Incidental Mutation 'R4627:Cep192'
ID |
348915 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cep192
|
Ensembl Gene |
ENSMUSG00000024542 |
Gene Name |
centrosomal protein 192 |
Synonyms |
D430014P18Rik, 4631422C13Rik |
MMRRC Submission |
041892-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4627 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
18 |
Chromosomal Location |
67933177-68018241 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to G
at 67945440 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Arginine
at position 180
(P180R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000025425
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025425]
|
AlphaFold |
E9Q4Y4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000025425
AA Change: P180R
PolyPhen 2
Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000025425 Gene: ENSMUSG00000024542 AA Change: P180R
Domain | Start | End | E-Value | Type |
low complexity region
|
70 |
84 |
N/A |
INTRINSIC |
low complexity region
|
195 |
217 |
N/A |
INTRINSIC |
low complexity region
|
975 |
991 |
N/A |
INTRINSIC |
low complexity region
|
1189 |
1204 |
N/A |
INTRINSIC |
low complexity region
|
2051 |
2069 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225077
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 95.4%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6a |
A |
T |
12: 113,508,569 (GRCm39) |
D314V |
probably benign |
Het |
Adamts18 |
C |
T |
8: 114,499,800 (GRCm39) |
W371* |
probably null |
Het |
Adamtsl2 |
T |
A |
2: 26,983,597 (GRCm39) |
L331Q |
probably damaging |
Het |
Akr1c13 |
G |
T |
13: 4,247,869 (GRCm39) |
V214F |
probably damaging |
Het |
Aldoart1 |
T |
C |
4: 72,770,680 (GRCm39) |
T43A |
probably benign |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Ano7 |
T |
C |
1: 93,302,907 (GRCm39) |
I15T |
probably benign |
Het |
Aopep |
T |
C |
13: 63,215,906 (GRCm39) |
S393P |
probably benign |
Het |
Aox3 |
A |
T |
1: 58,164,194 (GRCm39) |
T155S |
probably damaging |
Het |
Ap2a1 |
C |
T |
7: 44,553,843 (GRCm39) |
V535M |
probably damaging |
Het |
Apbb2 |
C |
T |
5: 66,557,419 (GRCm39) |
|
probably null |
Het |
Astn1 |
C |
A |
1: 158,329,821 (GRCm39) |
H225Q |
possibly damaging |
Het |
Atm |
A |
G |
9: 53,367,806 (GRCm39) |
I2439T |
possibly damaging |
Het |
Atp1b2 |
T |
A |
11: 69,492,160 (GRCm39) |
I263F |
probably damaging |
Het |
Ccdc184 |
A |
T |
15: 98,066,638 (GRCm39) |
N148Y |
probably benign |
Het |
Cdca7 |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGA |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAGA |
2: 72,312,205 (GRCm39) |
|
probably benign |
Het |
Cfap46 |
T |
C |
7: 139,237,197 (GRCm39) |
Y571C |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,260,843 (GRCm39) |
L85Q |
probably damaging |
Het |
Chchd6 |
G |
A |
6: 89,361,642 (GRCm39) |
L226F |
probably damaging |
Het |
Cnot6l |
A |
G |
5: 96,225,070 (GRCm39) |
V541A |
probably benign |
Het |
Cobl |
T |
C |
11: 12,201,093 (GRCm39) |
E1214G |
probably damaging |
Het |
Cpsf2 |
G |
A |
12: 101,956,154 (GRCm39) |
R319Q |
probably benign |
Het |
Csdc2 |
T |
C |
15: 81,833,324 (GRCm39) |
V107A |
probably benign |
Het |
Csmd1 |
A |
G |
8: 16,747,933 (GRCm39) |
W273R |
probably benign |
Het |
Dnah2 |
T |
A |
11: 69,356,202 (GRCm39) |
N2156I |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,352,617 (GRCm39) |
Y165C |
probably benign |
Het |
Exoc1 |
T |
C |
5: 76,690,075 (GRCm39) |
V205A |
probably benign |
Het |
Fam98c |
T |
C |
7: 28,854,693 (GRCm39) |
T49A |
possibly damaging |
Het |
Fbln2 |
G |
T |
6: 91,236,749 (GRCm39) |
V755L |
probably damaging |
Het |
Fhad1 |
A |
T |
4: 141,623,779 (GRCm39) |
V1371D |
possibly damaging |
Het |
Folh1 |
A |
T |
7: 86,422,460 (GRCm39) |
M59K |
probably benign |
Het |
Foxf2 |
A |
T |
13: 31,810,871 (GRCm39) |
H270L |
probably benign |
Het |
Gm14401 |
G |
A |
2: 176,778,109 (GRCm39) |
R65H |
probably benign |
Het |
Gpn1 |
C |
A |
5: 31,655,737 (GRCm39) |
Y592* |
probably null |
Het |
Hmcn1 |
T |
G |
1: 150,471,645 (GRCm39) |
D4903A |
probably benign |
Het |
Hnf1a |
T |
C |
5: 115,093,930 (GRCm39) |
R220G |
probably damaging |
Het |
Hoxd10 |
G |
A |
2: 74,522,636 (GRCm39) |
A105T |
probably benign |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Kidins220 |
C |
T |
12: 25,107,041 (GRCm39) |
T1498I |
possibly damaging |
Het |
Klhl2 |
G |
T |
8: 65,211,225 (GRCm39) |
Y274* |
probably null |
Het |
Lmbrd1 |
A |
G |
1: 24,745,080 (GRCm39) |
Y140C |
probably damaging |
Het |
Mapk8ip3 |
G |
A |
17: 25,122,267 (GRCm39) |
T706I |
probably benign |
Het |
Mast4 |
A |
C |
13: 103,470,529 (GRCm39) |
S58A |
possibly damaging |
Het |
Mcm6 |
T |
C |
1: 128,279,285 (GRCm39) |
D167G |
probably benign |
Het |
Mmachc |
A |
T |
4: 116,560,668 (GRCm39) |
S276T |
probably damaging |
Het |
Nfat5 |
A |
T |
8: 108,095,908 (GRCm39) |
Q1289L |
probably damaging |
Het |
Nlrc4 |
G |
T |
17: 74,753,623 (GRCm39) |
F253L |
probably damaging |
Het |
Nr1i3 |
C |
A |
1: 171,044,014 (GRCm39) |
A112E |
probably benign |
Het |
Or10ac1 |
T |
A |
6: 42,515,375 (GRCm39) |
T194S |
possibly damaging |
Het |
Or13a17 |
T |
A |
7: 140,271,291 (GRCm39) |
S158T |
probably benign |
Het |
Or2b28 |
T |
C |
13: 21,531,634 (GRCm39) |
F179L |
probably damaging |
Het |
Or7g33 |
G |
T |
9: 19,448,969 (GRCm39) |
Q86K |
possibly damaging |
Het |
Orc5 |
G |
T |
5: 22,753,003 (GRCm39) |
F10L |
probably benign |
Het |
Pde10a |
A |
C |
17: 9,200,484 (GRCm39) |
D779A |
probably damaging |
Het |
Pde4b |
T |
C |
4: 102,458,802 (GRCm39) |
L486S |
probably damaging |
Het |
Pex2 |
A |
T |
3: 5,626,341 (GRCm39) |
I156N |
probably damaging |
Het |
Phtf2 |
C |
T |
5: 20,978,738 (GRCm39) |
R63Q |
probably damaging |
Het |
Prag1 |
A |
G |
8: 36,570,446 (GRCm39) |
Y343C |
probably damaging |
Het |
Prdm16 |
A |
T |
4: 154,451,697 (GRCm39) |
Y170N |
probably damaging |
Het |
Prpf6 |
A |
C |
2: 181,243,267 (GRCm39) |
K5T |
probably damaging |
Het |
Ptpn1 |
A |
G |
2: 167,809,701 (GRCm39) |
K103R |
probably benign |
Het |
Ralgapa2 |
A |
G |
2: 146,203,373 (GRCm39) |
S1159P |
possibly damaging |
Het |
Rapgef3 |
G |
T |
15: 97,656,810 (GRCm39) |
D318E |
probably damaging |
Het |
Ripk4 |
A |
T |
16: 97,545,226 (GRCm39) |
S474T |
probably damaging |
Het |
Rmi1 |
A |
G |
13: 58,556,950 (GRCm39) |
R400G |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,319,405 (GRCm39) |
V1491A |
probably damaging |
Het |
Sec16a |
C |
T |
2: 26,321,080 (GRCm39) |
|
probably null |
Het |
Setd7 |
G |
T |
3: 51,450,086 (GRCm39) |
N113K |
probably damaging |
Het |
Shank2 |
C |
T |
7: 143,965,161 (GRCm39) |
T1502M |
probably damaging |
Het |
Skor1 |
A |
T |
9: 63,052,758 (GRCm39) |
C376S |
probably damaging |
Het |
Slc12a3 |
A |
T |
8: 95,056,012 (GRCm39) |
L49F |
probably benign |
Het |
Slc35d3 |
C |
T |
10: 19,725,077 (GRCm39) |
V260M |
probably damaging |
Het |
Slc46a1 |
T |
A |
11: 78,357,715 (GRCm39) |
V256E |
probably benign |
Het |
Slc6a1 |
T |
C |
6: 114,285,067 (GRCm39) |
S127P |
probably benign |
Het |
Syngr4 |
A |
G |
7: 45,536,452 (GRCm39) |
L190P |
probably damaging |
Het |
Tagap |
G |
A |
17: 8,145,773 (GRCm39) |
|
probably null |
Het |
Tamm41 |
A |
T |
6: 115,011,963 (GRCm39) |
N89K |
probably benign |
Het |
Tbc1d31 |
T |
A |
15: 57,831,308 (GRCm39) |
M922K |
probably benign |
Het |
Tbk1 |
T |
C |
10: 121,403,985 (GRCm39) |
N254S |
possibly damaging |
Het |
Tfec |
A |
G |
6: 16,840,478 (GRCm39) |
S140P |
probably damaging |
Het |
Tnrc18 |
T |
C |
5: 142,725,883 (GRCm39) |
E1802G |
unknown |
Het |
Tom1l2 |
C |
T |
11: 60,133,533 (GRCm39) |
|
probably null |
Het |
Tonsl |
T |
G |
15: 76,521,424 (GRCm39) |
K323Q |
probably damaging |
Het |
Tsnaxip1 |
A |
T |
8: 106,568,039 (GRCm39) |
E268D |
probably damaging |
Het |
Ttf1 |
C |
A |
2: 28,955,172 (GRCm39) |
H179N |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,556,517 (GRCm39) |
S30163G |
probably damaging |
Het |
Ube2c |
A |
G |
2: 164,614,093 (GRCm39) |
N143S |
possibly damaging |
Het |
Ugt1a10 |
G |
A |
1: 88,146,112 (GRCm39) |
R519Q |
probably damaging |
Het |
Utp25 |
T |
C |
1: 192,790,003 (GRCm39) |
T719A |
probably benign |
Het |
Vmn2r9 |
T |
C |
5: 108,995,463 (GRCm39) |
Y395C |
probably damaging |
Het |
Vwa8 |
G |
A |
14: 79,341,137 (GRCm39) |
|
probably null |
Het |
Zfp9 |
A |
G |
6: 118,441,937 (GRCm39) |
Y242H |
probably damaging |
Het |
|
Other mutations in Cep192 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Cep192
|
APN |
18 |
67,953,407 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00163:Cep192
|
APN |
18 |
68,013,871 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL00509:Cep192
|
APN |
18 |
67,991,939 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01012:Cep192
|
APN |
18 |
67,945,477 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01143:Cep192
|
APN |
18 |
67,937,445 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01302:Cep192
|
APN |
18 |
67,991,974 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01653:Cep192
|
APN |
18 |
67,986,043 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02202:Cep192
|
APN |
18 |
67,936,207 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02448:Cep192
|
APN |
18 |
68,002,518 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02494:Cep192
|
APN |
18 |
67,937,453 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02574:Cep192
|
APN |
18 |
67,974,350 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02624:Cep192
|
APN |
18 |
68,013,866 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02646:Cep192
|
APN |
18 |
67,995,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Cep192
|
APN |
18 |
67,991,921 (GRCm39) |
splice site |
probably benign |
|
IGL02684:Cep192
|
APN |
18 |
67,967,634 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02977:Cep192
|
APN |
18 |
67,985,976 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03000:Cep192
|
APN |
18 |
67,985,115 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03133:Cep192
|
APN |
18 |
67,943,176 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03139:Cep192
|
APN |
18 |
67,961,547 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03213:Cep192
|
APN |
18 |
67,998,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03250:Cep192
|
APN |
18 |
67,940,426 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03259:Cep192
|
APN |
18 |
67,953,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Cep192
|
UTSW |
18 |
67,983,808 (GRCm39) |
critical splice donor site |
probably null |
|
R0180:Cep192
|
UTSW |
18 |
67,968,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R0281:Cep192
|
UTSW |
18 |
67,961,553 (GRCm39) |
splice site |
probably benign |
|
R0374:Cep192
|
UTSW |
18 |
67,951,954 (GRCm39) |
nonsense |
probably null |
|
R0420:Cep192
|
UTSW |
18 |
67,946,964 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0479:Cep192
|
UTSW |
18 |
67,991,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Cep192
|
UTSW |
18 |
67,940,336 (GRCm39) |
missense |
probably benign |
0.04 |
R1024:Cep192
|
UTSW |
18 |
67,971,125 (GRCm39) |
missense |
probably benign |
0.37 |
R1382:Cep192
|
UTSW |
18 |
67,989,370 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1394:Cep192
|
UTSW |
18 |
67,991,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:Cep192
|
UTSW |
18 |
67,991,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R1641:Cep192
|
UTSW |
18 |
67,980,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1704:Cep192
|
UTSW |
18 |
67,989,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Cep192
|
UTSW |
18 |
67,984,838 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1835:Cep192
|
UTSW |
18 |
67,937,494 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1978:Cep192
|
UTSW |
18 |
67,936,228 (GRCm39) |
critical splice donor site |
probably null |
|
R2164:Cep192
|
UTSW |
18 |
67,953,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R2180:Cep192
|
UTSW |
18 |
67,957,813 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2307:Cep192
|
UTSW |
18 |
67,946,970 (GRCm39) |
missense |
probably benign |
0.07 |
R2442:Cep192
|
UTSW |
18 |
67,957,759 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2897:Cep192
|
UTSW |
18 |
67,988,341 (GRCm39) |
splice site |
probably null |
|
R2898:Cep192
|
UTSW |
18 |
67,988,341 (GRCm39) |
splice site |
probably null |
|
R2901:Cep192
|
UTSW |
18 |
68,002,512 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3433:Cep192
|
UTSW |
18 |
67,967,963 (GRCm39) |
missense |
probably benign |
0.08 |
R3620:Cep192
|
UTSW |
18 |
67,962,928 (GRCm39) |
missense |
probably benign |
0.00 |
R3621:Cep192
|
UTSW |
18 |
67,962,928 (GRCm39) |
missense |
probably benign |
0.00 |
R3712:Cep192
|
UTSW |
18 |
67,953,400 (GRCm39) |
missense |
probably benign |
0.00 |
R4559:Cep192
|
UTSW |
18 |
68,004,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Cep192
|
UTSW |
18 |
67,949,862 (GRCm39) |
nonsense |
probably null |
|
R4591:Cep192
|
UTSW |
18 |
67,968,039 (GRCm39) |
missense |
probably damaging |
0.99 |
R4604:Cep192
|
UTSW |
18 |
67,948,993 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4725:Cep192
|
UTSW |
18 |
67,949,837 (GRCm39) |
missense |
probably benign |
|
R4738:Cep192
|
UTSW |
18 |
68,017,901 (GRCm39) |
nonsense |
probably null |
|
R4739:Cep192
|
UTSW |
18 |
67,984,803 (GRCm39) |
missense |
probably benign |
0.02 |
R4927:Cep192
|
UTSW |
18 |
67,968,195 (GRCm39) |
missense |
probably benign |
0.16 |
R4948:Cep192
|
UTSW |
18 |
67,949,875 (GRCm39) |
missense |
probably benign |
0.00 |
R5090:Cep192
|
UTSW |
18 |
67,993,617 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5105:Cep192
|
UTSW |
18 |
67,999,612 (GRCm39) |
missense |
probably benign |
0.08 |
R5154:Cep192
|
UTSW |
18 |
67,983,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5192:Cep192
|
UTSW |
18 |
67,968,075 (GRCm39) |
missense |
probably benign |
0.03 |
R5735:Cep192
|
UTSW |
18 |
68,013,866 (GRCm39) |
missense |
probably benign |
0.20 |
R5812:Cep192
|
UTSW |
18 |
67,984,808 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5869:Cep192
|
UTSW |
18 |
67,948,935 (GRCm39) |
missense |
probably benign |
0.01 |
R5981:Cep192
|
UTSW |
18 |
67,993,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Cep192
|
UTSW |
18 |
67,971,068 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6335:Cep192
|
UTSW |
18 |
67,967,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:Cep192
|
UTSW |
18 |
67,945,506 (GRCm39) |
missense |
probably benign |
0.00 |
R6861:Cep192
|
UTSW |
18 |
67,974,699 (GRCm39) |
missense |
probably benign |
0.43 |
R7192:Cep192
|
UTSW |
18 |
67,983,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R7264:Cep192
|
UTSW |
18 |
67,953,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R7397:Cep192
|
UTSW |
18 |
67,989,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Cep192
|
UTSW |
18 |
67,967,874 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7696:Cep192
|
UTSW |
18 |
67,953,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R7756:Cep192
|
UTSW |
18 |
67,989,384 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7758:Cep192
|
UTSW |
18 |
67,989,384 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8247:Cep192
|
UTSW |
18 |
67,974,188 (GRCm39) |
missense |
probably benign |
0.02 |
R8695:Cep192
|
UTSW |
18 |
67,951,958 (GRCm39) |
nonsense |
probably null |
|
R8865:Cep192
|
UTSW |
18 |
67,967,703 (GRCm39) |
missense |
probably benign |
0.01 |
R8935:Cep192
|
UTSW |
18 |
67,995,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R9453:Cep192
|
UTSW |
18 |
67,989,354 (GRCm39) |
nonsense |
probably null |
|
R9571:Cep192
|
UTSW |
18 |
67,952,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R9581:Cep192
|
UTSW |
18 |
67,980,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R9599:Cep192
|
UTSW |
18 |
67,968,525 (GRCm39) |
missense |
probably benign |
0.19 |
R9779:Cep192
|
UTSW |
18 |
67,968,348 (GRCm39) |
missense |
probably damaging |
1.00 |
RF003:Cep192
|
UTSW |
18 |
67,971,027 (GRCm39) |
missense |
probably benign |
0.44 |
X0066:Cep192
|
UTSW |
18 |
67,945,520 (GRCm39) |
splice site |
probably null |
|
Z1176:Cep192
|
UTSW |
18 |
68,014,359 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CCTGCGTTTTAAGGTGGAGC -3'
(R):5'- GTCTTGTTACAGGTAGAAGGAAAC -3'
Sequencing Primer
(F):5'- GTAGGACAGGAAGGGATGCTACTAC -3'
(R):5'- TTACAGGTAGAAGGAAACGACAAAG -3'
|
Posted On |
2015-10-08 |