G |
15: 77,373,161 (GRCm39) |
I266V |
probably benign |
Het |
| Arhgef28 |
T |
C |
13: 98,121,896 (GRCm39) |
Y556C |
probably damaging |
Het |
| Brd8 |
T |
A |
18: 34,744,304 (GRCm39) |
T175S |
probably damaging |
Het |
| Camsap2 |
C |
T |
1: 136,208,937 (GRCm39) |
V852I |
probably benign |
Het |
| Cd55b |
G |
T |
1: 130,341,803 (GRCm39) |
P278Q |
probably damaging |
Het |
| Cep290 |
T |
A |
10: 100,367,028 (GRCm39) |
S1126R |
possibly damaging |
Het |
| Cfh |
C |
T |
1: 140,030,155 (GRCm39) |
C906Y |
probably damaging |
Het |
| Chst13 |
C |
A |
6: 90,286,260 (GRCm39) |
R234L |
probably damaging |
Het |
| Clcn7 |
T |
C |
17: 25,376,502 (GRCm39) |
F611L |
probably benign |
Het |
| Cntnap1 |
A |
G |
11: 101,075,441 (GRCm39) |
D873G |
probably damaging |
Het |
| Cntnap5b |
T |
C |
1: 100,091,871 (GRCm39) |
I518T |
probably damaging |
Het |
| Col28a1 |
T |
C |
6: 8,014,969 (GRCm39) |
E812G |
probably damaging |
Het |
| Cpa1 |
T |
C |
6: 30,640,953 (GRCm39) |
I148T |
probably damaging |
Het |
| Cyp11a1 |
A |
G |
9: 57,932,383 (GRCm39) |
N232S |
probably benign |
Het |
| Dhrs13 |
A |
G |
11: 77,923,519 (GRCm39) |
D79G |
probably damaging |
Het |
| Disp1 |
T |
C |
1: 182,868,712 (GRCm39) |
E1236G |
possibly damaging |
Het |
| Dnah1 |
A |
C |
14: 31,026,544 (GRCm39) |
L778R |
probably damaging |
Het |
| Dnah14 |
CTGTG |
CTG |
1: 181,412,589 (GRCm39) |
|
probably null |
Het |
| Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
| Dock9 |
A |
T |
14: 121,799,492 (GRCm39) |
I1729N |
probably damaging |
Het |
| Dysf |
T |
C |
6: 84,114,248 (GRCm39) |
V1192A |
possibly damaging |
Het |
| Enpp2 |
A |
G |
15: 54,762,742 (GRCm39) |
S169P |
probably damaging |
Het |
| Fam114a2 |
T |
G |
11: 57,404,972 (GRCm39) |
R43S |
probably damaging |
Het |
| Fam13a |
T |
C |
6: 58,917,239 (GRCm39) |
T546A |
probably benign |
Het |
| Fos |
A |
T |
12: 85,522,460 (GRCm39) |
D163V |
probably damaging |
Het |
| Fras1 |
T |
C |
5: 96,912,805 (GRCm39) |
Y3370H |
probably damaging |
Het |
| Fshr |
T |
C |
17: 89,507,961 (GRCm39) |
N27S |
probably null |
Het |
| Galnt6 |
A |
G |
15: 100,591,305 (GRCm39) |
S600P |
possibly damaging |
Het |
| Gars1 |
T |
A |
6: 55,032,809 (GRCm39) |
N260K |
probably damaging |
Het |
| Grep1 |
T |
C |
17: 23,925,124 (GRCm39) |
N495S |
possibly damaging |
Het |
| Grik3 |
A |
G |
4: 125,526,205 (GRCm39) |
D146G |
probably benign |
Het |
| Hdac4 |
T |
C |
1: 91,923,896 (GRCm39) |
T205A |
probably benign |
Het |
| Kcnq3 |
T |
C |
15: 65,876,643 (GRCm39) |
D500G |
probably benign |
Het |
| Kmt5c |
A |
G |
7: 4,749,480 (GRCm39) |
K333E |
probably benign |
Het |
| Krt81 |
A |
G |
15: 101,357,404 (GRCm39) |
S443P |
probably benign |
Het |
| M6pr |
T |
C |
6: 122,292,121 (GRCm39) |
|
probably null |
Het |
| Mccc2 |
T |
A |
13: 100,130,085 (GRCm39) |
I91L |
probably benign |
Het |
| Nip7 |
A |
G |
8: 107,785,055 (GRCm39) |
D110G |
probably damaging |
Het |
| Nol8 |
T |
A |
13: 49,829,829 (GRCm39) |
F1093I |
probably damaging |
Het |
| Nrxn1 |
T |
C |
17: 90,872,874 (GRCm39) |
T1027A |
possibly damaging |
Het |
| Ofcc1 |
T |
A |
13: 40,302,052 (GRCm39) |
M495L |
probably benign |
Het |
| Or13p10 |
A |
T |
4: 118,523,490 (GRCm39) |
M259L |
probably benign |
Het |
| Or7e178 |
A |
G |
9: 20,225,742 (GRCm39) |
M158T |
probably benign |
Het |
| Pafah1b2 |
A |
T |
9: 45,886,425 (GRCm39) |
V81D |
probably damaging |
Het |
| Pcdhga4 |
A |
T |
18: 37,818,966 (GRCm39) |
S172C |
probably damaging |
Het |
| Pds5a |
A |
G |
5: 65,813,639 (GRCm39) |
V282A |
probably damaging |
Het |
| Plat |
A |
G |
8: 23,262,282 (GRCm39) |
D102G |
possibly damaging |
Het |
| Plce1 |
C |
A |
19: 38,757,909 (GRCm39) |
Q1961K |
probably damaging |
Het |
| Plppr3 |
T |
A |
10: 79,697,566 (GRCm39) |
K444* |
probably null |
Het |
| Plscr3 |
A |
G |
11: 69,738,472 (GRCm39) |
|
probably null |
Het |
| Prtg |
A |
T |
9: 72,813,468 (GRCm39) |
T943S |
probably benign |
Het |
| Racgap1 |
A |
G |
15: 99,521,834 (GRCm39) |
F519L |
probably benign |
Het |
| Rbms2 |
A |
T |
10: 127,987,050 (GRCm39) |
|
probably null |
Het |
| Rfx7 |
A |
G |
9: 72,524,237 (GRCm39) |
T476A |
possibly damaging |
Het |
| Rnf150 |
T |
A |
8: 83,810,131 (GRCm39) |
L421Q |
possibly damaging |
Het |
| Sema3b |
A |
G |
9: 107,478,119 (GRCm39) |
L422P |
possibly damaging |
Het |
| Shank2 |
G |
A |
7: 143,963,417 (GRCm39) |
A921T |
probably benign |
Het |
| Skint3 |
A |
T |
4: 112,113,072 (GRCm39) |
E227D |
probably damaging |
Het |
| Slc25a19 |
G |
A |
11: 115,508,386 (GRCm39) |
R201C |
possibly damaging |
Het |
| Slc38a10 |
G |
T |
11: 120,038,645 (GRCm39) |
A40D |
probably damaging |
Het |
| Slc5a4b |
T |
C |
10: 75,917,185 (GRCm39) |
T284A |
probably benign |
Het |
| Smc1b |
A |
T |
15: 85,011,824 (GRCm39) |
F154I |
probably benign |
Het |
| Spry2 |
A |
T |
14: 106,130,418 (GRCm39) |
M256K |
possibly damaging |
Het |
| Stkld1 |
C |
T |
2: 26,833,899 (GRCm39) |
P129S |
probably damaging |
Het |
| Syce2 |
T |
C |
8: 85,599,371 (GRCm39) |
L13S |
possibly damaging |
Het |
| Tbc1d15 |
C |
A |
10: 115,069,148 (GRCm39) |
V74L |
possibly damaging |
Het |
| Tecpr2 |
T |
A |
12: 110,911,185 (GRCm39) |
V1074D |
probably damaging |
Het |
| Tex36 |
G |
A |
7: 133,197,054 (GRCm39) |
T21I |
probably benign |
Het |
| Ttn |
T |
G |
2: 76,554,454 (GRCm39) |
D30787A |
probably damaging |
Het |
| Ttn |
T |
A |
2: 76,622,264 (GRCm39) |
Q13710L |
probably benign |
Het |
| Usp34 |
T |
C |
11: 23,362,260 (GRCm39) |
F1569L |
possibly damaging |
Het |
| Vat1l |
C |
T |
8: 115,098,391 (GRCm39) |
A387V |
probably damaging |
Het |
| Vil1 |
G |
A |
1: 74,460,470 (GRCm39) |
G209D |
possibly damaging |
Het |
| Vmn1r113 |
G |
T |
7: 20,521,792 (GRCm39) |
D195Y |
probably damaging |
Het |
| Vmn2r69 |
A |
C |
7: 85,064,799 (GRCm39) |
I29R |
probably benign |
Het |
| Vti1b |
G |
A |
12: 79,207,323 (GRCm39) |
Q76* |
probably null |
Het |
| Zfp423 |
C |
A |
8: 88,508,662 (GRCm39) |
V540F |
possibly damaging |
Het |
| Zfp644 |
T |
C |
5: 106,785,990 (GRCm39) |
N186D |
probably damaging |
Het |
| Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
| Zfp787 |
G |
A |
7: 6,135,360 (GRCm39) |
A297V |
probably damaging |
Het |
| Zfp827 |
G |
T |
8: 79,787,324 (GRCm39) |
Q163H |
probably damaging |
Het |
| Zfp955b |
T |
A |
17: 33,522,160 (GRCm39) |
V543E |
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 |
|
R2151:Gpr158
|
UTSW |
2 |
21,832,325 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
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 |
|
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'- TTACAGTCCTTCCAACCTAAAAGTC -3'
(R):5'- ACACTCGCTTTCTTGAGGAGG -3'
Sequencing Primer
(F):5'- GTCCTTCCAACCTAAAAGTCATTTAC -3'
(R):5'- CAAATAATGGTGGAGCATCAAGC -3'
|
| Posted On |
2018-04-02 |
Incidental Mutation