Incidental Mutation 'R4880:Chd1'
ID |
375252 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Chd1
|
Ensembl Gene |
ENSMUSG00000023852 |
Gene Name |
chromodomain helicase DNA binding protein 1 |
Synonyms |
4930525N21Rik |
MMRRC Submission |
042489-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4880 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
17 |
Chromosomal Location |
15925229-15992872 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 17594916 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Serine
at position 17
(F17S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000156350
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000024620]
[ENSMUST00000232199]
[ENSMUST00000232396]
|
AlphaFold |
P40201 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000024620
AA Change: F17S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000024620 Gene: ENSMUSG00000116564 AA Change: F17S
Domain | Start | End | E-Value | Type |
Pfam:Rio2_N
|
9 |
91 |
9.5e-36 |
PFAM |
Pfam:Kdo
|
105 |
193 |
6.3e-8 |
PFAM |
Pfam:RIO1
|
108 |
284 |
1.7e-57 |
PFAM |
Pfam:APH
|
194 |
278 |
3.2e-8 |
PFAM |
low complexity region
|
326 |
340 |
N/A |
INTRINSIC |
low complexity region
|
501 |
518 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000232199
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232288
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000232396
AA Change: F17S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Meta Mutation Damage Score |
0.8721 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.5%
|
Validation Efficiency |
98% (89/91) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete embryonic lethality associated with arrest of epiblast development due to increased apoptosis and cell cycle defects, abnormal rostral-caudal axis patterning, and failure to gastrulate. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
T |
C |
7: 41,276,529 (GRCm39) |
I744T |
possibly damaging |
Het |
Adgrb1 |
T |
A |
15: 74,458,871 (GRCm39) |
F1324L |
possibly damaging |
Het |
Adm |
A |
G |
7: 110,228,326 (GRCm39) |
H230R |
probably benign |
Het |
Ank2 |
A |
T |
3: 126,840,475 (GRCm39) |
|
probably null |
Het |
Arih1 |
A |
T |
9: 59,344,168 (GRCm39) |
F156L |
possibly damaging |
Het |
Atf6b |
A |
G |
17: 34,873,529 (GRCm39) |
H660R |
probably damaging |
Het |
Bcl9l |
C |
A |
9: 44,420,007 (GRCm39) |
Q1101K |
probably benign |
Het |
Ccdc174 |
G |
A |
6: 91,876,572 (GRCm39) |
|
probably benign |
Het |
Ccdc65 |
A |
C |
15: 98,620,538 (GRCm39) |
|
probably null |
Het |
Cela2a |
T |
C |
4: 141,549,598 (GRCm39) |
N59S |
probably benign |
Het |
Cfap157 |
A |
T |
2: 32,668,261 (GRCm39) |
V393E |
probably damaging |
Het |
Cpne3 |
T |
C |
4: 19,540,827 (GRCm39) |
I183V |
probably benign |
Het |
Cyp2d11 |
C |
A |
15: 82,276,306 (GRCm39) |
V122L |
probably benign |
Het |
Dcaf8 |
C |
A |
1: 172,015,056 (GRCm39) |
|
probably benign |
Het |
Dchs1 |
T |
A |
7: 105,404,937 (GRCm39) |
D2535V |
probably benign |
Het |
Eif4a2 |
G |
T |
16: 22,927,650 (GRCm39) |
|
probably benign |
Het |
Fzd4 |
T |
A |
7: 89,057,109 (GRCm39) |
D385E |
probably benign |
Het |
Galnt13 |
C |
A |
2: 54,950,584 (GRCm39) |
Q422K |
probably damaging |
Het |
Gnptab |
C |
T |
10: 88,268,413 (GRCm39) |
Q507* |
probably null |
Het |
Hoxa7 |
A |
G |
6: 52,194,014 (GRCm39) |
|
probably benign |
Het |
Htra1 |
T |
A |
7: 130,563,813 (GRCm39) |
V228D |
probably damaging |
Het |
Idi2l |
A |
T |
13: 8,990,702 (GRCm39) |
|
probably null |
Het |
Ifi203 |
T |
A |
1: 173,756,716 (GRCm39) |
|
probably benign |
Het |
Iqca1l |
T |
C |
5: 24,754,750 (GRCm39) |
D340G |
probably benign |
Het |
Irs1 |
TGGGGTGGACATCGAACTGAAGGAG |
TG |
1: 82,265,453 (GRCm39) |
913 |
probably null |
Het |
Itga2b |
G |
T |
11: 102,348,548 (GRCm39) |
|
probably benign |
Het |
Itgb1 |
G |
T |
8: 129,442,631 (GRCm39) |
R272L |
probably damaging |
Het |
Kif9 |
A |
G |
9: 110,330,703 (GRCm39) |
E343G |
probably damaging |
Het |
Klhl5 |
T |
C |
5: 65,316,244 (GRCm39) |
V97A |
probably damaging |
Het |
Lama5 |
C |
A |
2: 179,818,861 (GRCm39) |
|
probably benign |
Het |
Lamb2 |
A |
G |
9: 108,361,226 (GRCm39) |
|
probably null |
Het |
Lrp1b |
T |
A |
2: 41,660,931 (GRCm39) |
Y59F |
probably benign |
Het |
Mmrn1 |
A |
G |
6: 60,953,423 (GRCm39) |
E568G |
probably benign |
Het |
Mreg |
A |
G |
1: 72,201,495 (GRCm39) |
Y166H |
probably damaging |
Het |
Myh7 |
C |
A |
14: 55,216,045 (GRCm39) |
V1323F |
probably benign |
Het |
Nr1i3 |
T |
A |
1: 171,043,951 (GRCm39) |
I91K |
probably damaging |
Het |
Nsfl1c |
T |
A |
2: 151,348,230 (GRCm39) |
D206E |
probably damaging |
Het |
Or11g24 |
T |
C |
14: 50,662,758 (GRCm39) |
Y261H |
possibly damaging |
Het |
Or13c3 |
A |
T |
4: 52,856,411 (GRCm39) |
M34K |
probably damaging |
Het |
Or2ak5 |
G |
A |
11: 58,611,107 (GRCm39) |
L256F |
probably benign |
Het |
Or4k44 |
A |
T |
2: 111,367,698 (GRCm39) |
L312* |
probably null |
Het |
Or5k17 |
A |
C |
16: 58,746,463 (GRCm39) |
L157W |
probably damaging |
Het |
Or8b54 |
T |
A |
9: 38,686,843 (GRCm39) |
C97* |
probably null |
Het |
Pcdhb7 |
C |
T |
18: 37,475,284 (GRCm39) |
T140I |
probably benign |
Het |
Pcdhgb5 |
T |
G |
18: 37,865,641 (GRCm39) |
S479A |
probably benign |
Het |
Pcsk5 |
T |
A |
19: 17,425,054 (GRCm39) |
Y1583F |
probably damaging |
Het |
Pias1 |
T |
C |
9: 62,820,080 (GRCm39) |
R296G |
probably benign |
Het |
Plscr1l1 |
A |
G |
9: 92,236,665 (GRCm39) |
E108G |
probably damaging |
Het |
Polr1e |
T |
A |
4: 45,022,280 (GRCm39) |
C100S |
probably damaging |
Het |
Rpap1 |
C |
A |
2: 119,614,346 (GRCm39) |
R17L |
probably damaging |
Het |
Rtn1 |
C |
T |
12: 72,264,232 (GRCm39) |
V192I |
possibly damaging |
Het |
Ryr2 |
G |
A |
13: 11,767,104 (GRCm39) |
P1262L |
probably damaging |
Het |
Slc4a7 |
G |
T |
14: 14,757,342 (GRCm38) |
D396Y |
probably damaging |
Het |
Slc5a8 |
T |
C |
10: 88,727,886 (GRCm39) |
Y118H |
probably damaging |
Het |
Slc7a6os |
T |
A |
8: 106,937,247 (GRCm39) |
Q71L |
probably benign |
Het |
Sphkap |
A |
G |
1: 83,266,538 (GRCm39) |
V127A |
probably damaging |
Het |
Srpk1 |
A |
G |
17: 28,810,199 (GRCm39) |
S580P |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,026,593 (GRCm39) |
I3474V |
probably damaging |
Het |
Tchh |
A |
G |
3: 93,351,130 (GRCm39) |
D190G |
possibly damaging |
Het |
Tenm4 |
T |
A |
7: 96,555,025 (GRCm39) |
|
probably null |
Het |
Tex14 |
T |
A |
11: 87,377,121 (GRCm39) |
I155N |
possibly damaging |
Het |
Tm7sf3 |
A |
T |
6: 146,511,358 (GRCm39) |
V377E |
possibly damaging |
Het |
Tnfsf9 |
T |
A |
17: 57,412,433 (GRCm39) |
M1K |
probably null |
Het |
Tns2 |
C |
T |
15: 102,020,474 (GRCm39) |
T780I |
probably damaging |
Het |
Trdn |
T |
A |
10: 33,347,575 (GRCm39) |
D639E |
probably benign |
Het |
Trmt10a |
A |
G |
3: 137,857,972 (GRCm39) |
E173G |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,649,119 (GRCm39) |
P10984S |
possibly damaging |
Het |
Tubb6 |
C |
T |
18: 67,534,386 (GRCm39) |
T95M |
possibly damaging |
Het |
Uroc1 |
G |
T |
6: 90,334,519 (GRCm39) |
R577L |
probably damaging |
Het |
Vmn2r86 |
T |
A |
10: 130,289,484 (GRCm39) |
D137V |
probably benign |
Het |
Xkr7 |
T |
C |
2: 152,896,873 (GRCm39) |
Y576H |
probably damaging |
Het |
Zfp410 |
A |
G |
12: 84,384,449 (GRCm39) |
N355D |
probably damaging |
Het |
Zfp59 |
C |
A |
7: 27,543,742 (GRCm39) |
D22E |
probably damaging |
Het |
Zfp64 |
C |
T |
2: 168,736,297 (GRCm39) |
R460H |
probably damaging |
Het |
Zfp655 |
T |
C |
5: 145,181,168 (GRCm39) |
V342A |
probably damaging |
Het |
Zfp990 |
G |
A |
4: 145,264,490 (GRCm39) |
G496E |
probably benign |
Het |
|
Other mutations in Chd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00704:Chd1
|
APN |
17 |
15,952,827 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01356:Chd1
|
APN |
17 |
15,970,127 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01369:Chd1
|
APN |
17 |
15,975,259 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01519:Chd1
|
APN |
17 |
17,598,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01604:Chd1
|
APN |
17 |
15,990,359 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01635:Chd1
|
APN |
17 |
17,598,858 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01721:Chd1
|
APN |
17 |
15,990,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01959:Chd1
|
APN |
17 |
15,962,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02367:Chd1
|
APN |
17 |
17,610,315 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02476:Chd1
|
APN |
17 |
15,954,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02756:Chd1
|
APN |
17 |
15,951,069 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02817:Chd1
|
APN |
17 |
15,969,762 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03084:Chd1
|
APN |
17 |
15,990,560 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03108:Chd1
|
APN |
17 |
15,945,543 (GRCm39) |
missense |
possibly damaging |
0.70 |
Holly
|
UTSW |
17 |
15,946,545 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0053:Chd1
|
UTSW |
17 |
15,967,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Chd1
|
UTSW |
17 |
15,967,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:Chd1
|
UTSW |
17 |
17,613,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Chd1
|
UTSW |
17 |
15,945,693 (GRCm39) |
missense |
probably benign |
|
R0285:Chd1
|
UTSW |
17 |
17,594,942 (GRCm39) |
splice site |
probably benign |
|
R0326:Chd1
|
UTSW |
17 |
15,988,830 (GRCm39) |
missense |
probably benign |
|
R0326:Chd1
|
UTSW |
17 |
15,988,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R0372:Chd1
|
UTSW |
17 |
17,607,552 (GRCm39) |
missense |
probably benign |
0.14 |
R0391:Chd1
|
UTSW |
17 |
15,970,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0486:Chd1
|
UTSW |
17 |
15,954,604 (GRCm39) |
missense |
probably damaging |
0.99 |
R0637:Chd1
|
UTSW |
17 |
15,962,550 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0675:Chd1
|
UTSW |
17 |
15,978,523 (GRCm39) |
unclassified |
probably benign |
|
R0701:Chd1
|
UTSW |
17 |
15,945,693 (GRCm39) |
missense |
probably benign |
|
R0788:Chd1
|
UTSW |
17 |
15,927,376 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0848:Chd1
|
UTSW |
17 |
15,990,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Chd1
|
UTSW |
17 |
15,945,693 (GRCm39) |
missense |
probably benign |
|
R1169:Chd1
|
UTSW |
17 |
15,955,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R1218:Chd1
|
UTSW |
17 |
15,945,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R1370:Chd1
|
UTSW |
17 |
17,607,742 (GRCm39) |
missense |
probably benign |
0.00 |
R1470:Chd1
|
UTSW |
17 |
15,946,545 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1470:Chd1
|
UTSW |
17 |
15,946,545 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1478:Chd1
|
UTSW |
17 |
15,959,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R1752:Chd1
|
UTSW |
17 |
15,963,494 (GRCm39) |
critical splice donor site |
probably null |
|
R1759:Chd1
|
UTSW |
17 |
17,607,533 (GRCm39) |
missense |
probably benign |
0.00 |
R1767:Chd1
|
UTSW |
17 |
15,990,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Chd1
|
UTSW |
17 |
15,982,748 (GRCm39) |
missense |
probably benign |
0.39 |
R2007:Chd1
|
UTSW |
17 |
15,951,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Chd1
|
UTSW |
17 |
15,962,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R3771:Chd1
|
UTSW |
17 |
17,594,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Chd1
|
UTSW |
17 |
17,594,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R3849:Chd1
|
UTSW |
17 |
15,952,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R4241:Chd1
|
UTSW |
17 |
15,990,289 (GRCm39) |
nonsense |
probably null |
|
R4242:Chd1
|
UTSW |
17 |
15,990,289 (GRCm39) |
nonsense |
probably null |
|
R4354:Chd1
|
UTSW |
17 |
17,610,263 (GRCm39) |
missense |
probably benign |
0.23 |
R4468:Chd1
|
UTSW |
17 |
15,980,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R4469:Chd1
|
UTSW |
17 |
15,980,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R4731:Chd1
|
UTSW |
17 |
17,598,079 (GRCm39) |
missense |
probably benign |
0.36 |
R4824:Chd1
|
UTSW |
17 |
15,953,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R4840:Chd1
|
UTSW |
17 |
15,989,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4840:Chd1
|
UTSW |
17 |
15,989,015 (GRCm39) |
nonsense |
probably null |
|
R4960:Chd1
|
UTSW |
17 |
15,962,493 (GRCm39) |
missense |
probably damaging |
0.96 |
R5071:Chd1
|
UTSW |
17 |
15,982,667 (GRCm39) |
missense |
probably benign |
|
R5078:Chd1
|
UTSW |
17 |
15,946,616 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5114:Chd1
|
UTSW |
17 |
15,948,460 (GRCm39) |
missense |
probably benign |
0.25 |
R5268:Chd1
|
UTSW |
17 |
15,956,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Chd1
|
UTSW |
17 |
15,990,530 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5304:Chd1
|
UTSW |
17 |
15,975,213 (GRCm39) |
missense |
probably benign |
0.01 |
R5307:Chd1
|
UTSW |
17 |
15,952,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Chd1
|
UTSW |
17 |
15,958,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R5553:Chd1
|
UTSW |
17 |
17,605,875 (GRCm39) |
missense |
probably benign |
0.17 |
R5623:Chd1
|
UTSW |
17 |
15,975,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R6022:Chd1
|
UTSW |
17 |
17,598,035 (GRCm39) |
missense |
probably benign |
0.39 |
R6137:Chd1
|
UTSW |
17 |
15,978,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Chd1
|
UTSW |
17 |
15,950,465 (GRCm39) |
splice site |
probably null |
|
R6373:Chd1
|
UTSW |
17 |
15,958,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6458:Chd1
|
UTSW |
17 |
15,950,864 (GRCm39) |
missense |
probably benign |
0.01 |
R6476:Chd1
|
UTSW |
17 |
17,601,250 (GRCm39) |
critical splice donor site |
probably null |
|
R6508:Chd1
|
UTSW |
17 |
15,958,895 (GRCm39) |
missense |
probably benign |
0.31 |
R6553:Chd1
|
UTSW |
17 |
15,945,692 (GRCm39) |
missense |
probably benign |
0.00 |
R6745:Chd1
|
UTSW |
17 |
17,607,429 (GRCm39) |
missense |
probably benign |
0.08 |
R7107:Chd1
|
UTSW |
17 |
15,981,628 (GRCm39) |
missense |
probably damaging |
0.98 |
R7230:Chd1
|
UTSW |
17 |
15,927,199 (GRCm39) |
splice site |
probably null |
|
R7317:Chd1
|
UTSW |
17 |
15,962,536 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7341:Chd1
|
UTSW |
17 |
15,990,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R7421:Chd1
|
UTSW |
17 |
15,969,660 (GRCm39) |
missense |
probably benign |
0.03 |
R7704:Chd1
|
UTSW |
17 |
15,987,737 (GRCm39) |
missense |
probably benign |
|
R7763:Chd1
|
UTSW |
17 |
15,953,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R8156:Chd1
|
UTSW |
17 |
15,981,666 (GRCm39) |
missense |
probably benign |
|
R8194:Chd1
|
UTSW |
17 |
17,594,737 (GRCm39) |
start gained |
probably benign |
|
R8261:Chd1
|
UTSW |
17 |
17,607,804 (GRCm39) |
missense |
probably benign |
0.02 |
R8338:Chd1
|
UTSW |
17 |
15,990,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R8401:Chd1
|
UTSW |
17 |
15,963,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Chd1
|
UTSW |
17 |
15,982,711 (GRCm39) |
missense |
probably damaging |
0.98 |
R9067:Chd1
|
UTSW |
17 |
15,951,107 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9184:Chd1
|
UTSW |
17 |
15,962,551 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9210:Chd1
|
UTSW |
17 |
15,950,767 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9212:Chd1
|
UTSW |
17 |
15,950,767 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9666:Chd1
|
UTSW |
17 |
15,955,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R9673:Chd1
|
UTSW |
17 |
15,989,023 (GRCm39) |
missense |
probably benign |
0.24 |
Z1176:Chd1
|
UTSW |
17 |
15,988,995 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Chd1
|
UTSW |
17 |
15,986,609 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Chd1
|
UTSW |
17 |
15,968,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCACGTGTTCTTACCTAGCG -3'
(R):5'- AGACGTAAGCACATCTGCAGC -3'
Sequencing Primer
(F):5'- GCACGTGTTCTTACCTAGCGATAAG -3'
(R):5'- GTAAGCACATCTGCAGCAAAAG -3'
|
Posted On |
2016-03-17 |