Incidental Mutation 'R3820:Zmynd8'
ID |
274845 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zmynd8
|
Ensembl Gene |
ENSMUSG00000039671 |
Gene Name |
zinc finger, MYND-type containing 8 |
Synonyms |
ZMYND8, RACK7, 1110013E22Rik, 2010005I16Rik, Prkcbp1, 3632413B07Rik |
MMRRC Submission |
040882-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R3820 (G1)
|
Quality Score |
170 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
165626072-165740896 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 165657381 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Stop codon
at position 521
(K521*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000136211
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000018050]
[ENSMUST00000088113]
[ENSMUST00000099084]
[ENSMUST00000109266]
[ENSMUST00000109269]
[ENSMUST00000170272]
[ENSMUST00000177633]
|
AlphaFold |
A2A484 |
Predicted Effect |
probably null
Transcript: ENSMUST00000018050
AA Change: K526*
|
SMART Domains |
Protein: ENSMUSP00000018050 Gene: ENSMUSG00000039671 AA Change: K526*
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
low complexity region
|
37 |
56 |
N/A |
INTRINSIC |
PHD
|
90 |
131 |
2.23e-11 |
SMART |
BROMO
|
147 |
254 |
1.77e-17 |
SMART |
Pfam:PWWP
|
275 |
349 |
4e-12 |
PFAM |
Pfam:DUF3544
|
412 |
624 |
9.8e-112 |
PFAM |
internal_repeat_2
|
640 |
701 |
9.06e-5 |
PROSPERO |
low complexity region
|
770 |
805 |
N/A |
INTRINSIC |
low complexity region
|
853 |
868 |
N/A |
INTRINSIC |
low complexity region
|
875 |
887 |
N/A |
INTRINSIC |
coiled coil region
|
916 |
978 |
N/A |
INTRINSIC |
Pfam:zf-MYND
|
988 |
1022 |
2.2e-7 |
PFAM |
low complexity region
|
1055 |
1075 |
N/A |
INTRINSIC |
low complexity region
|
1142 |
1156 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000088113
AA Change: K521*
|
SMART Domains |
Protein: ENSMUSP00000085436 Gene: ENSMUSG00000039671 AA Change: K521*
Domain | Start | End | E-Value | Type |
low complexity region
|
8 |
19 |
N/A |
INTRINSIC |
low complexity region
|
43 |
54 |
N/A |
INTRINSIC |
low complexity region
|
57 |
76 |
N/A |
INTRINSIC |
PHD
|
85 |
126 |
2.23e-11 |
SMART |
BROMO
|
142 |
249 |
1.77e-17 |
SMART |
Pfam:PWWP
|
271 |
346 |
2.7e-11 |
PFAM |
Pfam:DUF3544
|
408 |
617 |
2.1e-102 |
PFAM |
internal_repeat_2
|
635 |
696 |
4.2e-5 |
PROSPERO |
low complexity region
|
765 |
800 |
N/A |
INTRINSIC |
low complexity region
|
848 |
863 |
N/A |
INTRINSIC |
low complexity region
|
870 |
882 |
N/A |
INTRINSIC |
coiled coil region
|
911 |
973 |
N/A |
INTRINSIC |
low complexity region
|
1050 |
1070 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000099084
AA Change: K501*
|
SMART Domains |
Protein: ENSMUSP00000096683 Gene: ENSMUSG00000039671 AA Change: K501*
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
low complexity region
|
37 |
56 |
N/A |
INTRINSIC |
PHD
|
65 |
106 |
2.23e-11 |
SMART |
BROMO
|
122 |
229 |
1.77e-17 |
SMART |
Pfam:PWWP
|
250 |
324 |
4.1e-12 |
PFAM |
Pfam:DUF3544
|
387 |
599 |
1e-111 |
PFAM |
internal_repeat_2
|
615 |
676 |
4.95e-5 |
PROSPERO |
low complexity region
|
745 |
780 |
N/A |
INTRINSIC |
low complexity region
|
819 |
844 |
N/A |
INTRINSIC |
low complexity region
|
880 |
895 |
N/A |
INTRINSIC |
low complexity region
|
902 |
914 |
N/A |
INTRINSIC |
coiled coil region
|
943 |
1005 |
N/A |
INTRINSIC |
Pfam:zf-MYND
|
1015 |
1049 |
2.3e-7 |
PFAM |
low complexity region
|
1082 |
1102 |
N/A |
INTRINSIC |
low complexity region
|
1169 |
1183 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000109266
AA Change: K546*
|
SMART Domains |
Protein: ENSMUSP00000104889 Gene: ENSMUSG00000039671 AA Change: K546*
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
11 |
N/A |
INTRINSIC |
low complexity region
|
43 |
54 |
N/A |
INTRINSIC |
low complexity region
|
57 |
76 |
N/A |
INTRINSIC |
PHD
|
110 |
151 |
2.23e-11 |
SMART |
BROMO
|
167 |
274 |
1.77e-17 |
SMART |
Pfam:PWWP
|
295 |
369 |
4.1e-12 |
PFAM |
Pfam:DUF3544
|
432 |
644 |
1e-111 |
PFAM |
internal_repeat_2
|
660 |
721 |
8.36e-5 |
PROSPERO |
low complexity region
|
790 |
825 |
N/A |
INTRINSIC |
low complexity region
|
873 |
888 |
N/A |
INTRINSIC |
low complexity region
|
895 |
907 |
N/A |
INTRINSIC |
coiled coil region
|
936 |
998 |
N/A |
INTRINSIC |
Pfam:zf-MYND
|
1008 |
1042 |
2.3e-7 |
PFAM |
low complexity region
|
1075 |
1095 |
N/A |
INTRINSIC |
low complexity region
|
1162 |
1176 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000109269
AA Change: K530*
|
SMART Domains |
Protein: ENSMUSP00000104892 Gene: ENSMUSG00000039671 AA Change: K530*
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
38 |
N/A |
INTRINSIC |
low complexity region
|
41 |
60 |
N/A |
INTRINSIC |
PHD
|
94 |
135 |
2.23e-11 |
SMART |
BROMO
|
151 |
258 |
1.77e-17 |
SMART |
Pfam:PWWP
|
280 |
355 |
6.6e-11 |
PFAM |
Pfam:DUF3544
|
417 |
626 |
2.6e-102 |
PFAM |
internal_repeat_2
|
644 |
705 |
6.15e-5 |
PROSPERO |
low complexity region
|
774 |
809 |
N/A |
INTRINSIC |
low complexity region
|
848 |
873 |
N/A |
INTRINSIC |
low complexity region
|
909 |
924 |
N/A |
INTRINSIC |
low complexity region
|
931 |
943 |
N/A |
INTRINSIC |
coiled coil region
|
972 |
1034 |
N/A |
INTRINSIC |
low complexity region
|
1111 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1198 |
1212 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152682
|
Predicted Effect |
probably null
Transcript: ENSMUST00000170272
AA Change: K501*
|
SMART Domains |
Protein: ENSMUSP00000128680 Gene: ENSMUSG00000039671 AA Change: K501*
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
low complexity region
|
37 |
56 |
N/A |
INTRINSIC |
PHD
|
65 |
106 |
2.23e-11 |
SMART |
BROMO
|
122 |
229 |
1.77e-17 |
SMART |
Pfam:PWWP
|
250 |
324 |
1.1e-11 |
PFAM |
Pfam:DUF3544
|
387 |
599 |
1.9e-111 |
PFAM |
internal_repeat_2
|
615 |
676 |
7.92e-5 |
PROSPERO |
low complexity region
|
745 |
780 |
N/A |
INTRINSIC |
low complexity region
|
828 |
843 |
N/A |
INTRINSIC |
low complexity region
|
850 |
862 |
N/A |
INTRINSIC |
coiled coil region
|
891 |
953 |
N/A |
INTRINSIC |
Pfam:zf-MYND
|
963 |
997 |
1.1e-6 |
PFAM |
low complexity region
|
1030 |
1050 |
N/A |
INTRINSIC |
low complexity region
|
1117 |
1131 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000177633
AA Change: K521*
|
SMART Domains |
Protein: ENSMUSP00000136211 Gene: ENSMUSG00000039671 AA Change: K521*
Domain | Start | End | E-Value | Type |
low complexity region
|
8 |
19 |
N/A |
INTRINSIC |
low complexity region
|
43 |
54 |
N/A |
INTRINSIC |
low complexity region
|
57 |
76 |
N/A |
INTRINSIC |
PHD
|
85 |
126 |
2.23e-11 |
SMART |
BROMO
|
142 |
249 |
1.77e-17 |
SMART |
Pfam:PWWP
|
270 |
344 |
9.6e-12 |
PFAM |
Pfam:DUF3544
|
407 |
619 |
1.8e-111 |
PFAM |
internal_repeat_2
|
635 |
696 |
6.45e-5 |
PROSPERO |
low complexity region
|
765 |
800 |
N/A |
INTRINSIC |
low complexity region
|
848 |
863 |
N/A |
INTRINSIC |
low complexity region
|
870 |
882 |
N/A |
INTRINSIC |
coiled coil region
|
911 |
973 |
N/A |
INTRINSIC |
Pfam:zf-MYND
|
983 |
1017 |
6.7e-7 |
PFAM |
low complexity region
|
1050 |
1070 |
N/A |
INTRINSIC |
low complexity region
|
1137 |
1151 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.8%
- 10x: 97.8%
- 20x: 96.4%
|
Validation Efficiency |
96% (47/49) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a receptor for activated C-kinase (RACK) protein. The encoded protein has been shown to bind in vitro to activated protein kinase C beta I. In addition, this protein is a cutaneous T-cell lymphoma-associated antigen. Finally, the protein contains a bromodomain and two zinc fingers, and is thought to be a transcriptional regulator. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
G |
T |
18: 6,630,166 (GRCm39) |
|
probably null |
Het |
Aarsd1 |
T |
A |
11: 101,301,971 (GRCm39) |
I332F |
probably damaging |
Het |
Abcd2 |
C |
T |
15: 91,058,908 (GRCm39) |
G512D |
probably damaging |
Het |
Adam6a |
T |
C |
12: 113,507,798 (GRCm39) |
I57T |
probably benign |
Het |
Adam6b |
C |
T |
12: 113,453,984 (GRCm39) |
T267I |
probably benign |
Het |
Ap1g2 |
G |
A |
14: 55,338,030 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
G |
A |
14: 33,089,378 (GRCm39) |
E455K |
probably benign |
Het |
Bltp1 |
G |
A |
3: 37,094,583 (GRCm39) |
V917I |
probably damaging |
Het |
Ccdc93 |
T |
C |
1: 121,389,969 (GRCm39) |
I253T |
probably damaging |
Het |
Cd44 |
T |
C |
2: 102,731,738 (GRCm39) |
|
probably null |
Het |
Cnot6 |
A |
T |
11: 49,579,999 (GRCm39) |
S98T |
probably benign |
Het |
Dnah9 |
C |
A |
11: 65,741,829 (GRCm39) |
|
probably null |
Het |
Edar |
T |
C |
10: 58,457,185 (GRCm39) |
Y131C |
probably damaging |
Het |
Eif5 |
A |
T |
12: 111,506,618 (GRCm39) |
R43* |
probably null |
Het |
Eml4 |
C |
A |
17: 83,780,494 (GRCm39) |
T667K |
probably damaging |
Het |
Fchsd1 |
A |
G |
18: 38,102,510 (GRCm39) |
|
probably benign |
Het |
Flt1 |
A |
G |
5: 147,636,827 (GRCm39) |
|
probably benign |
Het |
Frem2 |
T |
A |
3: 53,424,270 (GRCm39) |
I3056F |
probably damaging |
Het |
Hivep1 |
A |
T |
13: 42,337,787 (GRCm39) |
H2622L |
possibly damaging |
Het |
Ido2 |
T |
C |
8: 25,023,771 (GRCm39) |
I356V |
probably benign |
Het |
Insyn2b |
T |
C |
11: 34,353,007 (GRCm39) |
S350P |
probably benign |
Het |
Itgb3 |
C |
A |
11: 104,524,438 (GRCm39) |
Y191* |
probably null |
Het |
Kcnma1 |
T |
C |
14: 23,350,006 (GRCm39) |
T1178A |
possibly damaging |
Het |
Kcnt1 |
A |
G |
2: 25,790,904 (GRCm39) |
H486R |
probably damaging |
Het |
Kif21a |
T |
C |
15: 90,852,277 (GRCm39) |
N950S |
probably benign |
Het |
Lama1 |
C |
A |
17: 68,086,041 (GRCm39) |
|
probably null |
Het |
Lrrc4b |
T |
A |
7: 44,111,982 (GRCm39) |
V618E |
probably damaging |
Het |
Micall2 |
C |
T |
5: 139,701,611 (GRCm39) |
G461D |
possibly damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Ncoa6 |
T |
A |
2: 155,248,858 (GRCm39) |
N1482I |
probably damaging |
Het |
Pcdhga10 |
A |
G |
18: 37,880,995 (GRCm39) |
N252S |
probably damaging |
Het |
Pcdhgb7 |
C |
A |
18: 37,885,286 (GRCm39) |
T152K |
possibly damaging |
Het |
Pds5a |
A |
G |
5: 65,811,419 (GRCm39) |
V338A |
possibly damaging |
Het |
Pds5b |
T |
C |
5: 150,659,802 (GRCm39) |
V255A |
possibly damaging |
Het |
Prkar2a |
T |
G |
9: 108,624,155 (GRCm39) |
F391V |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,986,328 (GRCm39) |
C1056R |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,218,862 (GRCm39) |
|
probably benign |
Het |
Serpinb5 |
T |
A |
1: 106,802,802 (GRCm39) |
Y112* |
probably null |
Het |
Slc17a4 |
C |
T |
13: 24,085,752 (GRCm39) |
R387H |
probably benign |
Het |
Tdrd5 |
A |
G |
1: 156,113,053 (GRCm39) |
V409A |
probably benign |
Het |
Tenm2 |
A |
T |
11: 35,915,147 (GRCm39) |
I2129N |
probably damaging |
Het |
Tmem8b |
C |
A |
4: 43,689,745 (GRCm39) |
H800N |
probably damaging |
Het |
Trpm3 |
A |
T |
19: 22,964,813 (GRCm39) |
N1436I |
probably benign |
Het |
Unc13c |
A |
T |
9: 73,838,240 (GRCm39) |
S870R |
probably benign |
Het |
Vmn2r16 |
C |
T |
5: 109,510,143 (GRCm39) |
P509S |
probably benign |
Het |
Vmn2r60 |
A |
T |
7: 41,785,125 (GRCm39) |
E112D |
probably damaging |
Het |
Xpnpep1 |
G |
A |
19: 52,992,250 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
A |
T |
13: 67,769,438 (GRCm39) |
C264S |
probably damaging |
Het |
|
Other mutations in Zmynd8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01288:Zmynd8
|
APN |
2 |
165,654,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01311:Zmynd8
|
APN |
2 |
165,647,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02317:Zmynd8
|
APN |
2 |
165,662,492 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02548:Zmynd8
|
APN |
2 |
165,675,325 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02798:Zmynd8
|
APN |
2 |
165,694,070 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02933:Zmynd8
|
APN |
2 |
165,670,238 (GRCm39) |
missense |
possibly damaging |
0.65 |
cain
|
UTSW |
2 |
165,699,973 (GRCm39) |
critical splice donor site |
probably null |
|
F5770:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
I1329:Zmynd8
|
UTSW |
2 |
165,670,145 (GRCm39) |
missense |
probably damaging |
1.00 |
P0031:Zmynd8
|
UTSW |
2 |
165,662,618 (GRCm39) |
splice site |
probably benign |
|
R0267:Zmynd8
|
UTSW |
2 |
165,670,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Zmynd8
|
UTSW |
2 |
165,629,078 (GRCm39) |
splice site |
probably null |
|
R1663:Zmynd8
|
UTSW |
2 |
165,649,805 (GRCm39) |
missense |
probably benign |
0.11 |
R2212:Zmynd8
|
UTSW |
2 |
165,657,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R3412:Zmynd8
|
UTSW |
2 |
165,657,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R3413:Zmynd8
|
UTSW |
2 |
165,657,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R3749:Zmynd8
|
UTSW |
2 |
165,647,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R3836:Zmynd8
|
UTSW |
2 |
165,700,019 (GRCm39) |
missense |
probably benign |
0.05 |
R3957:Zmynd8
|
UTSW |
2 |
165,654,395 (GRCm39) |
missense |
probably damaging |
0.99 |
R4379:Zmynd8
|
UTSW |
2 |
165,649,858 (GRCm39) |
splice site |
probably null |
|
R4526:Zmynd8
|
UTSW |
2 |
165,649,527 (GRCm39) |
intron |
probably benign |
|
R4739:Zmynd8
|
UTSW |
2 |
165,647,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Zmynd8
|
UTSW |
2 |
165,681,954 (GRCm39) |
nonsense |
probably null |
|
R4932:Zmynd8
|
UTSW |
2 |
165,676,871 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4933:Zmynd8
|
UTSW |
2 |
165,676,871 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4997:Zmynd8
|
UTSW |
2 |
165,634,736 (GRCm39) |
missense |
probably benign |
0.01 |
R5652:Zmynd8
|
UTSW |
2 |
165,649,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5741:Zmynd8
|
UTSW |
2 |
165,681,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:Zmynd8
|
UTSW |
2 |
165,684,707 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6242:Zmynd8
|
UTSW |
2 |
165,740,867 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6332:Zmynd8
|
UTSW |
2 |
165,680,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Zmynd8
|
UTSW |
2 |
165,687,943 (GRCm39) |
nonsense |
probably null |
|
R6772:Zmynd8
|
UTSW |
2 |
165,649,521 (GRCm39) |
missense |
probably benign |
0.35 |
R6970:Zmynd8
|
UTSW |
2 |
165,717,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R6986:Zmynd8
|
UTSW |
2 |
165,675,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7229:Zmynd8
|
UTSW |
2 |
165,699,973 (GRCm39) |
critical splice donor site |
probably null |
|
R7266:Zmynd8
|
UTSW |
2 |
165,649,492 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7296:Zmynd8
|
UTSW |
2 |
165,681,929 (GRCm39) |
missense |
probably damaging |
0.98 |
R7642:Zmynd8
|
UTSW |
2 |
165,654,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R7818:Zmynd8
|
UTSW |
2 |
165,684,751 (GRCm39) |
missense |
probably damaging |
0.97 |
R7821:Zmynd8
|
UTSW |
2 |
165,723,000 (GRCm39) |
intron |
probably benign |
|
R8135:Zmynd8
|
UTSW |
2 |
165,654,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8828:Zmynd8
|
UTSW |
2 |
165,654,466 (GRCm39) |
missense |
probably benign |
0.00 |
R9128:Zmynd8
|
UTSW |
2 |
165,700,058 (GRCm39) |
start codon destroyed |
probably null |
|
R9200:Zmynd8
|
UTSW |
2 |
165,682,005 (GRCm39) |
missense |
probably benign |
|
R9345:Zmynd8
|
UTSW |
2 |
165,654,668 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9478:Zmynd8
|
UTSW |
2 |
165,649,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9626:Zmynd8
|
UTSW |
2 |
165,654,268 (GRCm39) |
critical splice donor site |
probably null |
|
R9649:Zmynd8
|
UTSW |
2 |
165,680,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R9759:Zmynd8
|
UTSW |
2 |
165,680,746 (GRCm39) |
missense |
possibly damaging |
0.89 |
V7580:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
V7581:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
V7583:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
Z1088:Zmynd8
|
UTSW |
2 |
165,670,091 (GRCm39) |
missense |
probably benign |
|
Z1176:Zmynd8
|
UTSW |
2 |
165,670,108 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCATCTCCAGAGACTAGCAC -3'
(R):5'- GCAGCTGGGATAAGCATTTTC -3'
Sequencing Primer
(F):5'- CCTAGCTGTGCTTTGCAA -3'
(R):5'- GCAGCTGGGATAAGCATTTTCTATAC -3'
|
Posted On |
2015-04-02 |