Incidental Mutation 'R8797:Rgs12'
ID |
671305 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Rgs12
|
Ensembl Gene |
ENSMUSG00000029101 |
Gene Name |
regulator of G-protein signaling 12 |
Synonyms |
4632412M04Rik, 1200016K18Rik |
MMRRC Submission |
068638-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.247)
|
Stock # |
R8797 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
35106789-35196988 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 35186915 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Glycine
at position 194
(S194G)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030984]
[ENSMUST00000087684]
[ENSMUST00000114280]
[ENSMUST00000114281]
[ENSMUST00000114283]
[ENSMUST00000114284]
[ENSMUST00000114285]
|
AlphaFold |
Q8CGE9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000030984
|
SMART Domains |
Protein: ENSMUSP00000030984 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
PDZ
|
29 |
98 |
5.25e-18 |
SMART |
PTB
|
224 |
373 |
5.05e-28 |
SMART |
low complexity region
|
443 |
456 |
N/A |
INTRINSIC |
low complexity region
|
643 |
661 |
N/A |
INTRINSIC |
low complexity region
|
685 |
697 |
N/A |
INTRINSIC |
RGS
|
715 |
832 |
2.84e-41 |
SMART |
low complexity region
|
849 |
865 |
N/A |
INTRINSIC |
low complexity region
|
868 |
880 |
N/A |
INTRINSIC |
low complexity region
|
911 |
928 |
N/A |
INTRINSIC |
RBD
|
962 |
1032 |
3.12e-28 |
SMART |
RBD
|
1034 |
1104 |
2.44e-21 |
SMART |
GoLoco
|
1187 |
1209 |
9.74e-9 |
SMART |
low complexity region
|
1259 |
1280 |
N/A |
INTRINSIC |
low complexity region
|
1292 |
1308 |
N/A |
INTRINSIC |
low complexity region
|
1359 |
1378 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000087684
|
SMART Domains |
Protein: ENSMUSP00000084970 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
PDZ
|
29 |
98 |
5.25e-18 |
SMART |
PTB
|
224 |
373 |
5.05e-28 |
SMART |
low complexity region
|
443 |
456 |
N/A |
INTRINSIC |
low complexity region
|
643 |
661 |
N/A |
INTRINSIC |
low complexity region
|
685 |
697 |
N/A |
INTRINSIC |
RGS
|
715 |
832 |
2.84e-41 |
SMART |
Pfam:RGS12_us1
|
836 |
953 |
4.3e-61 |
PFAM |
RBD
|
962 |
1032 |
3.12e-28 |
SMART |
RBD
|
1034 |
1104 |
2.44e-21 |
SMART |
Pfam:RGS12_us2
|
1106 |
1180 |
2.4e-37 |
PFAM |
GoLoco
|
1187 |
1209 |
9.74e-9 |
SMART |
Pfam:RGS12_usC
|
1238 |
1379 |
9.2e-49 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000114280
|
SMART Domains |
Protein: ENSMUSP00000109919 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
39 |
N/A |
INTRINSIC |
RGS
|
57 |
174 |
2.84e-41 |
SMART |
low complexity region
|
191 |
207 |
N/A |
INTRINSIC |
low complexity region
|
210 |
222 |
N/A |
INTRINSIC |
low complexity region
|
253 |
270 |
N/A |
INTRINSIC |
RBD
|
304 |
374 |
3.12e-28 |
SMART |
RBD
|
376 |
446 |
2.44e-21 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000114281
|
SMART Domains |
Protein: ENSMUSP00000109920 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
39 |
N/A |
INTRINSIC |
RGS
|
57 |
174 |
2.84e-41 |
SMART |
low complexity region
|
191 |
207 |
N/A |
INTRINSIC |
low complexity region
|
210 |
222 |
N/A |
INTRINSIC |
low complexity region
|
253 |
270 |
N/A |
INTRINSIC |
RBD
|
304 |
374 |
3.12e-28 |
SMART |
RBD
|
376 |
446 |
2.44e-21 |
SMART |
GoLoco
|
529 |
551 |
9.74e-9 |
SMART |
low complexity region
|
601 |
622 |
N/A |
INTRINSIC |
low complexity region
|
634 |
650 |
N/A |
INTRINSIC |
low complexity region
|
701 |
720 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000114283
|
SMART Domains |
Protein: ENSMUSP00000109922 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
39 |
N/A |
INTRINSIC |
RGS
|
57 |
174 |
2.84e-41 |
SMART |
low complexity region
|
191 |
207 |
N/A |
INTRINSIC |
low complexity region
|
210 |
222 |
N/A |
INTRINSIC |
low complexity region
|
253 |
270 |
N/A |
INTRINSIC |
RBD
|
304 |
374 |
3.12e-28 |
SMART |
RBD
|
376 |
446 |
2.44e-21 |
SMART |
GoLoco
|
529 |
551 |
9.74e-9 |
SMART |
low complexity region
|
601 |
622 |
N/A |
INTRINSIC |
low complexity region
|
634 |
650 |
N/A |
INTRINSIC |
low complexity region
|
697 |
729 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000114284
|
SMART Domains |
Protein: ENSMUSP00000109923 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
low complexity region
|
37 |
49 |
N/A |
INTRINSIC |
RGS
|
67 |
184 |
2.84e-41 |
SMART |
low complexity region
|
201 |
217 |
N/A |
INTRINSIC |
low complexity region
|
220 |
232 |
N/A |
INTRINSIC |
low complexity region
|
263 |
280 |
N/A |
INTRINSIC |
RBD
|
314 |
384 |
3.12e-28 |
SMART |
RBD
|
386 |
456 |
2.44e-21 |
SMART |
GoLoco
|
539 |
561 |
9.74e-9 |
SMART |
low complexity region
|
611 |
632 |
N/A |
INTRINSIC |
low complexity region
|
644 |
660 |
N/A |
INTRINSIC |
low complexity region
|
711 |
730 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000114285
|
SMART Domains |
Protein: ENSMUSP00000109924 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
low complexity region
|
37 |
49 |
N/A |
INTRINSIC |
RGS
|
67 |
184 |
2.84e-41 |
SMART |
low complexity region
|
201 |
217 |
N/A |
INTRINSIC |
low complexity region
|
220 |
232 |
N/A |
INTRINSIC |
low complexity region
|
263 |
280 |
N/A |
INTRINSIC |
RBD
|
314 |
384 |
3.12e-28 |
SMART |
RBD
|
386 |
456 |
2.44e-21 |
SMART |
GoLoco
|
539 |
561 |
9.74e-9 |
SMART |
low complexity region
|
611 |
632 |
N/A |
INTRINSIC |
low complexity region
|
644 |
660 |
N/A |
INTRINSIC |
low complexity region
|
707 |
739 |
N/A |
INTRINSIC |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000116913 Gene: ENSMUSG00000029101 AA Change: S194G
Domain | Start | End | E-Value | Type |
RBD
|
21 |
91 |
3.12e-28 |
SMART |
RBD
|
93 |
163 |
2.44e-21 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150139
|
SMART Domains |
Protein: ENSMUSP00000117158 Gene: ENSMUSG00000029101
Domain | Start | End | E-Value | Type |
Blast:RBD
|
2 |
33 |
5e-13 |
BLAST |
Pfam:RGS12_us2
|
35 |
80 |
5.8e-13 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201936
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.9%
- 20x: 99.6%
|
Validation Efficiency |
100% (50/50) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the 'regulator of G protein signaling' (RGS) gene family. The encoded protein may function as a guanosine triphosphatase (GTPase)-activating protein as well as a transcriptional repressor. This protein may play a role in tumorigenesis. Multiple transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
C |
A |
7: 119,137,374 (GRCm39) |
P397T |
probably damaging |
Het |
Adamts14 |
C |
T |
10: 61,106,781 (GRCm39) |
R113K |
probably benign |
Het |
Baiap2 |
G |
A |
11: 119,897,201 (GRCm39) |
V519I |
probably benign |
Het |
Ccna1 |
C |
T |
3: 54,953,069 (GRCm39) |
A233T |
probably benign |
Het |
Cdon |
T |
C |
9: 35,389,931 (GRCm39) |
Y862H |
probably damaging |
Het |
Crygc |
C |
T |
1: 65,111,030 (GRCm39) |
A86T |
probably benign |
Het |
Cyb5d2 |
T |
G |
11: 72,669,662 (GRCm39) |
N232T |
probably benign |
Het |
Dnah14 |
C |
A |
1: 181,465,412 (GRCm39) |
H1193N |
probably benign |
Het |
Dnah17 |
T |
G |
11: 117,992,201 (GRCm39) |
E1170A |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,162,806 (GRCm39) |
Y384C |
probably damaging |
Het |
Fat4 |
G |
A |
3: 39,053,278 (GRCm39) |
V4091I |
probably benign |
Het |
Fbxl12 |
C |
A |
9: 20,550,160 (GRCm39) |
R165L |
possibly damaging |
Het |
G6pc2 |
A |
G |
2: 69,050,441 (GRCm39) |
Y22C |
probably benign |
Het |
Gpihbp1 |
A |
T |
15: 75,469,828 (GRCm39) |
Q181L |
possibly damaging |
Het |
H2bc4 |
C |
T |
13: 23,868,552 (GRCm39) |
S113L |
probably damaging |
Het |
Hhatl |
A |
T |
9: 121,619,965 (GRCm39) |
|
probably benign |
Het |
Iars1 |
C |
A |
13: 49,841,738 (GRCm39) |
S75R |
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,902,573 (GRCm39) |
I375F |
possibly damaging |
Het |
Itih4 |
A |
G |
14: 30,618,529 (GRCm39) |
I647V |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 67,060,616 (GRCm39) |
C703S |
probably benign |
Het |
L3mbtl2 |
C |
T |
15: 81,569,615 (GRCm39) |
T619I |
possibly damaging |
Het |
Lct |
T |
C |
1: 128,231,684 (GRCm39) |
T722A |
possibly damaging |
Het |
Meioc |
C |
T |
11: 102,567,686 (GRCm39) |
Q827* |
probably null |
Het |
Meis2 |
T |
C |
2: 115,694,986 (GRCm39) |
S386G |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,071,876 (GRCm39) |
D543V |
probably damaging |
Het |
Ms4a13 |
C |
T |
19: 11,161,200 (GRCm39) |
R113H |
probably benign |
Het |
Myrfl |
T |
C |
10: 116,613,325 (GRCm39) |
Y826C |
probably benign |
Het |
Nf1 |
T |
C |
11: 79,366,711 (GRCm39) |
|
probably benign |
Het |
Nrg3 |
A |
C |
14: 38,093,243 (GRCm39) |
L542R |
probably benign |
Het |
Or13j1 |
T |
C |
4: 43,706,455 (GRCm39) |
T38A |
probably damaging |
Het |
Or2y8 |
T |
A |
11: 52,036,340 (GRCm39) |
T6S |
probably benign |
Het |
Or6c65 |
T |
A |
10: 129,603,674 (GRCm39) |
I103K |
probably damaging |
Het |
Pcdh15 |
A |
G |
10: 74,419,978 (GRCm39) |
N1212S |
probably damaging |
Het |
Pcsk5 |
G |
A |
19: 17,443,472 (GRCm39) |
T1229I |
probably benign |
Het |
Pkd1l3 |
A |
T |
8: 110,374,946 (GRCm39) |
H1483L |
probably benign |
Het |
Polr3b |
T |
A |
10: 84,532,879 (GRCm39) |
L840* |
probably null |
Het |
Psd4 |
A |
T |
2: 24,287,440 (GRCm39) |
R457S |
probably benign |
Het |
Relch |
T |
C |
1: 105,678,121 (GRCm39) |
S1149P |
possibly damaging |
Het |
Rps3 |
A |
G |
7: 99,132,797 (GRCm39) |
|
probably null |
Het |
Saxo4 |
T |
C |
19: 10,455,602 (GRCm39) |
I216V |
probably benign |
Het |
Sgcb |
G |
T |
5: 73,793,036 (GRCm39) |
N255K |
probably benign |
Het |
Sla2 |
A |
G |
2: 156,717,799 (GRCm39) |
Y158H |
probably damaging |
Het |
Sla2 |
G |
A |
2: 156,717,823 (GRCm39) |
Q150* |
probably null |
Het |
Slc12a2 |
T |
A |
18: 58,012,455 (GRCm39) |
Y193N |
possibly damaging |
Het |
Supt16 |
G |
T |
14: 52,409,960 (GRCm39) |
T749K |
probably damaging |
Het |
Uqcrc2 |
A |
G |
7: 120,239,500 (GRCm39) |
E104G |
probably damaging |
Het |
Vasp |
T |
C |
7: 18,994,563 (GRCm39) |
N251S |
unknown |
Het |
Vmn1r72 |
A |
G |
7: 11,403,965 (GRCm39) |
M161T |
probably benign |
Het |
Zc3h18 |
T |
C |
8: 123,134,989 (GRCm39) |
|
probably benign |
Het |
Zfp981 |
T |
A |
4: 146,619,906 (GRCm39) |
L20* |
probably null |
Het |
|
Other mutations in Rgs12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01443:Rgs12
|
APN |
5 |
35,132,563 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02296:Rgs12
|
APN |
5 |
35,123,464 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02337:Rgs12
|
APN |
5 |
35,177,697 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02483:Rgs12
|
APN |
5 |
35,187,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02869:Rgs12
|
APN |
5 |
35,183,227 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02989:Rgs12
|
APN |
5 |
35,122,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Rgs12
|
UTSW |
5 |
35,180,120 (GRCm39) |
unclassified |
probably benign |
|
R0015:Rgs12
|
UTSW |
5 |
35,180,120 (GRCm39) |
unclassified |
probably benign |
|
R0046:Rgs12
|
UTSW |
5 |
35,122,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Rgs12
|
UTSW |
5 |
35,122,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0106:Rgs12
|
UTSW |
5 |
35,124,008 (GRCm39) |
missense |
probably benign |
0.03 |
R0106:Rgs12
|
UTSW |
5 |
35,124,008 (GRCm39) |
missense |
probably benign |
0.03 |
R0233:Rgs12
|
UTSW |
5 |
35,187,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Rgs12
|
UTSW |
5 |
35,187,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R0245:Rgs12
|
UTSW |
5 |
35,187,424 (GRCm39) |
missense |
probably benign |
0.01 |
R0611:Rgs12
|
UTSW |
5 |
35,176,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Rgs12
|
UTSW |
5 |
35,180,466 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0723:Rgs12
|
UTSW |
5 |
35,181,710 (GRCm39) |
unclassified |
probably benign |
|
R1174:Rgs12
|
UTSW |
5 |
35,123,809 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Rgs12
|
UTSW |
5 |
35,178,511 (GRCm39) |
missense |
probably damaging |
0.98 |
R1556:Rgs12
|
UTSW |
5 |
35,196,626 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1774:Rgs12
|
UTSW |
5 |
35,123,747 (GRCm39) |
missense |
probably benign |
0.34 |
R1791:Rgs12
|
UTSW |
5 |
35,123,456 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1866:Rgs12
|
UTSW |
5 |
35,123,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Rgs12
|
UTSW |
5 |
35,123,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R1923:Rgs12
|
UTSW |
5 |
35,189,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Rgs12
|
UTSW |
5 |
35,187,872 (GRCm39) |
missense |
probably benign |
0.00 |
R2107:Rgs12
|
UTSW |
5 |
35,124,079 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3730:Rgs12
|
UTSW |
5 |
35,189,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R3731:Rgs12
|
UTSW |
5 |
35,189,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R3808:Rgs12
|
UTSW |
5 |
35,189,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Rgs12
|
UTSW |
5 |
35,123,359 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3827:Rgs12
|
UTSW |
5 |
35,123,359 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3829:Rgs12
|
UTSW |
5 |
35,123,359 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3830:Rgs12
|
UTSW |
5 |
35,123,359 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4392:Rgs12
|
UTSW |
5 |
35,189,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4617:Rgs12
|
UTSW |
5 |
35,177,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5132:Rgs12
|
UTSW |
5 |
35,147,156 (GRCm39) |
intron |
probably benign |
|
R5213:Rgs12
|
UTSW |
5 |
35,122,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5296:Rgs12
|
UTSW |
5 |
35,178,448 (GRCm39) |
unclassified |
probably benign |
|
R5480:Rgs12
|
UTSW |
5 |
35,123,455 (GRCm39) |
missense |
probably benign |
0.09 |
R5510:Rgs12
|
UTSW |
5 |
35,123,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R5708:Rgs12
|
UTSW |
5 |
35,123,696 (GRCm39) |
missense |
probably benign |
0.41 |
R5987:Rgs12
|
UTSW |
5 |
35,177,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6053:Rgs12
|
UTSW |
5 |
35,123,296 (GRCm39) |
missense |
probably benign |
0.01 |
R6113:Rgs12
|
UTSW |
5 |
35,177,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R6401:Rgs12
|
UTSW |
5 |
35,177,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Rgs12
|
UTSW |
5 |
35,180,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R6807:Rgs12
|
UTSW |
5 |
35,180,515 (GRCm39) |
missense |
probably null |
0.27 |
R6857:Rgs12
|
UTSW |
5 |
35,187,366 (GRCm39) |
nonsense |
probably null |
|
R7082:Rgs12
|
UTSW |
5 |
35,124,050 (GRCm39) |
missense |
probably benign |
0.00 |
R7250:Rgs12
|
UTSW |
5 |
35,122,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R7276:Rgs12
|
UTSW |
5 |
35,183,715 (GRCm39) |
missense |
probably benign |
0.06 |
R7444:Rgs12
|
UTSW |
5 |
35,183,287 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7632:Rgs12
|
UTSW |
5 |
35,122,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R8049:Rgs12
|
UTSW |
5 |
35,183,374 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8089:Rgs12
|
UTSW |
5 |
35,177,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R8241:Rgs12
|
UTSW |
5 |
35,123,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8927:Rgs12
|
UTSW |
5 |
35,123,633 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8928:Rgs12
|
UTSW |
5 |
35,123,633 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9073:Rgs12
|
UTSW |
5 |
35,177,753 (GRCm39) |
unclassified |
probably benign |
|
R9211:Rgs12
|
UTSW |
5 |
35,123,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R9485:Rgs12
|
UTSW |
5 |
35,189,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R9550:Rgs12
|
UTSW |
5 |
35,196,665 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Rgs12
|
UTSW |
5 |
35,123,113 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Rgs12
|
UTSW |
5 |
35,183,696 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Rgs12
|
UTSW |
5 |
35,122,198 (GRCm39) |
start gained |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- ATGTGAATGGAACCCCTGGG -3'
(R):5'- TTGGGAAGCCAGATACCATATGC -3'
Sequencing Primer
(F):5'- CCCTGGGGCCAAGGGTG -3'
(R):5'- GAATGTGACATTAACTCCTGCC -3'
|
Posted On |
2021-04-30 |