Incidental Mutation 'R7831:Pik3c2b'
| ID |
605590 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Pik3c2b
|
| Ensembl Gene |
ENSMUSG00000026447 |
| Gene Name |
phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta |
| Synonyms |
PI3K-C2beta, C330011J12Rik |
| MMRRC Submission |
045885-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.253)
|
| Stock # |
R7831 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
132973410-133036429 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 132998980 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Asparagine
at position 367
(S367N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000076911
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077730]
[ENSMUST00000153707]
|
| AlphaFold |
E9QAN8 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000077730
AA Change: S367N
PolyPhen 2
Score 0.937 (Sensitivity: 0.80; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000076911
Gene: ENSMUSG00000026447
AA Change: S367N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
155 |
160 |
N/A |
INTRINSIC |
|
low complexity region
|
168 |
183 |
N/A |
INTRINSIC |
|
PI3K_rbd
|
363 |
465 |
2.15e-19 |
SMART |
|
PI3K_C2
|
618 |
726 |
6.17e-29 |
SMART |
|
PI3Ka
|
804 |
990 |
1.66e-84 |
SMART |
|
PI3Kc
|
1078 |
1340 |
3.45e-132 |
SMART |
|
PX
|
1364 |
1476 |
9.44e-27 |
SMART |
|
low complexity region
|
1481 |
1492 |
N/A |
INTRINSIC |
|
C2
|
1517 |
1622 |
1.82e-18 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000153707
|
| SMART Domains |
Protein: ENSMUSP00000115469
Gene: ENSMUSG00000026447
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
155 |
160 |
N/A |
INTRINSIC |
|
low complexity region
|
168 |
183 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
100% (87/87) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the phosphoinositide 3-kinase (PI3K) family. PI3-kinases play roles in signaling pathways involved in cell proliferation, oncogenic transformation, cell survival, cell migration, and intracellular protein trafficking. This protein contains a lipid kinase catalytic domain as well as a C-terminal C2 domain, a characteristic of class II PI3-kinases. C2 domains act as calcium-dependent phospholipid binding motifs that mediate translocation of proteins to membranes, and may also mediate protein-protein interactions. The PI3-kinase activity of this protein is sensitive to low nanomolar levels of the inhibitor wortmanin. The C2 domain of this protein was shown to bind phospholipids but not Ca2+, which suggests that this enzyme may function in a calcium-independent manner. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal epidermal growth, differentiation and function. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
G |
A |
11: 9,247,404 (GRCm39) |
V2384I |
possibly damaging |
Het |
| Acsl1 |
A |
G |
8: 46,972,043 (GRCm39) |
D297G |
probably benign |
Het |
| Ap2a1 |
C |
A |
7: 44,550,436 (GRCm39) |
R944L |
probably damaging |
Het |
| Apbb1ip |
A |
G |
2: 22,756,933 (GRCm39) |
Y398C |
probably damaging |
Het |
| Atp8a2 |
A |
T |
14: 60,011,202 (GRCm39) |
V968D |
probably damaging |
Het |
| Becn1 |
T |
C |
11: 101,181,279 (GRCm39) |
T341A |
probably benign |
Het |
| Card11 |
G |
T |
5: 140,859,167 (GRCm39) |
S1126R |
possibly damaging |
Het |
| Ccdc51 |
T |
C |
9: 108,921,058 (GRCm39) |
L315S |
probably damaging |
Het |
| Cdk12 |
T |
C |
11: 98,140,653 (GRCm39) |
L1298P |
unknown |
Het |
| Cep170b |
A |
T |
12: 112,711,234 (GRCm39) |
D1538V |
probably benign |
Het |
| Cfap52 |
A |
T |
11: 67,826,782 (GRCm39) |
F348I |
possibly damaging |
Het |
| Clip1 |
A |
T |
5: 123,751,342 (GRCm39) |
M813K |
|
Het |
| Col19a1 |
G |
A |
1: 24,565,563 (GRCm39) |
T256I |
unknown |
Het |
| Col6a3 |
A |
T |
1: 90,724,268 (GRCm39) |
C2027* |
probably null |
Het |
| Crisp4 |
A |
T |
1: 18,199,013 (GRCm39) |
N140K |
probably benign |
Het |
| Crocc2 |
G |
T |
1: 93,143,195 (GRCm39) |
A1266S |
probably benign |
Het |
| Cyfip2 |
G |
A |
11: 46,087,273 (GRCm39) |
R1206C |
probably damaging |
Het |
| Cyp24a1 |
T |
A |
2: 170,327,860 (GRCm39) |
M461L |
probably damaging |
Het |
| Cyp2a5 |
C |
T |
7: 26,534,940 (GRCm39) |
T51I |
possibly damaging |
Het |
| Cyp2b19 |
C |
T |
7: 26,466,565 (GRCm39) |
H398Y |
possibly damaging |
Het |
| Cyp4a29 |
G |
A |
4: 115,107,367 (GRCm39) |
V234I |
probably benign |
Het |
| Dicer1 |
T |
G |
12: 104,675,059 (GRCm39) |
K734N |
probably damaging |
Het |
| Dnai1 |
T |
C |
4: 41,614,695 (GRCm39) |
|
probably null |
Het |
| Entpd3 |
G |
A |
9: 120,373,025 (GRCm39) |
G14D |
probably damaging |
Het |
| Entrep3 |
G |
A |
3: 89,091,520 (GRCm39) |
|
probably null |
Het |
| Ermp1 |
T |
C |
19: 29,595,367 (GRCm39) |
T634A |
probably benign |
Het |
| Evc |
C |
T |
5: 37,476,427 (GRCm39) |
G374D |
probably damaging |
Het |
| Fcgbp |
C |
A |
7: 27,806,404 (GRCm39) |
T2124K |
probably damaging |
Het |
| Fgf8 |
G |
A |
19: 45,730,876 (GRCm39) |
P50S |
probably benign |
Het |
| Fmnl1 |
C |
T |
11: 103,088,999 (GRCm39) |
R1074W |
unknown |
Het |
| Galnt18 |
C |
T |
7: 111,155,665 (GRCm39) |
V223M |
possibly damaging |
Het |
| Galnt2 |
A |
G |
8: 125,058,817 (GRCm39) |
N295S |
probably benign |
Het |
| Grip1 |
T |
G |
10: 119,854,011 (GRCm39) |
V600G |
probably damaging |
Het |
| Insm2 |
T |
A |
12: 55,647,323 (GRCm39) |
C356S |
probably damaging |
Het |
| Itpr2 |
T |
A |
6: 146,193,082 (GRCm39) |
I1672F |
probably benign |
Het |
| Kdm1b |
T |
G |
13: 47,204,098 (GRCm39) |
N76K |
probably benign |
Het |
| Khnyn |
T |
A |
14: 56,125,303 (GRCm39) |
|
probably null |
Het |
| Kidins220 |
C |
T |
12: 25,111,230 (GRCm39) |
A1167V |
possibly damaging |
Het |
| Krt40 |
T |
C |
11: 99,432,087 (GRCm39) |
D208G |
probably benign |
Het |
| Lars1 |
T |
A |
18: 42,350,627 (GRCm39) |
D894V |
probably benign |
Het |
| Lmx1a |
A |
T |
1: 167,668,521 (GRCm39) |
N266I |
probably benign |
Het |
| Mrgprb5 |
T |
A |
7: 47,817,997 (GRCm39) |
K246M |
probably benign |
Het |
| Mrpl2 |
G |
A |
17: 46,959,598 (GRCm39) |
G176R |
possibly damaging |
Het |
| Muc21 |
T |
A |
17: 35,929,651 (GRCm39) |
T1512S |
unknown |
Het |
| Nell1 |
T |
A |
7: 49,632,548 (GRCm39) |
F60L |
possibly damaging |
Het |
| Nnt |
G |
A |
13: 119,506,630 (GRCm39) |
A453V |
possibly damaging |
Het |
| Opa1 |
A |
G |
16: 29,467,755 (GRCm39) |
K940R |
probably benign |
Het |
| Opn5 |
A |
C |
17: 42,891,510 (GRCm39) |
I309S |
probably null |
Het |
| Or1af1 |
C |
T |
2: 37,109,723 (GRCm39) |
T74I |
probably damaging |
Het |
| Or1r1 |
A |
C |
11: 73,875,257 (GRCm39) |
M59R |
probably damaging |
Het |
| Or2ag15 |
T |
A |
7: 106,340,620 (GRCm39) |
I174F |
probably damaging |
Het |
| P3h3 |
T |
G |
6: 124,832,118 (GRCm39) |
E256A |
possibly damaging |
Het |
| Pald1 |
G |
T |
10: 61,191,593 (GRCm39) |
T65K |
probably damaging |
Het |
| Pcnx3 |
T |
C |
19: 5,735,989 (GRCm39) |
Y279C |
probably damaging |
Het |
| Pik3cb |
T |
C |
9: 98,970,666 (GRCm39) |
T342A |
probably benign |
Het |
| Pkd1l3 |
A |
T |
8: 110,357,990 (GRCm39) |
E837D |
possibly damaging |
Het |
| Ppp2r2b |
T |
A |
18: 42,834,597 (GRCm39) |
Y191F |
probably benign |
Het |
| Ppp4r4 |
G |
A |
12: 103,557,080 (GRCm39) |
E439K |
possibly damaging |
Het |
| Ptprk |
A |
G |
10: 28,444,404 (GRCm39) |
I946V |
possibly damaging |
Het |
| Ror1 |
A |
G |
4: 100,298,295 (GRCm39) |
N556S |
probably benign |
Het |
| Ryr3 |
C |
T |
2: 112,757,183 (GRCm39) |
A391T |
possibly damaging |
Het |
| Selp |
G |
A |
1: 163,972,584 (GRCm39) |
|
probably null |
Het |
| Setx |
T |
C |
2: 29,047,120 (GRCm39) |
L1866S |
probably damaging |
Het |
| Setx |
T |
A |
2: 29,069,866 (GRCm39) |
V2557E |
possibly damaging |
Het |
| Slc66a3 |
T |
A |
12: 17,047,632 (GRCm39) |
|
probably null |
Het |
| Slit2 |
A |
G |
5: 48,402,025 (GRCm39) |
T805A |
probably benign |
Het |
| Sorbs3 |
T |
G |
14: 70,440,481 (GRCm39) |
N89T |
possibly damaging |
Het |
| Sorl1 |
C |
A |
9: 42,001,257 (GRCm39) |
V248L |
probably benign |
Het |
| Srebf2 |
T |
A |
15: 82,066,288 (GRCm39) |
V612E |
probably damaging |
Het |
| Sv2c |
T |
A |
13: 96,113,200 (GRCm39) |
Y583F |
probably damaging |
Het |
| Tada1 |
G |
T |
1: 166,217,442 (GRCm39) |
R193I |
probably damaging |
Het |
| Tnrc6b |
C |
G |
15: 80,764,580 (GRCm39) |
A694G |
possibly damaging |
Het |
| Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
| Ttn |
C |
T |
2: 76,711,425 (GRCm39) |
G8372D |
unknown |
Het |
| Ube2g2 |
A |
G |
10: 77,470,576 (GRCm39) |
T68A |
|
Het |
| Ubl7 |
T |
G |
9: 57,821,918 (GRCm39) |
V89G |
possibly damaging |
Het |
| Ush2a |
T |
A |
1: 188,492,038 (GRCm39) |
I3109N |
probably damaging |
Het |
| Utp20 |
T |
A |
10: 88,598,632 (GRCm39) |
K115* |
probably null |
Het |
| Vmn2r26 |
T |
A |
6: 124,016,758 (GRCm39) |
Y407* |
probably null |
Het |
| Yod1 |
G |
T |
1: 130,646,986 (GRCm39) |
V288F |
probably damaging |
Het |
| Zbed5 |
A |
C |
5: 129,930,798 (GRCm39) |
N249T |
possibly damaging |
Het |
| Zbtb5 |
T |
C |
4: 44,995,244 (GRCm39) |
T47A |
probably damaging |
Het |
| Zcchc14 |
T |
C |
8: 122,331,984 (GRCm39) |
T460A |
not run |
Het |
| Zfp712 |
A |
C |
13: 67,200,483 (GRCm39) |
|
probably null |
Het |
| Zfyve16 |
A |
T |
13: 92,658,836 (GRCm39) |
H358Q |
probably benign |
Het |
|
| Other mutations in Pik3c2b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01086:Pik3c2b
|
APN |
1 |
133,019,356 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01288:Pik3c2b
|
APN |
1 |
133,022,543 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01313:Pik3c2b
|
APN |
1 |
132,999,369 (GRCm39) |
nonsense |
probably null |
|
|
IGL01367:Pik3c2b
|
APN |
1 |
133,033,726 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02379:Pik3c2b
|
APN |
1 |
133,022,529 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02638:Pik3c2b
|
APN |
1 |
133,005,056 (GRCm39) |
splice site |
probably benign |
|
|
IGL02728:Pik3c2b
|
APN |
1 |
133,020,065 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL02992:Pik3c2b
|
APN |
1 |
132,994,718 (GRCm39) |
nonsense |
probably null |
|
|
IGL03121:Pik3c2b
|
APN |
1 |
133,007,483 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0453:Pik3c2b
|
UTSW |
1 |
133,005,134 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0518:Pik3c2b
|
UTSW |
1 |
133,033,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0616:Pik3c2b
|
UTSW |
1 |
133,028,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0659:Pik3c2b
|
UTSW |
1 |
132,998,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1542:Pik3c2b
|
UTSW |
1 |
133,017,772 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1716:Pik3c2b
|
UTSW |
1 |
133,022,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1728:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1729:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1730:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1739:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1762:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1783:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1784:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1785:Pik3c2b
|
UTSW |
1 |
132,994,365 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1816:Pik3c2b
|
UTSW |
1 |
133,029,108 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1897:Pik3c2b
|
UTSW |
1 |
132,994,654 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R2006:Pik3c2b
|
UTSW |
1 |
132,994,282 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2067:Pik3c2b
|
UTSW |
1 |
133,027,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2271:Pik3c2b
|
UTSW |
1 |
133,031,166 (GRCm39) |
missense |
probably benign |
|
|
R2294:Pik3c2b
|
UTSW |
1 |
132,994,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2320:Pik3c2b
|
UTSW |
1 |
133,031,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4735:Pik3c2b
|
UTSW |
1 |
132,994,787 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4926:Pik3c2b
|
UTSW |
1 |
133,027,364 (GRCm39) |
nonsense |
probably null |
|
|
R4948:Pik3c2b
|
UTSW |
1 |
133,027,453 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4997:Pik3c2b
|
UTSW |
1 |
133,032,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5304:Pik3c2b
|
UTSW |
1 |
132,998,146 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R5461:Pik3c2b
|
UTSW |
1 |
133,027,440 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5722:Pik3c2b
|
UTSW |
1 |
133,031,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5971:Pik3c2b
|
UTSW |
1 |
133,002,365 (GRCm39) |
splice site |
probably null |
|
|
R5980:Pik3c2b
|
UTSW |
1 |
133,016,046 (GRCm39) |
missense |
probably benign |
0.43 |
|
R6036:Pik3c2b
|
UTSW |
1 |
133,018,451 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6138:Pik3c2b
|
UTSW |
1 |
133,002,365 (GRCm39) |
splice site |
probably null |
|
|
R6223:Pik3c2b
|
UTSW |
1 |
132,998,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6273:Pik3c2b
|
UTSW |
1 |
132,994,449 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6742:Pik3c2b
|
UTSW |
1 |
133,003,559 (GRCm39) |
missense |
probably benign |
|
|
R6954:Pik3c2b
|
UTSW |
1 |
132,994,041 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6998:Pik3c2b
|
UTSW |
1 |
133,030,110 (GRCm39) |
missense |
probably benign |
0.23 |
|
R7103:Pik3c2b
|
UTSW |
1 |
133,033,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7133:Pik3c2b
|
UTSW |
1 |
133,017,972 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R7161:Pik3c2b
|
UTSW |
1 |
133,033,850 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7183:Pik3c2b
|
UTSW |
1 |
132,994,203 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7193:Pik3c2b
|
UTSW |
1 |
133,007,512 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7252:Pik3c2b
|
UTSW |
1 |
133,022,472 (GRCm39) |
missense |
probably benign |
0.19 |
|
R7263:Pik3c2b
|
UTSW |
1 |
133,017,940 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7404:Pik3c2b
|
UTSW |
1 |
133,018,444 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7709:Pik3c2b
|
UTSW |
1 |
133,007,579 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7712:Pik3c2b
|
UTSW |
1 |
133,013,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7823:Pik3c2b
|
UTSW |
1 |
133,030,043 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7913:Pik3c2b
|
UTSW |
1 |
133,017,799 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7916:Pik3c2b
|
UTSW |
1 |
133,028,642 (GRCm39) |
missense |
probably benign |
0.30 |
|
R7960:Pik3c2b
|
UTSW |
1 |
133,031,587 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7981:Pik3c2b
|
UTSW |
1 |
133,003,547 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R8346:Pik3c2b
|
UTSW |
1 |
133,017,984 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8938:Pik3c2b
|
UTSW |
1 |
133,016,068 (GRCm39) |
missense |
probably benign |
0.19 |
|
R8997:Pik3c2b
|
UTSW |
1 |
133,018,517 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9416:Pik3c2b
|
UTSW |
1 |
133,005,187 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9598:Pik3c2b
|
UTSW |
1 |
133,012,725 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9621:Pik3c2b
|
UTSW |
1 |
132,999,345 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9742:Pik3c2b
|
UTSW |
1 |
133,022,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9776:Pik3c2b
|
UTSW |
1 |
133,018,588 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9786:Pik3c2b
|
UTSW |
1 |
133,019,338 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
U15987:Pik3c2b
|
UTSW |
1 |
133,002,365 (GRCm39) |
splice site |
probably null |
|
|
X0060:Pik3c2b
|
UTSW |
1 |
133,012,674 (GRCm39) |
missense |
probably benign |
0.18 |
|
Z1176:Pik3c2b
|
UTSW |
1 |
133,027,424 (GRCm39) |
nonsense |
probably null |
|
|
Z1176:Pik3c2b
|
UTSW |
1 |
132,994,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGACTGTAGCAGAGATGACCAG -3'
(R):5'- TTCATTCAGGCGACAGAGTG -3'
Sequencing Primer
(F):5'- AGCCTAGCCCACAGGTCAG -3'
(R):5'- TGAGGTGAGAAACAAAGTTCCC -3'
|
| Posted On |
2019-12-20 |
Incidental Mutation