Incidental Mutation 'R7806:Clca4b'
ID |
600760 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Clca4b
|
Ensembl Gene |
ENSMUSG00000074195 |
Gene Name |
chloride channel accessory 4B |
Synonyms |
AI747448 |
MMRRC Submission |
045861-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.060)
|
Stock # |
R7806 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
144616682-144638290 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 144638157 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 35
(D35G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000096149
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098549]
|
AlphaFold |
Q3UW98 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000098549
AA Change: D35G
PolyPhen 2
Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
|
SMART Domains |
Protein: ENSMUSP00000096149 Gene: ENSMUSG00000074195 AA Change: D35G
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
VWA
|
306 |
480 |
1.03e-15 |
SMART |
Blast:VWA
|
513 |
552 |
6e-16 |
BLAST |
Blast:FN3
|
757 |
838 |
5e-35 |
BLAST |
low complexity region
|
882 |
906 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.8%
- 20x: 99.3%
|
Validation Efficiency |
98% (83/85) |
MGI Phenotype |
PHENOTYPE: No notable phenotype was detected in a high throughput screen of homozyogus mutant null mice. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810004N23Rik |
C |
A |
8: 125,569,143 (GRCm39) |
V144F |
probably benign |
Het |
Aar2 |
T |
A |
2: 156,393,031 (GRCm39) |
I140N |
possibly damaging |
Het |
Abca15 |
A |
G |
7: 119,932,059 (GRCm39) |
N104S |
probably damaging |
Het |
Adam22 |
A |
T |
5: 8,142,825 (GRCm39) |
N803K |
probably damaging |
Het |
Adk |
A |
G |
14: 21,376,679 (GRCm39) |
N26S |
|
Het |
Ak9 |
A |
C |
10: 41,309,080 (GRCm39) |
|
probably null |
Het |
Alpk2 |
T |
C |
18: 65,482,487 (GRCm39) |
D40G |
probably benign |
Het |
Ankrd65 |
A |
T |
4: 155,877,437 (GRCm39) |
H316L |
probably benign |
Het |
Cabp7 |
C |
T |
11: 4,688,889 (GRCm39) |
A194T |
probably damaging |
Het |
Ccdc180 |
A |
C |
4: 45,912,801 (GRCm39) |
K593N |
possibly damaging |
Het |
Cd80 |
A |
G |
16: 38,294,315 (GRCm39) |
D66G |
probably benign |
Het |
Cdh5 |
T |
C |
8: 104,867,448 (GRCm39) |
V575A |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,737,809 (GRCm39) |
Q2678R |
probably benign |
Het |
Cideb |
G |
A |
14: 55,992,625 (GRCm39) |
T97M |
probably damaging |
Het |
Clpx |
T |
C |
9: 65,207,213 (GRCm39) |
V37A |
probably benign |
Het |
Cmya5 |
A |
C |
13: 93,230,770 (GRCm39) |
S1439R |
probably benign |
Het |
Cndp2 |
T |
A |
18: 84,688,945 (GRCm39) |
H279L |
probably benign |
Het |
Cngb1 |
A |
T |
8: 96,025,432 (GRCm39) |
|
probably null |
Het |
Cpq |
T |
A |
15: 33,497,443 (GRCm39) |
N394K |
possibly damaging |
Het |
Dedd |
T |
C |
1: 171,166,062 (GRCm39) |
L60P |
probably benign |
Het |
Dennd3 |
C |
A |
15: 73,442,624 (GRCm39) |
L1216M |
possibly damaging |
Het |
Dntt |
A |
T |
19: 41,018,071 (GRCm39) |
N65I |
probably benign |
Het |
Fap |
T |
A |
2: 62,333,758 (GRCm39) |
E662V |
probably damaging |
Het |
Fasn |
A |
T |
11: 120,700,821 (GRCm39) |
M2066K |
probably benign |
Het |
Fggy |
G |
A |
4: 95,489,203 (GRCm39) |
G69E |
probably benign |
Het |
Foxc1 |
G |
T |
13: 31,992,739 (GRCm39) |
G517C |
unknown |
Het |
Gas2l3 |
A |
G |
10: 89,249,232 (GRCm39) |
Y629H |
probably benign |
Het |
Gcnt2 |
A |
G |
13: 41,071,717 (GRCm39) |
N120S |
probably damaging |
Het |
Gfpt2 |
A |
G |
11: 49,714,142 (GRCm39) |
T300A |
probably benign |
Het |
Glud1 |
A |
G |
14: 34,065,606 (GRCm39) |
R535G |
probably damaging |
Het |
Gm3248 |
T |
A |
14: 5,943,883 (GRCm38) |
I114L |
probably benign |
Het |
Gm3278 |
G |
A |
14: 16,082,211 (GRCm39) |
|
probably null |
Het |
Gm3402 |
A |
C |
5: 146,451,090 (GRCm39) |
K44Q |
probably damaging |
Het |
Gm3696 |
C |
G |
14: 18,433,094 (GRCm39) |
R188S |
probably benign |
Het |
Gm3696 |
C |
A |
14: 18,433,095 (GRCm39) |
R188M |
probably benign |
Het |
Gmppa |
T |
C |
1: 75,415,581 (GRCm39) |
L113P |
probably damaging |
Het |
Gmps |
A |
G |
3: 63,890,091 (GRCm39) |
|
probably null |
Het |
Gnal |
T |
A |
18: 67,346,145 (GRCm39) |
M275K |
probably damaging |
Het |
Gopc |
G |
C |
10: 52,229,525 (GRCm39) |
N231K |
probably damaging |
Het |
Gpr152 |
T |
C |
19: 4,193,487 (GRCm39) |
S343P |
probably benign |
Het |
Gpr17 |
T |
C |
18: 32,080,593 (GRCm39) |
I157V |
probably benign |
Het |
Grm7 |
T |
A |
6: 111,223,314 (GRCm39) |
Y451* |
probably null |
Het |
Ikbke |
T |
C |
1: 131,199,635 (GRCm39) |
E286G |
probably damaging |
Het |
Inpp5b |
A |
T |
4: 124,678,881 (GRCm39) |
|
probably null |
Het |
Iqgap2 |
G |
A |
13: 95,818,765 (GRCm39) |
L664F |
probably benign |
Het |
Kif17 |
A |
G |
4: 138,015,507 (GRCm39) |
E552G |
possibly damaging |
Het |
Lamtor1 |
T |
A |
7: 101,555,220 (GRCm39) |
Y5* |
probably null |
Het |
Lpin2 |
A |
G |
17: 71,552,166 (GRCm39) |
I829V |
probably damaging |
Het |
Lrg1 |
T |
G |
17: 56,426,967 (GRCm39) |
D335A |
probably benign |
Het |
Lrriq3 |
T |
C |
3: 154,804,444 (GRCm39) |
Y35H |
probably damaging |
Het |
Mkx |
T |
A |
18: 7,000,607 (GRCm39) |
M112L |
probably benign |
Het |
Mlxipl |
A |
C |
5: 135,163,397 (GRCm39) |
D760A |
possibly damaging |
Het |
Muc6 |
T |
C |
7: 141,217,387 (GRCm39) |
T2429A |
possibly damaging |
Het |
N4bp2l2 |
A |
G |
5: 150,566,715 (GRCm39) |
C134R |
unknown |
Het |
Nanos1 |
A |
G |
19: 60,744,972 (GRCm39) |
E90G |
probably benign |
Het |
Nckap1 |
T |
C |
2: 80,371,843 (GRCm39) |
D329G |
probably damaging |
Het |
Or13a18 |
T |
C |
7: 140,190,685 (GRCm39) |
I194T |
probably benign |
Het |
Or14j9 |
A |
C |
17: 37,875,112 (GRCm39) |
L30R |
probably damaging |
Het |
Or8b12c |
T |
C |
9: 37,715,872 (GRCm39) |
S222P |
probably damaging |
Het |
Or8g51 |
G |
T |
9: 38,609,567 (GRCm39) |
L32I |
probably benign |
Het |
Osbpl7 |
A |
G |
11: 96,946,954 (GRCm39) |
H419R |
probably benign |
Het |
Otog |
C |
T |
7: 45,935,200 (GRCm39) |
T1395I |
probably benign |
Het |
Pigq |
T |
A |
17: 26,150,700 (GRCm39) |
I451F |
probably benign |
Het |
Ptgfrn |
A |
G |
3: 100,984,448 (GRCm39) |
V248A |
possibly damaging |
Het |
Rdh19 |
G |
T |
10: 127,692,740 (GRCm39) |
V136L |
probably damaging |
Het |
Rfesd |
T |
C |
13: 76,156,308 (GRCm39) |
T33A |
possibly damaging |
Het |
Rnf213 |
G |
A |
11: 119,302,371 (GRCm39) |
V432M |
|
Het |
Rpl22l1 |
T |
A |
3: 28,860,962 (GRCm39) |
L60Q |
probably benign |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,127 (GRCm39) |
|
probably benign |
Het |
Samd3 |
A |
G |
10: 26,120,425 (GRCm39) |
T140A |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,189,623 (GRCm39) |
V419A |
possibly damaging |
Het |
Serpinb6a |
T |
C |
13: 34,119,548 (GRCm39) |
|
probably null |
Het |
Slc22a4 |
A |
G |
11: 53,881,476 (GRCm39) |
L414P |
probably damaging |
Het |
Smarcd3 |
A |
T |
5: 24,798,260 (GRCm39) |
V420D |
probably benign |
Het |
Tcaim |
A |
G |
9: 122,663,995 (GRCm39) |
D495G |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,074,266 (GRCm39) |
V1873A |
possibly damaging |
Het |
Tmcc2 |
T |
C |
1: 132,288,527 (GRCm39) |
N387D |
probably damaging |
Het |
Tmed8 |
A |
T |
12: 87,219,204 (GRCm39) |
I322N |
probably damaging |
Het |
Tmod4 |
A |
C |
3: 95,034,915 (GRCm39) |
D168A |
probably benign |
Het |
Trgc2 |
A |
T |
13: 19,491,390 (GRCm39) |
|
probably benign |
Het |
Trp53bp1 |
C |
T |
2: 121,035,542 (GRCm39) |
E1520K |
probably damaging |
Het |
Trpv5 |
T |
A |
6: 41,651,867 (GRCm39) |
I183F |
probably damaging |
Het |
Vmn2r70 |
A |
T |
7: 85,208,401 (GRCm39) |
I692K |
probably benign |
Het |
Vmn2r87 |
T |
A |
10: 130,315,679 (GRCm39) |
Y129F |
probably benign |
Het |
Vps8 |
A |
G |
16: 21,278,501 (GRCm39) |
D253G |
probably damaging |
Het |
Ythdc2 |
T |
C |
18: 44,977,353 (GRCm39) |
I383T |
possibly damaging |
Het |
Ythdc2 |
T |
C |
18: 44,983,491 (GRCm39) |
S553P |
probably benign |
Het |
Zfyve26 |
A |
G |
12: 79,327,129 (GRCm39) |
|
probably null |
Het |
Zic1 |
G |
A |
9: 91,247,024 (GRCm39) |
T16I |
probably damaging |
Het |
|
Other mutations in Clca4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00228:Clca4b
|
APN |
3 |
144,638,152 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00391:Clca4b
|
APN |
3 |
144,621,322 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00576:Clca4b
|
APN |
3 |
144,631,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01484:Clca4b
|
APN |
3 |
144,633,996 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01539:Clca4b
|
APN |
3 |
144,631,918 (GRCm39) |
missense |
probably benign |
|
IGL01726:Clca4b
|
APN |
3 |
144,634,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01903:Clca4b
|
APN |
3 |
144,634,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01967:Clca4b
|
APN |
3 |
144,633,951 (GRCm39) |
splice site |
probably benign |
|
IGL02002:Clca4b
|
APN |
3 |
144,638,194 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02323:Clca4b
|
APN |
3 |
144,619,082 (GRCm39) |
missense |
probably benign |
|
IGL02379:Clca4b
|
APN |
3 |
144,627,619 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02638:Clca4b
|
APN |
3 |
144,631,939 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02859:Clca4b
|
APN |
3 |
144,617,800 (GRCm39) |
missense |
probably benign |
|
R0110:Clca4b
|
UTSW |
3 |
144,619,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R0266:Clca4b
|
UTSW |
3 |
144,628,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R0311:Clca4b
|
UTSW |
3 |
144,638,257 (GRCm39) |
missense |
probably benign |
0.04 |
R0348:Clca4b
|
UTSW |
3 |
144,627,741 (GRCm39) |
missense |
probably damaging |
0.96 |
R0450:Clca4b
|
UTSW |
3 |
144,619,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Clca4b
|
UTSW |
3 |
144,619,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Clca4b
|
UTSW |
3 |
144,627,717 (GRCm39) |
missense |
probably benign |
0.15 |
R0551:Clca4b
|
UTSW |
3 |
144,634,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Clca4b
|
UTSW |
3 |
144,622,536 (GRCm39) |
missense |
probably benign |
|
R0570:Clca4b
|
UTSW |
3 |
144,631,110 (GRCm39) |
missense |
probably benign |
0.01 |
R0591:Clca4b
|
UTSW |
3 |
144,621,353 (GRCm39) |
nonsense |
probably null |
|
R0627:Clca4b
|
UTSW |
3 |
144,634,020 (GRCm39) |
missense |
probably benign |
0.20 |
R0729:Clca4b
|
UTSW |
3 |
144,634,111 (GRCm39) |
splice site |
probably benign |
|
R0844:Clca4b
|
UTSW |
3 |
144,622,532 (GRCm39) |
missense |
probably damaging |
0.96 |
R0964:Clca4b
|
UTSW |
3 |
144,621,337 (GRCm39) |
missense |
probably benign |
|
R1388:Clca4b
|
UTSW |
3 |
144,622,415 (GRCm39) |
missense |
probably benign |
|
R1479:Clca4b
|
UTSW |
3 |
144,621,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R1603:Clca4b
|
UTSW |
3 |
144,627,780 (GRCm39) |
missense |
probably benign |
0.20 |
R2045:Clca4b
|
UTSW |
3 |
144,630,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Clca4b
|
UTSW |
3 |
144,634,348 (GRCm39) |
missense |
probably benign |
0.19 |
R2185:Clca4b
|
UTSW |
3 |
144,634,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R2241:Clca4b
|
UTSW |
3 |
144,616,987 (GRCm39) |
missense |
probably benign |
0.00 |
R2300:Clca4b
|
UTSW |
3 |
144,622,432 (GRCm39) |
missense |
probably benign |
0.02 |
R2321:Clca4b
|
UTSW |
3 |
144,638,134 (GRCm39) |
missense |
probably benign |
0.00 |
R2359:Clca4b
|
UTSW |
3 |
144,631,003 (GRCm39) |
missense |
probably damaging |
0.96 |
R3105:Clca4b
|
UTSW |
3 |
144,622,432 (GRCm39) |
missense |
probably benign |
0.02 |
R3151:Clca4b
|
UTSW |
3 |
144,621,272 (GRCm39) |
missense |
probably benign |
0.05 |
R3158:Clca4b
|
UTSW |
3 |
144,617,878 (GRCm39) |
missense |
probably benign |
0.04 |
R3177:Clca4b
|
UTSW |
3 |
144,617,120 (GRCm39) |
missense |
probably benign |
0.15 |
R3277:Clca4b
|
UTSW |
3 |
144,617,120 (GRCm39) |
missense |
probably benign |
0.15 |
R3981:Clca4b
|
UTSW |
3 |
144,631,797 (GRCm39) |
missense |
probably benign |
0.27 |
R4601:Clca4b
|
UTSW |
3 |
144,632,945 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4646:Clca4b
|
UTSW |
3 |
144,634,286 (GRCm39) |
missense |
probably benign |
0.00 |
R4647:Clca4b
|
UTSW |
3 |
144,634,286 (GRCm39) |
missense |
probably benign |
0.00 |
R4696:Clca4b
|
UTSW |
3 |
144,617,146 (GRCm39) |
missense |
probably benign |
0.00 |
R4893:Clca4b
|
UTSW |
3 |
144,630,934 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4998:Clca4b
|
UTSW |
3 |
144,621,269 (GRCm39) |
missense |
probably benign |
0.00 |
R5053:Clca4b
|
UTSW |
3 |
144,616,882 (GRCm39) |
missense |
probably benign |
0.01 |
R5060:Clca4b
|
UTSW |
3 |
144,617,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R5319:Clca4b
|
UTSW |
3 |
144,630,940 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5409:Clca4b
|
UTSW |
3 |
144,622,452 (GRCm39) |
nonsense |
probably null |
|
R5534:Clca4b
|
UTSW |
3 |
144,621,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Clca4b
|
UTSW |
3 |
144,638,196 (GRCm39) |
missense |
probably benign |
0.04 |
R5667:Clca4b
|
UTSW |
3 |
144,627,624 (GRCm39) |
missense |
probably benign |
|
R5671:Clca4b
|
UTSW |
3 |
144,627,624 (GRCm39) |
missense |
probably benign |
|
R5715:Clca4b
|
UTSW |
3 |
144,619,018 (GRCm39) |
missense |
probably benign |
0.01 |
R5875:Clca4b
|
UTSW |
3 |
144,628,650 (GRCm39) |
missense |
probably benign |
0.38 |
R5876:Clca4b
|
UTSW |
3 |
144,617,821 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6122:Clca4b
|
UTSW |
3 |
144,631,927 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6294:Clca4b
|
UTSW |
3 |
144,630,946 (GRCm39) |
missense |
probably null |
|
R6408:Clca4b
|
UTSW |
3 |
144,625,036 (GRCm39) |
missense |
probably benign |
0.00 |
R6418:Clca4b
|
UTSW |
3 |
144,633,996 (GRCm39) |
missense |
probably benign |
0.02 |
R6458:Clca4b
|
UTSW |
3 |
144,617,088 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6536:Clca4b
|
UTSW |
3 |
144,622,490 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6567:Clca4b
|
UTSW |
3 |
144,638,100 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6781:Clca4b
|
UTSW |
3 |
144,628,562 (GRCm39) |
missense |
probably benign |
|
R6799:Clca4b
|
UTSW |
3 |
144,621,388 (GRCm39) |
splice site |
probably null |
|
R7046:Clca4b
|
UTSW |
3 |
144,621,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R7365:Clca4b
|
UTSW |
3 |
144,628,529 (GRCm39) |
missense |
not run |
|
R7431:Clca4b
|
UTSW |
3 |
144,616,894 (GRCm39) |
missense |
probably benign |
0.28 |
R7462:Clca4b
|
UTSW |
3 |
144,628,621 (GRCm39) |
missense |
probably benign |
0.00 |
R7611:Clca4b
|
UTSW |
3 |
144,627,757 (GRCm39) |
missense |
probably benign |
0.03 |
R7918:Clca4b
|
UTSW |
3 |
144,619,033 (GRCm39) |
missense |
probably damaging |
0.99 |
R7962:Clca4b
|
UTSW |
3 |
144,622,421 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7990:Clca4b
|
UTSW |
3 |
144,634,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R8198:Clca4b
|
UTSW |
3 |
144,638,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8327:Clca4b
|
UTSW |
3 |
144,627,762 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8370:Clca4b
|
UTSW |
3 |
144,631,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8434:Clca4b
|
UTSW |
3 |
144,631,917 (GRCm39) |
missense |
probably benign |
0.00 |
R8493:Clca4b
|
UTSW |
3 |
144,617,911 (GRCm39) |
missense |
probably benign |
|
R9027:Clca4b
|
UTSW |
3 |
144,617,827 (GRCm39) |
nonsense |
probably null |
|
R9211:Clca4b
|
UTSW |
3 |
144,638,214 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9371:Clca4b
|
UTSW |
3 |
144,631,845 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9400:Clca4b
|
UTSW |
3 |
144,616,953 (GRCm39) |
missense |
probably benign |
0.00 |
R9446:Clca4b
|
UTSW |
3 |
144,638,134 (GRCm39) |
missense |
probably benign |
0.01 |
R9474:Clca4b
|
UTSW |
3 |
144,616,927 (GRCm39) |
missense |
probably benign |
0.04 |
R9479:Clca4b
|
UTSW |
3 |
144,617,100 (GRCm39) |
missense |
probably benign |
0.44 |
R9493:Clca4b
|
UTSW |
3 |
144,632,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9730:Clca4b
|
UTSW |
3 |
144,632,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R9733:Clca4b
|
UTSW |
3 |
144,621,272 (GRCm39) |
missense |
probably benign |
0.05 |
|
Predicted Primers |
PCR Primer
(F):5'- CCTTCATCTGGAATGTCTTAGAGC -3'
(R):5'- TCCCACAATCAGCTAACAGGTG -3'
Sequencing Primer
(F):5'- GGAATGTCTTAGAGCTTTCATCTCAC -3'
(R):5'- TGATGGCTTTCTCCAGAG -3'
|
Posted On |
2019-11-26 |