Incidental Mutation 'R0279:Ipo9'
ID |
65343 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ipo9
|
Ensembl Gene |
ENSMUSG00000041879 |
Gene Name |
importin 9 |
Synonyms |
0710008K06Rik, Imp9 |
MMRRC Submission |
038501-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0279 (G1)
|
Quality Score |
122 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
135310050-135358237 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
A to T
at 135348101 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125646
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041023]
[ENSMUST00000161032]
[ENSMUST00000161189]
[ENSMUST00000161838]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000041023
|
SMART Domains |
Protein: ENSMUSP00000036093 Gene: ENSMUSG00000041879
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
10 |
N/A |
INTRINSIC |
IBN_N
|
43 |
119 |
3.83e-7 |
SMART |
low complexity region
|
911 |
922 |
N/A |
INTRINSIC |
low complexity region
|
978 |
990 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159173
|
SMART Domains |
Protein: ENSMUSP00000123869 Gene: ENSMUSG00000041879
Domain | Start | End | E-Value | Type |
low complexity region
|
1 |
7 |
N/A |
INTRINSIC |
SCOP:d1i6la_
|
18 |
49 |
3e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161032
|
SMART Domains |
Protein: ENSMUSP00000124779 Gene: ENSMUSG00000041879
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
10 |
N/A |
INTRINSIC |
IBN_N
|
43 |
119 |
3.83e-7 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161135
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161189
|
SMART Domains |
Protein: ENSMUSP00000124492 Gene: ENSMUSG00000041879
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
10 |
N/A |
INTRINSIC |
SCOP:d1i6la_
|
21 |
52 |
4e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161838
|
SMART Domains |
Protein: ENSMUSP00000125646 Gene: ENSMUSG00000041879
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
10 |
N/A |
INTRINSIC |
SCOP:d1i6la_
|
21 |
52 |
4e-3 |
SMART |
|
Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.7%
- 10x: 95.1%
- 20x: 89.6%
|
Validation Efficiency |
99% (82/83) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit embryonic lethality at E7. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610528J11Rik |
A |
T |
4: 118,386,490 (GRCm39) |
M1L |
probably benign |
Het |
5730596B20Rik |
T |
A |
6: 52,156,182 (GRCm39) |
|
probably benign |
Het |
Acrbp |
T |
C |
6: 125,030,917 (GRCm39) |
|
probably null |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Acss3 |
A |
G |
10: 106,920,732 (GRCm39) |
I126T |
possibly damaging |
Het |
Aff3 |
T |
C |
1: 38,574,650 (GRCm39) |
E110G |
probably damaging |
Het |
Aldh1a3 |
T |
C |
7: 66,059,000 (GRCm39) |
I113V |
probably benign |
Het |
Aplp2 |
T |
C |
9: 31,069,086 (GRCm39) |
E525G |
probably damaging |
Het |
Atp2b4 |
A |
G |
1: 133,657,440 (GRCm39) |
|
probably benign |
Het |
Atp8a1 |
C |
T |
5: 67,970,435 (GRCm39) |
|
probably null |
Het |
Bhmt |
A |
G |
13: 93,761,972 (GRCm39) |
C104R |
probably damaging |
Het |
Cct5 |
T |
G |
15: 31,591,177 (GRCm39) |
E508A |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,787,065 (GRCm39) |
E2761D |
probably benign |
Het |
Clstn1 |
T |
C |
4: 149,728,131 (GRCm39) |
S600P |
probably damaging |
Het |
Cnppd1 |
A |
G |
1: 75,113,573 (GRCm39) |
S232P |
probably damaging |
Het |
Crybb3 |
T |
C |
5: 113,227,619 (GRCm39) |
|
probably null |
Het |
Csmd1 |
A |
G |
8: 16,273,249 (GRCm39) |
I861T |
probably damaging |
Het |
Cyp2d10 |
A |
C |
15: 82,289,540 (GRCm39) |
S191A |
possibly damaging |
Het |
Ddx10 |
T |
C |
9: 53,146,604 (GRCm39) |
D206G |
probably damaging |
Het |
Dnah1 |
G |
T |
14: 31,024,332 (GRCm39) |
H916N |
possibly damaging |
Het |
Dnah9 |
A |
G |
11: 65,802,615 (GRCm39) |
|
probably null |
Het |
Epb42 |
G |
A |
2: 120,859,525 (GRCm39) |
|
probably benign |
Het |
Etnppl |
A |
G |
3: 130,423,062 (GRCm39) |
R248G |
probably damaging |
Het |
Eya3 |
T |
C |
4: 132,446,558 (GRCm39) |
F369L |
probably damaging |
Het |
Fam170b |
T |
C |
14: 32,556,025 (GRCm39) |
|
probably benign |
Het |
Fli1 |
A |
T |
9: 32,372,723 (GRCm39) |
V105D |
probably damaging |
Het |
Fmo1 |
T |
C |
1: 162,657,841 (GRCm39) |
I433M |
possibly damaging |
Het |
Fndc3b |
C |
A |
3: 27,511,155 (GRCm39) |
C785F |
probably benign |
Het |
Foxe3 |
T |
C |
4: 114,782,765 (GRCm39) |
D149G |
probably damaging |
Het |
Gk5 |
T |
C |
9: 96,056,857 (GRCm39) |
|
probably benign |
Het |
Gm14226 |
A |
G |
2: 154,867,372 (GRCm39) |
D443G |
possibly damaging |
Het |
Gm9796 |
C |
T |
11: 95,588,821 (GRCm39) |
|
noncoding transcript |
Het |
Golga4 |
A |
T |
9: 118,398,061 (GRCm39) |
R52S |
probably benign |
Het |
Hey2 |
C |
A |
10: 30,710,006 (GRCm39) |
C249F |
probably damaging |
Het |
Ireb2 |
C |
A |
9: 54,793,877 (GRCm39) |
T269K |
probably benign |
Het |
Kansl3 |
A |
G |
1: 36,391,050 (GRCm39) |
V274A |
probably damaging |
Het |
Kcnk2 |
C |
T |
1: 188,942,169 (GRCm39) |
A352T |
possibly damaging |
Het |
Lamc2 |
T |
C |
1: 153,006,442 (GRCm39) |
E903G |
probably benign |
Het |
Lepr |
A |
G |
4: 101,607,541 (GRCm39) |
K253R |
probably benign |
Het |
Lmntd2 |
T |
C |
7: 140,793,536 (GRCm39) |
|
probably benign |
Het |
Lrrc39 |
A |
T |
3: 116,371,952 (GRCm39) |
T240S |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,635,085 (GRCm39) |
|
probably null |
Het |
Maf |
T |
C |
8: 116,432,495 (GRCm39) |
M370V |
possibly damaging |
Het |
Mib2 |
G |
A |
4: 155,745,673 (GRCm39) |
S46L |
possibly damaging |
Het |
Mms22l |
C |
T |
4: 24,497,867 (GRCm39) |
T63I |
probably damaging |
Het |
Morc2a |
T |
A |
11: 3,633,989 (GRCm39) |
S700R |
probably benign |
Het |
Mpz |
A |
G |
1: 170,987,498 (GRCm39) |
|
probably benign |
Het |
Ncam2 |
T |
C |
16: 81,420,225 (GRCm39) |
|
probably benign |
Het |
Niban1 |
T |
C |
1: 151,584,957 (GRCm39) |
|
probably null |
Het |
Nudt14 |
C |
T |
12: 112,902,037 (GRCm39) |
A123T |
probably damaging |
Het |
Odad3 |
A |
G |
9: 21,901,543 (GRCm39) |
|
probably benign |
Het |
Or10h1 |
C |
T |
17: 33,418,298 (GRCm39) |
T92I |
probably benign |
Het |
Or2a7 |
G |
A |
6: 43,151,692 (GRCm39) |
M257I |
probably benign |
Het |
Or9g20 |
A |
T |
2: 85,629,879 (GRCm39) |
I245N |
possibly damaging |
Het |
Otoa |
T |
C |
7: 120,710,302 (GRCm39) |
|
probably benign |
Het |
Pik3cg |
G |
A |
12: 32,254,790 (GRCm39) |
T399I |
probably damaging |
Het |
Pkn3 |
C |
T |
2: 29,973,309 (GRCm39) |
A377V |
probably benign |
Het |
Ppan |
A |
G |
9: 20,802,825 (GRCm39) |
N327S |
probably benign |
Het |
Prkca |
T |
C |
11: 107,944,937 (GRCm39) |
|
probably benign |
Het |
Prrc2c |
A |
T |
1: 162,543,033 (GRCm39) |
V320E |
probably damaging |
Het |
Ptprq |
A |
G |
10: 107,444,278 (GRCm39) |
V1442A |
probably damaging |
Het |
Rapgef1 |
C |
T |
2: 29,616,239 (GRCm39) |
R834C |
probably damaging |
Het |
Rbms1 |
G |
T |
2: 60,672,754 (GRCm39) |
N44K |
probably damaging |
Het |
Rfwd3 |
A |
C |
8: 112,009,365 (GRCm39) |
F404V |
probably benign |
Het |
Rimbp3 |
G |
T |
16: 17,027,317 (GRCm39) |
R247L |
probably benign |
Het |
Serpinb1b |
T |
C |
13: 33,277,696 (GRCm39) |
S310P |
possibly damaging |
Het |
Smtn |
C |
A |
11: 3,480,235 (GRCm39) |
V329L |
probably damaging |
Het |
Snapc2 |
T |
C |
8: 4,304,979 (GRCm39) |
|
probably benign |
Het |
Spam1 |
A |
T |
6: 24,800,418 (GRCm39) |
M386L |
probably benign |
Het |
Syne2 |
A |
G |
12: 76,142,387 (GRCm39) |
E6208G |
probably damaging |
Het |
Teddm1a |
T |
C |
1: 153,768,369 (GRCm39) |
Y278H |
probably damaging |
Het |
Tnfaip6 |
A |
T |
2: 51,945,928 (GRCm39) |
N258I |
possibly damaging |
Het |
Trpm4 |
C |
T |
7: 44,971,472 (GRCm39) |
R188Q |
probably damaging |
Het |
Ttbk2 |
A |
T |
2: 120,579,441 (GRCm39) |
H491Q |
probably benign |
Het |
Urgcp |
C |
T |
11: 5,666,989 (GRCm39) |
E450K |
probably benign |
Het |
Vmn1r228 |
T |
C |
17: 20,996,637 (GRCm39) |
N294D |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,015,958 (GRCm39) |
C2606S |
probably damaging |
Het |
Wdr33 |
T |
A |
18: 32,021,377 (GRCm39) |
H642Q |
unknown |
Het |
Zbtb46 |
A |
G |
2: 181,053,567 (GRCm39) |
S382P |
possibly damaging |
Het |
Zfp217 |
A |
G |
2: 169,961,700 (GRCm39) |
I209T |
probably benign |
Het |
Zranb3 |
T |
A |
1: 127,891,510 (GRCm39) |
N822I |
probably benign |
Het |
|
Other mutations in Ipo9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00896:Ipo9
|
APN |
1 |
135,327,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01611:Ipo9
|
APN |
1 |
135,314,431 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01941:Ipo9
|
APN |
1 |
135,335,811 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01944:Ipo9
|
APN |
1 |
135,333,624 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01959:Ipo9
|
APN |
1 |
135,348,093 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02649:Ipo9
|
APN |
1 |
135,313,672 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02697:Ipo9
|
APN |
1 |
135,318,314 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03286:Ipo9
|
APN |
1 |
135,334,816 (GRCm39) |
intron |
probably benign |
|
FR4304:Ipo9
|
UTSW |
1 |
135,314,017 (GRCm39) |
nonsense |
probably null |
|
FR4304:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Ipo9
|
UTSW |
1 |
135,314,009 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Ipo9
|
UTSW |
1 |
135,314,007 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Ipo9
|
UTSW |
1 |
135,314,019 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Ipo9
|
UTSW |
1 |
135,314,004 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Ipo9
|
UTSW |
1 |
135,314,019 (GRCm39) |
small insertion |
probably benign |
|
R0111:Ipo9
|
UTSW |
1 |
135,333,662 (GRCm39) |
missense |
probably damaging |
0.97 |
R0238:Ipo9
|
UTSW |
1 |
135,332,074 (GRCm39) |
splice site |
probably benign |
|
R0239:Ipo9
|
UTSW |
1 |
135,332,074 (GRCm39) |
splice site |
probably benign |
|
R0704:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small deletion |
probably benign |
|
R1070:Ipo9
|
UTSW |
1 |
135,334,281 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1282:Ipo9
|
UTSW |
1 |
135,330,030 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1467:Ipo9
|
UTSW |
1 |
135,334,281 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1467:Ipo9
|
UTSW |
1 |
135,334,281 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1728:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1728:Ipo9
|
UTSW |
1 |
135,314,009 (GRCm39) |
small insertion |
probably benign |
|
R1728:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1729:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1729:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1730:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1730:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1739:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1739:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1762:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1762:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1783:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1783:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1784:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1784:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1785:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R1785:Ipo9
|
UTSW |
1 |
135,314,019 (GRCm39) |
small insertion |
probably benign |
|
R1785:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R1899:Ipo9
|
UTSW |
1 |
135,327,884 (GRCm39) |
missense |
probably damaging |
0.99 |
R2049:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2049:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2130:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2130:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2131:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2131:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2133:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2133:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
R2133:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2136:Ipo9
|
UTSW |
1 |
135,322,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R2141:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2141:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,314,020 (GRCm39) |
small insertion |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,329,988 (GRCm39) |
missense |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,314,006 (GRCm39) |
small insertion |
probably benign |
|
R2142:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
R2356:Ipo9
|
UTSW |
1 |
135,334,555 (GRCm39) |
missense |
probably benign |
0.00 |
R2923:Ipo9
|
UTSW |
1 |
135,327,867 (GRCm39) |
missense |
probably benign |
0.25 |
R3161:Ipo9
|
UTSW |
1 |
135,337,214 (GRCm39) |
missense |
probably benign |
0.43 |
R3162:Ipo9
|
UTSW |
1 |
135,337,214 (GRCm39) |
missense |
probably benign |
0.43 |
R3162:Ipo9
|
UTSW |
1 |
135,337,214 (GRCm39) |
missense |
probably benign |
0.43 |
R4086:Ipo9
|
UTSW |
1 |
135,316,428 (GRCm39) |
unclassified |
probably benign |
|
R4679:Ipo9
|
UTSW |
1 |
135,321,907 (GRCm39) |
missense |
probably benign |
|
R4816:Ipo9
|
UTSW |
1 |
135,334,288 (GRCm39) |
missense |
probably benign |
0.21 |
R4956:Ipo9
|
UTSW |
1 |
135,331,960 (GRCm39) |
critical splice donor site |
probably null |
|
R5052:Ipo9
|
UTSW |
1 |
135,316,349 (GRCm39) |
splice site |
probably null |
|
R5055:Ipo9
|
UTSW |
1 |
135,330,097 (GRCm39) |
nonsense |
probably null |
|
R5230:Ipo9
|
UTSW |
1 |
135,347,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R5240:Ipo9
|
UTSW |
1 |
135,317,344 (GRCm39) |
unclassified |
probably benign |
|
R5257:Ipo9
|
UTSW |
1 |
135,313,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R5340:Ipo9
|
UTSW |
1 |
135,313,170 (GRCm39) |
missense |
probably benign |
0.00 |
R5560:Ipo9
|
UTSW |
1 |
135,329,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R5602:Ipo9
|
UTSW |
1 |
135,329,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R5604:Ipo9
|
UTSW |
1 |
135,329,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R5654:Ipo9
|
UTSW |
1 |
135,313,210 (GRCm39) |
nonsense |
probably null |
|
R6018:Ipo9
|
UTSW |
1 |
135,318,274 (GRCm39) |
critical splice donor site |
probably null |
|
R6128:Ipo9
|
UTSW |
1 |
135,318,311 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6841:Ipo9
|
UTSW |
1 |
135,314,046 (GRCm39) |
missense |
probably benign |
|
R7230:Ipo9
|
UTSW |
1 |
135,334,496 (GRCm39) |
critical splice donor site |
probably benign |
|
R7255:Ipo9
|
UTSW |
1 |
135,313,726 (GRCm39) |
missense |
probably benign |
0.01 |
R7383:Ipo9
|
UTSW |
1 |
135,316,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R7844:Ipo9
|
UTSW |
1 |
135,322,062 (GRCm39) |
missense |
probably benign |
0.00 |
R7889:Ipo9
|
UTSW |
1 |
135,334,591 (GRCm39) |
missense |
probably benign |
0.22 |
R8125:Ipo9
|
UTSW |
1 |
135,331,078 (GRCm39) |
missense |
probably benign |
0.00 |
R8823:Ipo9
|
UTSW |
1 |
135,347,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R8889:Ipo9
|
UTSW |
1 |
135,314,544 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8892:Ipo9
|
UTSW |
1 |
135,314,544 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8906:Ipo9
|
UTSW |
1 |
135,321,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R8926:Ipo9
|
UTSW |
1 |
135,313,952 (GRCm39) |
splice site |
probably benign |
|
R9084:Ipo9
|
UTSW |
1 |
135,334,563 (GRCm39) |
missense |
probably benign |
0.01 |
R9215:Ipo9
|
UTSW |
1 |
135,347,033 (GRCm39) |
missense |
probably benign |
0.05 |
R9756:Ipo9
|
UTSW |
1 |
135,314,057 (GRCm39) |
missense |
probably benign |
0.00 |
Y5405:Ipo9
|
UTSW |
1 |
135,314,022 (GRCm39) |
small insertion |
probably benign |
|
Y5405:Ipo9
|
UTSW |
1 |
135,314,013 (GRCm39) |
small insertion |
probably benign |
|
Y5405:Ipo9
|
UTSW |
1 |
135,314,007 (GRCm39) |
small insertion |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- CAAGAGGCGGGACTTATTTCCACAC -3'
(R):5'- GCACATTGAAAACTGTTCTCTGCAACC -3'
Sequencing Primer
(F):5'- GATACACTTGAATCATCTAAGGCTG -3'
(R):5'- CTGCAACCCTTGTTTTGTTTTGG -3'
|
Posted On |
2013-08-08 |