Incidental Mutation 'R9211:Polr1a'
ID |
698858 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Polr1a
|
Ensembl Gene |
ENSMUSG00000049553 |
Gene Name |
polymerase (RNA) I polypeptide A |
Synonyms |
2900087K15Rik, 3010014K16Rik, 194kDa, mRPA1, Rpo1-4, RPA194 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R9211 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
71886037-71956419 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 71943521 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 1252
(I1252T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000060858
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055296]
|
AlphaFold |
O35134 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000055296
AA Change: I1252T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000060858 Gene: ENSMUSG00000049553 AA Change: I1252T
Domain | Start | End | E-Value | Type |
RPOLA_N
|
302 |
649 |
8.97e-137 |
SMART |
Pfam:RNA_pol_Rpb1_4
|
846 |
958 |
1.3e-26 |
PFAM |
Pfam:RNA_pol_Rpb1_5
|
965 |
1669 |
7e-103 |
PFAM |
low complexity region
|
1698 |
1708 |
N/A |
INTRINSIC |
|
Predicted Effect |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
Validation Efficiency |
99% (86/87) |
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 the largest subunit of the RNA polymerase I complex. The encoded protein represents the catalytic subunit of the complex, which transcribes DNA into ribosomal RNA precursors. Defects in this gene are a cause of the Cincinnati type of acrofacial dysostosis. [provided by RefSeq, May 2016]
|
Allele List at MGI |
All alleles(18) : Gene trapped(18) |
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
G |
T |
1: 120,099,161 (GRCm39) |
D85Y |
possibly damaging |
Het |
Accs |
T |
C |
2: 93,668,614 (GRCm39) |
R315G |
probably damaging |
Het |
Adam3 |
A |
C |
8: 25,177,910 (GRCm39) |
W668G |
probably benign |
Het |
Adgrb2 |
T |
A |
4: 129,886,199 (GRCm39) |
V113E |
probably benign |
Het |
Anapc4 |
C |
T |
5: 53,007,994 (GRCm39) |
T391I |
possibly damaging |
Het |
Angpt2 |
C |
T |
8: 18,748,078 (GRCm39) |
G394D |
probably benign |
Het |
Ankrd31 |
C |
G |
13: 97,029,551 (GRCm39) |
L1662V |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,612,370 (GRCm39) |
D1234G |
possibly damaging |
Het |
Ankrd6 |
C |
T |
4: 32,806,580 (GRCm39) |
V558M |
probably damaging |
Het |
Ankrd61 |
T |
A |
5: 143,828,358 (GRCm39) |
M206L |
probably benign |
Het |
Arhgap33 |
C |
T |
7: 30,223,023 (GRCm39) |
G970R |
possibly damaging |
Het |
Atf7 |
A |
G |
15: 102,437,117 (GRCm39) |
V115A |
unknown |
Het |
Atp2c2 |
A |
T |
8: 120,446,032 (GRCm39) |
R65S |
probably benign |
Het |
Atp8b5 |
T |
A |
4: 43,367,960 (GRCm39) |
M861K |
probably damaging |
Het |
Bmi1 |
T |
C |
2: 18,689,152 (GRCm39) |
S279P |
probably benign |
Het |
Bptf |
T |
G |
11: 106,946,124 (GRCm39) |
S2372R |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,879,308 (GRCm39) |
I15L |
unknown |
Het |
Card11 |
A |
G |
5: 140,869,375 (GRCm39) |
M807T |
probably benign |
Het |
Ccdc175 |
A |
T |
12: 72,153,458 (GRCm39) |
D704E |
probably damaging |
Het |
Cd300ld |
T |
A |
11: 114,878,386 (GRCm39) |
Y42F |
probably damaging |
Het |
Cdh1 |
A |
T |
8: 107,390,962 (GRCm39) |
T693S |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,638,214 (GRCm39) |
Y16C |
possibly damaging |
Het |
Col4a4 |
A |
G |
1: 82,506,501 (GRCm39) |
I273T |
unknown |
Het |
Coro2b |
C |
A |
9: 62,427,662 (GRCm39) |
V9L |
probably benign |
Het |
Crnkl1 |
T |
C |
2: 145,774,773 (GRCm39) |
D55G |
probably damaging |
Het |
Dcps |
T |
A |
9: 35,035,872 (GRCm39) |
N338I |
probably damaging |
Het |
Dusp2 |
A |
T |
2: 127,179,311 (GRCm39) |
H222L |
probably benign |
Het |
Dync1li1 |
C |
A |
9: 114,518,012 (GRCm39) |
Y21* |
probably null |
Het |
Efhb |
T |
G |
17: 53,756,507 (GRCm39) |
Q381H |
probably damaging |
Het |
Elac2 |
A |
T |
11: 64,869,864 (GRCm39) |
|
probably benign |
Het |
Etaa1 |
A |
G |
11: 17,896,053 (GRCm39) |
V688A |
possibly damaging |
Het |
Fam120c |
C |
T |
X: 150,127,495 (GRCm39) |
H84Y |
probably benign |
Het |
Fbxl7 |
T |
A |
15: 26,789,616 (GRCm39) |
N37I |
probably damaging |
Het |
Fndc3b |
A |
T |
3: 27,523,086 (GRCm39) |
W498R |
probably damaging |
Het |
Galc |
G |
A |
12: 98,173,699 (GRCm39) |
A621V |
probably benign |
Het |
Gch1 |
A |
T |
14: 47,426,519 (GRCm39) |
I69N |
probably damaging |
Het |
Gdpd4 |
T |
C |
7: 97,615,466 (GRCm39) |
V97A |
possibly damaging |
Het |
Hirip3 |
C |
T |
7: 126,463,567 (GRCm39) |
R485* |
probably null |
Het |
Hmgcs2 |
C |
T |
3: 98,204,748 (GRCm39) |
T302I |
possibly damaging |
Het |
Ing5 |
A |
T |
1: 93,740,409 (GRCm39) |
K137I |
possibly damaging |
Het |
Kcnh8 |
T |
A |
17: 53,146,236 (GRCm39) |
Y375N |
probably damaging |
Het |
Kdm3a |
C |
A |
6: 71,573,674 (GRCm39) |
W963L |
probably benign |
Het |
Klra17 |
T |
G |
6: 129,842,651 (GRCm39) |
I216L |
possibly damaging |
Het |
Kmt2e |
A |
G |
5: 23,669,770 (GRCm39) |
K86E |
possibly damaging |
Het |
Krt42 |
T |
C |
11: 100,155,867 (GRCm39) |
N293S |
possibly damaging |
Het |
Lrrc8d |
T |
A |
5: 105,960,216 (GRCm39) |
W209R |
probably damaging |
Het |
Mettl23 |
C |
T |
11: 116,734,469 (GRCm39) |
P13S |
unknown |
Het |
Ncln |
T |
C |
10: 81,323,527 (GRCm39) |
Y540C |
probably damaging |
Het |
Neb |
C |
G |
2: 52,135,360 (GRCm39) |
G3250A |
probably damaging |
Het |
Nebl |
A |
G |
2: 17,393,501 (GRCm39) |
|
probably null |
Het |
Nqo2 |
A |
T |
13: 34,156,399 (GRCm39) |
T38S |
probably benign |
Het |
Obscn |
A |
T |
11: 59,026,693 (GRCm39) |
I170N |
probably benign |
Het |
Or2bd2 |
G |
T |
7: 6,443,417 (GRCm39) |
G173W |
probably damaging |
Het |
Or4c100 |
A |
G |
2: 88,356,170 (GRCm39) |
D81G |
probably benign |
Het |
Or5af2 |
A |
T |
11: 58,708,709 (GRCm39) |
N292Y |
probably damaging |
Het |
Or5p6 |
C |
T |
7: 107,630,798 (GRCm39) |
V251I |
probably damaging |
Het |
Or7g28 |
T |
A |
9: 19,271,824 (GRCm39) |
I276F |
possibly damaging |
Het |
Or8k38 |
A |
T |
2: 86,488,024 (GRCm39) |
Y259* |
probably null |
Het |
Pacs1 |
A |
T |
19: 5,189,057 (GRCm39) |
V775E |
probably damaging |
Het |
Pheta2 |
A |
T |
15: 82,225,227 (GRCm39) |
|
probably benign |
Het |
Pmfbp1 |
T |
C |
8: 110,262,445 (GRCm39) |
I713T |
probably benign |
Het |
Pnma8b |
A |
G |
7: 16,679,589 (GRCm39) |
D191G |
unknown |
Het |
Prss16 |
A |
T |
13: 22,192,754 (GRCm39) |
M110K |
probably benign |
Het |
Pygo2 |
T |
C |
3: 89,338,038 (GRCm39) |
|
probably null |
Het |
Rab5b |
C |
A |
10: 128,519,063 (GRCm39) |
|
probably null |
Het |
Reln |
G |
T |
5: 22,549,200 (GRCm39) |
Y69* |
probably null |
Het |
Rgs12 |
T |
A |
5: 35,123,165 (GRCm39) |
M316K |
probably damaging |
Het |
Rmi2 |
T |
C |
16: 10,657,743 (GRCm39) |
C118R |
possibly damaging |
Het |
Rnf223 |
T |
A |
4: 156,216,834 (GRCm39) |
C70S |
probably damaging |
Het |
Rxrb |
T |
A |
17: 34,255,626 (GRCm39) |
F371Y |
probably damaging |
Het |
Smurf2 |
T |
A |
11: 106,759,463 (GRCm39) |
S78C |
probably damaging |
Het |
Sorbs1 |
A |
T |
19: 40,332,798 (GRCm39) |
|
probably null |
Het |
Spag17 |
C |
T |
3: 100,032,614 (GRCm39) |
|
probably benign |
Het |
Spidr |
T |
C |
16: 15,871,319 (GRCm39) |
H217R |
probably benign |
Het |
Tiam2 |
T |
G |
17: 3,498,729 (GRCm39) |
V835G |
possibly damaging |
Het |
Tm2d2 |
C |
T |
8: 25,510,548 (GRCm39) |
R136* |
probably null |
Het |
Tnks |
C |
T |
8: 35,316,489 (GRCm39) |
D877N |
probably damaging |
Het |
Tns1 |
A |
G |
1: 73,956,948 (GRCm39) |
L491P |
possibly damaging |
Het |
Trps1 |
A |
G |
15: 50,694,840 (GRCm39) |
I485T |
probably damaging |
Het |
Tubgcp5 |
A |
G |
7: 55,456,331 (GRCm39) |
S308G |
probably benign |
Het |
Ugt8a |
T |
C |
3: 125,661,130 (GRCm39) |
H454R |
probably damaging |
Het |
Usp32 |
G |
T |
11: 84,913,559 (GRCm39) |
T924K |
probably damaging |
Het |
Vmn2r91 |
A |
T |
17: 18,356,819 (GRCm39) |
K829* |
probably null |
Het |
Zfc3h1 |
T |
C |
10: 115,248,328 (GRCm39) |
F1146L |
possibly damaging |
Het |
Zfp729a |
G |
T |
13: 67,767,820 (GRCm39) |
A803E |
probably benign |
Het |
Zfp990 |
A |
G |
4: 145,264,171 (GRCm39) |
T390A |
probably damaging |
Het |
|
Other mutations in Polr1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01363:Polr1a
|
APN |
6 |
71,925,470 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01834:Polr1a
|
APN |
6 |
71,925,446 (GRCm39) |
missense |
probably benign |
|
IGL01902:Polr1a
|
APN |
6 |
71,940,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02101:Polr1a
|
APN |
6 |
71,927,786 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02325:Polr1a
|
APN |
6 |
71,897,641 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02398:Polr1a
|
APN |
6 |
71,913,540 (GRCm39) |
splice site |
probably benign |
|
IGL02528:Polr1a
|
APN |
6 |
71,941,701 (GRCm39) |
missense |
probably benign |
|
IGL02555:Polr1a
|
APN |
6 |
71,897,441 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02613:Polr1a
|
APN |
6 |
71,944,304 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02693:Polr1a
|
APN |
6 |
71,940,830 (GRCm39) |
splice site |
probably benign |
|
IGL02892:Polr1a
|
APN |
6 |
71,908,680 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03059:Polr1a
|
APN |
6 |
71,913,496 (GRCm39) |
missense |
probably benign |
|
IGL03174:Polr1a
|
APN |
6 |
71,954,331 (GRCm39) |
missense |
possibly damaging |
0.82 |
D4043:Polr1a
|
UTSW |
6 |
71,918,401 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0092:Polr1a
|
UTSW |
6 |
71,944,439 (GRCm39) |
splice site |
probably benign |
|
R0217:Polr1a
|
UTSW |
6 |
71,940,687 (GRCm39) |
missense |
probably benign |
0.19 |
R0267:Polr1a
|
UTSW |
6 |
71,951,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R0329:Polr1a
|
UTSW |
6 |
71,943,400 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0330:Polr1a
|
UTSW |
6 |
71,943,400 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0352:Polr1a
|
UTSW |
6 |
71,897,747 (GRCm39) |
splice site |
probably benign |
|
R0411:Polr1a
|
UTSW |
6 |
71,955,405 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0446:Polr1a
|
UTSW |
6 |
71,927,648 (GRCm39) |
critical splice donor site |
probably null |
|
R0846:Polr1a
|
UTSW |
6 |
71,901,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R1035:Polr1a
|
UTSW |
6 |
71,944,900 (GRCm39) |
missense |
probably benign |
|
R1294:Polr1a
|
UTSW |
6 |
71,889,886 (GRCm39) |
missense |
probably damaging |
0.99 |
R1460:Polr1a
|
UTSW |
6 |
71,918,368 (GRCm39) |
missense |
probably damaging |
0.99 |
R1657:Polr1a
|
UTSW |
6 |
71,918,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R1846:Polr1a
|
UTSW |
6 |
71,953,172 (GRCm39) |
missense |
probably damaging |
0.98 |
R1862:Polr1a
|
UTSW |
6 |
71,886,187 (GRCm39) |
missense |
probably damaging |
0.96 |
R1865:Polr1a
|
UTSW |
6 |
71,943,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Polr1a
|
UTSW |
6 |
71,944,898 (GRCm39) |
missense |
probably benign |
0.02 |
R1937:Polr1a
|
UTSW |
6 |
71,913,536 (GRCm39) |
critical splice donor site |
probably null |
|
R2063:Polr1a
|
UTSW |
6 |
71,913,269 (GRCm39) |
splice site |
probably null |
|
R2071:Polr1a
|
UTSW |
6 |
71,953,058 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2084:Polr1a
|
UTSW |
6 |
71,927,793 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2377:Polr1a
|
UTSW |
6 |
71,949,810 (GRCm39) |
critical splice donor site |
probably null |
|
R2410:Polr1a
|
UTSW |
6 |
71,951,866 (GRCm39) |
missense |
probably benign |
|
R3001:Polr1a
|
UTSW |
6 |
71,890,000 (GRCm39) |
missense |
probably benign |
0.01 |
R3001:Polr1a
|
UTSW |
6 |
71,942,628 (GRCm39) |
missense |
probably benign |
0.02 |
R3002:Polr1a
|
UTSW |
6 |
71,942,628 (GRCm39) |
missense |
probably benign |
0.02 |
R3002:Polr1a
|
UTSW |
6 |
71,890,000 (GRCm39) |
missense |
probably benign |
0.01 |
R3924:Polr1a
|
UTSW |
6 |
71,906,434 (GRCm39) |
missense |
probably benign |
0.00 |
R4105:Polr1a
|
UTSW |
6 |
71,953,175 (GRCm39) |
missense |
probably damaging |
0.98 |
R4125:Polr1a
|
UTSW |
6 |
71,942,690 (GRCm39) |
missense |
probably benign |
0.00 |
R4271:Polr1a
|
UTSW |
6 |
71,930,006 (GRCm39) |
missense |
probably benign |
0.02 |
R4440:Polr1a
|
UTSW |
6 |
71,927,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R4667:Polr1a
|
UTSW |
6 |
71,894,805 (GRCm39) |
missense |
probably benign |
0.30 |
R4769:Polr1a
|
UTSW |
6 |
71,927,852 (GRCm39) |
missense |
probably benign |
0.01 |
R4801:Polr1a
|
UTSW |
6 |
71,953,054 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Polr1a
|
UTSW |
6 |
71,953,054 (GRCm39) |
missense |
probably benign |
0.00 |
R4828:Polr1a
|
UTSW |
6 |
71,943,385 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4911:Polr1a
|
UTSW |
6 |
71,886,213 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5071:Polr1a
|
UTSW |
6 |
71,908,693 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5165:Polr1a
|
UTSW |
6 |
71,944,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R5223:Polr1a
|
UTSW |
6 |
71,944,891 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5239:Polr1a
|
UTSW |
6 |
71,890,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Polr1a
|
UTSW |
6 |
71,906,350 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5599:Polr1a
|
UTSW |
6 |
71,944,346 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5696:Polr1a
|
UTSW |
6 |
71,906,410 (GRCm39) |
missense |
probably benign |
0.05 |
R5850:Polr1a
|
UTSW |
6 |
71,903,667 (GRCm39) |
missense |
probably benign |
0.00 |
R6274:Polr1a
|
UTSW |
6 |
71,931,874 (GRCm39) |
splice site |
probably null |
|
R6526:Polr1a
|
UTSW |
6 |
71,906,427 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6578:Polr1a
|
UTSW |
6 |
71,953,025 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6660:Polr1a
|
UTSW |
6 |
71,944,358 (GRCm39) |
missense |
probably damaging |
0.98 |
R6892:Polr1a
|
UTSW |
6 |
71,941,696 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7274:Polr1a
|
UTSW |
6 |
71,897,500 (GRCm39) |
nonsense |
probably null |
|
R7291:Polr1a
|
UTSW |
6 |
71,918,440 (GRCm39) |
missense |
probably benign |
0.02 |
R7311:Polr1a
|
UTSW |
6 |
71,927,863 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7431:Polr1a
|
UTSW |
6 |
71,903,643 (GRCm39) |
missense |
probably benign |
0.14 |
R7479:Polr1a
|
UTSW |
6 |
71,913,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R7607:Polr1a
|
UTSW |
6 |
71,890,005 (GRCm39) |
missense |
probably benign |
|
R7739:Polr1a
|
UTSW |
6 |
71,931,819 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7746:Polr1a
|
UTSW |
6 |
71,918,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R7764:Polr1a
|
UTSW |
6 |
71,930,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R7835:Polr1a
|
UTSW |
6 |
71,892,126 (GRCm39) |
missense |
probably benign |
0.02 |
R8029:Polr1a
|
UTSW |
6 |
71,889,940 (GRCm39) |
nonsense |
probably null |
|
R8057:Polr1a
|
UTSW |
6 |
71,908,644 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8144:Polr1a
|
UTSW |
6 |
71,927,600 (GRCm39) |
missense |
probably benign |
|
R8170:Polr1a
|
UTSW |
6 |
71,897,733 (GRCm39) |
missense |
probably benign |
|
R8320:Polr1a
|
UTSW |
6 |
71,918,368 (GRCm39) |
missense |
probably damaging |
0.99 |
R8328:Polr1a
|
UTSW |
6 |
71,897,718 (GRCm39) |
missense |
probably benign |
|
R8331:Polr1a
|
UTSW |
6 |
71,953,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Polr1a
|
UTSW |
6 |
71,941,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8511:Polr1a
|
UTSW |
6 |
71,897,504 (GRCm39) |
missense |
probably benign |
0.01 |
R8709:Polr1a
|
UTSW |
6 |
71,951,832 (GRCm39) |
missense |
probably benign |
|
R8745:Polr1a
|
UTSW |
6 |
71,931,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R8784:Polr1a
|
UTSW |
6 |
71,927,612 (GRCm39) |
missense |
probably benign |
|
R9055:Polr1a
|
UTSW |
6 |
71,892,053 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9088:Polr1a
|
UTSW |
6 |
71,908,767 (GRCm39) |
missense |
probably benign |
0.26 |
R9228:Polr1a
|
UTSW |
6 |
71,931,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R9240:Polr1a
|
UTSW |
6 |
71,940,661 (GRCm39) |
nonsense |
probably null |
|
R9267:Polr1a
|
UTSW |
6 |
71,942,542 (GRCm39) |
missense |
probably benign |
|
R9302:Polr1a
|
UTSW |
6 |
71,901,683 (GRCm39) |
critical splice donor site |
probably null |
|
R9744:Polr1a
|
UTSW |
6 |
71,906,372 (GRCm39) |
missense |
probably benign |
0.05 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGATAGCCTAACACTTGCTCC -3'
(R):5'- CCTGATGATGTGGCAGAAGG -3'
Sequencing Primer
(F):5'- GATAGCCTAACACTTGCTCCTGATTC -3'
(R):5'- CTGATGATGTGGCAGAAGGATACAC -3'
|
Posted On |
2022-02-07 |