Incidental Mutation 'RF010:Ttbk2'
| ID |
603115 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ttbk2
|
| Ensembl Gene |
ENSMUSG00000090100 |
| Gene Name |
tau tubulin kinase 2 |
| Synonyms |
2610507N02Rik, B930008N24Rik, TTK |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
RF010 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
120563297-120681085 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
A to T
at 120620820 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Stop codon
at position 147
(C147*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000028740
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028740]
[ENSMUST00000057135]
[ENSMUST00000085840]
[ENSMUST00000131389]
[ENSMUST00000143051]
|
| AlphaFold |
Q3UVR3 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000028740
AA Change: C147*
|
| SMART Domains |
Protein: ENSMUSP00000028740
Gene: ENSMUSG00000090100
AA Change: C147*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
90 |
347 |
7e-31 |
PFAM |
|
Pfam:Pkinase_Tyr
|
90 |
348 |
8.2e-19 |
PFAM |
|
low complexity region
|
369 |
383 |
N/A |
INTRINSIC |
|
low complexity region
|
1143 |
1156 |
N/A |
INTRINSIC |
|
low complexity region
|
1205 |
1242 |
N/A |
INTRINSIC |
|
low complexity region
|
1254 |
1271 |
N/A |
INTRINSIC |
|
low complexity region
|
1285 |
1309 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000057135
AA Change: C78*
|
| SMART Domains |
Protein: ENSMUSP00000055032
Gene: ENSMUSG00000090100
AA Change: C78*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
21 |
274 |
1.2e-32 |
PFAM |
|
Pfam:Pkinase_Tyr
|
21 |
280 |
3.8e-19 |
PFAM |
|
low complexity region
|
300 |
314 |
N/A |
INTRINSIC |
|
low complexity region
|
1074 |
1087 |
N/A |
INTRINSIC |
|
low complexity region
|
1136 |
1173 |
N/A |
INTRINSIC |
|
low complexity region
|
1185 |
1202 |
N/A |
INTRINSIC |
|
low complexity region
|
1216 |
1240 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000085840
AA Change: C78*
|
| SMART Domains |
Protein: ENSMUSP00000083001
Gene: ENSMUSG00000090100
AA Change: C78*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
21 |
274 |
1.2e-32 |
PFAM |
|
Pfam:Pkinase_Tyr
|
21 |
280 |
3.8e-19 |
PFAM |
|
low complexity region
|
300 |
314 |
N/A |
INTRINSIC |
|
low complexity region
|
1074 |
1087 |
N/A |
INTRINSIC |
|
low complexity region
|
1136 |
1173 |
N/A |
INTRINSIC |
|
low complexity region
|
1185 |
1202 |
N/A |
INTRINSIC |
|
low complexity region
|
1216 |
1240 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000131389
AA Change: C78*
|
| SMART Domains |
Protein: ENSMUSP00000118905
Gene: ENSMUSG00000090100
AA Change: C78*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
21 |
145 |
1.3e-18 |
PFAM |
|
Pfam:Pkinase_Tyr
|
21 |
148 |
9.7e-12 |
PFAM |
|
Pfam:Pkinase
|
145 |
239 |
1.2e-5 |
PFAM |
|
low complexity region
|
265 |
279 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000143051
AA Change: C78*
|
| SMART Domains |
Protein: ENSMUSP00000121996
Gene: ENSMUSG00000090100
AA Change: C78*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
21 |
274 |
2.4e-32 |
PFAM |
|
Pfam:Pkinase_Tyr
|
21 |
280 |
7.7e-19 |
PFAM |
|
low complexity region
|
300 |
314 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.4%
- 20x: 98.8%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem. [provided by RefSeq, Aug 2009]
PHENOTYPE: Mice homozygous for a knock-in allele exhibit complete preweaning lethality, decreased embryo size, growth retardation, and incomplete turning. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 70 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2300002M23Rik |
GGGTTATGGTCAGTACCCCCCAGTAGGGACCTGGGGCGGTTATGGTCAGTACCCCCCAGTAGGGCCCTGGGGCGGTTATGGTCAGTACCCCCCAGTAGGGACCTGGGG |
GGGTTATGGTCAGTACCCCCCAGTAGGGCCCTGGGGCGGTTATGGTCAGTACCCCCCAGTAGGGACCTGGGG |
17: 35,879,473 (GRCm39) |
|
probably benign |
Het |
| Acap3 |
CCTGGGCTGCTG |
CCTGGGCTGCTGCATACTGGGCTGCTG |
4: 155,989,553 (GRCm39) |
|
probably benign |
Het |
| Ankrd28 |
A |
G |
14: 31,500,943 (GRCm39) |
I16T |
probably damaging |
Het |
| AY761185 |
GCACTGTGGGC |
G |
8: 21,433,927 (GRCm39) |
|
probably null |
Het |
| Bend3 |
T |
A |
10: 43,386,180 (GRCm39) |
F191Y |
possibly damaging |
Het |
| Calhm1 |
GTGGC |
GTGGCTGTGGCTATGGC |
19: 47,129,712 (GRCm39) |
|
probably benign |
Het |
| Camkv |
CGCTGCTGC |
CGC |
9: 107,825,059 (GRCm39) |
|
probably benign |
Het |
| Cfap251 |
TCTCA |
T |
5: 123,412,224 (GRCm39) |
|
probably benign |
Het |
| Chga |
GCA |
GCATCA |
12: 102,527,662 (GRCm39) |
|
probably benign |
Het |
| Cngb1 |
CTCTGGCTCTGGCTCTGGCTCTG |
C |
8: 96,030,278 (GRCm39) |
|
probably null |
Het |
| Cnot3 |
T |
C |
7: 3,659,068 (GRCm39) |
V438A |
probably benign |
Het |
| Cntnap5c |
T |
A |
17: 58,593,790 (GRCm39) |
W710R |
probably damaging |
Het |
| Dyrk1a |
A |
G |
16: 94,478,422 (GRCm39) |
S404G |
probably benign |
Het |
| Efhd2 |
GCCGCC |
GCCGCCTCCGCC |
4: 141,602,075 (GRCm39) |
|
probably benign |
Het |
| Flywch1 |
GTGT |
GTGTGGGGAGGCTACGTACTCACCCACACCTGTTGT |
17: 23,981,149 (GRCm39) |
|
probably null |
Het |
| Fmn2 |
T |
A |
1: 174,409,581 (GRCm39) |
S605T |
unknown |
Het |
| Gab3 |
TCT |
TCTGCT |
X: 74,043,617 (GRCm39) |
|
probably benign |
Het |
| Gabre |
GCTC |
GCTCCGTCTC |
X: 71,313,666 (GRCm39) |
|
probably benign |
Het |
| Gli3 |
A |
G |
13: 15,900,954 (GRCm39) |
Y1447C |
probably damaging |
Het |
| Hibch |
T |
C |
1: 52,952,891 (GRCm39) |
V297A |
probably benign |
Het |
| Ifi213 |
C |
G |
1: 173,409,719 (GRCm39) |
D462H |
probably damaging |
Het |
| Kcnh8 |
G |
A |
17: 53,285,267 (GRCm39) |
R1079H |
probably benign |
Het |
| Lce1m |
GCTGCTGCC |
GCTGCTGCCCCCACTGCTGCC |
3: 92,925,597 (GRCm39) |
|
probably benign |
Het |
| Lpo |
A |
G |
11: 87,711,928 (GRCm39) |
V43A |
probably benign |
Het |
| Map1a |
A |
AGCTCCAGCTCCAGCCCCACCTCCAGCTCCC |
2: 121,136,799 (GRCm39) |
|
probably benign |
Het |
| Mapk9 |
A |
G |
11: 49,745,083 (GRCm39) |
|
probably benign |
Het |
| Mep1a |
G |
A |
17: 43,797,126 (GRCm39) |
H314Y |
probably damaging |
Het |
| Myh3 |
ATTAC |
ATTACTTAC |
11: 66,977,182 (GRCm39) |
|
probably null |
Het |
| Myh3 |
AC |
ACTTCC |
11: 66,977,185 (GRCm39) |
|
probably null |
Het |
| Nusap1 |
ACGTTAGCAGTGAGGAGCAA |
ACGTTAGCAGTGAGGAGCAAACTGAGATACTCGTTAGCAGTGAGGAGCAA |
2: 119,458,065 (GRCm39) |
|
probably benign |
Het |
| Or10ag56 |
T |
A |
2: 87,139,184 (GRCm39) |
V37E |
possibly damaging |
Het |
| Or14a259 |
T |
C |
7: 86,012,594 (GRCm39) |
Q317R |
probably benign |
Het |
| Pdcd11 |
AGGAGG |
A |
19: 47,101,890 (GRCm39) |
|
probably null |
Het |
| Pfkm |
T |
A |
15: 98,027,674 (GRCm39) |
I651N |
possibly damaging |
Het |
| Phldb3 |
CCCCCGCCCC |
CCCCC |
7: 24,325,920 (GRCm39) |
|
probably null |
Het |
| Polr1has |
CACCACCAC |
CACCACCACCACCACCACCACTACCACCAC |
17: 37,275,955 (GRCm39) |
|
probably benign |
Het |
| Prkce |
T |
C |
17: 86,795,627 (GRCm39) |
V288A |
probably damaging |
Het |
| Pxmp4 |
A |
G |
2: 154,434,183 (GRCm39) |
S93P |
probably damaging |
Het |
| Rfc4 |
T |
C |
16: 22,946,232 (GRCm39) |
T17A |
probably benign |
Het |
| Rfx4 |
CTCTCTCT |
CTCTCTCTCTCTCTCTATCTCTCT |
10: 84,694,351 (GRCm39) |
|
probably benign |
Het |
| Ryr3 |
G |
T |
2: 112,606,015 (GRCm39) |
A2415E |
probably damaging |
Het |
| Sbp |
ACAAAGATGCTGACAACAAAGATGCTGACA |
ACAAAGATGCTGACACCAAAGATGCTGACAACAAAGATGCTGACA |
17: 24,164,325 (GRCm39) |
|
probably benign |
Het |
| Sec24c |
T |
A |
14: 20,738,783 (GRCm39) |
|
probably null |
Het |
| Sec63 |
C |
A |
10: 42,682,620 (GRCm39) |
A437E |
probably benign |
Het |
| Six3 |
GCG |
GCGTCG |
17: 85,928,783 (GRCm39) |
|
probably benign |
Het |
| Slco5a1 |
G |
A |
1: 12,942,171 (GRCm39) |
T825I |
probably damaging |
Het |
| Spmap2l |
CAG |
CAGCGATCCTCCCCAGTCCCGCAAGGCGAG |
5: 77,164,274 (GRCm39) |
|
probably benign |
Het |
| Stard8 |
GGA |
GGAAGA |
X: 98,110,123 (GRCm39) |
|
probably benign |
Het |
| Stxbp1 |
A |
G |
2: 32,711,927 (GRCm39) |
V30A |
probably benign |
Het |
| Supt20 |
AGCAGC |
AGCAGCGGCAGC |
3: 54,635,083 (GRCm39) |
|
probably benign |
Het |
| Syne1 |
T |
A |
10: 5,196,386 (GRCm39) |
D3882V |
possibly damaging |
Het |
| T |
A |
G |
17: 8,660,540 (GRCm39) |
T384A |
probably benign |
Het |
| Tbc1d12 |
CGGGGCGG |
CG |
19: 38,825,384 (GRCm39) |
|
probably benign |
Het |
| Tcof1 |
CAG |
CAGAAG |
18: 60,968,816 (GRCm39) |
|
probably benign |
Het |
| Tcstv5 |
A |
T |
13: 120,411,582 (GRCm39) |
V8E |
probably benign |
Het |
| Tfeb |
GCA |
GCAACA |
17: 48,097,019 (GRCm39) |
|
probably benign |
Het |
| Tfeb |
CAG |
CAGAAG |
17: 48,097,032 (GRCm39) |
|
probably benign |
Het |
| Thumpd3 |
C |
T |
6: 113,033,006 (GRCm39) |
A248V |
probably damaging |
Het |
| Tlcd4 |
T |
A |
3: 121,022,533 (GRCm39) |
I103L |
probably benign |
Het |
| Tmem181a |
T |
C |
17: 6,330,978 (GRCm39) |
|
probably null |
Het |
| Trim41 |
A |
T |
11: 48,698,165 (GRCm39) |
H600Q |
probably damaging |
Het |
| Ttll2 |
C |
T |
17: 7,618,737 (GRCm39) |
A397T |
probably benign |
Het |
| Unc79 |
T |
A |
12: 103,079,046 (GRCm39) |
L1737Q |
probably benign |
Het |
| Usp47 |
T |
A |
7: 111,692,145 (GRCm39) |
V869E |
probably damaging |
Het |
| Vmn1r231 |
T |
A |
17: 21,110,255 (GRCm39) |
Q220L |
probably damaging |
Het |
| Vmn2r26 |
C |
T |
6: 124,016,448 (GRCm39) |
T304I |
possibly damaging |
Het |
| Wrn |
T |
C |
8: 33,778,793 (GRCm39) |
N839S |
probably benign |
Het |
| Zfp384 |
GCCCAGGCCCAGGCCCAGGCCCAG |
GCCCAGGCCCAGTCCCAGGCCCAGGCCCAGGCCCAG |
6: 125,013,434 (GRCm39) |
|
probably benign |
Het |
| Zfp384 |
GGCCCAGG |
GGCCCAGGAGCACGCCCAGG |
6: 125,013,451 (GRCm39) |
|
probably benign |
Het |
| Zfyve26 |
C |
T |
12: 79,302,112 (GRCm39) |
C1828Y |
probably damaging |
Het |
|
| Other mutations in Ttbk2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00091:Ttbk2
|
APN |
2 |
120,579,314 (GRCm39) |
nonsense |
probably null |
|
|
IGL00484:Ttbk2
|
APN |
2 |
120,604,367 (GRCm39) |
nonsense |
probably null |
|
|
IGL00767:Ttbk2
|
APN |
2 |
120,576,226 (GRCm39) |
missense |
probably benign |
|
|
IGL00809:Ttbk2
|
APN |
2 |
120,590,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01484:Ttbk2
|
APN |
2 |
120,570,314 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01974:Ttbk2
|
APN |
2 |
120,616,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02488:Ttbk2
|
APN |
2 |
120,586,352 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02874:Ttbk2
|
APN |
2 |
120,576,193 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02893:Ttbk2
|
APN |
2 |
120,614,210 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03210:Ttbk2
|
APN |
2 |
120,652,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0279:Ttbk2
|
UTSW |
2 |
120,579,441 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0362:Ttbk2
|
UTSW |
2 |
120,576,264 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0376:Ttbk2
|
UTSW |
2 |
120,608,062 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0400:Ttbk2
|
UTSW |
2 |
120,580,723 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0601:Ttbk2
|
UTSW |
2 |
120,655,777 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R0606:Ttbk2
|
UTSW |
2 |
120,604,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0664:Ttbk2
|
UTSW |
2 |
120,579,302 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0718:Ttbk2
|
UTSW |
2 |
120,579,056 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0718:Ttbk2
|
UTSW |
2 |
120,575,641 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0783:Ttbk2
|
UTSW |
2 |
120,570,458 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0906:Ttbk2
|
UTSW |
2 |
120,614,262 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1141:Ttbk2
|
UTSW |
2 |
120,637,332 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1363:Ttbk2
|
UTSW |
2 |
120,637,389 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1420:Ttbk2
|
UTSW |
2 |
120,576,393 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1734:Ttbk2
|
UTSW |
2 |
120,586,319 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2033:Ttbk2
|
UTSW |
2 |
120,637,330 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2047:Ttbk2
|
UTSW |
2 |
120,579,397 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2893:Ttbk2
|
UTSW |
2 |
120,576,091 (GRCm39) |
splice site |
probably null |
|
|
R3783:Ttbk2
|
UTSW |
2 |
120,604,296 (GRCm39) |
splice site |
probably benign |
|
|
R3785:Ttbk2
|
UTSW |
2 |
120,604,296 (GRCm39) |
splice site |
probably benign |
|
|
R3870:Ttbk2
|
UTSW |
2 |
120,570,500 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4024:Ttbk2
|
UTSW |
2 |
120,590,736 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4039:Ttbk2
|
UTSW |
2 |
120,576,276 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4060:Ttbk2
|
UTSW |
2 |
120,579,465 (GRCm39) |
missense |
probably benign |
0.26 |
|
R4624:Ttbk2
|
UTSW |
2 |
120,603,804 (GRCm39) |
missense |
probably benign |
0.19 |
|
R4634:Ttbk2
|
UTSW |
2 |
120,570,673 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4708:Ttbk2
|
UTSW |
2 |
120,570,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4727:Ttbk2
|
UTSW |
2 |
120,575,851 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4811:Ttbk2
|
UTSW |
2 |
120,570,551 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4962:Ttbk2
|
UTSW |
2 |
120,575,631 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4964:Ttbk2
|
UTSW |
2 |
120,603,758 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4966:Ttbk2
|
UTSW |
2 |
120,603,758 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5369:Ttbk2
|
UTSW |
2 |
120,655,743 (GRCm39) |
start gained |
probably benign |
|
|
R5430:Ttbk2
|
UTSW |
2 |
120,608,046 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5607:Ttbk2
|
UTSW |
2 |
120,637,305 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5812:Ttbk2
|
UTSW |
2 |
120,653,040 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5898:Ttbk2
|
UTSW |
2 |
120,575,521 (GRCm39) |
missense |
probably benign |
0.08 |
|
R5951:Ttbk2
|
UTSW |
2 |
120,603,764 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6135:Ttbk2
|
UTSW |
2 |
120,580,798 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6889:Ttbk2
|
UTSW |
2 |
120,603,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6907:Ttbk2
|
UTSW |
2 |
120,655,751 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7013:Ttbk2
|
UTSW |
2 |
120,576,265 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7128:Ttbk2
|
UTSW |
2 |
120,576,569 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7173:Ttbk2
|
UTSW |
2 |
120,570,592 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7358:Ttbk2
|
UTSW |
2 |
120,620,791 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7475:Ttbk2
|
UTSW |
2 |
120,579,121 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7891:Ttbk2
|
UTSW |
2 |
120,616,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8529:Ttbk2
|
UTSW |
2 |
120,604,338 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R9050:Ttbk2
|
UTSW |
2 |
120,637,319 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9051:Ttbk2
|
UTSW |
2 |
120,575,911 (GRCm39) |
nonsense |
probably null |
|
|
R9372:Ttbk2
|
UTSW |
2 |
120,603,766 (GRCm39) |
missense |
probably benign |
0.31 |
|
R9485:Ttbk2
|
UTSW |
2 |
120,575,986 (GRCm39) |
missense |
probably benign |
0.32 |
|
R9675:Ttbk2
|
UTSW |
2 |
120,637,241 (GRCm39) |
missense |
probably benign |
0.14 |
|
RF021:Ttbk2
|
UTSW |
2 |
120,579,115 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ACGCACTTCATCTGTTCAGC -3'
(R):5'- CCTTACTGTATCTGCTCAGGG -3'
Sequencing Primer
(F):5'- CACTTCATCTGTTCAGCATACATAAG -3'
(R):5'- TTATTTGAGTATTCAAGGAGCAGAGG -3'
|
| Posted On |
2019-12-04 |
Incidental Mutation