Incidental Mutation 'R1784:Igfn1'
ID |
195940 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Igfn1
|
Ensembl Gene |
ENSMUSG00000051985 |
Gene Name |
immunoglobulin-like and fibronectin type III domain containing 1 |
Synonyms |
9830123M21Rik |
MMRRC Submission |
039815-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.099)
|
Stock # |
R1784 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
135881316-135934080 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 135926363 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 29
(E29G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129680
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000166193]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000166193
AA Change: E29G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000129680 Gene: ENSMUSG00000051985 AA Change: E29G
Domain | Start | End | E-Value | Type |
low complexity region
|
90 |
101 |
N/A |
INTRINSIC |
IG
|
193 |
279 |
1.29e-6 |
SMART |
PDB:2LHU|A
|
302 |
365 |
8e-7 |
PDB |
IG_like
|
378 |
464 |
5.45e1 |
SMART |
IG
|
474 |
555 |
1.79e0 |
SMART |
low complexity region
|
724 |
739 |
N/A |
INTRINSIC |
internal_repeat_2
|
838 |
1006 |
9.98e-5 |
PROSPERO |
low complexity region
|
1067 |
1084 |
N/A |
INTRINSIC |
internal_repeat_2
|
1812 |
1967 |
9.98e-5 |
PROSPERO |
Pfam:I-set
|
2054 |
2139 |
6.2e-8 |
PFAM |
IG
|
2153 |
2239 |
4.86e-2 |
SMART |
FN3
|
2242 |
2326 |
3.99e-10 |
SMART |
FN3
|
2342 |
2425 |
9.1e-14 |
SMART |
FN3
|
2443 |
2526 |
1.5e-14 |
SMART |
IG
|
2553 |
2636 |
6.41e-2 |
SMART |
FN3
|
2639 |
2721 |
3.2e-9 |
SMART |
IGc2
|
2767 |
2834 |
4.89e-7 |
SMART |
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.5%
- 20x: 93.2%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 186 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930453N24Rik |
T |
C |
16: 64,589,385 (GRCm39) |
I90V |
probably damaging |
Het |
Acacb |
TGGGG |
TGGG |
5: 114,347,828 (GRCm39) |
|
probably null |
Het |
Adamts17 |
C |
T |
7: 66,799,704 (GRCm39) |
R1060* |
probably null |
Het |
Adamts5 |
T |
A |
16: 85,674,803 (GRCm39) |
K454* |
probably null |
Het |
Adgrg6 |
T |
C |
10: 14,315,526 (GRCm39) |
T593A |
probably damaging |
Het |
Aldh4a1 |
A |
G |
4: 139,371,472 (GRCm39) |
Y462C |
probably damaging |
Het |
Ankrd12 |
G |
T |
17: 66,291,071 (GRCm39) |
P1454Q |
probably benign |
Het |
Ap1m1 |
T |
A |
8: 73,006,693 (GRCm39) |
S230T |
probably benign |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Atp6ap1l |
T |
A |
13: 91,053,400 (GRCm39) |
K4N |
probably damaging |
Het |
Boc |
T |
C |
16: 44,316,782 (GRCm39) |
T454A |
probably benign |
Het |
Bola1 |
C |
T |
3: 96,104,426 (GRCm39) |
G56D |
probably benign |
Het |
C4bp |
C |
G |
1: 130,570,725 (GRCm39) |
V284L |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,046,454 (GRCm39) |
F1761S |
probably benign |
Het |
Camsap2 |
C |
T |
1: 136,209,053 (GRCm39) |
R802Q |
probably benign |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cbs |
G |
T |
17: 31,839,923 (GRCm39) |
A337E |
probably benign |
Het |
Ccdc186 |
A |
C |
19: 56,797,652 (GRCm39) |
H306Q |
probably benign |
Het |
Cd180 |
T |
C |
13: 102,842,367 (GRCm39) |
L471P |
probably damaging |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cd55 |
C |
A |
1: 130,387,370 (GRCm39) |
A143S |
probably benign |
Het |
Cdk12 |
T |
C |
11: 98,140,796 (GRCm39) |
|
probably benign |
Het |
Cfh |
C |
T |
1: 140,075,435 (GRCm39) |
V268I |
possibly damaging |
Het |
Cfhr2 |
A |
G |
1: 139,741,180 (GRCm39) |
M265T |
probably benign |
Het |
Cfhr2 |
A |
C |
1: 139,741,197 (GRCm39) |
N259K |
probably benign |
Het |
Chi3l1 |
C |
T |
1: 134,116,267 (GRCm39) |
A250V |
probably damaging |
Het |
Chit1 |
A |
G |
1: 134,077,132 (GRCm39) |
R312G |
possibly damaging |
Het |
Chrna6 |
A |
T |
8: 27,896,812 (GRCm39) |
M355K |
possibly damaging |
Het |
Clcn1 |
T |
A |
6: 42,276,448 (GRCm39) |
F360Y |
possibly damaging |
Het |
Copa |
T |
A |
1: 171,939,554 (GRCm39) |
F597Y |
probably benign |
Het |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
probably benign |
Het |
Crb1 |
G |
A |
1: 139,168,876 (GRCm39) |
P881S |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,170,733 (GRCm39) |
G825R |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,171,155 (GRCm39) |
R684H |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,162,517 (GRCm39) |
M1214V |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,880,015 (GRCm39) |
Q391L |
probably damaging |
Het |
Cwh43 |
T |
C |
5: 73,565,561 (GRCm39) |
L42P |
probably damaging |
Het |
Cxcr4 |
C |
T |
1: 128,517,014 (GRCm39) |
V216I |
probably benign |
Het |
Cyb5r1 |
C |
T |
1: 134,335,405 (GRCm39) |
R147W |
probably damaging |
Het |
Ddx59 |
T |
C |
1: 136,344,791 (GRCm39) |
V154A |
probably benign |
Het |
Dnah17 |
C |
T |
11: 117,960,345 (GRCm39) |
C2572Y |
possibly damaging |
Het |
Dnah9 |
G |
A |
11: 65,975,846 (GRCm39) |
T1401I |
possibly damaging |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
Elf2 |
A |
T |
3: 51,164,993 (GRCm39) |
V277D |
probably damaging |
Het |
Etnk2 |
C |
A |
1: 133,293,325 (GRCm39) |
D89E |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,293,503 (GRCm39) |
G149W |
probably damaging |
Het |
Etnk2 |
C |
T |
1: 133,293,554 (GRCm39) |
R166* |
probably null |
Het |
Etnk2 |
G |
A |
1: 133,293,555 (GRCm39) |
R166Q |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,304,653 (GRCm39) |
V292E |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,304,784 (GRCm39) |
A336S |
probably benign |
Het |
Etnk2 |
C |
T |
1: 133,291,628 (GRCm39) |
P43S |
probably benign |
Het |
Fam72a |
C |
T |
1: 131,466,633 (GRCm39) |
T139M |
probably benign |
Het |
Fam72a |
T |
C |
1: 131,458,406 (GRCm39) |
I56T |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,907,611 (GRCm39) |
V2797G |
possibly damaging |
Het |
Fbxl6 |
C |
T |
15: 76,422,258 (GRCm39) |
R137H |
probably damaging |
Het |
Fcamr |
A |
G |
1: 130,739,317 (GRCm39) |
I206V |
probably benign |
Het |
Fcamr |
G |
A |
1: 130,740,366 (GRCm39) |
G262S |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,429 (GRCm39) |
I283V |
probably benign |
Het |
Fcamr |
T |
C |
1: 130,740,475 (GRCm39) |
V298A |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,546 (GRCm39) |
M322V |
probably benign |
Het |
Fcamr |
C |
T |
1: 130,740,553 (GRCm39) |
P324L |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,742,334 (GRCm39) |
N574D |
probably benign |
Het |
Fcamr |
A |
C |
1: 130,732,364 (GRCm39) |
N117T |
probably benign |
Het |
Fcmr |
T |
C |
1: 130,806,006 (GRCm39) |
S321P |
probably benign |
Het |
Fcmr |
A |
G |
1: 130,803,711 (GRCm39) |
T172A |
probably benign |
Het |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Galnt17 |
A |
T |
5: 131,179,801 (GRCm39) |
H115Q |
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Glrx2 |
C |
T |
1: 143,615,478 (GRCm39) |
A27V |
possibly damaging |
Het |
Gm10563 |
C |
T |
4: 155,720,337 (GRCm39) |
|
probably benign |
Het |
Gm12887 |
T |
A |
4: 121,473,715 (GRCm39) |
D45V |
probably benign |
Het |
Gse1 |
G |
A |
8: 121,294,992 (GRCm39) |
|
probably benign |
Het |
Guk1 |
A |
T |
11: 59,076,138 (GRCm39) |
V100E |
probably damaging |
Het |
Heatr4 |
T |
C |
12: 84,014,346 (GRCm39) |
I630M |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,439,902 (GRCm39) |
Y1134F |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Ikbke |
C |
A |
1: 131,193,674 (GRCm39) |
A459S |
probably benign |
Het |
Ikbke |
T |
C |
1: 131,197,560 (GRCm39) |
S447G |
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Itprid1 |
T |
C |
6: 55,945,526 (GRCm39) |
F749S |
probably benign |
Het |
Kcnh5 |
T |
C |
12: 75,184,465 (GRCm39) |
D86G |
probably benign |
Het |
Kcnt2 |
G |
A |
1: 140,282,285 (GRCm39) |
S90N |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,713 (GRCm39) |
K340E |
probably damaging |
Het |
Kif14 |
G |
A |
1: 136,406,103 (GRCm39) |
A556T |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,418,070 (GRCm39) |
S868G |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,431,169 (GRCm39) |
L1189F |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,443,699 (GRCm39) |
F1291L |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,453,521 (GRCm39) |
V1433A |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kif18b |
A |
G |
11: 102,806,367 (GRCm39) |
|
probably null |
Het |
Kif21b |
A |
G |
1: 136,087,859 (GRCm39) |
I983V |
possibly damaging |
Het |
Kpna3 |
T |
A |
14: 61,605,150 (GRCm39) |
E499V |
probably benign |
Het |
Kremen1 |
GGG |
GGGTGG |
11: 5,151,792 (GRCm39) |
|
probably benign |
Het |
Krt23 |
A |
T |
11: 99,383,790 (GRCm39) |
V34D |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,761 (GRCm39) |
R346C |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,119 (GRCm39) |
P132S |
possibly damaging |
Het |
Lax1 |
T |
C |
1: 133,608,307 (GRCm39) |
N145D |
probably benign |
Het |
Lax1 |
G |
A |
1: 133,611,372 (GRCm39) |
P67S |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,607,716 (GRCm39) |
R342G |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,914,826 (GRCm39) |
V641I |
probably benign |
Het |
Lgr6 |
A |
T |
1: 134,915,747 (GRCm39) |
S334T |
probably benign |
Het |
Lgr6 |
G |
T |
1: 134,918,373 (GRCm39) |
H263N |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,931,214 (GRCm39) |
S3N |
probably benign |
Het |
Lima1 |
G |
T |
15: 99,678,344 (GRCm39) |
P539Q |
possibly damaging |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Megf10 |
T |
C |
18: 57,373,864 (GRCm39) |
|
probably null |
Het |
Mrgbp |
T |
A |
2: 180,227,242 (GRCm39) |
N192K |
probably damaging |
Het |
Mrgpra2b |
A |
G |
7: 47,114,627 (GRCm39) |
I35T |
probably benign |
Het |
Mroh3 |
G |
C |
1: 136,119,882 (GRCm39) |
Q440E |
possibly damaging |
Het |
Mrpl3 |
C |
T |
9: 104,934,266 (GRCm39) |
H130Y |
probably benign |
Het |
Mybph |
C |
T |
1: 134,125,218 (GRCm39) |
R249C |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,392,614 (GRCm39) |
C3206S |
probably damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Nbeal2 |
T |
A |
9: 110,459,925 (GRCm39) |
K1844* |
probably null |
Het |
Ndufaf7 |
A |
T |
17: 79,245,058 (GRCm39) |
K59M |
probably damaging |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
C |
G |
1: 133,832,908 (GRCm39) |
S64T |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or8b12i |
A |
T |
9: 20,082,209 (GRCm39) |
Y219* |
probably null |
Het |
Otoa |
T |
C |
7: 120,724,662 (GRCm39) |
V447A |
probably benign |
Het |
Papss1 |
A |
G |
3: 131,311,728 (GRCm39) |
N319D |
probably benign |
Het |
Pcdhb3 |
G |
A |
18: 37,434,931 (GRCm39) |
G299D |
probably damaging |
Het |
Pcsk4 |
T |
C |
10: 80,159,404 (GRCm39) |
D432G |
probably damaging |
Het |
Pde4b |
T |
C |
4: 102,462,457 (GRCm39) |
I711T |
probably benign |
Het |
Pde5a |
G |
T |
3: 122,541,889 (GRCm39) |
L126F |
probably damaging |
Het |
Pigr |
C |
T |
1: 130,772,259 (GRCm39) |
A159V |
possibly damaging |
Het |
Pik3c2b |
C |
T |
1: 132,994,365 (GRCm39) |
P110S |
probably benign |
Het |
Pinx1 |
A |
G |
14: 64,115,559 (GRCm39) |
|
probably null |
Het |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Ppfia4 |
G |
A |
1: 134,227,059 (GRCm39) |
P1159S |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Prrx1 |
T |
A |
1: 163,089,536 (GRCm39) |
N97I |
probably damaging |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
probably benign |
Het |
Ptprc |
T |
G |
1: 138,027,414 (GRCm39) |
N478T |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,039,992 (GRCm39) |
K212E |
possibly damaging |
Het |
Ptprc |
A |
G |
1: 138,035,575 (GRCm39) |
V400A |
probably benign |
Het |
Ptprc |
C |
A |
1: 138,035,562 (GRCm39) |
E402D |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,561 (GRCm39) |
S405P |
probably benign |
Het |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Rbsn |
A |
T |
6: 92,167,000 (GRCm39) |
L548Q |
possibly damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Ren1 |
C |
G |
1: 133,287,745 (GRCm39) |
L360V |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,287,721 (GRCm39) |
N352Y |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,286,817 (GRCm39) |
E315D |
probably benign |
Het |
Ren1 |
A |
C |
1: 133,284,195 (GRCm39) |
K187Q |
probably benign |
Het |
Ren1 |
C |
T |
1: 133,281,975 (GRCm39) |
T32I |
probably benign |
Het |
Ren1 |
T |
A |
1: 133,281,944 (GRCm39) |
W22R |
probably damaging |
Het |
Rgs22 |
T |
A |
15: 36,087,582 (GRCm39) |
K445N |
probably damaging |
Het |
Rint1 |
T |
A |
5: 24,014,841 (GRCm39) |
D352E |
probably benign |
Het |
Rnpep |
C |
T |
1: 135,190,834 (GRCm39) |
A571T |
possibly damaging |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Ro60 |
C |
T |
1: 143,635,752 (GRCm39) |
V465I |
probably benign |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Sis |
A |
T |
3: 72,872,978 (GRCm39) |
C53* |
probably null |
Het |
Slain2 |
A |
G |
5: 73,114,957 (GRCm39) |
H396R |
probably damaging |
Het |
Slc22a5 |
G |
A |
11: 53,757,177 (GRCm39) |
P491L |
probably damaging |
Het |
Slc26a9 |
C |
A |
1: 131,693,750 (GRCm39) |
R747S |
probably benign |
Het |
Slc26a9 |
C |
T |
1: 131,691,608 (GRCm39) |
A617V |
probably benign |
Het |
Stab2 |
T |
G |
10: 86,773,903 (GRCm39) |
R809S |
probably benign |
Het |
Tbc1d19 |
T |
G |
5: 53,986,714 (GRCm39) |
I41S |
probably damaging |
Het |
Tbc1d31 |
T |
A |
15: 57,827,316 (GRCm39) |
H919Q |
possibly damaging |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
probably benign |
Het |
Thsd7b |
A |
C |
1: 130,044,368 (GRCm39) |
Q1116P |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,556,628 (GRCm39) |
T328I |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 129,595,674 (GRCm39) |
F498Y |
probably benign |
Het |
Tnfrsf25 |
T |
A |
4: 152,202,761 (GRCm39) |
|
probably null |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Traf7 |
A |
G |
17: 24,731,353 (GRCm39) |
F228L |
probably damaging |
Het |
Trim32 |
T |
A |
4: 65,532,634 (GRCm39) |
I397N |
probably damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,577,968 (GRCm39) |
T779A |
probably benign |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Upf2 |
A |
T |
2: 6,032,261 (GRCm39) |
S191C |
probably damaging |
Het |
Usp42 |
T |
C |
5: 143,700,381 (GRCm39) |
D1214G |
probably damaging |
Het |
Vcam1 |
T |
A |
3: 115,908,164 (GRCm39) |
I633L |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,507,086 (GRCm39) |
Y742C |
probably damaging |
Het |
Vmn2r81 |
C |
A |
10: 79,106,489 (GRCm39) |
T489K |
probably benign |
Het |
Ypel1 |
C |
G |
16: 16,907,283 (GRCm39) |
|
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zfp169 |
C |
T |
13: 48,643,295 (GRCm39) |
A611T |
possibly damaging |
Het |
Zfp281 |
GCGGCAGCTCCGGCAGC |
GCGGCAGCTCCGGCAGCTCCGGCAGC |
1: 136,553,091 (GRCm39) |
|
probably benign |
Het |
Zp3r |
A |
G |
1: 130,524,551 (GRCm39) |
L164P |
probably benign |
Het |
Zp3r |
C |
A |
1: 130,547,151 (GRCm39) |
E8D |
possibly damaging |
Het |
|
Other mutations in Igfn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00753:Igfn1
|
APN |
1 |
135,894,464 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Igfn1
|
APN |
1 |
135,881,755 (GRCm39) |
utr 3 prime |
probably benign |
|
Bounty
|
UTSW |
1 |
135,904,655 (GRCm39) |
critical splice donor site |
probably null |
|
R2276_Igfn1_773
|
UTSW |
1 |
135,892,479 (GRCm39) |
missense |
probably damaging |
0.98 |
R4058_Igfn1_315
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R0144:Igfn1
|
UTSW |
1 |
135,889,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R0190:Igfn1
|
UTSW |
1 |
135,889,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0350:Igfn1
|
UTSW |
1 |
135,884,505 (GRCm39) |
nonsense |
probably null |
|
R0413:Igfn1
|
UTSW |
1 |
135,895,334 (GRCm39) |
missense |
probably benign |
0.23 |
R0504:Igfn1
|
UTSW |
1 |
135,896,267 (GRCm39) |
missense |
probably benign |
0.00 |
R0606:Igfn1
|
UTSW |
1 |
135,887,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0681:Igfn1
|
UTSW |
1 |
135,891,591 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0825:Igfn1
|
UTSW |
1 |
135,890,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Igfn1
|
UTSW |
1 |
135,882,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R1066:Igfn1
|
UTSW |
1 |
135,898,463 (GRCm39) |
missense |
probably benign |
|
R1078:Igfn1
|
UTSW |
1 |
135,902,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1224:Igfn1
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R1569:Igfn1
|
UTSW |
1 |
135,896,771 (GRCm39) |
missense |
probably benign |
|
R1626:Igfn1
|
UTSW |
1 |
135,896,705 (GRCm39) |
missense |
probably benign |
0.29 |
R1663:Igfn1
|
UTSW |
1 |
135,896,046 (GRCm39) |
missense |
probably benign |
0.15 |
R1677:Igfn1
|
UTSW |
1 |
135,898,839 (GRCm39) |
missense |
probably damaging |
0.99 |
R1709:Igfn1
|
UTSW |
1 |
135,883,311 (GRCm39) |
missense |
probably benign |
0.24 |
R1728:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1728:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1728:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1729:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1729:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1730:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1739:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1739:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1746:Igfn1
|
UTSW |
1 |
135,897,561 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1762:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1762:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1783:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1783:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1783:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1784:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1784:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,926,421 (GRCm39) |
missense |
unknown |
|
R1785:Igfn1
|
UTSW |
1 |
135,887,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Igfn1
|
UTSW |
1 |
135,895,937 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,898,149 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,899,865 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,907,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Igfn1
|
UTSW |
1 |
135,910,213 (GRCm39) |
missense |
probably benign |
|
R1785:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R1847:Igfn1
|
UTSW |
1 |
135,897,126 (GRCm39) |
missense |
probably benign |
|
R1866:Igfn1
|
UTSW |
1 |
135,902,606 (GRCm39) |
splice site |
probably null |
|
R1921:Igfn1
|
UTSW |
1 |
135,893,801 (GRCm39) |
critical splice donor site |
probably null |
|
R1984:Igfn1
|
UTSW |
1 |
135,889,782 (GRCm39) |
missense |
probably benign |
0.39 |
R2049:Igfn1
|
UTSW |
1 |
135,902,590 (GRCm39) |
splice site |
probably benign |
|
R2049:Igfn1
|
UTSW |
1 |
135,898,376 (GRCm39) |
missense |
probably benign |
|
R2098:Igfn1
|
UTSW |
1 |
135,906,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Igfn1
|
UTSW |
1 |
135,902,590 (GRCm39) |
splice site |
probably benign |
|
R2141:Igfn1
|
UTSW |
1 |
135,902,590 (GRCm39) |
splice site |
probably benign |
|
R2276:Igfn1
|
UTSW |
1 |
135,892,479 (GRCm39) |
missense |
probably damaging |
0.98 |
R2425:Igfn1
|
UTSW |
1 |
135,890,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Igfn1
|
UTSW |
1 |
135,897,275 (GRCm39) |
missense |
probably benign |
|
R2504:Igfn1
|
UTSW |
1 |
135,897,054 (GRCm39) |
missense |
probably benign |
0.07 |
R3109:Igfn1
|
UTSW |
1 |
135,925,586 (GRCm39) |
missense |
probably benign |
0.12 |
R3421:Igfn1
|
UTSW |
1 |
135,904,655 (GRCm39) |
critical splice donor site |
probably null |
|
R3423:Igfn1
|
UTSW |
1 |
135,926,379 (GRCm39) |
missense |
probably benign |
0.01 |
R3705:Igfn1
|
UTSW |
1 |
135,896,147 (GRCm39) |
missense |
probably benign |
|
R3871:Igfn1
|
UTSW |
1 |
135,896,574 (GRCm39) |
missense |
probably benign |
0.03 |
R3875:Igfn1
|
UTSW |
1 |
135,882,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:Igfn1
|
UTSW |
1 |
135,894,918 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3955:Igfn1
|
UTSW |
1 |
135,894,918 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3957:Igfn1
|
UTSW |
1 |
135,894,918 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3965:Igfn1
|
UTSW |
1 |
135,895,557 (GRCm39) |
missense |
probably benign |
|
R4006:Igfn1
|
UTSW |
1 |
135,910,100 (GRCm39) |
splice site |
probably null |
|
R4058:Igfn1
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R4059:Igfn1
|
UTSW |
1 |
135,897,494 (GRCm39) |
missense |
probably benign |
0.07 |
R4370:Igfn1
|
UTSW |
1 |
135,895,844 (GRCm39) |
missense |
probably benign |
0.00 |
R4380:Igfn1
|
UTSW |
1 |
135,895,509 (GRCm39) |
missense |
probably benign |
0.00 |
R4495:Igfn1
|
UTSW |
1 |
135,897,416 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4628:Igfn1
|
UTSW |
1 |
135,887,468 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4672:Igfn1
|
UTSW |
1 |
135,893,107 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4682:Igfn1
|
UTSW |
1 |
135,926,363 (GRCm39) |
missense |
probably benign |
|
R4702:Igfn1
|
UTSW |
1 |
135,894,947 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4744:Igfn1
|
UTSW |
1 |
135,910,196 (GRCm39) |
missense |
probably benign |
0.07 |
R4777:Igfn1
|
UTSW |
1 |
135,882,600 (GRCm39) |
missense |
probably benign |
|
R4806:Igfn1
|
UTSW |
1 |
135,895,095 (GRCm39) |
missense |
probably benign |
0.01 |
R4840:Igfn1
|
UTSW |
1 |
135,895,778 (GRCm39) |
missense |
probably benign |
0.00 |
R4894:Igfn1
|
UTSW |
1 |
135,882,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Igfn1
|
UTSW |
1 |
135,882,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Igfn1
|
UTSW |
1 |
135,892,564 (GRCm39) |
missense |
probably benign |
|
R5108:Igfn1
|
UTSW |
1 |
135,910,179 (GRCm39) |
missense |
probably benign |
|
R5120:Igfn1
|
UTSW |
1 |
135,901,240 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5127:Igfn1
|
UTSW |
1 |
135,887,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R5231:Igfn1
|
UTSW |
1 |
135,894,474 (GRCm39) |
missense |
probably benign |
0.26 |
R5286:Igfn1
|
UTSW |
1 |
135,895,599 (GRCm39) |
missense |
probably benign |
0.10 |
R5307:Igfn1
|
UTSW |
1 |
135,892,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Igfn1
|
UTSW |
1 |
135,893,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R5553:Igfn1
|
UTSW |
1 |
135,895,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R5660:Igfn1
|
UTSW |
1 |
135,898,152 (GRCm39) |
missense |
probably benign |
0.01 |
R5779:Igfn1
|
UTSW |
1 |
135,894,578 (GRCm39) |
missense |
probably benign |
0.16 |
R5818:Igfn1
|
UTSW |
1 |
135,893,864 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5832:Igfn1
|
UTSW |
1 |
135,902,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R5933:Igfn1
|
UTSW |
1 |
135,898,341 (GRCm39) |
nonsense |
probably null |
|
R5966:Igfn1
|
UTSW |
1 |
135,893,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R6116:Igfn1
|
UTSW |
1 |
135,898,205 (GRCm39) |
missense |
probably benign |
0.00 |
R6297:Igfn1
|
UTSW |
1 |
135,892,399 (GRCm39) |
critical splice donor site |
probably null |
|
R6652:Igfn1
|
UTSW |
1 |
135,891,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Igfn1
|
UTSW |
1 |
135,897,605 (GRCm39) |
missense |
probably benign |
|
R6816:Igfn1
|
UTSW |
1 |
135,887,466 (GRCm39) |
missense |
probably benign |
0.02 |
R6886:Igfn1
|
UTSW |
1 |
135,901,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Igfn1
|
UTSW |
1 |
135,910,218 (GRCm39) |
missense |
probably benign |
0.33 |
R6975:Igfn1
|
UTSW |
1 |
135,896,183 (GRCm39) |
missense |
probably damaging |
0.96 |
R7105:Igfn1
|
UTSW |
1 |
135,911,956 (GRCm39) |
missense |
probably benign |
0.11 |
R7114:Igfn1
|
UTSW |
1 |
135,894,519 (GRCm39) |
missense |
probably benign |
0.01 |
R7233:Igfn1
|
UTSW |
1 |
135,897,873 (GRCm39) |
missense |
probably benign |
0.41 |
R7276:Igfn1
|
UTSW |
1 |
135,926,376 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7354:Igfn1
|
UTSW |
1 |
135,903,770 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7358:Igfn1
|
UTSW |
1 |
135,891,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7380:Igfn1
|
UTSW |
1 |
135,889,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Igfn1
|
UTSW |
1 |
135,894,785 (GRCm39) |
missense |
probably benign |
0.00 |
R7513:Igfn1
|
UTSW |
1 |
135,887,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R7718:Igfn1
|
UTSW |
1 |
135,896,774 (GRCm39) |
missense |
probably benign |
|
R7769:Igfn1
|
UTSW |
1 |
135,910,143 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7810:Igfn1
|
UTSW |
1 |
135,902,527 (GRCm39) |
missense |
probably damaging |
0.98 |
R7917:Igfn1
|
UTSW |
1 |
135,899,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R7952:Igfn1
|
UTSW |
1 |
135,891,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R8041:Igfn1
|
UTSW |
1 |
135,895,797 (GRCm39) |
nonsense |
probably null |
|
R8233:Igfn1
|
UTSW |
1 |
135,895,782 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Igfn1
|
UTSW |
1 |
135,887,619 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8363:Igfn1
|
UTSW |
1 |
135,891,625 (GRCm39) |
missense |
probably benign |
0.01 |
R8428:Igfn1
|
UTSW |
1 |
135,895,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R8731:Igfn1
|
UTSW |
1 |
135,925,574 (GRCm39) |
missense |
probably benign |
0.02 |
R8756:Igfn1
|
UTSW |
1 |
135,895,698 (GRCm39) |
missense |
probably benign |
0.10 |
R8797:Igfn1
|
UTSW |
1 |
135,902,573 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8913:Igfn1
|
UTSW |
1 |
135,891,579 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8927:Igfn1
|
UTSW |
1 |
135,905,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Igfn1
|
UTSW |
1 |
135,905,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9087:Igfn1
|
UTSW |
1 |
135,902,606 (GRCm39) |
splice site |
probably null |
|
R9109:Igfn1
|
UTSW |
1 |
135,926,327 (GRCm39) |
missense |
probably benign |
0.26 |
R9113:Igfn1
|
UTSW |
1 |
135,883,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Igfn1
|
UTSW |
1 |
135,902,528 (GRCm39) |
missense |
probably benign |
0.03 |
R9205:Igfn1
|
UTSW |
1 |
135,903,695 (GRCm39) |
missense |
probably damaging |
0.96 |
R9251:Igfn1
|
UTSW |
1 |
135,894,409 (GRCm39) |
splice site |
probably benign |
|
R9260:Igfn1
|
UTSW |
1 |
135,907,694 (GRCm39) |
missense |
probably benign |
0.45 |
R9275:Igfn1
|
UTSW |
1 |
135,901,185 (GRCm39) |
missense |
probably damaging |
0.96 |
R9277:Igfn1
|
UTSW |
1 |
135,887,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R9278:Igfn1
|
UTSW |
1 |
135,901,185 (GRCm39) |
missense |
probably damaging |
0.96 |
R9287:Igfn1
|
UTSW |
1 |
135,925,544 (GRCm39) |
missense |
probably benign |
0.33 |
R9298:Igfn1
|
UTSW |
1 |
135,926,327 (GRCm39) |
missense |
probably benign |
0.26 |
R9356:Igfn1
|
UTSW |
1 |
135,899,825 (GRCm39) |
nonsense |
probably null |
|
R9371:Igfn1
|
UTSW |
1 |
135,906,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9532:Igfn1
|
UTSW |
1 |
135,897,229 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9653:Igfn1
|
UTSW |
1 |
135,883,323 (GRCm39) |
nonsense |
probably null |
|
R9666:Igfn1
|
UTSW |
1 |
135,897,692 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9741:Igfn1
|
UTSW |
1 |
135,895,383 (GRCm39) |
missense |
probably benign |
0.00 |
R9748:Igfn1
|
UTSW |
1 |
135,926,336 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9796:Igfn1
|
UTSW |
1 |
135,897,611 (GRCm39) |
missense |
probably benign |
0.26 |
Z1176:Igfn1
|
UTSW |
1 |
135,899,738 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Igfn1
|
UTSW |
1 |
135,897,305 (GRCm39) |
missense |
probably benign |
0.26 |
Z1177:Igfn1
|
UTSW |
1 |
135,883,547 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Igfn1
|
UTSW |
1 |
135,910,164 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Predicted Primers |
PCR Primer
(F):5'- TGATGGGGCACCAAGTCCTCAATG -3'
(R):5'- CAGGGGAGCAAATTGGACCCTAAAC -3'
Sequencing Primer
(F):5'- ACCAAGTCCTCAATGTCAGCTTC -3'
(R):5'- gcacaatacatggcatatggtag -3'
|
Posted On |
2014-05-23 |