Incidental Mutation 'R7381:Gsap'
ID |
572704 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Gsap
|
Ensembl Gene |
ENSMUSG00000039934 |
Gene Name |
gamma-secretase activating protein |
Synonyms |
A530088I07Rik, Pion |
MMRRC Submission |
045463-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.125)
|
Stock # |
R7381 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
21391253-21520130 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 21431785 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 228
(I228N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000043679
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036031]
[ENSMUST00000195969]
[ENSMUST00000198014]
[ENSMUST00000198071]
[ENSMUST00000198937]
|
AlphaFold |
Q3TCV3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000036031
AA Change: I228N
PolyPhen 2
Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000043679 Gene: ENSMUSG00000039934 AA Change: I228N
Domain | Start | End | E-Value | Type |
low complexity region
|
386 |
398 |
N/A |
INTRINSIC |
Pfam:GSAP-16
|
646 |
753 |
6.8e-43 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195969
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000198014
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000198071
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000198937
AA Change: I228N
PolyPhen 2
Score 0.917 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000142986 Gene: ENSMUSG00000039934 AA Change: I228N
Domain | Start | End | E-Value | Type |
low complexity region
|
355 |
367 |
N/A |
INTRINSIC |
Pfam:GSAP-16
|
608 |
722 |
1.6e-42 |
PFAM |
|
Meta Mutation Damage Score |
0.5579 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
Validation Efficiency |
98% (88/90) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Accumulation of neurotoxic amyloid-beta is a major hallmark of Alzheimer disease (AD; MIM 104300). Formation of amyloid-beta is catalyzed by gamma-secretase (see PSEN1; MIM 104311), a protease with numerous substrates. PION, or GSAP, selectively increases amyloid-beta production through a mechanism involving its interaction with both gamma-secretase and its substrate, the amyloid-beta precursor protein (APP; MIM 104760) C-terminal fragment (APP-CTF) (He et al., 2010 [PubMed 20811458]).[supplied by OMIM, Nov 2010]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
T |
C |
9: 53,323,122 (GRCm39) |
Y53H |
probably damaging |
Het |
Abca8a |
A |
T |
11: 109,920,913 (GRCm39) |
|
probably null |
Het |
Acads |
C |
A |
5: 115,249,057 (GRCm39) |
Q365H |
probably damaging |
Het |
Acsm3 |
A |
G |
7: 119,380,049 (GRCm39) |
D462G |
probably damaging |
Het |
Adam39 |
T |
A |
8: 41,279,000 (GRCm39) |
C464S |
probably damaging |
Het |
Adgra3 |
A |
G |
5: 50,216,116 (GRCm39) |
M1T |
probably null |
Het |
AI182371 |
T |
C |
2: 34,975,371 (GRCm39) |
Y276C |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,730,277 (GRCm39) |
H719L |
possibly damaging |
Het |
Ano7 |
G |
A |
1: 93,323,057 (GRCm39) |
V466I |
probably benign |
Het |
Art5 |
A |
G |
7: 101,747,377 (GRCm39) |
L134P |
probably damaging |
Het |
Atcay |
A |
G |
10: 81,046,431 (GRCm39) |
Y298H |
possibly damaging |
Het |
Atp1a4 |
A |
T |
1: 172,067,682 (GRCm39) |
F527Y |
possibly damaging |
Het |
Bpifb2 |
A |
T |
2: 153,734,268 (GRCm39) |
M428L |
probably benign |
Het |
Brinp2 |
A |
C |
1: 158,073,913 (GRCm39) |
V736G |
probably benign |
Het |
Cdc5l |
C |
T |
17: 45,722,849 (GRCm39) |
A437T |
probably benign |
Het |
Cdx2 |
G |
A |
5: 147,243,440 (GRCm39) |
P118L |
possibly damaging |
Het |
Chpt1 |
G |
A |
10: 88,311,193 (GRCm39) |
|
probably null |
Het |
Creb3l2 |
T |
A |
6: 37,312,783 (GRCm39) |
E417V |
probably damaging |
Het |
Csnk2a1 |
A |
G |
2: 152,100,614 (GRCm39) |
T129A |
probably benign |
Het |
Dennd6b |
A |
T |
15: 89,070,376 (GRCm39) |
L431Q |
possibly damaging |
Het |
Dgkz |
C |
T |
2: 91,775,180 (GRCm39) |
A260T |
probably benign |
Het |
Dhx34 |
T |
A |
7: 15,949,373 (GRCm39) |
T352S |
probably benign |
Het |
Elp4 |
C |
T |
2: 105,622,652 (GRCm39) |
R349Q |
not run |
Het |
Emsy |
A |
C |
7: 98,240,010 (GRCm39) |
F1228V |
probably damaging |
Het |
Eps8l1 |
T |
A |
7: 4,473,437 (GRCm39) |
|
probably null |
Het |
Faf1 |
T |
A |
4: 109,719,134 (GRCm39) |
D413E |
probably damaging |
Het |
Fat3 |
T |
C |
9: 16,158,283 (GRCm39) |
Y1109C |
probably damaging |
Het |
Fbp1 |
T |
C |
13: 63,012,867 (GRCm39) |
K314E |
probably benign |
Het |
Fbxl20 |
A |
G |
11: 97,981,614 (GRCm39) |
V358A |
probably benign |
Het |
Fbxo34 |
C |
G |
14: 47,767,992 (GRCm39) |
R502G |
probably benign |
Het |
Fxr2 |
G |
A |
11: 69,532,875 (GRCm39) |
C151Y |
possibly damaging |
Het |
Garin5b |
C |
A |
7: 4,760,681 (GRCm39) |
R677L |
|
Het |
Gja8 |
T |
C |
3: 96,827,338 (GRCm39) |
D108G |
probably benign |
Het |
Gm10722 |
C |
A |
9: 3,001,235 (GRCm39) |
L104I |
probably benign |
Het |
Grsf1 |
A |
G |
5: 88,813,666 (GRCm39) |
V361A |
probably benign |
Het |
Hagh |
T |
C |
17: 25,075,686 (GRCm39) |
I131T |
probably damaging |
Het |
Heca |
A |
T |
10: 17,791,272 (GRCm39) |
Y261* |
probably null |
Het |
Hipk3 |
A |
G |
2: 104,269,696 (GRCm39) |
F498L |
probably damaging |
Het |
Hps4 |
T |
A |
5: 112,523,324 (GRCm39) |
I614N |
possibly damaging |
Het |
Icam1 |
T |
C |
9: 20,938,886 (GRCm39) |
S450P |
probably benign |
Het |
Il22 |
G |
A |
10: 118,041,069 (GRCm39) |
M58I |
possibly damaging |
Het |
Khdrbs2 |
T |
A |
1: 32,372,883 (GRCm39) |
S186T |
not run |
Het |
Kif16b |
A |
G |
2: 142,699,343 (GRCm39) |
F79S |
probably damaging |
Het |
Kntc1 |
C |
A |
5: 123,948,971 (GRCm39) |
F1905L |
probably benign |
Het |
Liat1 |
A |
T |
11: 75,893,833 (GRCm39) |
D70V |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 40,692,929 (GRCm39) |
G3423D |
|
Het |
Lrp5 |
G |
T |
19: 3,643,588 (GRCm39) |
Q1346K |
probably benign |
Het |
Map3k21 |
A |
C |
8: 126,671,717 (GRCm39) |
T1002P |
possibly damaging |
Het |
Mdga2 |
G |
T |
12: 66,615,670 (GRCm39) |
R646S |
probably benign |
Het |
Mex3b |
G |
T |
7: 82,518,073 (GRCm39) |
M129I |
possibly damaging |
Het |
Mfsd10 |
G |
T |
5: 34,793,770 (GRCm39) |
N85K |
probably damaging |
Het |
Mios |
A |
G |
6: 8,216,064 (GRCm39) |
D420G |
probably damaging |
Het |
Mogs |
C |
A |
6: 83,092,613 (GRCm39) |
P18T |
unknown |
Het |
Mrgpre |
A |
G |
7: 143,335,150 (GRCm39) |
C118R |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,601,285 (GRCm39) |
H1321L |
|
Het |
Nkapl |
T |
C |
13: 21,651,759 (GRCm39) |
K285E |
probably damaging |
Het |
Nphp4 |
C |
T |
4: 152,583,460 (GRCm39) |
P200S |
possibly damaging |
Het |
Piezo1 |
A |
G |
8: 123,228,397 (GRCm39) |
F297L |
|
Het |
Pkhd1 |
T |
G |
1: 20,271,197 (GRCm39) |
S3119R |
probably damaging |
Het |
Pla2g15 |
G |
A |
8: 106,889,576 (GRCm39) |
V283I |
probably benign |
Het |
Ppp1r13l |
T |
A |
7: 19,102,786 (GRCm39) |
|
probably null |
Het |
Prex1 |
A |
G |
2: 166,429,047 (GRCm39) |
Y849H |
probably damaging |
Het |
Psg27 |
C |
A |
7: 18,301,008 (GRCm39) |
W15L |
probably benign |
Het |
Ptar1 |
A |
T |
19: 23,686,334 (GRCm39) |
|
probably null |
Het |
Ptpn6 |
G |
A |
6: 124,705,135 (GRCm39) |
R264C |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,177,038 (GRCm39) |
I988V |
probably benign |
Het |
Ptpro |
G |
A |
6: 137,376,559 (GRCm39) |
V680I |
possibly damaging |
Het |
Rnf170 |
C |
T |
8: 26,613,876 (GRCm39) |
P28S |
probably benign |
Het |
Rnpepl1 |
A |
G |
1: 92,846,917 (GRCm39) |
S580G |
possibly damaging |
Het |
Rtel1 |
C |
T |
2: 180,972,608 (GRCm39) |
R29* |
probably null |
Het |
Rtkn |
T |
C |
6: 83,128,726 (GRCm39) |
L26P |
probably damaging |
Het |
Sdk2 |
A |
C |
11: 113,729,315 (GRCm39) |
S1087R |
probably damaging |
Het |
Sema7a |
C |
T |
9: 57,860,852 (GRCm39) |
P71L |
probably benign |
Het |
Sgpp1 |
C |
T |
12: 75,763,038 (GRCm39) |
C381Y |
probably damaging |
Het |
Sis |
A |
T |
3: 72,820,625 (GRCm39) |
|
probably null |
Het |
Slc24a5 |
A |
C |
2: 124,910,869 (GRCm39) |
D100A |
probably benign |
Het |
Slc25a23 |
A |
T |
17: 57,360,587 (GRCm39) |
I251K |
probably damaging |
Het |
Slc6a5 |
T |
A |
7: 49,579,804 (GRCm39) |
L394H |
probably damaging |
Het |
Slc7a4 |
A |
T |
16: 17,392,920 (GRCm39) |
M293K |
probably damaging |
Het |
Syne2 |
T |
A |
12: 75,973,263 (GRCm39) |
S1089T |
probably benign |
Het |
Tanc1 |
A |
T |
2: 59,615,670 (GRCm39) |
T226S |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,936,984 (GRCm39) |
T1355A |
probably benign |
Het |
Tmem101 |
A |
G |
11: 102,044,176 (GRCm39) |
M237T |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,749,359 (GRCm39) |
H3897Y |
possibly damaging |
Het |
Tubb4a |
C |
T |
17: 57,387,698 (GRCm39) |
V443M |
unknown |
Het |
Ucp2 |
G |
A |
7: 100,147,576 (GRCm39) |
R185H |
possibly damaging |
Het |
Vmn1r116 |
G |
T |
7: 20,606,436 (GRCm39) |
E86* |
probably null |
Het |
Vmn2r37 |
T |
C |
7: 9,213,032 (GRCm39) |
E530G |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,333,125 (GRCm39) |
T1293A |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,260,535 (GRCm39) |
Y1711N |
probably benign |
Het |
Zfp873 |
A |
T |
10: 81,896,805 (GRCm39) |
E512V |
probably damaging |
Het |
Zfyve16 |
T |
A |
13: 92,657,654 (GRCm39) |
K752N |
probably damaging |
Het |
Zhx1 |
T |
C |
15: 57,916,561 (GRCm39) |
N562D |
possibly damaging |
Het |
|
Other mutations in Gsap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00788:Gsap
|
APN |
5 |
21,459,022 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00788:Gsap
|
APN |
5 |
21,426,303 (GRCm39) |
splice site |
probably benign |
|
IGL01344:Gsap
|
APN |
5 |
21,447,881 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01347:Gsap
|
APN |
5 |
21,431,318 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01618:Gsap
|
APN |
5 |
21,431,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Gsap
|
APN |
5 |
21,495,152 (GRCm39) |
unclassified |
probably benign |
|
IGL02061:Gsap
|
APN |
5 |
21,486,609 (GRCm39) |
splice site |
probably benign |
|
IGL02161:Gsap
|
APN |
5 |
21,458,377 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02259:Gsap
|
APN |
5 |
21,391,398 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02635:Gsap
|
APN |
5 |
21,494,814 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02684:Gsap
|
APN |
5 |
21,447,801 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02822:Gsap
|
APN |
5 |
21,422,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03231:Gsap
|
APN |
5 |
21,434,164 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4305001:Gsap
|
UTSW |
5 |
21,391,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R0012:Gsap
|
UTSW |
5 |
21,431,227 (GRCm39) |
splice site |
probably benign |
|
R0012:Gsap
|
UTSW |
5 |
21,431,227 (GRCm39) |
splice site |
probably benign |
|
R0019:Gsap
|
UTSW |
5 |
21,475,620 (GRCm39) |
splice site |
probably benign |
|
R0019:Gsap
|
UTSW |
5 |
21,475,620 (GRCm39) |
splice site |
probably benign |
|
R0045:Gsap
|
UTSW |
5 |
21,431,830 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0054:Gsap
|
UTSW |
5 |
21,455,933 (GRCm39) |
splice site |
probably benign |
|
R0054:Gsap
|
UTSW |
5 |
21,455,933 (GRCm39) |
splice site |
probably benign |
|
R0409:Gsap
|
UTSW |
5 |
21,427,443 (GRCm39) |
splice site |
probably benign |
|
R0507:Gsap
|
UTSW |
5 |
21,474,961 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0624:Gsap
|
UTSW |
5 |
21,458,949 (GRCm39) |
splice site |
probably null |
|
R1037:Gsap
|
UTSW |
5 |
21,456,163 (GRCm39) |
splice site |
probably benign |
|
R1076:Gsap
|
UTSW |
5 |
21,492,692 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1459:Gsap
|
UTSW |
5 |
21,412,236 (GRCm39) |
splice site |
probably benign |
|
R1757:Gsap
|
UTSW |
5 |
21,486,035 (GRCm39) |
missense |
probably damaging |
0.98 |
R1852:Gsap
|
UTSW |
5 |
21,495,543 (GRCm39) |
splice site |
probably null |
|
R2034:Gsap
|
UTSW |
5 |
21,475,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Gsap
|
UTSW |
5 |
21,431,837 (GRCm39) |
splice site |
probably benign |
|
R2125:Gsap
|
UTSW |
5 |
21,447,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Gsap
|
UTSW |
5 |
21,427,438 (GRCm39) |
critical splice donor site |
probably null |
|
R2310:Gsap
|
UTSW |
5 |
21,401,088 (GRCm39) |
nonsense |
probably null |
|
R2337:Gsap
|
UTSW |
5 |
21,493,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3442:Gsap
|
UTSW |
5 |
21,483,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R4229:Gsap
|
UTSW |
5 |
21,451,975 (GRCm39) |
missense |
probably benign |
0.00 |
R4271:Gsap
|
UTSW |
5 |
21,431,348 (GRCm39) |
critical splice donor site |
probably null |
|
R4551:Gsap
|
UTSW |
5 |
21,495,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R4553:Gsap
|
UTSW |
5 |
21,495,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Gsap
|
UTSW |
5 |
21,431,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Gsap
|
UTSW |
5 |
21,451,969 (GRCm39) |
utr 3 prime |
probably benign |
|
R4799:Gsap
|
UTSW |
5 |
21,455,941 (GRCm39) |
missense |
probably benign |
0.05 |
R4857:Gsap
|
UTSW |
5 |
21,492,797 (GRCm39) |
splice site |
probably null |
|
R4973:Gsap
|
UTSW |
5 |
21,459,037 (GRCm39) |
missense |
probably benign |
0.04 |
R5015:Gsap
|
UTSW |
5 |
21,427,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R5031:Gsap
|
UTSW |
5 |
21,447,824 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5120:Gsap
|
UTSW |
5 |
21,474,934 (GRCm39) |
missense |
probably damaging |
0.96 |
R5451:Gsap
|
UTSW |
5 |
21,422,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R5469:Gsap
|
UTSW |
5 |
21,495,542 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5519:Gsap
|
UTSW |
5 |
21,494,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Gsap
|
UTSW |
5 |
21,456,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5650:Gsap
|
UTSW |
5 |
21,456,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R6064:Gsap
|
UTSW |
5 |
21,434,223 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6139:Gsap
|
UTSW |
5 |
21,486,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R6148:Gsap
|
UTSW |
5 |
21,475,575 (GRCm39) |
missense |
probably benign |
0.39 |
R6148:Gsap
|
UTSW |
5 |
21,431,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Gsap
|
UTSW |
5 |
21,422,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Gsap
|
UTSW |
5 |
21,486,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R6977:Gsap
|
UTSW |
5 |
21,476,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Gsap
|
UTSW |
5 |
21,476,235 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7013:Gsap
|
UTSW |
5 |
21,483,108 (GRCm39) |
missense |
probably benign |
0.39 |
R7159:Gsap
|
UTSW |
5 |
21,475,618 (GRCm39) |
splice site |
probably null |
|
R7181:Gsap
|
UTSW |
5 |
21,458,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7234:Gsap
|
UTSW |
5 |
21,391,433 (GRCm39) |
missense |
probably benign |
|
R7332:Gsap
|
UTSW |
5 |
21,495,119 (GRCm39) |
missense |
probably benign |
0.00 |
R8047:Gsap
|
UTSW |
5 |
21,462,866 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8062:Gsap
|
UTSW |
5 |
21,399,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R8126:Gsap
|
UTSW |
5 |
21,475,010 (GRCm39) |
missense |
probably benign |
0.04 |
R8219:Gsap
|
UTSW |
5 |
21,456,113 (GRCm39) |
missense |
probably benign |
0.00 |
R8355:Gsap
|
UTSW |
5 |
21,456,017 (GRCm39) |
nonsense |
probably null |
|
R8472:Gsap
|
UTSW |
5 |
21,427,432 (GRCm39) |
nonsense |
probably null |
|
R8715:Gsap
|
UTSW |
5 |
21,431,245 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8745:Gsap
|
UTSW |
5 |
21,474,949 (GRCm39) |
missense |
probably benign |
0.05 |
R8798:Gsap
|
UTSW |
5 |
21,476,248 (GRCm39) |
critical splice donor site |
probably null |
|
R9080:Gsap
|
UTSW |
5 |
21,399,410 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9120:Gsap
|
UTSW |
5 |
21,458,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9178:Gsap
|
UTSW |
5 |
21,422,471 (GRCm39) |
missense |
probably damaging |
0.98 |
R9209:Gsap
|
UTSW |
5 |
21,433,064 (GRCm39) |
missense |
probably benign |
0.10 |
R9404:Gsap
|
UTSW |
5 |
21,474,919 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Gsap
|
UTSW |
5 |
21,456,030 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- ATGTTGACATCATTGCTGTGTC -3'
(R):5'- TTAGAGAGCTGAGGCCTTGTGAC -3'
Sequencing Primer
(F):5'- TTACAGATGGTTAGGCGCCAC -3'
(R):5'- TGACAGCACAAGCCACGTTATTTG -3'
|
Posted On |
2019-09-13 |