Incidental Mutation 'R9187:Abcb1a'
ID |
697428 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abcb1a
|
Ensembl Gene |
ENSMUSG00000040584 |
Gene Name |
ATP-binding cassette, sub-family B member 1A |
Synonyms |
Evi32, multiple drug resistant 1a, Pgp, MDR3, Pgy-3, Mdr1a, P-glycoprotein, P-gp, Pgy3, mdr-3 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.172)
|
Stock # |
R9187 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
8710077-8798575 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 8765016 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Serine
at position 669
(C669S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000041204
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047753]
|
AlphaFold |
P21447 |
PDB Structure |
Structure of P-glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [X-RAY DIFFRACTION]
Structure of P-glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [X-RAY DIFFRACTION]
Structure of P-glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [X-RAY DIFFRACTION]
Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain [X-RAY DIFFRACTION]
Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain [X-RAY DIFFRACTION]
Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain [X-RAY DIFFRACTION]
Structure of Mouse P-Glycoprotein [X-RAY DIFFRACTION]
Corrected Structure of Mouse P-glycoprotein [X-RAY DIFFRACTION]
Corrected Structure of Mouse P-glycoprotein bound to QZ59-RRR [X-RAY DIFFRACTION]
Corrected Structure of Mouse P-glycoprotein bound to QZ59-SSS [X-RAY DIFFRACTION]
>> 5 additional structures at PDB <<
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000047753
AA Change: C669S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000041204 Gene: ENSMUSG00000040584 AA Change: C669S
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
Pfam:ABC_membrane
|
50 |
339 |
8.3e-97 |
PFAM |
AAA
|
415 |
607 |
1.22e-20 |
SMART |
Pfam:ABC_membrane
|
707 |
982 |
4.8e-79 |
PFAM |
AAA
|
1058 |
1246 |
8.85e-18 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.5%
|
Validation Efficiency |
97% (70/72) |
MGI Phenotype |
FUNCTION: The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This gene encodes a p-glycoprotein which actively transports a variety of hydrophobic amphipathic drugs and plays a major role in the blood-brain barrier permeability of certain drugs. [provided by RefSeq, Jul 2008] PHENOTYPE: Mutations in this gene result in increased sensitivity to various drugs, including avermectins and vinblastine. Mice with a null allele develop spontanous colitis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,200,961 (GRCm39) |
|
probably null |
Het |
Abcc3 |
A |
G |
11: 94,255,913 (GRCm39) |
L524P |
probably damaging |
Het |
Akap5 |
A |
T |
12: 76,376,745 (GRCm39) |
K726* |
probably null |
Het |
Aldh16a1 |
T |
C |
7: 44,791,441 (GRCm39) |
E778G |
probably damaging |
Het |
Ankle2 |
G |
A |
5: 110,400,610 (GRCm39) |
V649M |
possibly damaging |
Het |
Apon |
A |
G |
10: 128,090,832 (GRCm39) |
N170S |
probably benign |
Het |
Baiap2l1 |
T |
C |
5: 144,217,764 (GRCm39) |
Y274C |
probably benign |
Het |
Bub1 |
A |
T |
2: 127,656,856 (GRCm39) |
N425K |
possibly damaging |
Het |
Camsap1 |
A |
G |
2: 25,820,028 (GRCm39) |
C1487R |
probably damaging |
Het |
Cd4 |
A |
C |
6: 124,844,651 (GRCm39) |
V378G |
probably damaging |
Het |
Cenpa |
C |
A |
5: 30,824,380 (GRCm39) |
P3Q |
unknown |
Het |
Cfap44 |
T |
C |
16: 44,225,144 (GRCm39) |
|
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,956,517 (GRCm39) |
M1021L |
probably benign |
Het |
Ddx39a |
G |
T |
8: 84,449,113 (GRCm39) |
M300I |
probably benign |
Het |
Dgkh |
T |
C |
14: 78,832,601 (GRCm39) |
R819G |
probably damaging |
Het |
Dlc1 |
A |
T |
8: 37,405,786 (GRCm39) |
M1K |
probably null |
Het |
Dnah9 |
A |
G |
11: 65,895,972 (GRCm39) |
W2468R |
probably benign |
Het |
Ebag9 |
A |
T |
15: 44,503,706 (GRCm39) |
K177I |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,101,184 (GRCm39) |
I249V |
probably damaging |
Het |
Fam171b |
T |
C |
2: 83,710,365 (GRCm39) |
V679A |
probably damaging |
Het |
Gabbr2 |
G |
A |
4: 46,674,533 (GRCm39) |
T818I |
probably damaging |
Het |
Gcn1 |
T |
C |
5: 115,752,177 (GRCm39) |
S2098P |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,302,991 (GRCm39) |
I609T |
probably damaging |
Het |
Gm5916 |
T |
G |
9: 36,032,020 (GRCm39) |
H88P |
probably benign |
Het |
Gon4l |
T |
C |
3: 88,786,618 (GRCm39) |
S586P |
probably benign |
Het |
Gzmg |
T |
A |
14: 56,394,714 (GRCm39) |
T185S |
probably benign |
Het |
Hipk3 |
T |
A |
2: 104,276,936 (GRCm39) |
D381V |
probably damaging |
Het |
Hnrnpul2 |
C |
A |
19: 8,808,319 (GRCm39) |
N681K |
probably benign |
Het |
Hpdl |
C |
A |
4: 116,678,372 (GRCm39) |
G30C |
probably damaging |
Het |
Iws1 |
G |
A |
18: 32,213,213 (GRCm39) |
E214K |
possibly damaging |
Het |
Krt82 |
C |
A |
15: 101,450,260 (GRCm39) |
V479L |
probably benign |
Het |
Lama4 |
G |
A |
10: 38,924,124 (GRCm39) |
|
probably null |
Het |
Lamc1 |
C |
A |
1: 153,097,434 (GRCm39) |
E1537* |
probably null |
Het |
Mab21l3 |
G |
A |
3: 101,730,594 (GRCm39) |
T215M |
probably benign |
Het |
Magi3 |
C |
A |
3: 103,923,073 (GRCm39) |
V1215F |
possibly damaging |
Het |
Mical2 |
T |
A |
7: 111,902,797 (GRCm39) |
C89* |
probably null |
Het |
Mitf |
T |
A |
6: 97,994,835 (GRCm39) |
V427D |
probably benign |
Het |
Muc4 |
T |
C |
16: 32,589,102 (GRCm39) |
V753A |
|
Het |
Myo16 |
G |
A |
8: 10,492,233 (GRCm39) |
R725H |
unknown |
Het |
Ncapg2 |
T |
A |
12: 116,402,287 (GRCm39) |
D706E |
probably damaging |
Het |
Ndst1 |
T |
C |
18: 60,824,268 (GRCm39) |
D803G |
probably benign |
Het |
Neb |
A |
T |
2: 52,096,115 (GRCm39) |
V5065D |
probably damaging |
Het |
Npm3 |
G |
A |
19: 45,737,941 (GRCm39) |
R19* |
probably null |
Het |
Ntrk3 |
A |
C |
7: 77,896,966 (GRCm39) |
N690K |
possibly damaging |
Het |
Or7g32 |
T |
C |
9: 19,389,166 (GRCm39) |
I127V |
probably benign |
Het |
Or7g35 |
T |
C |
9: 19,495,950 (GRCm39) |
I39T |
probably benign |
Het |
Or8d4 |
C |
A |
9: 40,038,886 (GRCm39) |
V124L |
possibly damaging |
Het |
P3h2 |
G |
A |
16: 25,924,186 (GRCm39) |
A83V |
probably benign |
Het |
Pdia2 |
A |
G |
17: 26,415,910 (GRCm39) |
S362P |
probably damaging |
Het |
Pmp22 |
C |
T |
11: 63,025,268 (GRCm39) |
H34Y |
probably benign |
Het |
Pmp22 |
T |
C |
11: 63,025,317 (GRCm39) |
V50A |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,255,006 (GRCm39) |
D283G |
probably damaging |
Het |
Pramel58 |
T |
C |
5: 94,831,755 (GRCm39) |
V254A |
probably benign |
Het |
Prss55 |
T |
A |
14: 64,314,531 (GRCm39) |
Q213L |
probably null |
Het |
Rgsl1 |
C |
T |
1: 153,669,613 (GRCm39) |
E258K |
possibly damaging |
Het |
Ripor2 |
T |
C |
13: 24,897,632 (GRCm39) |
F777L |
probably benign |
Het |
Rsf1 |
GGC |
GGCGGCGGCCGC |
7: 97,229,140 (GRCm39) |
|
probably benign |
Het |
Sgce |
G |
A |
6: 4,711,362 (GRCm39) |
R173C |
probably benign |
Het |
Sncaip |
T |
G |
18: 53,040,011 (GRCm39) |
M735R |
probably benign |
Het |
Snrpd2 |
T |
A |
7: 18,886,505 (GRCm39) |
I96N |
probably damaging |
Het |
Spryd3 |
T |
G |
15: 102,039,110 (GRCm39) |
D121A |
probably damaging |
Het |
Srsf3-ps |
A |
G |
11: 98,516,187 (GRCm39) |
V62A |
possibly damaging |
Het |
Sspo |
T |
C |
6: 48,472,223 (GRCm39) |
C149R |
probably damaging |
Het |
Tbc1d10b |
A |
T |
7: 126,807,105 (GRCm39) |
M144K |
probably benign |
Het |
Tbc1d31 |
T |
A |
15: 57,779,485 (GRCm39) |
I66N |
probably damaging |
Het |
Tssk1 |
A |
G |
16: 17,712,457 (GRCm39) |
T81A |
possibly damaging |
Het |
Ttc28 |
A |
G |
5: 111,249,902 (GRCm39) |
Y284C |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,573,755 (GRCm39) |
T25713A |
probably benign |
Het |
Vmn2r125 |
T |
C |
4: 156,703,554 (GRCm39) |
W311R |
probably damaging |
Het |
Vmn2r80 |
A |
T |
10: 79,030,438 (GRCm39) |
T755S |
probably benign |
Het |
Vmn2r98 |
T |
C |
17: 19,301,481 (GRCm39) |
C828R |
probably damaging |
Het |
Wwox |
T |
C |
8: 115,438,978 (GRCm39) |
F348S |
probably damaging |
Het |
Zeb2 |
T |
A |
2: 45,000,040 (GRCm39) |
R65W |
possibly damaging |
Het |
Zfp712 |
T |
A |
13: 67,188,637 (GRCm39) |
H630L |
probably damaging |
Het |
Zfp764 |
G |
T |
7: 127,004,608 (GRCm39) |
H174Q |
probably damaging |
Het |
|
Other mutations in Abcb1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00704:Abcb1a
|
APN |
5 |
8,736,257 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00898:Abcb1a
|
APN |
5 |
8,783,690 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01064:Abcb1a
|
APN |
5 |
8,782,388 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01118:Abcb1a
|
APN |
5 |
8,724,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01150:Abcb1a
|
APN |
5 |
8,752,550 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01584:Abcb1a
|
APN |
5 |
8,748,637 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01654:Abcb1a
|
APN |
5 |
8,765,065 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01820:Abcb1a
|
APN |
5 |
8,765,896 (GRCm39) |
splice site |
probably benign |
|
IGL02499:Abcb1a
|
APN |
5 |
8,776,807 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02711:Abcb1a
|
APN |
5 |
8,773,245 (GRCm39) |
splice site |
probably null |
|
IGL02954:Abcb1a
|
APN |
5 |
8,782,341 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03018:Abcb1a
|
APN |
5 |
8,752,451 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03119:Abcb1a
|
APN |
5 |
8,764,887 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03292:Abcb1a
|
APN |
5 |
8,765,827 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03338:Abcb1a
|
APN |
5 |
8,744,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R0418:Abcb1a
|
UTSW |
5 |
8,763,281 (GRCm39) |
missense |
probably damaging |
0.96 |
R0559:Abcb1a
|
UTSW |
5 |
8,748,535 (GRCm39) |
missense |
probably benign |
0.01 |
R0595:Abcb1a
|
UTSW |
5 |
8,790,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Abcb1a
|
UTSW |
5 |
8,748,539 (GRCm39) |
missense |
probably benign |
0.13 |
R0811:Abcb1a
|
UTSW |
5 |
8,763,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R0812:Abcb1a
|
UTSW |
5 |
8,763,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R0894:Abcb1a
|
UTSW |
5 |
8,724,856 (GRCm39) |
splice site |
probably benign |
|
R0948:Abcb1a
|
UTSW |
5 |
8,790,621 (GRCm39) |
splice site |
probably null |
|
R1292:Abcb1a
|
UTSW |
5 |
8,763,343 (GRCm39) |
missense |
probably benign |
0.00 |
R1318:Abcb1a
|
UTSW |
5 |
8,751,621 (GRCm39) |
missense |
probably benign |
0.31 |
R1459:Abcb1a
|
UTSW |
5 |
8,752,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Abcb1a
|
UTSW |
5 |
8,736,300 (GRCm39) |
critical splice donor site |
probably null |
|
R1514:Abcb1a
|
UTSW |
5 |
8,724,791 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2100:Abcb1a
|
UTSW |
5 |
8,763,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R2409:Abcb1a
|
UTSW |
5 |
8,788,747 (GRCm39) |
missense |
probably benign |
0.30 |
R2844:Abcb1a
|
UTSW |
5 |
8,736,164 (GRCm39) |
missense |
probably benign |
0.02 |
R3709:Abcb1a
|
UTSW |
5 |
8,788,738 (GRCm39) |
missense |
probably benign |
0.03 |
R3755:Abcb1a
|
UTSW |
5 |
8,797,403 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4193:Abcb1a
|
UTSW |
5 |
8,765,068 (GRCm39) |
splice site |
probably null |
|
R4401:Abcb1a
|
UTSW |
5 |
8,752,390 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4463:Abcb1a
|
UTSW |
5 |
8,769,981 (GRCm39) |
splice site |
probably benign |
|
R4539:Abcb1a
|
UTSW |
5 |
8,765,793 (GRCm39) |
missense |
probably benign |
|
R4635:Abcb1a
|
UTSW |
5 |
8,764,927 (GRCm39) |
missense |
probably benign |
|
R4740:Abcb1a
|
UTSW |
5 |
8,752,280 (GRCm39) |
critical splice donor site |
probably null |
|
R4757:Abcb1a
|
UTSW |
5 |
8,787,632 (GRCm39) |
missense |
probably damaging |
0.99 |
R4764:Abcb1a
|
UTSW |
5 |
8,765,732 (GRCm39) |
splice site |
probably null |
|
R4792:Abcb1a
|
UTSW |
5 |
8,796,657 (GRCm39) |
critical splice donor site |
probably null |
|
R4829:Abcb1a
|
UTSW |
5 |
8,773,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R4935:Abcb1a
|
UTSW |
5 |
8,787,773 (GRCm39) |
critical splice donor site |
probably null |
|
R5140:Abcb1a
|
UTSW |
5 |
8,752,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R5181:Abcb1a
|
UTSW |
5 |
8,764,937 (GRCm39) |
missense |
probably benign |
|
R5355:Abcb1a
|
UTSW |
5 |
8,776,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5406:Abcb1a
|
UTSW |
5 |
8,752,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R5496:Abcb1a
|
UTSW |
5 |
8,724,818 (GRCm39) |
missense |
probably benign |
|
R5557:Abcb1a
|
UTSW |
5 |
8,764,949 (GRCm39) |
missense |
probably benign |
0.01 |
R5572:Abcb1a
|
UTSW |
5 |
8,765,108 (GRCm39) |
splice site |
probably null |
|
R5702:Abcb1a
|
UTSW |
5 |
8,787,752 (GRCm39) |
missense |
probably benign |
0.15 |
R5753:Abcb1a
|
UTSW |
5 |
8,773,160 (GRCm39) |
missense |
probably damaging |
0.98 |
R5769:Abcb1a
|
UTSW |
5 |
8,733,426 (GRCm39) |
missense |
probably benign |
0.01 |
R5895:Abcb1a
|
UTSW |
5 |
8,752,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R6536:Abcb1a
|
UTSW |
5 |
8,769,030 (GRCm39) |
missense |
probably benign |
0.01 |
R6555:Abcb1a
|
UTSW |
5 |
8,752,468 (GRCm39) |
missense |
probably damaging |
0.97 |
R6798:Abcb1a
|
UTSW |
5 |
8,782,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Abcb1a
|
UTSW |
5 |
8,751,628 (GRCm39) |
missense |
probably benign |
0.28 |
R7000:Abcb1a
|
UTSW |
5 |
8,752,823 (GRCm39) |
missense |
probably benign |
0.19 |
R7102:Abcb1a
|
UTSW |
5 |
8,744,072 (GRCm39) |
missense |
probably benign |
0.01 |
R7172:Abcb1a
|
UTSW |
5 |
8,752,399 (GRCm39) |
missense |
probably benign |
0.00 |
R7313:Abcb1a
|
UTSW |
5 |
8,773,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Abcb1a
|
UTSW |
5 |
8,765,771 (GRCm39) |
nonsense |
probably null |
|
R7718:Abcb1a
|
UTSW |
5 |
8,765,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7816:Abcb1a
|
UTSW |
5 |
8,736,132 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7829:Abcb1a
|
UTSW |
5 |
8,748,623 (GRCm39) |
missense |
probably benign |
0.06 |
R7943:Abcb1a
|
UTSW |
5 |
8,736,222 (GRCm39) |
missense |
probably benign |
|
R8040:Abcb1a
|
UTSW |
5 |
8,765,035 (GRCm39) |
missense |
probably benign |
0.00 |
R8086:Abcb1a
|
UTSW |
5 |
8,724,833 (GRCm39) |
missense |
probably benign |
|
R8271:Abcb1a
|
UTSW |
5 |
8,736,212 (GRCm39) |
missense |
probably benign |
0.41 |
R8367:Abcb1a
|
UTSW |
5 |
8,736,221 (GRCm39) |
missense |
probably benign |
0.00 |
R8520:Abcb1a
|
UTSW |
5 |
8,735,346 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8680:Abcb1a
|
UTSW |
5 |
8,735,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R8820:Abcb1a
|
UTSW |
5 |
8,773,204 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8996:Abcb1a
|
UTSW |
5 |
8,769,069 (GRCm39) |
missense |
probably benign |
0.00 |
R9114:Abcb1a
|
UTSW |
5 |
8,788,702 (GRCm39) |
nonsense |
probably null |
|
R9127:Abcb1a
|
UTSW |
5 |
8,724,707 (GRCm39) |
missense |
probably benign |
|
R9294:Abcb1a
|
UTSW |
5 |
8,736,171 (GRCm39) |
missense |
probably benign |
0.02 |
R9459:Abcb1a
|
UTSW |
5 |
8,735,414 (GRCm39) |
critical splice donor site |
probably null |
|
R9581:Abcb1a
|
UTSW |
5 |
8,790,428 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9617:Abcb1a
|
UTSW |
5 |
8,797,353 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9676:Abcb1a
|
UTSW |
5 |
8,714,548 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9682:Abcb1a
|
UTSW |
5 |
8,752,507 (GRCm39) |
missense |
probably benign |
0.44 |
R9790:Abcb1a
|
UTSW |
5 |
8,748,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9791:Abcb1a
|
UTSW |
5 |
8,748,604 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Abcb1a
|
UTSW |
5 |
8,796,544 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- CCAACATGTGACACAAGATGG -3'
(R):5'- TTTCTGGAACACTCTGGAGAAC -3'
Sequencing Primer
(F):5'- TGAATTAGGAAATGAAGCTTG -3'
(R):5'- AACAGAGTTCCCACGTCT -3'
|
Posted On |
2022-02-07 |