Incidental Mutation 'R8784:Dzip3'
ID |
670523 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dzip3
|
Ensembl Gene |
ENSMUSG00000064061 |
Gene Name |
DAZ interacting protein 3, zinc finger |
Synonyms |
2A-HUB, 2310047C04Rik, 6430549P11Rik |
MMRRC Submission |
068606-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R8784 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
48744591-48814505 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 48751628 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Glutamic Acid
at position 767
(V767E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000110161
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000114516]
[ENSMUST00000121869]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000114516
AA Change: V767E
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000110161 Gene: ENSMUSG00000064061 AA Change: V767E
Domain | Start | End | E-Value | Type |
low complexity region
|
451 |
472 |
N/A |
INTRINSIC |
coiled coil region
|
548 |
568 |
N/A |
INTRINSIC |
coiled coil region
|
599 |
650 |
N/A |
INTRINSIC |
low complexity region
|
743 |
754 |
N/A |
INTRINSIC |
low complexity region
|
883 |
891 |
N/A |
INTRINSIC |
RING
|
938 |
977 |
2.09e-7 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000121869
AA Change: V973E
PolyPhen 2
Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000113344 Gene: ENSMUSG00000064061 AA Change: V973E
Domain | Start | End | E-Value | Type |
low complexity region
|
657 |
678 |
N/A |
INTRINSIC |
coiled coil region
|
754 |
774 |
N/A |
INTRINSIC |
coiled coil region
|
805 |
856 |
N/A |
INTRINSIC |
low complexity region
|
949 |
960 |
N/A |
INTRINSIC |
low complexity region
|
1089 |
1097 |
N/A |
INTRINSIC |
RING
|
1144 |
1183 |
2.09e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000151950
|
SMART Domains |
Protein: ENSMUSP00000117675 Gene: ENSMUSG00000064061
Domain | Start | End | E-Value | Type |
low complexity region
|
82 |
90 |
N/A |
INTRINSIC |
SCOP:d1ldjb_
|
113 |
161 |
1e-3 |
SMART |
Blast:RING
|
137 |
161 |
4e-10 |
BLAST |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
Validation Efficiency |
100% (87/87) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for an ENU-indcued allele exhibit embryonic lethality. [provided by MGI curators]
|
Allele List at MGI |
All alleles(23) : Gene trapped(23)
|
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
A |
T |
7: 45,652,025 (GRCm39) |
M614K |
probably benign |
Het |
Adamts7 |
G |
T |
9: 90,075,918 (GRCm39) |
V1217L |
probably null |
Het |
Adcyap1r1 |
T |
A |
6: 55,458,100 (GRCm39) |
N300K |
probably damaging |
Het |
Atf7ip |
A |
G |
6: 136,576,648 (GRCm39) |
D1017G |
probably damaging |
Het |
Atg2b |
A |
C |
12: 105,605,500 (GRCm39) |
D1488E |
probably damaging |
Het |
Atxn2 |
A |
G |
5: 121,933,091 (GRCm39) |
T805A |
probably benign |
Het |
Azi2 |
A |
T |
9: 117,884,960 (GRCm39) |
H223L |
probably benign |
Het |
Banp |
T |
A |
8: 122,727,852 (GRCm39) |
S349T |
probably damaging |
Het |
Bicra |
A |
T |
7: 15,705,875 (GRCm39) |
I1522N |
probably damaging |
Het |
Brca2 |
A |
T |
5: 150,472,126 (GRCm39) |
R2342* |
probably null |
Het |
C6 |
T |
C |
15: 4,822,622 (GRCm39) |
C623R |
probably damaging |
Het |
Cc2d2a |
T |
C |
5: 43,860,645 (GRCm39) |
Y574H |
possibly damaging |
Het |
Cdk5rap3 |
C |
T |
11: 96,803,212 (GRCm39) |
C115Y |
probably benign |
Het |
Chrm4 |
T |
A |
2: 91,758,033 (GRCm39) |
M147K |
probably benign |
Het |
Cit |
A |
T |
5: 115,984,442 (GRCm39) |
K5* |
probably null |
Het |
Ciz1 |
T |
A |
2: 32,260,262 (GRCm39) |
S231T |
probably benign |
Het |
Crebrf |
A |
G |
17: 26,961,520 (GRCm39) |
I206V |
probably benign |
Het |
Cyc1 |
T |
C |
15: 76,227,863 (GRCm39) |
S34P |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,388,097 (GRCm39) |
I3185M |
probably benign |
Het |
Dtnbp1 |
T |
C |
13: 45,075,702 (GRCm39) |
D347G |
unknown |
Het |
Gdf3 |
A |
T |
6: 122,583,279 (GRCm39) |
C363S |
probably damaging |
Het |
Glb1l |
T |
C |
1: 75,176,975 (GRCm39) |
K487R |
probably damaging |
Het |
Gm9747 |
T |
C |
1: 82,212,002 (GRCm39) |
V67A |
unknown |
Het |
Hoxb2 |
A |
G |
11: 96,242,736 (GRCm39) |
T34A |
possibly damaging |
Het |
Ifnk |
C |
T |
4: 35,152,383 (GRCm39) |
R104C |
probably damaging |
Het |
Igfbp1 |
A |
T |
11: 7,151,952 (GRCm39) |
I252F |
probably damaging |
Het |
Ighv1-74 |
T |
C |
12: 115,766,480 (GRCm39) |
T47A |
probably benign |
Het |
Igkv4-62 |
A |
T |
6: 69,376,946 (GRCm39) |
W68R |
probably damaging |
Het |
Il23r |
A |
G |
6: 67,443,401 (GRCm39) |
I234T |
probably damaging |
Het |
Ints2 |
T |
A |
11: 86,112,963 (GRCm39) |
I852F |
probably damaging |
Het |
Ints2 |
G |
A |
11: 86,115,941 (GRCm39) |
Q763* |
probably null |
Het |
Jhy |
T |
G |
9: 40,872,182 (GRCm39) |
H109P |
probably benign |
Het |
Katna1 |
T |
A |
10: 7,614,579 (GRCm39) |
V29D |
possibly damaging |
Het |
Kcng4 |
T |
A |
8: 120,352,970 (GRCm39) |
E313D |
probably benign |
Het |
Klf14 |
T |
A |
6: 30,935,049 (GRCm39) |
H195L |
probably damaging |
Het |
Lama3 |
A |
G |
18: 12,554,212 (GRCm39) |
N472S |
probably benign |
Het |
Layn |
A |
T |
9: 50,970,781 (GRCm39) |
V254E |
possibly damaging |
Het |
Lrba |
A |
T |
3: 86,283,235 (GRCm39) |
S1850C |
probably damaging |
Het |
Map1s |
A |
G |
8: 71,358,909 (GRCm39) |
I2V |
unknown |
Het |
Map3k12 |
T |
A |
15: 102,413,797 (GRCm39) |
Q58L |
possibly damaging |
Het |
Minpp1 |
T |
C |
19: 32,491,396 (GRCm39) |
V358A |
probably benign |
Het |
Mymk |
C |
G |
2: 26,961,947 (GRCm39) |
K27N |
possibly damaging |
Het |
Nek8 |
T |
C |
11: 78,063,375 (GRCm39) |
K130E |
probably damaging |
Het |
Ngef |
T |
A |
1: 87,405,293 (GRCm39) |
S706C |
probably damaging |
Het |
Nsun6 |
G |
A |
2: 15,001,306 (GRCm39) |
Q417* |
probably null |
Het |
Ntsr2 |
G |
T |
12: 16,706,852 (GRCm39) |
Q293H |
probably damaging |
Het |
Ocln |
T |
A |
13: 100,676,050 (GRCm39) |
I148F |
probably damaging |
Het |
Or12d12 |
A |
G |
17: 37,610,701 (GRCm39) |
I204T |
probably benign |
Het |
Or4p19 |
A |
T |
2: 88,242,091 (GRCm39) |
Y304N |
probably benign |
Het |
Or8g30 |
T |
A |
9: 39,229,989 (GRCm39) |
Q307L |
probably benign |
Het |
Pank3 |
T |
G |
11: 35,672,412 (GRCm39) |
F272V |
probably damaging |
Het |
Piezo1 |
A |
T |
8: 123,223,328 (GRCm39) |
|
probably benign |
Het |
Plppr4 |
G |
A |
3: 117,116,190 (GRCm39) |
R556* |
probably null |
Het |
Polr1a |
G |
T |
6: 71,927,612 (GRCm39) |
R821L |
probably benign |
Het |
Ppp1r36 |
C |
T |
12: 76,485,967 (GRCm39) |
T375I |
probably benign |
Het |
Ptprj |
T |
A |
2: 90,290,856 (GRCm39) |
I628F |
possibly damaging |
Het |
Puf60 |
C |
A |
15: 75,949,525 (GRCm39) |
V29F |
unknown |
Het |
R3hdm2 |
T |
G |
10: 127,293,521 (GRCm39) |
S142A |
probably damaging |
Het |
Rassf1 |
A |
G |
9: 107,435,041 (GRCm39) |
S179G |
probably benign |
Het |
Rbm6 |
A |
G |
9: 107,665,337 (GRCm39) |
S772P |
possibly damaging |
Het |
Rnf103 |
T |
G |
6: 71,486,982 (GRCm39) |
S538A |
probably benign |
Het |
Scoc |
C |
A |
8: 84,164,245 (GRCm39) |
V58L |
probably benign |
Het |
Secisbp2l |
G |
A |
2: 125,602,263 (GRCm39) |
Q366* |
probably null |
Het |
Slc16a14 |
T |
C |
1: 84,890,784 (GRCm39) |
T174A |
probably benign |
Het |
Slc25a22 |
A |
C |
7: 141,011,020 (GRCm39) |
*324G |
probably null |
Het |
Smarca2 |
C |
T |
19: 26,753,558 (GRCm39) |
T197I |
probably benign |
Het |
Speg |
T |
C |
1: 75,381,793 (GRCm39) |
|
probably benign |
Het |
Srgap2 |
T |
A |
1: 131,223,212 (GRCm39) |
N858I |
unknown |
Het |
Syna |
C |
T |
5: 134,588,723 (GRCm39) |
M75I |
probably benign |
Het |
Tbc1d22b |
T |
C |
17: 29,818,918 (GRCm39) |
I424T |
probably damaging |
Het |
Tcaf1 |
T |
G |
6: 42,656,221 (GRCm39) |
T252P |
probably benign |
Het |
Thbs1 |
A |
G |
2: 117,943,613 (GRCm39) |
D77G |
probably damaging |
Het |
Tlcd3a |
T |
C |
11: 76,098,941 (GRCm39) |
F237S |
probably damaging |
Het |
Trim21 |
T |
C |
7: 102,208,675 (GRCm39) |
E348G |
probably benign |
Het |
Trpm3 |
A |
G |
19: 22,896,040 (GRCm39) |
D959G |
probably benign |
Het |
Ttc24 |
A |
T |
3: 87,980,033 (GRCm39) |
C182* |
probably null |
Het |
Tti1 |
T |
C |
2: 157,850,514 (GRCm39) |
T242A |
probably benign |
Het |
Ube2q2l |
G |
A |
6: 136,378,729 (GRCm39) |
Q34* |
probably null |
Het |
Ube3b |
G |
T |
5: 114,526,800 (GRCm39) |
C100F |
probably damaging |
Het |
Vmn1r26 |
T |
A |
6: 57,985,440 (GRCm39) |
T250S |
possibly damaging |
Het |
Vnn1 |
A |
G |
10: 23,780,526 (GRCm39) |
T505A |
probably benign |
Het |
Vps13a |
C |
A |
19: 16,642,153 (GRCm39) |
W2158L |
probably damaging |
Het |
Vwa1 |
A |
T |
4: 155,857,345 (GRCm39) |
V151E |
probably damaging |
Het |
Zfp14 |
A |
G |
7: 29,742,961 (GRCm39) |
S46P |
probably damaging |
Het |
Zfp773 |
C |
A |
7: 7,135,570 (GRCm39) |
C342F |
probably benign |
Het |
Zscan12 |
T |
A |
13: 21,547,991 (GRCm39) |
S58T |
possibly damaging |
Het |
|
Other mutations in Dzip3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00825:Dzip3
|
APN |
16 |
48,748,778 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00931:Dzip3
|
APN |
16 |
48,755,860 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01109:Dzip3
|
APN |
16 |
48,750,037 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01121:Dzip3
|
APN |
16 |
48,765,244 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01328:Dzip3
|
APN |
16 |
48,792,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01729:Dzip3
|
APN |
16 |
48,748,726 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02044:Dzip3
|
APN |
16 |
48,768,790 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02051:Dzip3
|
APN |
16 |
48,792,617 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02115:Dzip3
|
APN |
16 |
48,768,848 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02125:Dzip3
|
APN |
16 |
48,747,959 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Dzip3
|
APN |
16 |
48,747,945 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02244:Dzip3
|
APN |
16 |
48,801,351 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02253:Dzip3
|
APN |
16 |
48,765,287 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02412:Dzip3
|
APN |
16 |
48,778,820 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02452:Dzip3
|
APN |
16 |
48,758,900 (GRCm39) |
splice site |
probably benign |
|
IGL02481:Dzip3
|
APN |
16 |
48,795,914 (GRCm39) |
splice site |
probably benign |
|
IGL02499:Dzip3
|
APN |
16 |
48,754,213 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02511:Dzip3
|
APN |
16 |
48,757,343 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02519:Dzip3
|
APN |
16 |
48,748,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02610:Dzip3
|
APN |
16 |
48,772,016 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03129:Dzip3
|
APN |
16 |
48,762,446 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03342:Dzip3
|
APN |
16 |
48,749,986 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03493:Dzip3
|
APN |
16 |
48,772,059 (GRCm39) |
missense |
probably benign |
0.32 |
corvette
|
UTSW |
16 |
48,747,903 (GRCm39) |
critical splice donor site |
probably null |
|
dazwick
|
UTSW |
16 |
48,778,828 (GRCm39) |
missense |
possibly damaging |
0.90 |
1mM(1):Dzip3
|
UTSW |
16 |
48,771,920 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4651001:Dzip3
|
UTSW |
16 |
48,765,241 (GRCm39) |
missense |
probably benign |
|
R0313:Dzip3
|
UTSW |
16 |
48,757,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R0483:Dzip3
|
UTSW |
16 |
48,768,076 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0504:Dzip3
|
UTSW |
16 |
48,780,006 (GRCm39) |
splice site |
probably benign |
|
R0744:Dzip3
|
UTSW |
16 |
48,780,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Dzip3
|
UTSW |
16 |
48,774,171 (GRCm39) |
splice site |
probably benign |
|
R0927:Dzip3
|
UTSW |
16 |
48,795,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R0931:Dzip3
|
UTSW |
16 |
48,771,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Dzip3
|
UTSW |
16 |
48,781,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R1203:Dzip3
|
UTSW |
16 |
48,772,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Dzip3
|
UTSW |
16 |
48,772,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Dzip3
|
UTSW |
16 |
48,765,985 (GRCm39) |
missense |
probably benign |
0.19 |
R1526:Dzip3
|
UTSW |
16 |
48,757,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1560:Dzip3
|
UTSW |
16 |
48,771,903 (GRCm39) |
splice site |
probably null |
|
R1585:Dzip3
|
UTSW |
16 |
48,798,241 (GRCm39) |
splice site |
probably benign |
|
R1682:Dzip3
|
UTSW |
16 |
48,778,780 (GRCm39) |
critical splice donor site |
probably null |
|
R1957:Dzip3
|
UTSW |
16 |
48,747,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R2472:Dzip3
|
UTSW |
16 |
48,774,150 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2571:Dzip3
|
UTSW |
16 |
48,792,581 (GRCm39) |
splice site |
probably null |
|
R3040:Dzip3
|
UTSW |
16 |
48,748,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Dzip3
|
UTSW |
16 |
48,747,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R3615:Dzip3
|
UTSW |
16 |
48,757,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R3616:Dzip3
|
UTSW |
16 |
48,757,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R3786:Dzip3
|
UTSW |
16 |
48,795,906 (GRCm39) |
missense |
probably benign |
0.08 |
R3851:Dzip3
|
UTSW |
16 |
48,770,376 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4097:Dzip3
|
UTSW |
16 |
48,778,852 (GRCm39) |
nonsense |
probably null |
|
R4371:Dzip3
|
UTSW |
16 |
48,763,818 (GRCm39) |
critical splice donor site |
probably null |
|
R4612:Dzip3
|
UTSW |
16 |
48,772,403 (GRCm39) |
nonsense |
probably null |
|
R4671:Dzip3
|
UTSW |
16 |
48,799,953 (GRCm39) |
nonsense |
probably null |
|
R4695:Dzip3
|
UTSW |
16 |
48,771,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R4696:Dzip3
|
UTSW |
16 |
48,746,332 (GRCm39) |
unclassified |
probably benign |
|
R4769:Dzip3
|
UTSW |
16 |
48,758,837 (GRCm39) |
missense |
probably damaging |
0.97 |
R5063:Dzip3
|
UTSW |
16 |
48,774,117 (GRCm39) |
nonsense |
probably null |
|
R5321:Dzip3
|
UTSW |
16 |
48,778,038 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5764:Dzip3
|
UTSW |
16 |
48,747,724 (GRCm39) |
intron |
probably benign |
|
R6020:Dzip3
|
UTSW |
16 |
48,772,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Dzip3
|
UTSW |
16 |
48,778,828 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6300:Dzip3
|
UTSW |
16 |
48,772,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R6365:Dzip3
|
UTSW |
16 |
48,751,636 (GRCm39) |
missense |
probably damaging |
0.96 |
R6778:Dzip3
|
UTSW |
16 |
48,802,446 (GRCm39) |
missense |
probably benign |
0.00 |
R6915:Dzip3
|
UTSW |
16 |
48,762,488 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7047:Dzip3
|
UTSW |
16 |
48,802,489 (GRCm39) |
missense |
probably benign |
0.04 |
R7059:Dzip3
|
UTSW |
16 |
48,801,305 (GRCm39) |
missense |
probably benign |
0.34 |
R7095:Dzip3
|
UTSW |
16 |
48,748,153 (GRCm39) |
missense |
probably benign |
|
R7227:Dzip3
|
UTSW |
16 |
48,771,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R7319:Dzip3
|
UTSW |
16 |
48,747,903 (GRCm39) |
critical splice donor site |
probably null |
|
R7436:Dzip3
|
UTSW |
16 |
48,772,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7469:Dzip3
|
UTSW |
16 |
48,765,242 (GRCm39) |
missense |
probably benign |
|
R7526:Dzip3
|
UTSW |
16 |
48,795,837 (GRCm39) |
missense |
probably damaging |
0.99 |
R7964:Dzip3
|
UTSW |
16 |
48,772,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R8131:Dzip3
|
UTSW |
16 |
48,754,156 (GRCm39) |
critical splice donor site |
probably null |
|
R8188:Dzip3
|
UTSW |
16 |
48,772,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8209:Dzip3
|
UTSW |
16 |
48,798,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R8750:Dzip3
|
UTSW |
16 |
48,801,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R8758:Dzip3
|
UTSW |
16 |
48,798,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R9086:Dzip3
|
UTSW |
16 |
48,781,493 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9157:Dzip3
|
UTSW |
16 |
48,748,124 (GRCm39) |
missense |
probably benign |
|
R9170:Dzip3
|
UTSW |
16 |
48,772,401 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9762:Dzip3
|
UTSW |
16 |
48,748,707 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- ACTGCAATTTCAAGGTCTCAGTAG -3'
(R):5'- TGGCATTCAAAGGTATACAAGCC -3'
Sequencing Primer
(F):5'- TCACTTAATTATCATCATCACCAGC -3'
(R):5'- GGTATACAAGCCAGTTCTTCTATCAC -3'
|
Posted On |
2021-04-30 |