Incidental Mutation 'R7034:Herc3'
| ID |
546522 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Herc3
|
| Ensembl Gene |
ENSMUSG00000029804 |
| Gene Name |
hect domain and RLD 3 |
| Synonyms |
5730409F18Rik |
| MMRRC Submission |
045135-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7034 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
58808450-58897383 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 58853840 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Leucine
at position 629
(M629L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000031823
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031823]
[ENSMUST00000041401]
|
| AlphaFold |
A6H6S0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000031823
AA Change: M629L
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
| SMART Domains |
Protein: ENSMUSP00000031823
Gene: ENSMUSG00000029804
AA Change: M629L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:RCC1_2
|
36 |
65 |
3.3e-11 |
PFAM |
|
Pfam:RCC1
|
52 |
99 |
3.6e-15 |
PFAM |
|
Pfam:RCC1_2
|
86 |
115 |
1.1e-10 |
PFAM |
|
Pfam:RCC1
|
102 |
152 |
1.4e-16 |
PFAM |
|
Pfam:RCC1_2
|
139 |
168 |
2.1e-9 |
PFAM |
|
Pfam:RCC1
|
155 |
205 |
2.6e-16 |
PFAM |
|
Pfam:RCC1_2
|
193 |
221 |
1.5e-9 |
PFAM |
|
Pfam:RCC1
|
208 |
257 |
4.7e-17 |
PFAM |
|
Pfam:RCC1_2
|
244 |
273 |
8e-9 |
PFAM |
|
Pfam:RCC1
|
260 |
309 |
2.6e-16 |
PFAM |
|
Pfam:RCC1_2
|
296 |
326 |
2.3e-7 |
PFAM |
|
Pfam:RCC1
|
313 |
377 |
3.8e-9 |
PFAM |
|
HECTc
|
721 |
913 |
2.08e-12 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000041401
AA Change: M629L
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000040025
Gene: ENSMUSG00000029804
AA Change: M629L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:RCC1_2
|
36 |
65 |
1.7e-11 |
PFAM |
|
Pfam:RCC1
|
52 |
99 |
1.6e-15 |
PFAM |
|
Pfam:RCC1_2
|
86 |
115 |
1.1e-10 |
PFAM |
|
Pfam:RCC1
|
102 |
152 |
7.3e-16 |
PFAM |
|
Pfam:RCC1_2
|
139 |
168 |
1.3e-9 |
PFAM |
|
Pfam:RCC1
|
155 |
205 |
1.4e-16 |
PFAM |
|
Pfam:RCC1_2
|
193 |
221 |
5e-10 |
PFAM |
|
Pfam:RCC1
|
208 |
257 |
1.4e-16 |
PFAM |
|
Pfam:RCC1_2
|
244 |
273 |
6.1e-8 |
PFAM |
|
Pfam:RCC1
|
260 |
309 |
1.7e-14 |
PFAM |
|
Pfam:RCC1_2
|
296 |
326 |
1.1e-7 |
PFAM |
|
Pfam:RCC1
|
313 |
377 |
6.6e-11 |
PFAM |
|
HECTc
|
721 |
1050 |
5.79e-157 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member the HERC ubiquitin ligase family. The encoded protein is located in the cytosol and binds ubiquitin via a HECT domain. Mutations in this gene have been associated with colorectal and gastric carcinomas. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]
PHENOTYPE: Mice homozygous for a null allele exhibit abnormal hair follicle bulge morphology. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700017N19Rik |
T |
A |
10: 100,445,118 (GRCm39) |
|
probably null |
Het |
| Adamts1 |
T |
A |
16: 85,599,634 (GRCm39) |
|
probably benign |
Het |
| Aff4 |
A |
G |
11: 53,299,236 (GRCm39) |
K979E |
probably damaging |
Het |
| Aftph |
A |
T |
11: 20,642,498 (GRCm39) |
M845K |
probably damaging |
Het |
| Akt2 |
T |
C |
7: 27,336,437 (GRCm39) |
|
probably null |
Het |
| Aldh1a7 |
A |
T |
19: 20,685,542 (GRCm39) |
L336Q |
possibly damaging |
Het |
| Ank3 |
C |
T |
10: 69,835,209 (GRCm39) |
T680M |
probably damaging |
Het |
| Apeh |
T |
C |
9: 107,971,470 (GRCm39) |
E59G |
possibly damaging |
Het |
| Armc8 |
C |
T |
9: 99,366,018 (GRCm39) |
|
probably null |
Het |
| Armh3 |
A |
G |
19: 45,953,688 (GRCm39) |
I195T |
probably damaging |
Het |
| Atp2b1 |
C |
T |
10: 98,823,172 (GRCm39) |
T244I |
probably damaging |
Het |
| Btaf1 |
C |
A |
19: 36,981,869 (GRCm39) |
T1633K |
probably benign |
Het |
| Cacng8 |
A |
G |
7: 3,463,819 (GRCm39) |
S324G |
probably benign |
Het |
| Calcr |
T |
A |
6: 3,692,543 (GRCm39) |
Q400L |
probably damaging |
Het |
| Caprin2 |
G |
A |
6: 148,749,703 (GRCm39) |
P536S |
possibly damaging |
Het |
| Ccdc54 |
A |
T |
16: 50,410,951 (GRCm39) |
M105K |
probably benign |
Het |
| Ccna1 |
T |
C |
3: 54,953,460 (GRCm39) |
E381G |
possibly damaging |
Het |
| Cd2ap |
A |
T |
17: 43,109,490 (GRCm39) |
L623Q |
probably damaging |
Het |
| Cdkl3 |
A |
G |
11: 51,918,042 (GRCm39) |
E415G |
probably benign |
Het |
| Chd5 |
C |
A |
4: 152,445,398 (GRCm39) |
L430I |
possibly damaging |
Het |
| Clspn |
G |
A |
4: 126,474,775 (GRCm39) |
E975K |
possibly damaging |
Het |
| Cobl |
C |
A |
11: 12,204,177 (GRCm39) |
V835F |
probably damaging |
Het |
| D430041D05Rik |
C |
A |
2: 104,022,883 (GRCm39) |
R1037L |
probably damaging |
Het |
| Derl1 |
A |
G |
15: 57,742,443 (GRCm39) |
|
probably null |
Het |
| Dhrs9 |
T |
G |
2: 69,223,520 (GRCm39) |
N89K |
probably benign |
Het |
| Erich1 |
A |
G |
8: 14,114,330 (GRCm39) |
I60T |
probably benign |
Het |
| Fam184a |
A |
T |
10: 53,570,910 (GRCm39) |
S408T |
possibly damaging |
Het |
| Fcgr4 |
T |
A |
1: 170,847,657 (GRCm39) |
M85K |
probably benign |
Het |
| Foxj3 |
A |
G |
4: 119,476,497 (GRCm39) |
E259G |
probably damaging |
Het |
| Galnt11 |
T |
C |
5: 25,463,811 (GRCm39) |
I361T |
probably damaging |
Het |
| Gck |
A |
G |
11: 5,851,747 (GRCm39) |
S441P |
probably damaging |
Het |
| Gdap1l1 |
G |
T |
2: 163,288,065 (GRCm39) |
V98F |
probably damaging |
Het |
| Gramd1a |
A |
G |
7: 30,832,181 (GRCm39) |
|
probably null |
Het |
| H2ac21 |
C |
T |
3: 96,127,304 (GRCm39) |
Q25* |
probably null |
Het |
| Hoxc12 |
G |
A |
15: 102,846,795 (GRCm39) |
G229D |
probably damaging |
Het |
| Hycc2 |
T |
A |
1: 58,574,696 (GRCm39) |
M282L |
probably benign |
Het |
| Itga9 |
T |
C |
9: 118,527,433 (GRCm39) |
L528P |
probably benign |
Het |
| Krt39 |
A |
C |
11: 99,412,062 (GRCm39) |
V8G |
probably benign |
Het |
| Krt71 |
A |
G |
15: 101,646,772 (GRCm39) |
I312T |
probably benign |
Het |
| Lrrc37 |
T |
A |
11: 103,506,638 (GRCm39) |
|
probably benign |
Het |
| Mllt11 |
A |
G |
3: 95,127,744 (GRCm39) |
Y9H |
probably damaging |
Het |
| Mrgpra3 |
G |
T |
7: 47,239,838 (GRCm39) |
N29K |
possibly damaging |
Het |
| Mug1 |
A |
G |
6: 121,850,603 (GRCm39) |
T700A |
probably benign |
Het |
| Myl1 |
T |
C |
1: 66,969,395 (GRCm39) |
N79S |
probably damaging |
Het |
| Myo18b |
G |
A |
5: 112,871,770 (GRCm39) |
Q2104* |
probably null |
Het |
| Nalf1 |
G |
A |
8: 9,820,589 (GRCm39) |
P144S |
possibly damaging |
Het |
| Ndufs2 |
T |
C |
1: 171,065,877 (GRCm39) |
D256G |
probably benign |
Het |
| Nek5 |
T |
C |
8: 22,597,739 (GRCm39) |
N280S |
probably benign |
Het |
| Nwd2 |
A |
T |
5: 63,962,258 (GRCm39) |
N614I |
probably damaging |
Het |
| Or6c88 |
G |
A |
10: 129,406,941 (GRCm39) |
C139Y |
possibly damaging |
Het |
| Parp1 |
G |
T |
1: 180,425,817 (GRCm39) |
K849N |
possibly damaging |
Het |
| Pcnx2 |
T |
C |
8: 126,512,041 (GRCm39) |
T1422A |
probably damaging |
Het |
| Plce1 |
A |
G |
19: 38,727,801 (GRCm39) |
N1520S |
probably damaging |
Het |
| Ppcdc |
T |
C |
9: 57,322,453 (GRCm39) |
T149A |
probably damaging |
Het |
| Ppl |
A |
G |
16: 4,905,366 (GRCm39) |
V1643A |
probably benign |
Het |
| Pramel23 |
A |
T |
4: 143,423,898 (GRCm39) |
I297N |
probably damaging |
Het |
| Prrx1 |
T |
A |
1: 163,075,907 (GRCm39) |
M220L |
probably benign |
Het |
| Pspc1 |
A |
C |
14: 56,996,085 (GRCm39) |
|
probably null |
Het |
| Ptpn20 |
A |
G |
14: 33,336,392 (GRCm39) |
*44W |
probably null |
Het |
| Qars1 |
T |
A |
9: 108,391,976 (GRCm39) |
V83E |
probably damaging |
Het |
| Rbm33 |
T |
C |
5: 28,599,496 (GRCm39) |
M956T |
unknown |
Het |
| Sash1 |
C |
A |
10: 8,605,847 (GRCm39) |
E848* |
probably null |
Het |
| Scai |
T |
A |
2: 39,011,147 (GRCm39) |
Y163F |
probably damaging |
Het |
| Serpinf2 |
A |
T |
11: 75,329,244 (GRCm39) |
|
probably benign |
Het |
| Sgo2b |
T |
A |
8: 64,379,868 (GRCm39) |
H988L |
probably benign |
Het |
| Sh2b2 |
G |
A |
5: 136,247,739 (GRCm39) |
T604I |
probably benign |
Het |
| Skint4 |
A |
T |
4: 112,015,281 (GRCm39) |
I449F |
possibly damaging |
Het |
| Slc30a2 |
A |
G |
4: 134,074,653 (GRCm39) |
I88V |
possibly damaging |
Het |
| Smug1 |
A |
G |
15: 103,064,369 (GRCm39) |
L184P |
probably damaging |
Het |
| Spatc1 |
A |
G |
15: 76,168,080 (GRCm39) |
T180A |
probably benign |
Het |
| Ssr1 |
A |
T |
13: 38,178,001 (GRCm39) |
L20Q |
probably null |
Het |
| Supt4a |
A |
G |
11: 87,634,084 (GRCm39) |
E100G |
probably damaging |
Het |
| Teddm2 |
T |
C |
1: 153,726,320 (GRCm39) |
I132V |
probably benign |
Het |
| Tmem131 |
C |
T |
1: 36,832,054 (GRCm39) |
G1861E |
possibly damaging |
Het |
| Tpr |
A |
T |
1: 150,299,358 (GRCm39) |
H1186L |
probably benign |
Het |
| Trim34b |
A |
T |
7: 103,978,743 (GRCm39) |
|
probably benign |
Het |
| Trpm2 |
T |
C |
10: 77,748,426 (GRCm39) |
M1415V |
probably benign |
Het |
| Ttll12 |
A |
G |
15: 83,471,086 (GRCm39) |
F264S |
probably benign |
Het |
| Vmn2r59 |
T |
C |
7: 41,695,644 (GRCm39) |
E256G |
probably benign |
Het |
| Vmn2r93 |
A |
T |
17: 18,546,672 (GRCm39) |
H848L |
probably benign |
Het |
| Vps35l |
T |
C |
7: 118,372,315 (GRCm39) |
S290P |
probably damaging |
Het |
| Wdfy3 |
G |
A |
5: 102,055,384 (GRCm39) |
T1562I |
probably damaging |
Het |
| Ybey |
T |
C |
10: 76,304,197 (GRCm39) |
S2G |
possibly damaging |
Het |
| Zfp346 |
A |
T |
13: 55,280,200 (GRCm39) |
Q308L |
probably benign |
Het |
|
| Other mutations in Herc3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00228:Herc3
|
APN |
6 |
58,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00423:Herc3
|
APN |
6 |
58,845,700 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00468:Herc3
|
APN |
6 |
58,895,751 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL01153:Herc3
|
APN |
6 |
58,837,321 (GRCm39) |
missense |
probably benign |
0.21 |
|
IGL01468:Herc3
|
APN |
6 |
58,831,880 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01696:Herc3
|
APN |
6 |
58,837,371 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
IGL01975:Herc3
|
APN |
6 |
58,893,561 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL02797:Herc3
|
APN |
6 |
58,845,679 (GRCm39) |
missense |
probably benign |
|
|
IGL02953:Herc3
|
APN |
6 |
58,834,718 (GRCm39) |
nonsense |
probably null |
|
|
aegean
|
UTSW |
6 |
58,832,745 (GRCm39) |
nonsense |
probably null |
|
|
PIT4519001:Herc3
|
UTSW |
6 |
58,853,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0019:Herc3
|
UTSW |
6 |
58,862,050 (GRCm39) |
splice site |
probably benign |
|
|
R0019:Herc3
|
UTSW |
6 |
58,862,050 (GRCm39) |
splice site |
probably benign |
|
|
R0025:Herc3
|
UTSW |
6 |
58,851,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0025:Herc3
|
UTSW |
6 |
58,851,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0268:Herc3
|
UTSW |
6 |
58,845,613 (GRCm39) |
splice site |
probably benign |
|
|
R0334:Herc3
|
UTSW |
6 |
58,895,802 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0344:Herc3
|
UTSW |
6 |
58,845,613 (GRCm39) |
splice site |
probably benign |
|
|
R0853:Herc3
|
UTSW |
6 |
58,853,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0927:Herc3
|
UTSW |
6 |
58,845,748 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R1333:Herc3
|
UTSW |
6 |
58,864,478 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1432:Herc3
|
UTSW |
6 |
58,893,827 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R1450:Herc3
|
UTSW |
6 |
58,853,500 (GRCm39) |
nonsense |
probably null |
|
|
R1594:Herc3
|
UTSW |
6 |
58,864,569 (GRCm39) |
unclassified |
probably benign |
|
|
R1757:Herc3
|
UTSW |
6 |
58,893,455 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1765:Herc3
|
UTSW |
6 |
58,865,645 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1932:Herc3
|
UTSW |
6 |
58,853,778 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1945:Herc3
|
UTSW |
6 |
58,864,424 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1988:Herc3
|
UTSW |
6 |
58,861,960 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2172:Herc3
|
UTSW |
6 |
58,864,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3080:Herc3
|
UTSW |
6 |
58,833,631 (GRCm39) |
splice site |
probably null |
|
|
R3545:Herc3
|
UTSW |
6 |
58,833,670 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3767:Herc3
|
UTSW |
6 |
58,853,587 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3767:Herc3
|
UTSW |
6 |
58,839,973 (GRCm39) |
missense |
probably benign |
|
|
R3805:Herc3
|
UTSW |
6 |
58,893,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3806:Herc3
|
UTSW |
6 |
58,893,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4049:Herc3
|
UTSW |
6 |
58,853,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4250:Herc3
|
UTSW |
6 |
58,893,501 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4469:Herc3
|
UTSW |
6 |
58,853,794 (GRCm39) |
nonsense |
probably null |
|
|
R4534:Herc3
|
UTSW |
6 |
58,837,332 (GRCm39) |
missense |
probably benign |
|
|
R4573:Herc3
|
UTSW |
6 |
58,871,098 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4887:Herc3
|
UTSW |
6 |
58,864,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5047:Herc3
|
UTSW |
6 |
58,832,745 (GRCm39) |
nonsense |
probably null |
|
|
R5049:Herc3
|
UTSW |
6 |
58,871,524 (GRCm39) |
splice site |
probably null |
|
|
R5062:Herc3
|
UTSW |
6 |
58,832,745 (GRCm39) |
nonsense |
probably null |
|
|
R5063:Herc3
|
UTSW |
6 |
58,832,745 (GRCm39) |
nonsense |
probably null |
|
|
R5288:Herc3
|
UTSW |
6 |
58,851,263 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5297:Herc3
|
UTSW |
6 |
58,833,626 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5386:Herc3
|
UTSW |
6 |
58,851,263 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5435:Herc3
|
UTSW |
6 |
58,832,791 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5576:Herc3
|
UTSW |
6 |
58,865,710 (GRCm39) |
missense |
probably benign |
0.08 |
|
R5605:Herc3
|
UTSW |
6 |
58,834,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5719:Herc3
|
UTSW |
6 |
58,871,528 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R5743:Herc3
|
UTSW |
6 |
58,895,784 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5870:Herc3
|
UTSW |
6 |
58,893,435 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6460:Herc3
|
UTSW |
6 |
58,867,108 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6930:Herc3
|
UTSW |
6 |
58,893,444 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7131:Herc3
|
UTSW |
6 |
58,864,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7187:Herc3
|
UTSW |
6 |
58,833,616 (GRCm39) |
missense |
probably benign |
0.42 |
|
R7212:Herc3
|
UTSW |
6 |
58,895,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7335:Herc3
|
UTSW |
6 |
58,853,773 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7349:Herc3
|
UTSW |
6 |
58,835,971 (GRCm39) |
missense |
probably benign |
|
|
R7568:Herc3
|
UTSW |
6 |
58,820,795 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7857:Herc3
|
UTSW |
6 |
58,820,637 (GRCm39) |
nonsense |
probably null |
|
|
R8321:Herc3
|
UTSW |
6 |
58,820,754 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8672:Herc3
|
UTSW |
6 |
58,850,786 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8684:Herc3
|
UTSW |
6 |
58,864,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8968:Herc3
|
UTSW |
6 |
58,867,183 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8994:Herc3
|
UTSW |
6 |
58,851,328 (GRCm39) |
missense |
probably benign |
0.11 |
|
R9219:Herc3
|
UTSW |
6 |
58,871,552 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9434:Herc3
|
UTSW |
6 |
58,853,846 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9562:Herc3
|
UTSW |
6 |
58,835,999 (GRCm39) |
missense |
probably null |
0.01 |
|
R9565:Herc3
|
UTSW |
6 |
58,835,999 (GRCm39) |
missense |
probably null |
0.01 |
|
Z1176:Herc3
|
UTSW |
6 |
58,820,843 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- AGAAGTTGTACAAGGTATCCCTGG -3'
(R):5'- CAAGAATTCCAAAGTCAACTGAGTG -3'
Sequencing Primer
(F):5'- CCTGGGGGATGGAGAGTG -3'
(R):5'- TGAAATAGATAGGTGTGTTAGCAGC -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation