Incidental Mutation 'R7831:Ppp4r4'
ID |
605650 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ppp4r4
|
Ensembl Gene |
ENSMUSG00000021209 |
Gene Name |
protein phosphatase 4, regulatory subunit 4 |
Synonyms |
8430415E04Rik |
MMRRC Submission |
045885-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.154)
|
Stock # |
R7831 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
103498542-103580090 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 103557080 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Lysine
at position 439
(E439K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000021631
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021631]
[ENSMUST00000187155]
[ENSMUST00000189871]
[ENSMUST00000190664]
|
AlphaFold |
Q8C0Y0 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000021631
AA Change: E439K
PolyPhen 2
Score 0.760 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000021631 Gene: ENSMUSG00000021209 AA Change: E439K
Domain | Start | End | E-Value | Type |
SCOP:d1gw5a_
|
55 |
577 |
6e-27 |
SMART |
PDB:3FGA|A
|
178 |
666 |
8e-6 |
PDB |
coiled coil region
|
690 |
726 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000187155
AA Change: E330K
PolyPhen 2
Score 0.760 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000140874 Gene: ENSMUSG00000021209 AA Change: E330K
Domain | Start | End | E-Value | Type |
Pfam:HEAT
|
145 |
175 |
2.8e-3 |
PFAM |
low complexity region
|
484 |
495 |
N/A |
INTRINSIC |
coiled coil region
|
581 |
617 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000189871
AA Change: E439K
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000139786 Gene: ENSMUSG00000021209 AA Change: E439K
Domain | Start | End | E-Value | Type |
SCOP:d1gw5a_
|
95 |
577 |
7e-26 |
SMART |
PDB:1B3U|B
|
178 |
666 |
2e-6 |
PDB |
coiled coil region
|
690 |
726 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000190664
|
SMART Domains |
Protein: ENSMUSP00000140295 Gene: ENSMUSG00000021209
Domain | Start | End | E-Value | Type |
Pfam:HEAT
|
38 |
68 |
5.8e-4 |
PFAM |
|
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 is a HEAT-like repeat-containing protein. The HEAT repeat is a tandemly repeated, 37-47 amino acid long module occurring in a number of cytoplasmic proteins. Arrays of HEAT repeats form a rod-like helical structure and appear to function as protein-protein interaction surfaces. The repeat-containing region of this protein has some similarity to the constant regulatory domain of the protein phosphatase 2A PR65/A subunit. The encoded protein binds protein serine/threonine phosphatase 4c in the cytoplasm. [provided by RefSeq, Jan 2017]
|
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 |
Pik3c2b |
G |
A |
1: 132,998,980 (GRCm39) |
S367N |
possibly 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 |
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 Ppp4r4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00827:Ppp4r4
|
APN |
12 |
103,545,335 (GRCm39) |
missense |
probably benign |
|
IGL01388:Ppp4r4
|
APN |
12 |
103,543,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01662:Ppp4r4
|
APN |
12 |
103,569,225 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01768:Ppp4r4
|
APN |
12 |
103,547,664 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01894:Ppp4r4
|
APN |
12 |
103,559,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01921:Ppp4r4
|
APN |
12 |
103,542,569 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
IGL01960:Ppp4r4
|
APN |
12 |
103,547,753 (GRCm39) |
splice site |
probably benign |
|
IGL02084:Ppp4r4
|
APN |
12 |
103,566,657 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02287:Ppp4r4
|
APN |
12 |
103,553,747 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02315:Ppp4r4
|
APN |
12 |
103,566,620 (GRCm39) |
splice site |
probably benign |
|
IGL03137:Ppp4r4
|
APN |
12 |
103,547,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03170:Ppp4r4
|
APN |
12 |
103,557,033 (GRCm39) |
intron |
probably benign |
|
cataract
|
UTSW |
12 |
103,579,074 (GRCm39) |
nonsense |
probably null |
|
downfall
|
UTSW |
12 |
103,559,357 (GRCm39) |
missense |
probably benign |
0.00 |
R0114:Ppp4r4
|
UTSW |
12 |
103,542,633 (GRCm39) |
missense |
probably benign |
0.00 |
R0390:Ppp4r4
|
UTSW |
12 |
103,567,619 (GRCm39) |
splice site |
probably benign |
|
R0403:Ppp4r4
|
UTSW |
12 |
103,550,361 (GRCm39) |
missense |
probably benign |
|
R0548:Ppp4r4
|
UTSW |
12 |
103,579,074 (GRCm39) |
nonsense |
probably null |
|
R0601:Ppp4r4
|
UTSW |
12 |
103,566,779 (GRCm39) |
splice site |
probably benign |
|
R0894:Ppp4r4
|
UTSW |
12 |
103,566,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R1127:Ppp4r4
|
UTSW |
12 |
103,545,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R1177:Ppp4r4
|
UTSW |
12 |
103,542,582 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1378:Ppp4r4
|
UTSW |
12 |
103,547,751 (GRCm39) |
splice site |
probably benign |
|
R1442:Ppp4r4
|
UTSW |
12 |
103,564,504 (GRCm39) |
missense |
probably damaging |
0.97 |
R1497:Ppp4r4
|
UTSW |
12 |
103,573,204 (GRCm39) |
missense |
probably benign |
0.07 |
R1651:Ppp4r4
|
UTSW |
12 |
103,550,331 (GRCm39) |
missense |
probably benign |
0.01 |
R1797:Ppp4r4
|
UTSW |
12 |
103,564,410 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1880:Ppp4r4
|
UTSW |
12 |
103,571,294 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2008:Ppp4r4
|
UTSW |
12 |
103,552,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R2038:Ppp4r4
|
UTSW |
12 |
103,542,539 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2404:Ppp4r4
|
UTSW |
12 |
103,547,749 (GRCm39) |
splice site |
probably null |
|
R2696:Ppp4r4
|
UTSW |
12 |
103,547,653 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2849:Ppp4r4
|
UTSW |
12 |
103,573,192 (GRCm39) |
missense |
probably benign |
0.00 |
R2965:Ppp4r4
|
UTSW |
12 |
103,579,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R3030:Ppp4r4
|
UTSW |
12 |
103,573,215 (GRCm39) |
missense |
probably benign |
|
R3805:Ppp4r4
|
UTSW |
12 |
103,566,625 (GRCm39) |
missense |
probably damaging |
0.99 |
R3862:Ppp4r4
|
UTSW |
12 |
103,562,680 (GRCm39) |
nonsense |
probably null |
|
R4194:Ppp4r4
|
UTSW |
12 |
103,524,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R4320:Ppp4r4
|
UTSW |
12 |
103,564,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R4558:Ppp4r4
|
UTSW |
12 |
103,573,192 (GRCm39) |
missense |
probably benign |
0.00 |
R4783:Ppp4r4
|
UTSW |
12 |
103,557,117 (GRCm39) |
critical splice donor site |
probably null |
|
R4866:Ppp4r4
|
UTSW |
12 |
103,566,706 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4903:Ppp4r4
|
UTSW |
12 |
103,557,030 (GRCm39) |
splice site |
probably null |
|
R5309:Ppp4r4
|
UTSW |
12 |
103,573,147 (GRCm39) |
splice site |
probably null |
|
R5312:Ppp4r4
|
UTSW |
12 |
103,573,147 (GRCm39) |
splice site |
probably null |
|
R5381:Ppp4r4
|
UTSW |
12 |
103,559,357 (GRCm39) |
missense |
probably benign |
0.00 |
R5383:Ppp4r4
|
UTSW |
12 |
103,550,427 (GRCm39) |
missense |
probably benign |
0.14 |
R5447:Ppp4r4
|
UTSW |
12 |
103,550,410 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5942:Ppp4r4
|
UTSW |
12 |
103,553,706 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6339:Ppp4r4
|
UTSW |
12 |
103,571,228 (GRCm39) |
nonsense |
probably null |
|
R6386:Ppp4r4
|
UTSW |
12 |
103,559,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R6712:Ppp4r4
|
UTSW |
12 |
103,562,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6755:Ppp4r4
|
UTSW |
12 |
103,551,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Ppp4r4
|
UTSW |
12 |
103,557,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R6879:Ppp4r4
|
UTSW |
12 |
103,518,179 (GRCm39) |
splice site |
probably null |
|
R7355:Ppp4r4
|
UTSW |
12 |
103,570,841 (GRCm39) |
nonsense |
probably null |
|
R7397:Ppp4r4
|
UTSW |
12 |
103,579,065 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7447:Ppp4r4
|
UTSW |
12 |
103,551,985 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7576:Ppp4r4
|
UTSW |
12 |
103,562,708 (GRCm39) |
missense |
probably damaging |
0.97 |
R7653:Ppp4r4
|
UTSW |
12 |
103,550,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R7683:Ppp4r4
|
UTSW |
12 |
103,553,364 (GRCm39) |
nonsense |
probably null |
|
R7748:Ppp4r4
|
UTSW |
12 |
103,571,320 (GRCm39) |
critical splice donor site |
probably null |
|
R7833:Ppp4r4
|
UTSW |
12 |
103,564,407 (GRCm39) |
missense |
probably benign |
0.03 |
R8238:Ppp4r4
|
UTSW |
12 |
103,557,066 (GRCm39) |
missense |
probably benign |
0.20 |
R8559:Ppp4r4
|
UTSW |
12 |
103,559,420 (GRCm39) |
missense |
probably benign |
0.04 |
R8674:Ppp4r4
|
UTSW |
12 |
103,562,720 (GRCm39) |
missense |
probably damaging |
0.97 |
R8799:Ppp4r4
|
UTSW |
12 |
103,567,623 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8847:Ppp4r4
|
UTSW |
12 |
103,562,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Ppp4r4
|
UTSW |
12 |
103,566,706 (GRCm39) |
missense |
probably benign |
0.00 |
R9075:Ppp4r4
|
UTSW |
12 |
103,570,290 (GRCm39) |
nonsense |
probably null |
|
R9106:Ppp4r4
|
UTSW |
12 |
103,570,315 (GRCm39) |
missense |
probably benign |
0.01 |
R9393:Ppp4r4
|
UTSW |
12 |
103,571,296 (GRCm39) |
nonsense |
probably null |
|
R9508:Ppp4r4
|
UTSW |
12 |
103,542,561 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9520:Ppp4r4
|
UTSW |
12 |
103,500,378 (GRCm39) |
missense |
probably benign |
0.00 |
R9636:Ppp4r4
|
UTSW |
12 |
103,564,688 (GRCm39) |
missense |
unknown |
|
R9641:Ppp4r4
|
UTSW |
12 |
103,567,811 (GRCm39) |
missense |
probably benign |
0.15 |
R9765:Ppp4r4
|
UTSW |
12 |
103,550,346 (GRCm39) |
nonsense |
probably null |
|
R9766:Ppp4r4
|
UTSW |
12 |
103,562,735 (GRCm39) |
missense |
probably benign |
0.40 |
X0025:Ppp4r4
|
UTSW |
12 |
103,566,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GTCGTGGCAGGAAACACATATATG -3'
(R):5'- AGTGCTTTCATTGAAGCTTCTC -3'
Sequencing Primer
(F):5'- GGAAACACATATATGCAGCTAAATT -3'
(R):5'- TCATTGAAGCTTCTCTTTTGTGTAC -3'
|
Posted On |
2019-12-20 |