Incidental Mutation 'R6520:Tet1'
ID |
521171 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tet1
|
Ensembl Gene |
ENSMUSG00000047146 |
Gene Name |
tet methylcytosine dioxygenase 1 |
Synonyms |
Cxxc6, D10Ertd17e, 2510010B09Rik, BB001228 |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R6520 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
10 |
Chromosomal Location |
62640349-62723242 bp(-) (GRCm39) |
Type of Mutation |
start codon destroyed |
DNA Base Change (assembly) |
A to G
at 62715792 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Threonine
at position 1
(M1T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133279
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050826]
[ENSMUST00000174189]
[ENSMUST00000218438]
[ENSMUST00000218782]
[ENSMUST00000227494]
[ENSMUST00000228901]
|
AlphaFold |
Q3URK3 |
Predicted Effect |
probably null
Transcript: ENSMUST00000050826
AA Change: M1T
PolyPhen 2
Score 0.131 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000059527 Gene: ENSMUSG00000047146 AA Change: M1T
Domain | Start | End | E-Value | Type |
low complexity region
|
8 |
21 |
N/A |
INTRINSIC |
low complexity region
|
118 |
132 |
N/A |
INTRINSIC |
low complexity region
|
553 |
564 |
N/A |
INTRINSIC |
Pfam:zf-CXXC
|
566 |
607 |
2.5e-11 |
PFAM |
low complexity region
|
884 |
902 |
N/A |
INTRINSIC |
low complexity region
|
1087 |
1106 |
N/A |
INTRINSIC |
Tet_JBP
|
1528 |
1931 |
1e-171 |
SMART |
low complexity region
|
1944 |
1956 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000174189
AA Change: M1T
PolyPhen 2
Score 0.533 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000133279 Gene: ENSMUSG00000047146 AA Change: M1T
Domain | Start | End | E-Value | Type |
low complexity region
|
8 |
21 |
N/A |
INTRINSIC |
low complexity region
|
118 |
132 |
N/A |
INTRINSIC |
low complexity region
|
553 |
564 |
N/A |
INTRINSIC |
Pfam:zf-CXXC
|
566 |
607 |
2.7e-10 |
PFAM |
low complexity region
|
884 |
902 |
N/A |
INTRINSIC |
low complexity region
|
1087 |
1106 |
N/A |
INTRINSIC |
Tet_JBP
|
1528 |
1963 |
7.36e-170 |
SMART |
low complexity region
|
1976 |
1988 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000218438
AA Change: M1T
|
Predicted Effect |
probably null
Transcript: ENSMUST00000218782
AA Change: M1T
|
Predicted Effect |
probably null
Transcript: ENSMUST00000227494
AA Change: M1T
|
Predicted Effect |
probably null
Transcript: ENSMUST00000228901
AA Change: M1T
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.5%
- 10x: 97.5%
- 20x: 92.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] DNA methylation is an epigenetic mechanism that is important for controlling gene expression. The protein encoded by this gene is a demethylase that belongs to the TET (ten-eleven translocation) family. Members of the TET protein family play a role in the DNA methylation process and gene activation. [provided by RefSeq, Sep 2015] PHENOTYPE: Mice homozygous for a knock-out allele exhibit background sensitive lethality, abnormal forebrain development, abnormal female reproductive organs and decreased litter size. Mice homozygous for a different knock-out allele exhibit impaired adult neurogenesis, impaired spatial learning and impaired short-term memory retention. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
T |
C |
11: 23,467,285 (GRCm39) |
D116G |
possibly damaging |
Het |
Adam22 |
C |
T |
5: 8,166,635 (GRCm39) |
V699M |
probably damaging |
Het |
Adh7 |
A |
G |
3: 137,929,771 (GRCm39) |
Y149C |
probably damaging |
Het |
Adissp |
G |
T |
2: 130,989,174 (GRCm39) |
H111N |
probably damaging |
Het |
Angptl3 |
A |
C |
4: 98,926,085 (GRCm39) |
N405T |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,824,217 (GRCm39) |
H180R |
probably damaging |
Het |
Apob |
T |
A |
12: 8,033,124 (GRCm39) |
I159N |
probably damaging |
Het |
Arhgap24 |
T |
C |
5: 103,028,659 (GRCm39) |
V185A |
probably benign |
Het |
Atf6 |
A |
T |
1: 170,695,238 (GRCm39) |
H11Q |
probably benign |
Het |
Atxn3 |
C |
A |
12: 101,900,660 (GRCm39) |
D208Y |
probably damaging |
Het |
Brd9 |
G |
A |
13: 74,090,913 (GRCm39) |
R273K |
probably benign |
Het |
Cbfa2t3 |
T |
A |
8: 123,362,540 (GRCm39) |
R302W |
probably benign |
Het |
Ccdc175 |
C |
A |
12: 72,186,804 (GRCm39) |
G347C |
probably damaging |
Het |
Ccdc87 |
A |
G |
19: 4,891,817 (GRCm39) |
K770E |
probably damaging |
Het |
Ccl17 |
T |
C |
8: 95,537,178 (GRCm39) |
F27L |
probably benign |
Het |
Cd3g |
A |
T |
9: 44,882,613 (GRCm39) |
|
probably null |
Het |
Cep350 |
A |
G |
1: 155,809,082 (GRCm39) |
V498A |
probably benign |
Het |
Cfap45 |
A |
G |
1: 172,368,151 (GRCm39) |
D381G |
probably damaging |
Het |
Cfap46 |
A |
G |
7: 139,194,321 (GRCm39) |
|
probably null |
Het |
Cnrip1 |
T |
A |
11: 17,028,536 (GRCm39) |
M156K |
probably damaging |
Het |
Col23a1 |
T |
C |
11: 51,440,552 (GRCm39) |
|
probably null |
Het |
Col4a1 |
C |
T |
8: 11,269,152 (GRCm39) |
G933S |
probably damaging |
Het |
Col5a3 |
C |
T |
9: 20,685,348 (GRCm39) |
V1443I |
unknown |
Het |
Col6a6 |
T |
C |
9: 105,663,024 (GRCm39) |
E171G |
possibly damaging |
Het |
Dennd1a |
A |
T |
2: 37,851,759 (GRCm39) |
|
probably null |
Het |
Dlk2 |
C |
T |
17: 46,613,438 (GRCm39) |
T188I |
probably damaging |
Het |
Dusp8 |
A |
G |
7: 141,637,418 (GRCm39) |
I203T |
probably damaging |
Het |
Eno2 |
C |
T |
6: 124,744,678 (GRCm39) |
R56H |
probably damaging |
Het |
Erich3 |
A |
T |
3: 154,469,102 (GRCm39) |
T1185S |
probably damaging |
Het |
Evi5l |
A |
T |
8: 4,255,906 (GRCm39) |
Q575L |
possibly damaging |
Het |
Fam187a |
T |
A |
11: 102,776,701 (GRCm39) |
H168Q |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,175,814 (GRCm39) |
E1633V |
probably damaging |
Het |
Fbln2 |
G |
A |
6: 91,236,641 (GRCm39) |
D719N |
probably damaging |
Het |
Fbn2 |
A |
T |
18: 58,235,462 (GRCm39) |
S672T |
probably damaging |
Het |
Gas8 |
C |
G |
8: 124,253,213 (GRCm39) |
A187G |
probably benign |
Het |
Gm2696 |
G |
A |
10: 77,672,332 (GRCm39) |
|
probably benign |
Het |
Gnl1 |
A |
T |
17: 36,293,845 (GRCm39) |
K272M |
probably benign |
Het |
Gtf2h3 |
C |
T |
5: 124,722,360 (GRCm39) |
T121I |
probably benign |
Het |
Hemgn |
T |
G |
4: 46,396,466 (GRCm39) |
K257Q |
probably damaging |
Het |
Hgsnat |
T |
C |
8: 26,443,328 (GRCm39) |
Y474C |
probably damaging |
Het |
Hoxc4 |
T |
C |
15: 102,943,380 (GRCm39) |
S78P |
probably benign |
Het |
Igkv14-100 |
T |
A |
6: 68,496,218 (GRCm39) |
L37Q |
probably damaging |
Het |
Iqck |
A |
T |
7: 118,540,854 (GRCm39) |
K251M |
probably damaging |
Het |
Itgal |
A |
T |
7: 126,929,503 (GRCm39) |
Q1140L |
probably benign |
Het |
Itpka |
A |
G |
2: 119,581,259 (GRCm39) |
R431G |
probably benign |
Het |
Jade1 |
A |
G |
3: 41,558,917 (GRCm39) |
N333D |
possibly damaging |
Het |
Jmjd7 |
A |
G |
2: 119,861,800 (GRCm39) |
H181R |
probably damaging |
Het |
Jmy |
A |
G |
13: 93,590,547 (GRCm39) |
S519P |
probably benign |
Het |
Klra10 |
T |
A |
6: 130,252,755 (GRCm39) |
H173L |
probably benign |
Het |
Krt72 |
T |
G |
15: 101,689,481 (GRCm39) |
I284L |
probably benign |
Het |
Krt78 |
C |
A |
15: 101,860,206 (GRCm39) |
V237F |
probably benign |
Het |
Mapkapk3 |
G |
A |
9: 107,134,648 (GRCm39) |
T296M |
probably damaging |
Het |
Mcmbp |
A |
C |
7: 128,314,451 (GRCm39) |
V255G |
possibly damaging |
Het |
Mcoln1 |
T |
G |
8: 3,555,855 (GRCm39) |
M50R |
probably damaging |
Het |
Mocos |
T |
A |
18: 24,799,447 (GRCm39) |
V227E |
probably benign |
Het |
Mpeg1 |
A |
G |
19: 12,439,322 (GRCm39) |
E260G |
probably benign |
Het |
Mrc1 |
A |
T |
2: 14,312,760 (GRCm39) |
N894I |
probably damaging |
Het |
Mroh7 |
A |
G |
4: 106,578,460 (GRCm39) |
S73P |
probably benign |
Het |
Myo3a |
A |
T |
2: 22,404,737 (GRCm39) |
I690L |
possibly damaging |
Het |
Naa50 |
T |
G |
16: 43,979,872 (GRCm39) |
F87V |
probably damaging |
Het |
Ndufs6 |
G |
T |
13: 73,476,471 (GRCm39) |
T32K |
probably damaging |
Het |
Nfe2l2 |
A |
G |
2: 75,506,912 (GRCm39) |
V396A |
probably benign |
Het |
Nptn |
A |
G |
9: 58,551,017 (GRCm39) |
E348G |
probably damaging |
Het |
Nsun4 |
A |
T |
4: 115,901,935 (GRCm39) |
L177Q |
probably damaging |
Het |
Or56b1b |
A |
G |
7: 108,164,046 (GRCm39) |
*319Q |
probably null |
Het |
Or8d6 |
T |
C |
9: 39,853,658 (GRCm39) |
I34T |
possibly damaging |
Het |
Or8k36-ps1 |
A |
G |
2: 86,437,462 (GRCm39) |
L151P |
unknown |
Het |
Plekha7 |
A |
G |
7: 115,763,717 (GRCm39) |
V233A |
probably benign |
Het |
Polq |
C |
A |
16: 36,880,739 (GRCm39) |
Q968K |
possibly damaging |
Het |
Prmt7 |
C |
T |
8: 106,961,516 (GRCm39) |
T143M |
probably damaging |
Het |
Ptprc |
G |
A |
1: 138,007,881 (GRCm39) |
Q886* |
probably null |
Het |
Rbp7 |
C |
A |
4: 149,537,371 (GRCm39) |
V36L |
possibly damaging |
Het |
Rev3l |
A |
T |
10: 39,698,698 (GRCm39) |
N1065I |
probably benign |
Het |
Scamp5 |
A |
T |
9: 57,354,489 (GRCm39) |
|
probably null |
Het |
Sec16a |
A |
G |
2: 26,316,118 (GRCm39) |
S1698P |
probably damaging |
Het |
Spr |
C |
A |
6: 85,114,474 (GRCm39) |
R85L |
probably benign |
Het |
Sptlc2 |
A |
C |
12: 87,402,436 (GRCm39) |
N163K |
probably benign |
Het |
Stk10 |
C |
T |
11: 32,538,839 (GRCm39) |
T226M |
probably damaging |
Het |
Sv2c |
A |
G |
13: 96,123,229 (GRCm39) |
Y415H |
probably benign |
Het |
Tnnt1 |
T |
A |
7: 4,512,060 (GRCm39) |
K150* |
probably null |
Het |
Trappc10 |
C |
T |
10: 78,037,287 (GRCm39) |
V839M |
probably benign |
Het |
Ubap2 |
T |
C |
4: 41,195,155 (GRCm39) |
N1131S |
probably damaging |
Het |
Upk2 |
T |
C |
9: 44,364,803 (GRCm39) |
E132G |
probably damaging |
Het |
Vmn2r117 |
A |
T |
17: 23,679,193 (GRCm39) |
V677D |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,702,943 (GRCm39) |
L670H |
probably damaging |
Het |
Wwc1 |
C |
T |
11: 35,744,264 (GRCm39) |
E853K |
probably benign |
Het |
Zfp512 |
G |
A |
5: 31,623,984 (GRCm39) |
R67H |
probably damaging |
Het |
Zfp804b |
T |
A |
5: 6,819,283 (GRCm39) |
H1260L |
probably damaging |
Het |
Zzef1 |
C |
A |
11: 72,716,891 (GRCm39) |
N360K |
probably damaging |
Het |
|
Other mutations in Tet1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00539:Tet1
|
APN |
10 |
62,650,276 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01079:Tet1
|
APN |
10 |
62,715,252 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01109:Tet1
|
APN |
10 |
62,715,553 (GRCm39) |
missense |
probably benign |
|
IGL01634:Tet1
|
APN |
10 |
62,714,367 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02003:Tet1
|
APN |
10 |
62,652,179 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02081:Tet1
|
APN |
10 |
62,649,597 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02100:Tet1
|
APN |
10 |
62,648,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02228:Tet1
|
APN |
10 |
62,649,513 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02524:Tet1
|
APN |
10 |
62,714,425 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02539:Tet1
|
APN |
10 |
62,648,798 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02608:Tet1
|
APN |
10 |
62,674,866 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02608:Tet1
|
APN |
10 |
62,715,388 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02702:Tet1
|
APN |
10 |
62,715,531 (GRCm39) |
missense |
possibly damaging |
0.83 |
K7371:Tet1
|
UTSW |
10 |
62,714,955 (GRCm39) |
missense |
probably benign |
|
R0166:Tet1
|
UTSW |
10 |
62,676,058 (GRCm39) |
missense |
probably benign |
0.05 |
R0371:Tet1
|
UTSW |
10 |
62,714,178 (GRCm39) |
missense |
probably damaging |
0.97 |
R0373:Tet1
|
UTSW |
10 |
62,713,988 (GRCm39) |
nonsense |
probably null |
|
R0391:Tet1
|
UTSW |
10 |
62,650,325 (GRCm39) |
splice site |
probably null |
|
R0445:Tet1
|
UTSW |
10 |
62,715,720 (GRCm39) |
missense |
probably benign |
0.08 |
R1016:Tet1
|
UTSW |
10 |
62,715,729 (GRCm39) |
missense |
probably benign |
|
R1344:Tet1
|
UTSW |
10 |
62,650,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R1546:Tet1
|
UTSW |
10 |
62,648,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Tet1
|
UTSW |
10 |
62,715,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Tet1
|
UTSW |
10 |
62,650,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1752:Tet1
|
UTSW |
10 |
62,648,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R1834:Tet1
|
UTSW |
10 |
62,649,444 (GRCm39) |
missense |
probably damaging |
0.99 |
R1964:Tet1
|
UTSW |
10 |
62,648,726 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2239:Tet1
|
UTSW |
10 |
62,715,513 (GRCm39) |
missense |
probably benign |
0.01 |
R2962:Tet1
|
UTSW |
10 |
62,650,323 (GRCm39) |
nonsense |
probably null |
|
R3084:Tet1
|
UTSW |
10 |
62,715,400 (GRCm39) |
missense |
probably benign |
0.34 |
R3086:Tet1
|
UTSW |
10 |
62,715,400 (GRCm39) |
missense |
probably benign |
0.34 |
R3972:Tet1
|
UTSW |
10 |
62,649,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R4622:Tet1
|
UTSW |
10 |
62,655,253 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4674:Tet1
|
UTSW |
10 |
62,674,627 (GRCm39) |
missense |
probably damaging |
0.97 |
R4687:Tet1
|
UTSW |
10 |
62,674,570 (GRCm39) |
missense |
probably benign |
0.04 |
R4718:Tet1
|
UTSW |
10 |
62,649,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R4801:Tet1
|
UTSW |
10 |
62,658,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R4802:Tet1
|
UTSW |
10 |
62,658,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R4903:Tet1
|
UTSW |
10 |
62,658,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Tet1
|
UTSW |
10 |
62,714,357 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5193:Tet1
|
UTSW |
10 |
62,674,026 (GRCm39) |
missense |
probably benign |
0.22 |
R5225:Tet1
|
UTSW |
10 |
62,674,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Tet1
|
UTSW |
10 |
62,650,230 (GRCm39) |
missense |
probably benign |
0.01 |
R5465:Tet1
|
UTSW |
10 |
62,675,556 (GRCm39) |
missense |
probably benign |
|
R5535:Tet1
|
UTSW |
10 |
62,668,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Tet1
|
UTSW |
10 |
62,714,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Tet1
|
UTSW |
10 |
62,675,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R5788:Tet1
|
UTSW |
10 |
62,675,737 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5818:Tet1
|
UTSW |
10 |
62,652,187 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5860:Tet1
|
UTSW |
10 |
62,648,399 (GRCm39) |
splice site |
probably null |
|
R5975:Tet1
|
UTSW |
10 |
62,715,552 (GRCm39) |
missense |
probably benign |
0.37 |
R6041:Tet1
|
UTSW |
10 |
62,649,152 (GRCm39) |
missense |
probably damaging |
0.98 |
R6092:Tet1
|
UTSW |
10 |
62,649,494 (GRCm39) |
missense |
probably benign |
0.10 |
R6132:Tet1
|
UTSW |
10 |
62,649,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R6157:Tet1
|
UTSW |
10 |
62,675,749 (GRCm39) |
missense |
probably damaging |
0.98 |
R7210:Tet1
|
UTSW |
10 |
62,650,280 (GRCm39) |
missense |
probably null |
0.95 |
R7223:Tet1
|
UTSW |
10 |
62,649,450 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7255:Tet1
|
UTSW |
10 |
62,658,415 (GRCm39) |
missense |
probably benign |
0.15 |
R7323:Tet1
|
UTSW |
10 |
62,715,818 (GRCm39) |
start gained |
probably benign |
|
R7472:Tet1
|
UTSW |
10 |
62,649,129 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7507:Tet1
|
UTSW |
10 |
62,668,671 (GRCm39) |
critical splice donor site |
probably null |
|
R7522:Tet1
|
UTSW |
10 |
62,654,762 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7849:Tet1
|
UTSW |
10 |
62,655,252 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7879:Tet1
|
UTSW |
10 |
62,714,825 (GRCm39) |
missense |
probably benign |
0.03 |
R8073:Tet1
|
UTSW |
10 |
62,649,132 (GRCm39) |
missense |
probably damaging |
0.98 |
R8098:Tet1
|
UTSW |
10 |
62,714,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R8147:Tet1
|
UTSW |
10 |
62,714,586 (GRCm39) |
missense |
probably benign |
0.01 |
R8355:Tet1
|
UTSW |
10 |
62,652,229 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8545:Tet1
|
UTSW |
10 |
62,648,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Tet1
|
UTSW |
10 |
62,675,985 (GRCm39) |
missense |
probably benign |
0.37 |
R8936:Tet1
|
UTSW |
10 |
62,676,063 (GRCm39) |
nonsense |
probably null |
|
R9173:Tet1
|
UTSW |
10 |
62,676,065 (GRCm39) |
missense |
probably benign |
|
R9414:Tet1
|
UTSW |
10 |
62,674,935 (GRCm39) |
missense |
probably benign |
0.01 |
R9584:Tet1
|
UTSW |
10 |
62,655,306 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tet1
|
UTSW |
10 |
62,654,764 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
Predicted Primers |
PCR Primer
(F):5'- AACTTGGTTTCGATCCCGATTC -3'
(R):5'- ACTCAGTCTCCCAAATGCTGG -3'
Sequencing Primer
(F):5'- TCGCGTCAGAAAACTCGG -3'
(R):5'- GCAACACCTCCAGATTCT -3'
|
Posted On |
2018-06-06 |