Incidental Mutation 'R1927:Nbr1'
ID |
214971 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nbr1
|
Ensembl Gene |
ENSMUSG00000017119 |
Gene Name |
NBR1, autophagy cargo receptor |
Synonyms |
|
MMRRC Submission |
039945-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1927 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
101442975-101472777 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 101458040 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Cysteine
at position 273
(Y273C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000102836
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071537]
[ENSMUST00000103098]
[ENSMUST00000103099]
[ENSMUST00000107208]
[ENSMUST00000107212]
[ENSMUST00000107213]
[ENSMUST00000107218]
[ENSMUST00000123558]
|
AlphaFold |
P97432 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000071537
AA Change: Y273C
PolyPhen 2
Score 0.627 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000071467 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
2.05e-8 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
Pfam:N_BRCA1_IG
|
378 |
479 |
7.1e-34 |
PFAM |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
714 |
744 |
N/A |
INTRINSIC |
PDB:2MJ5|B
|
935 |
981 |
2e-24 |
PDB |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000103098
AA Change: Y273C
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000099387 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
7.02e-16 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
PDB:4OLE|D
|
368 |
486 |
5e-77 |
PDB |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
714 |
744 |
N/A |
INTRINSIC |
PDB:2MJ5|B
|
935 |
981 |
2e-24 |
PDB |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000103099
AA Change: Y273C
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000099388 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
7.02e-16 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
PDB:4OLE|D
|
368 |
486 |
5e-77 |
PDB |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
714 |
744 |
N/A |
INTRINSIC |
PDB:2MJ5|B
|
935 |
981 |
2e-24 |
PDB |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107208
AA Change: Y273C
PolyPhen 2
Score 0.627 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000102826 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
7.02e-16 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
PDB:4OLE|D
|
368 |
486 |
1e-77 |
PDB |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
714 |
744 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107212
AA Change: Y273C
PolyPhen 2
Score 0.627 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000102830 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
7.02e-16 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
PDB:4OLE|D
|
368 |
486 |
3e-77 |
PDB |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
689 |
719 |
N/A |
INTRINSIC |
PDB:2MJ5|B
|
910 |
956 |
2e-24 |
PDB |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107213
AA Change: Y273C
PolyPhen 2
Score 0.627 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000102831 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
7.02e-16 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
PDB:4OLE|D
|
368 |
486 |
2e-77 |
PDB |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
677 |
707 |
N/A |
INTRINSIC |
PDB:2MJ5|B
|
898 |
944 |
2e-24 |
PDB |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107218
AA Change: Y273C
PolyPhen 2
Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000102836 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
7.02e-16 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
PDB:4OLE|D
|
368 |
486 |
5e-77 |
PDB |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
714 |
744 |
N/A |
INTRINSIC |
PDB:2MJ5|B
|
935 |
981 |
2e-24 |
PDB |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000123558
AA Change: Y273C
PolyPhen 2
Score 0.627 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000133619 Gene: ENSMUSG00000017119 AA Change: Y273C
Domain | Start | End | E-Value | Type |
PB1
|
4 |
86 |
7.02e-16 |
SMART |
ZnF_ZZ
|
212 |
257 |
1.21e-13 |
SMART |
coiled coil region
|
291 |
330 |
N/A |
INTRINSIC |
PDB:4OLE|D
|
368 |
486 |
2e-77 |
PDB |
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
coiled coil region
|
714 |
744 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000149019
AA Change: Y32C
|
SMART Domains |
Protein: ENSMUSP00000119900 Gene: ENSMUSG00000017119 AA Change: Y32C
Domain | Start | End | E-Value | Type |
coiled coil region
|
50 |
89 |
N/A |
INTRINSIC |
Pfam:N_BRCA1_IG
|
138 |
239 |
2.3e-34 |
PFAM |
low complexity region
|
267 |
278 |
N/A |
INTRINSIC |
coiled coil region
|
473 |
500 |
N/A |
INTRINSIC |
PDB:2MJ5|B
|
659 |
705 |
1e-24 |
PDB |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149170
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144517
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000174013
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146452
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127871
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B-box/coiled-coil motif, which is present in many genes with transformation potential. It functions as a specific autophagy receptor for the selective autophagic degradation of peroxisomes by forming intracellular inclusions with ubiquitylated autophagic substrates. This gene is located on a region of chromosome 17q21.1 that is in close proximity to the BRCA1 tumor suppressor gene. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014] PHENOTYPE: Homozygous mice of the genetic truncation allele had an age-dependent increase in bone mass and bone mineral density. Mice homozygous for a floxed allele activated in T cells exhibit decreased ovalbumin-induced inflammation and defective Th2 polarization. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
C |
6: 121,613,338 (GRCm39) |
S31P |
probably damaging |
Het |
Abca12 |
G |
T |
1: 71,283,999 (GRCm39) |
H2524Q |
probably damaging |
Het |
Acsl5 |
T |
C |
19: 55,266,586 (GRCm39) |
V135A |
probably benign |
Het |
Actl11 |
T |
G |
9: 107,806,736 (GRCm39) |
L353R |
possibly damaging |
Het |
Adcy6 |
G |
T |
15: 98,496,379 (GRCm39) |
|
probably null |
Het |
B230104I21Rik |
A |
G |
4: 154,425,694 (GRCm39) |
I697T |
probably damaging |
Het |
BC061237 |
G |
A |
14: 44,738,700 (GRCm39) |
R33K |
possibly damaging |
Het |
Brf1 |
C |
A |
12: 112,963,964 (GRCm39) |
V5F |
possibly damaging |
Het |
Chmp2a |
C |
T |
7: 12,767,863 (GRCm39) |
A21T |
possibly damaging |
Het |
Cwh43 |
A |
G |
5: 73,610,417 (GRCm39) |
N607S |
probably benign |
Het |
Ddhd2 |
G |
A |
8: 26,231,688 (GRCm39) |
L445F |
possibly damaging |
Het |
Dicer1 |
C |
A |
12: 104,669,143 (GRCm39) |
D1180Y |
possibly damaging |
Het |
Dnaaf4 |
A |
T |
9: 72,867,909 (GRCm39) |
I57L |
probably damaging |
Het |
Dock5 |
A |
T |
14: 68,083,511 (GRCm39) |
S133T |
possibly damaging |
Het |
Efs |
A |
T |
14: 55,154,620 (GRCm39) |
C540S |
possibly damaging |
Het |
Ehd4 |
C |
T |
2: 119,921,973 (GRCm39) |
G428S |
probably benign |
Het |
Eml1 |
C |
T |
12: 108,504,476 (GRCm39) |
R812* |
probably null |
Het |
Enpp1 |
C |
T |
10: 24,530,786 (GRCm39) |
D557N |
possibly damaging |
Het |
Fn3krp |
A |
G |
11: 121,315,803 (GRCm39) |
T65A |
probably damaging |
Het |
Galnt5 |
A |
G |
2: 57,888,615 (GRCm39) |
R72G |
probably benign |
Het |
Gfod1 |
C |
T |
13: 43,354,336 (GRCm39) |
R213H |
possibly damaging |
Het |
Gm10518 |
A |
G |
1: 179,631,210 (GRCm39) |
|
probably benign |
Het |
Gm5431 |
A |
G |
11: 48,780,082 (GRCm39) |
F558S |
probably damaging |
Het |
Got1 |
C |
T |
19: 43,504,119 (GRCm39) |
|
probably null |
Het |
Gucy2g |
C |
T |
19: 55,226,191 (GRCm39) |
V242I |
probably benign |
Het |
Hdgfl2 |
T |
A |
17: 56,406,874 (GRCm39) |
V606E |
possibly damaging |
Het |
Hoxa3 |
T |
C |
6: 52,146,979 (GRCm39) |
|
probably benign |
Het |
Iqub |
T |
A |
6: 24,491,670 (GRCm39) |
I339L |
probably benign |
Het |
Kdm4c |
C |
T |
4: 74,263,720 (GRCm39) |
T668I |
probably benign |
Het |
Klhl32 |
T |
C |
4: 24,617,474 (GRCm39) |
I592V |
probably benign |
Het |
Mfsd12 |
G |
T |
10: 81,197,921 (GRCm39) |
M296I |
probably benign |
Het |
Mfsd4b4 |
C |
T |
10: 39,768,437 (GRCm39) |
A219T |
probably damaging |
Het |
Mrpl52 |
T |
C |
14: 54,664,414 (GRCm39) |
S9P |
possibly damaging |
Het |
Ncf4 |
G |
T |
15: 78,144,846 (GRCm39) |
G217V |
probably damaging |
Het |
Neo1 |
T |
C |
9: 58,897,668 (GRCm39) |
E96G |
probably benign |
Het |
Nid2 |
T |
A |
14: 19,818,344 (GRCm39) |
N279K |
probably damaging |
Het |
Nr5a2 |
A |
G |
1: 136,872,732 (GRCm39) |
Y56H |
probably damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Nynrin |
A |
G |
14: 56,101,049 (GRCm39) |
T280A |
probably benign |
Het |
Or1o2 |
A |
G |
17: 37,542,434 (GRCm39) |
Y276H |
probably damaging |
Het |
Or2b28 |
T |
A |
13: 21,531,116 (GRCm39) |
I6N |
probably benign |
Het |
Or2w2 |
A |
G |
13: 21,758,426 (GRCm39) |
F67L |
probably benign |
Het |
Or55b10 |
A |
G |
7: 102,143,266 (GRCm39) |
S239P |
possibly damaging |
Het |
Or5b109 |
T |
C |
19: 13,212,393 (GRCm39) |
Y260H |
probably damaging |
Het |
Otog |
G |
A |
7: 45,895,707 (GRCm39) |
C107Y |
probably damaging |
Het |
Ptprn |
A |
G |
1: 75,230,766 (GRCm39) |
V565A |
probably benign |
Het |
Rbm6 |
T |
G |
9: 107,730,102 (GRCm39) |
D182A |
probably damaging |
Het |
Rhbg |
A |
G |
3: 88,151,859 (GRCm39) |
F400L |
probably benign |
Het |
Rpl22l1 |
T |
A |
3: 28,860,738 (GRCm39) |
N33K |
possibly damaging |
Het |
Rtp1 |
T |
A |
16: 23,249,959 (GRCm39) |
I108N |
probably damaging |
Het |
Sema6b |
A |
T |
17: 56,439,797 (GRCm39) |
F15I |
probably benign |
Het |
Sirpa |
C |
T |
2: 129,458,296 (GRCm39) |
T304I |
possibly damaging |
Het |
Slc22a29 |
A |
G |
19: 8,184,430 (GRCm39) |
I257T |
probably benign |
Het |
Slc41a1 |
T |
C |
1: 131,768,938 (GRCm39) |
I256T |
probably damaging |
Het |
Smg6 |
A |
G |
11: 75,033,674 (GRCm39) |
K1208R |
probably damaging |
Het |
Sorcs1 |
G |
T |
19: 50,210,633 (GRCm39) |
P744Q |
probably damaging |
Het |
Sptbn5 |
T |
C |
2: 119,900,943 (GRCm39) |
T213A |
probably benign |
Het |
St18 |
A |
G |
1: 6,872,936 (GRCm39) |
T224A |
probably benign |
Het |
Stat3 |
T |
C |
11: 100,785,655 (GRCm39) |
N465S |
probably damaging |
Het |
Stmn2 |
T |
A |
3: 8,610,636 (GRCm39) |
M40K |
probably benign |
Het |
Tespa1 |
A |
G |
10: 130,184,108 (GRCm39) |
D63G |
probably benign |
Het |
Thrb |
T |
A |
14: 18,008,674 (GRCm38) |
C133S |
probably damaging |
Het |
Tmem25 |
C |
T |
9: 44,707,780 (GRCm39) |
V172M |
possibly damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trhde |
T |
A |
10: 114,636,754 (GRCm39) |
Y151F |
probably damaging |
Het |
Trp53bp2 |
A |
G |
1: 182,280,229 (GRCm39) |
T912A |
probably damaging |
Het |
Unc79 |
C |
A |
12: 103,135,951 (GRCm39) |
A2269E |
probably damaging |
Het |
Zfp507 |
C |
T |
7: 35,493,150 (GRCm39) |
R631Q |
probably damaging |
Het |
Zfp758 |
T |
G |
17: 22,594,823 (GRCm39) |
S436R |
probably damaging |
Het |
Zfp791 |
G |
T |
8: 85,837,312 (GRCm39) |
T184K |
probably benign |
Het |
Znrf3 |
A |
G |
11: 5,231,062 (GRCm39) |
V817A |
probably benign |
Het |
|
Other mutations in Nbr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02187:Nbr1
|
APN |
11 |
101,460,185 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02192:Nbr1
|
APN |
11 |
101,460,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02259:Nbr1
|
APN |
11 |
101,468,816 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02951:Nbr1
|
APN |
11 |
101,462,805 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02994:Nbr1
|
APN |
11 |
101,447,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R0087:Nbr1
|
UTSW |
11 |
101,455,519 (GRCm39) |
missense |
probably benign |
0.16 |
R0630:Nbr1
|
UTSW |
11 |
101,457,913 (GRCm39) |
unclassified |
probably benign |
|
R0723:Nbr1
|
UTSW |
11 |
101,467,145 (GRCm39) |
nonsense |
probably null |
|
R0733:Nbr1
|
UTSW |
11 |
101,467,197 (GRCm39) |
missense |
probably benign |
0.00 |
R1482:Nbr1
|
UTSW |
11 |
101,463,667 (GRCm39) |
missense |
probably benign |
0.34 |
R1567:Nbr1
|
UTSW |
11 |
101,466,037 (GRCm39) |
missense |
probably damaging |
0.98 |
R1570:Nbr1
|
UTSW |
11 |
101,455,656 (GRCm39) |
unclassified |
probably benign |
|
R1668:Nbr1
|
UTSW |
11 |
101,460,592 (GRCm39) |
missense |
probably benign |
0.00 |
R1759:Nbr1
|
UTSW |
11 |
101,450,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Nbr1
|
UTSW |
11 |
101,465,978 (GRCm39) |
missense |
probably damaging |
0.98 |
R2131:Nbr1
|
UTSW |
11 |
101,457,017 (GRCm39) |
splice site |
probably null |
|
R2211:Nbr1
|
UTSW |
11 |
101,458,090 (GRCm39) |
critical splice donor site |
probably null |
|
R2255:Nbr1
|
UTSW |
11 |
101,463,643 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4270:Nbr1
|
UTSW |
11 |
101,458,048 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4271:Nbr1
|
UTSW |
11 |
101,458,048 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4710:Nbr1
|
UTSW |
11 |
101,466,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Nbr1
|
UTSW |
11 |
101,465,903 (GRCm39) |
missense |
probably benign |
0.06 |
R5468:Nbr1
|
UTSW |
11 |
101,463,290 (GRCm39) |
missense |
probably benign |
0.10 |
R5554:Nbr1
|
UTSW |
11 |
101,455,633 (GRCm39) |
missense |
probably benign |
0.34 |
R5771:Nbr1
|
UTSW |
11 |
101,450,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R6119:Nbr1
|
UTSW |
11 |
101,457,938 (GRCm39) |
splice site |
probably null |
|
R6400:Nbr1
|
UTSW |
11 |
101,456,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R6603:Nbr1
|
UTSW |
11 |
101,446,931 (GRCm39) |
unclassified |
probably benign |
|
R6943:Nbr1
|
UTSW |
11 |
101,468,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R7347:Nbr1
|
UTSW |
11 |
101,460,147 (GRCm39) |
nonsense |
probably null |
|
R7472:Nbr1
|
UTSW |
11 |
101,462,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R7501:Nbr1
|
UTSW |
11 |
101,457,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Nbr1
|
UTSW |
11 |
101,447,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R7744:Nbr1
|
UTSW |
11 |
101,460,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R7795:Nbr1
|
UTSW |
11 |
101,460,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Nbr1
|
UTSW |
11 |
101,455,520 (GRCm39) |
missense |
probably benign |
0.00 |
R9377:Nbr1
|
UTSW |
11 |
101,456,590 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9615:Nbr1
|
UTSW |
11 |
101,465,978 (GRCm39) |
missense |
probably benign |
0.02 |
R9667:Nbr1
|
UTSW |
11 |
101,451,261 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9801:Nbr1
|
UTSW |
11 |
101,447,025 (GRCm39) |
missense |
probably damaging |
0.99 |
X0019:Nbr1
|
UTSW |
11 |
101,457,950 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Nbr1
|
UTSW |
11 |
101,463,380 (GRCm39) |
missense |
probably benign |
0.04 |
|
Predicted Primers |
PCR Primer
(F):5'- TCAGGGACTTCTTGCTGCAT -3'
(R):5'- GTGCTGGGGATTACATCTGATTT -3'
Sequencing Primer
(F):5'- GGACTTCTTGCTGCATAGTTTTTAC -3'
(R):5'- ACTCTGCACCTTTGGAAGAG -3'
|
Posted On |
2014-07-14 |