Incidental Mutation 'R8817:Rpgrip1'
ID |
672839 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Rpgrip1
|
Ensembl Gene |
ENSMUSG00000057132 |
Gene Name |
retinitis pigmentosa GTPase regulator interacting protein 1 |
Synonyms |
A930002K18Rik, 4930505G06Rik, nmf247, 4930401L23Rik |
MMRRC Submission |
068727-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.232)
|
Stock # |
R8817 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
52348161-52401003 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 52378056 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 468
(V468A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000107230
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000111600]
[ENSMUST00000111603]
[ENSMUST00000180646]
[ENSMUST00000181401]
|
AlphaFold |
Q9EPQ2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000111600
AA Change: V468A
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000107227 Gene: ENSMUSG00000057132 AA Change: V468A
Domain | Start | End | E-Value | Type |
low complexity region
|
98 |
119 |
N/A |
INTRINSIC |
coiled coil region
|
248 |
348 |
N/A |
INTRINSIC |
coiled coil region
|
499 |
542 |
N/A |
INTRINSIC |
C2
|
602 |
707 |
1.08e-2 |
SMART |
coiled coil region
|
746 |
795 |
N/A |
INTRINSIC |
Blast:C2
|
958 |
1086 |
1e-37 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000111603
AA Change: V468A
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000107230 Gene: ENSMUSG00000057132 AA Change: V468A
Domain | Start | End | E-Value | Type |
low complexity region
|
98 |
119 |
N/A |
INTRINSIC |
coiled coil region
|
248 |
348 |
N/A |
INTRINSIC |
coiled coil region
|
499 |
543 |
N/A |
INTRINSIC |
Pfam:C2-C2_1
|
582 |
721 |
1.9e-49 |
PFAM |
C2
|
764 |
869 |
7.3e-5 |
SMART |
coiled coil region
|
910 |
999 |
N/A |
INTRINSIC |
Blast:C2
|
1162 |
1290 |
2e-37 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000180513
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000180646
|
SMART Domains |
Protein: ENSMUSP00000137751 Gene: ENSMUSG00000057132
Domain | Start | End | E-Value | Type |
low complexity region
|
98 |
119 |
N/A |
INTRINSIC |
coiled coil region
|
248 |
276 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000181401
AA Change: V468A
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000138027 Gene: ENSMUSG00000057132 AA Change: V468A
Domain | Start | End | E-Value | Type |
low complexity region
|
98 |
119 |
N/A |
INTRINSIC |
coiled coil region
|
248 |
348 |
N/A |
INTRINSIC |
coiled coil region
|
499 |
547 |
N/A |
INTRINSIC |
Pfam:DUF3250
|
605 |
710 |
2.8e-46 |
PFAM |
C2
|
753 |
858 |
1.08e-2 |
SMART |
coiled coil region
|
899 |
988 |
N/A |
INTRINSIC |
Blast:C2
|
1151 |
1279 |
1e-37 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000181627
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000181709
|
Meta Mutation Damage Score |
0.0682 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.8%
- 20x: 99.4%
|
Validation Efficiency |
99% (77/78) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008] PHENOTYPE: Homozygous mutation of this gene results in photoreceptor cell dysmorphology. By 3 months of age mutant animals show near complete loss of photoreceptor cells. [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 |
Aadacl4fm4 |
A |
G |
4: 144,400,361 (GRCm39) |
V139A |
probably benign |
Het |
Aass |
A |
T |
6: 23,097,195 (GRCm39) |
Y41* |
probably null |
Het |
AI429214 |
G |
A |
8: 37,461,268 (GRCm39) |
V139I |
probably benign |
Het |
Cacna1a |
G |
A |
8: 85,365,426 (GRCm39) |
A2190T |
probably benign |
Het |
Cstpp1 |
A |
G |
2: 91,107,343 (GRCm39) |
Y320H |
probably benign |
Het |
Cutc |
T |
C |
19: 43,744,113 (GRCm39) |
V38A |
probably benign |
Het |
Cxcl10 |
G |
T |
5: 92,495,230 (GRCm39) |
P98H |
probably damaging |
Het |
Dop1a |
T |
C |
9: 86,396,003 (GRCm39) |
S822P |
possibly damaging |
Het |
Dusp19 |
T |
C |
2: 80,454,631 (GRCm39) |
L117P |
probably damaging |
Het |
Emc3 |
A |
G |
6: 113,492,868 (GRCm39) |
F261S |
probably damaging |
Het |
Ephx2 |
T |
C |
14: 66,344,725 (GRCm39) |
T200A |
probably benign |
Het |
Eri1 |
A |
C |
8: 35,945,792 (GRCm39) |
D164E |
probably damaging |
Het |
Ethe1 |
T |
C |
7: 24,305,727 (GRCm39) |
I158T |
probably damaging |
Het |
Fancm |
C |
T |
12: 65,167,331 (GRCm39) |
R1547C |
probably damaging |
Het |
Fer1l4 |
T |
A |
2: 155,890,143 (GRCm39) |
T261S |
probably damaging |
Het |
Fyb2 |
A |
G |
4: 104,802,652 (GRCm39) |
R185G |
probably benign |
Het |
Gabrp |
A |
T |
11: 33,504,464 (GRCm39) |
S284T |
possibly damaging |
Het |
Gga2 |
G |
A |
7: 121,590,845 (GRCm39) |
R488* |
probably null |
Het |
Gm9758 |
A |
G |
5: 14,962,230 (GRCm39) |
L126S |
probably damaging |
Het |
Gse1 |
T |
C |
8: 121,294,542 (GRCm39) |
F290L |
probably damaging |
Het |
Hdgfl1 |
A |
G |
13: 26,954,068 (GRCm39) |
S2P |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
Huwe1 |
A |
G |
X: 150,669,993 (GRCm39) |
K1482R |
probably benign |
Het |
Lama2 |
A |
T |
10: 27,063,869 (GRCm39) |
W1307R |
probably damaging |
Het |
Map3k6 |
A |
G |
4: 132,974,071 (GRCm39) |
K517E |
probably benign |
Het |
Mbl1 |
T |
A |
14: 40,875,555 (GRCm39) |
L3Q |
unknown |
Het |
Mepe |
G |
T |
5: 104,485,151 (GRCm39) |
R97L |
probably benign |
Het |
Minpp1 |
T |
A |
19: 32,463,747 (GRCm39) |
M136K |
possibly damaging |
Het |
Mrgprb1 |
T |
A |
7: 48,097,070 (GRCm39) |
I281F |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,349,207 (GRCm39) |
I1374V |
probably benign |
Het |
Or14j8 |
A |
G |
17: 38,263,273 (GRCm39) |
I214T |
probably damaging |
Het |
Or4c12 |
A |
G |
2: 89,773,790 (GRCm39) |
L223S |
probably damaging |
Het |
Or52e19b |
A |
T |
7: 103,032,825 (GRCm39) |
I128N |
probably damaging |
Het |
Or8g34 |
C |
T |
9: 39,373,387 (GRCm39) |
S217F |
probably damaging |
Het |
Or8g37 |
G |
T |
9: 39,730,939 (GRCm39) |
M1I |
probably null |
Het |
Pamr1 |
T |
G |
2: 102,464,766 (GRCm39) |
V305G |
probably benign |
Het |
Pcbp3 |
T |
C |
10: 76,625,670 (GRCm39) |
T125A |
probably benign |
Het |
Peli2 |
G |
A |
14: 48,490,130 (GRCm39) |
E201K |
possibly damaging |
Het |
Pitpnm3 |
T |
C |
11: 71,941,894 (GRCm39) |
E971G |
possibly damaging |
Het |
Pkdrej |
A |
G |
15: 85,702,774 (GRCm39) |
V1054A |
probably damaging |
Het |
Plcb1 |
G |
A |
2: 135,175,429 (GRCm39) |
|
probably benign |
Het |
Prpf40a |
T |
C |
2: 53,042,971 (GRCm39) |
K480E |
probably damaging |
Het |
Psd3 |
A |
G |
8: 68,413,135 (GRCm39) |
I465T |
possibly damaging |
Het |
Pskh1 |
C |
T |
8: 106,656,352 (GRCm39) |
R343W |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,007,371 (GRCm39) |
T1645S |
probably damaging |
Het |
Rasal1 |
T |
C |
5: 120,808,416 (GRCm39) |
F483L |
probably damaging |
Het |
Rbm28 |
T |
C |
6: 29,155,023 (GRCm39) |
|
probably benign |
Het |
Recql |
G |
A |
6: 142,304,612 (GRCm39) |
|
probably benign |
Het |
Rnf40 |
T |
C |
7: 127,196,332 (GRCm39) |
V760A |
probably damaging |
Het |
Rp1l1 |
A |
T |
14: 64,268,085 (GRCm39) |
R1224W |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,750,509 (GRCm39) |
I1921F |
possibly damaging |
Het |
Sirpa |
G |
A |
2: 129,435,558 (GRCm39) |
G9D |
unknown |
Het |
Slc28a2b |
A |
T |
2: 122,348,988 (GRCm39) |
T305S |
possibly damaging |
Het |
Slc40a1 |
A |
C |
1: 45,948,699 (GRCm39) |
V527G |
probably damaging |
Het |
Smarca4 |
T |
A |
9: 21,547,497 (GRCm39) |
M260K |
probably benign |
Het |
Smarca5 |
A |
T |
8: 81,460,379 (GRCm39) |
M119K |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,758,887 (GRCm39) |
V2206A |
unknown |
Het |
Sp4 |
A |
T |
12: 118,225,624 (GRCm39) |
V580D |
possibly damaging |
Het |
Spata31d1c |
G |
A |
13: 65,182,376 (GRCm39) |
C75Y |
probably damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Srcap |
T |
C |
7: 127,152,395 (GRCm39) |
S2220P |
probably benign |
Het |
Stra6 |
G |
T |
9: 58,059,265 (GRCm39) |
V543F |
possibly damaging |
Het |
Tenm4 |
T |
A |
7: 96,523,335 (GRCm39) |
F1626I |
probably benign |
Het |
Tjp1 |
T |
C |
7: 64,952,810 (GRCm39) |
N1508S |
probably benign |
Het |
Trrap |
T |
A |
5: 144,782,348 (GRCm39) |
L3298Q |
probably damaging |
Het |
Tsn |
A |
G |
1: 118,232,470 (GRCm39) |
L135P |
probably damaging |
Het |
Ttl |
A |
T |
2: 128,910,778 (GRCm39) |
H54L |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,660,251 (GRCm39) |
T12110S |
unknown |
Het |
Uba6 |
T |
C |
5: 86,296,772 (GRCm39) |
I306V |
probably null |
Het |
Ubap2 |
A |
G |
4: 41,223,425 (GRCm39) |
S204P |
possibly damaging |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Ush2a |
A |
T |
1: 187,995,231 (GRCm39) |
M1L |
probably benign |
Het |
Vmn1r159 |
C |
A |
7: 22,542,559 (GRCm39) |
V158F |
probably benign |
Het |
Wif1 |
A |
G |
10: 120,932,621 (GRCm39) |
H333R |
possibly damaging |
Het |
Zfp282 |
T |
A |
6: 47,881,760 (GRCm39) |
N482K |
probably benign |
Het |
|
Other mutations in Rpgrip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00333:Rpgrip1
|
APN |
14 |
52,387,895 (GRCm39) |
splice site |
probably null |
|
IGL01016:Rpgrip1
|
APN |
14 |
52,383,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01019:Rpgrip1
|
APN |
14 |
52,368,633 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01382:Rpgrip1
|
APN |
14 |
52,382,934 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01433:Rpgrip1
|
APN |
14 |
52,363,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01528:Rpgrip1
|
APN |
14 |
52,349,634 (GRCm39) |
nonsense |
probably null |
|
IGL01548:Rpgrip1
|
APN |
14 |
52,363,728 (GRCm39) |
splice site |
probably benign |
|
IGL01652:Rpgrip1
|
APN |
14 |
52,382,949 (GRCm39) |
unclassified |
probably benign |
|
IGL02040:Rpgrip1
|
APN |
14 |
52,358,476 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02113:Rpgrip1
|
APN |
14 |
52,371,301 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02121:Rpgrip1
|
APN |
14 |
52,384,831 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02185:Rpgrip1
|
APN |
14 |
52,349,685 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02234:Rpgrip1
|
APN |
14 |
52,368,766 (GRCm39) |
splice site |
probably benign |
|
IGL02322:Rpgrip1
|
APN |
14 |
52,387,499 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02379:Rpgrip1
|
APN |
14 |
52,376,345 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02524:Rpgrip1
|
APN |
14 |
52,358,511 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02836:Rpgrip1
|
APN |
14 |
52,382,714 (GRCm39) |
splice site |
probably null |
|
IGL03264:Rpgrip1
|
APN |
14 |
52,378,109 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03410:Rpgrip1
|
APN |
14 |
52,395,823 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Rpgrip1
|
UTSW |
14 |
52,387,001 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4976:Rpgrip1
|
UTSW |
14 |
52,386,851 (GRCm39) |
utr 3 prime |
probably benign |
|
R0045:Rpgrip1
|
UTSW |
14 |
52,378,601 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0045:Rpgrip1
|
UTSW |
14 |
52,378,601 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0089:Rpgrip1
|
UTSW |
14 |
52,386,841 (GRCm39) |
utr 3 prime |
probably benign |
|
R0498:Rpgrip1
|
UTSW |
14 |
52,368,771 (GRCm39) |
splice site |
probably benign |
|
R0602:Rpgrip1
|
UTSW |
14 |
52,371,313 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0776:Rpgrip1
|
UTSW |
14 |
52,378,626 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1139:Rpgrip1
|
UTSW |
14 |
52,384,678 (GRCm39) |
missense |
probably benign |
0.33 |
R1528:Rpgrip1
|
UTSW |
14 |
52,349,681 (GRCm39) |
missense |
probably benign |
0.01 |
R1715:Rpgrip1
|
UTSW |
14 |
52,378,148 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1934:Rpgrip1
|
UTSW |
14 |
52,352,101 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2087:Rpgrip1
|
UTSW |
14 |
52,374,079 (GRCm39) |
splice site |
probably null |
|
R2114:Rpgrip1
|
UTSW |
14 |
52,387,024 (GRCm39) |
missense |
probably benign |
0.27 |
R3406:Rpgrip1
|
UTSW |
14 |
52,382,666 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3835:Rpgrip1
|
UTSW |
14 |
52,384,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R4084:Rpgrip1
|
UTSW |
14 |
52,386,808 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4124:Rpgrip1
|
UTSW |
14 |
52,389,781 (GRCm39) |
splice site |
probably null |
|
R4381:Rpgrip1
|
UTSW |
14 |
52,387,906 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4407:Rpgrip1
|
UTSW |
14 |
52,384,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R4520:Rpgrip1
|
UTSW |
14 |
52,389,746 (GRCm39) |
missense |
probably benign |
0.08 |
R4904:Rpgrip1
|
UTSW |
14 |
52,397,586 (GRCm39) |
missense |
probably damaging |
0.97 |
R4904:Rpgrip1
|
UTSW |
14 |
52,358,544 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5284:Rpgrip1
|
UTSW |
14 |
52,386,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R5342:Rpgrip1
|
UTSW |
14 |
52,382,666 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5377:Rpgrip1
|
UTSW |
14 |
52,397,652 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5499:Rpgrip1
|
UTSW |
14 |
52,378,042 (GRCm39) |
missense |
probably benign |
0.00 |
R5729:Rpgrip1
|
UTSW |
14 |
52,397,617 (GRCm39) |
missense |
probably benign |
0.28 |
R5834:Rpgrip1
|
UTSW |
14 |
52,395,839 (GRCm39) |
missense |
probably damaging |
0.99 |
R6157:Rpgrip1
|
UTSW |
14 |
52,349,631 (GRCm39) |
missense |
probably benign |
0.00 |
R6455:Rpgrip1
|
UTSW |
14 |
52,378,646 (GRCm39) |
missense |
probably damaging |
0.97 |
R6796:Rpgrip1
|
UTSW |
14 |
52,387,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Rpgrip1
|
UTSW |
14 |
52,378,650 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7173:Rpgrip1
|
UTSW |
14 |
52,349,633 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7302:Rpgrip1
|
UTSW |
14 |
52,387,012 (GRCm39) |
missense |
unknown |
|
R7315:Rpgrip1
|
UTSW |
14 |
52,358,458 (GRCm39) |
missense |
not run |
|
R7320:Rpgrip1
|
UTSW |
14 |
52,368,673 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7344:Rpgrip1
|
UTSW |
14 |
52,378,116 (GRCm39) |
missense |
probably damaging |
0.98 |
R7459:Rpgrip1
|
UTSW |
14 |
52,378,016 (GRCm39) |
missense |
probably benign |
0.18 |
R7797:Rpgrip1
|
UTSW |
14 |
52,371,277 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7852:Rpgrip1
|
UTSW |
14 |
52,383,337 (GRCm39) |
missense |
probably benign |
0.01 |
R7916:Rpgrip1
|
UTSW |
14 |
52,368,641 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7990:Rpgrip1
|
UTSW |
14 |
52,366,975 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8041:Rpgrip1
|
UTSW |
14 |
52,356,702 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8344:Rpgrip1
|
UTSW |
14 |
52,387,819 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8403:Rpgrip1
|
UTSW |
14 |
52,389,658 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8559:Rpgrip1
|
UTSW |
14 |
52,386,714 (GRCm39) |
missense |
unknown |
|
R8679:Rpgrip1
|
UTSW |
14 |
52,396,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R8890:Rpgrip1
|
UTSW |
14 |
52,382,501 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9197:Rpgrip1
|
UTSW |
14 |
52,382,857 (GRCm39) |
missense |
possibly damaging |
0.51 |
RF028:Rpgrip1
|
UTSW |
14 |
52,386,855 (GRCm39) |
nonsense |
probably null |
|
RF034:Rpgrip1
|
UTSW |
14 |
52,386,983 (GRCm39) |
utr 3 prime |
probably benign |
|
RF035:Rpgrip1
|
UTSW |
14 |
52,386,850 (GRCm39) |
utr 3 prime |
probably benign |
|
RF036:Rpgrip1
|
UTSW |
14 |
52,386,998 (GRCm39) |
frame shift |
probably null |
|
RF040:Rpgrip1
|
UTSW |
14 |
52,386,994 (GRCm39) |
frame shift |
probably null |
|
RF043:Rpgrip1
|
UTSW |
14 |
52,386,852 (GRCm39) |
utr 3 prime |
probably benign |
|
X0024:Rpgrip1
|
UTSW |
14 |
52,378,665 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0026:Rpgrip1
|
UTSW |
14 |
52,384,678 (GRCm39) |
missense |
probably benign |
0.33 |
|
Predicted Primers |
PCR Primer
(F):5'- TCTGCTGTGACACACTGACTG -3'
(R):5'- GCACTTGCCGTTTTATGAGC -3'
Sequencing Primer
(F):5'- TGACACACTGACTGGGGGC -3'
(R):5'- CTTAGCTGACTTCTGGGGCCAG -3'
|
Posted On |
2021-04-30 |