Incidental Mutation 'R0238:Ipo9'
ID |
59087 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ipo9
|
Ensembl Gene |
ENSMUSG00000041879 |
Gene Name |
importin 9 |
Synonyms |
0710008K06Rik, Imp9 |
MMRRC Submission |
038476-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0238 (G1)
|
Quality Score |
213 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
135310050-135358237 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to G
at 135332074 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 |
noncoding transcript
Transcript: ENSMUST00000159017
|
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 |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161704
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161258
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.8%
- 10x: 97.4%
- 20x: 94.7%
|
Validation Efficiency |
98% (105/107) |
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: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aar2 |
T |
G |
2: 156,392,893 (GRCm39) |
V94G |
probably benign |
Het |
Acp5 |
A |
T |
9: 22,041,218 (GRCm39) |
S70T |
possibly damaging |
Het |
Adcy1 |
C |
G |
11: 7,089,162 (GRCm39) |
N525K |
possibly damaging |
Het |
Adra1d |
C |
A |
2: 131,388,134 (GRCm39) |
V474F |
probably benign |
Het |
Aknad1 |
A |
G |
3: 108,688,555 (GRCm39) |
M628V |
probably benign |
Het |
Alg8 |
A |
T |
7: 97,032,891 (GRCm39) |
|
probably null |
Het |
Cacna1d |
A |
G |
14: 29,845,453 (GRCm39) |
V572A |
probably benign |
Het |
Ccdc158 |
A |
C |
5: 92,809,977 (GRCm39) |
M177R |
probably benign |
Het |
Ccdc191 |
A |
T |
16: 43,767,859 (GRCm39) |
R678* |
probably null |
Het |
Cdkn2d |
C |
A |
9: 21,202,288 (GRCm39) |
|
probably benign |
Het |
Cdx2 |
G |
T |
5: 147,240,097 (GRCm39) |
T193K |
probably damaging |
Het |
Cfap44 |
T |
A |
16: 44,242,681 (GRCm39) |
M695K |
probably benign |
Het |
Cfap70 |
A |
C |
14: 20,498,673 (GRCm39) |
S5A |
probably benign |
Het |
Chd9 |
T |
C |
8: 91,659,456 (GRCm39) |
S139P |
probably damaging |
Het |
Chmp7 |
A |
G |
14: 69,958,446 (GRCm39) |
V241A |
probably damaging |
Het |
Cnga1 |
A |
G |
5: 72,762,374 (GRCm39) |
I380T |
probably damaging |
Het |
Col4a1 |
C |
T |
8: 11,268,780 (GRCm39) |
|
probably benign |
Het |
Cts6 |
T |
A |
13: 61,349,633 (GRCm39) |
E53D |
probably damaging |
Het |
Cul2 |
A |
G |
18: 3,414,115 (GRCm39) |
|
probably benign |
Het |
Dclk3 |
A |
T |
9: 111,311,696 (GRCm39) |
N646I |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,370,738 (GRCm39) |
S4673G |
probably benign |
Het |
Dock4 |
G |
T |
12: 40,787,539 (GRCm39) |
S818I |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,041,461 (GRCm39) |
Q156* |
probably null |
Het |
Espnl |
T |
C |
1: 91,250,009 (GRCm39) |
V52A |
probably damaging |
Het |
Fam163b |
T |
C |
2: 27,002,646 (GRCm39) |
N117S |
probably damaging |
Het |
Fam89a |
A |
G |
8: 125,467,971 (GRCm39) |
Y114H |
probably damaging |
Het |
Flcn |
T |
C |
11: 59,691,902 (GRCm39) |
N249S |
probably benign |
Het |
Gnai1 |
A |
G |
5: 18,478,548 (GRCm39) |
S206P |
probably damaging |
Het |
H1f6 |
G |
T |
13: 23,880,307 (GRCm39) |
K153N |
possibly damaging |
Het |
Hal |
T |
C |
10: 93,339,344 (GRCm39) |
S478P |
possibly damaging |
Het |
Haus3 |
G |
A |
5: 34,323,600 (GRCm39) |
P337S |
possibly damaging |
Het |
Hectd1 |
T |
A |
12: 51,816,101 (GRCm39) |
M1324L |
possibly damaging |
Het |
Hpn |
G |
T |
7: 30,798,815 (GRCm39) |
|
probably benign |
Het |
Hspa9 |
A |
T |
18: 35,079,699 (GRCm39) |
Y243* |
probably null |
Het |
Htr3a |
T |
C |
9: 48,817,686 (GRCm39) |
T96A |
probably benign |
Het |
Ift140 |
C |
A |
17: 25,264,497 (GRCm39) |
C557* |
probably null |
Het |
Il4ra |
T |
C |
7: 125,174,371 (GRCm39) |
|
probably benign |
Het |
Irag2 |
G |
A |
6: 145,117,704 (GRCm39) |
|
probably benign |
Het |
Jph3 |
A |
G |
8: 122,480,459 (GRCm39) |
Q379R |
possibly damaging |
Het |
Kcnb1 |
A |
G |
2: 166,946,889 (GRCm39) |
V653A |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,455,131 (GRCm39) |
E1551G |
probably damaging |
Het |
Krt17 |
G |
A |
11: 100,151,704 (GRCm39) |
R30* |
probably null |
Het |
Lamb3 |
A |
T |
1: 193,003,361 (GRCm39) |
D100V |
probably damaging |
Het |
Map2 |
A |
G |
1: 66,455,265 (GRCm39) |
D1385G |
probably damaging |
Het |
Map3k21 |
A |
G |
8: 126,671,709 (GRCm39) |
D999G |
possibly damaging |
Het |
Marf1 |
T |
C |
16: 13,969,147 (GRCm39) |
I109V |
probably benign |
Het |
Mcam |
T |
G |
9: 44,051,502 (GRCm39) |
|
probably null |
Het |
Med18 |
T |
C |
4: 132,187,337 (GRCm39) |
H99R |
probably damaging |
Het |
Mettl25 |
C |
T |
10: 105,662,386 (GRCm39) |
V195I |
probably damaging |
Het |
Micu2 |
G |
A |
14: 58,154,835 (GRCm39) |
|
probably benign |
Het |
Mpl |
A |
G |
4: 118,314,060 (GRCm39) |
|
probably benign |
Het |
Myh8 |
A |
G |
11: 67,192,518 (GRCm39) |
T1466A |
probably benign |
Het |
Myo1e |
A |
T |
9: 70,249,408 (GRCm39) |
I503F |
possibly damaging |
Het |
Myo3b |
T |
A |
2: 69,935,769 (GRCm39) |
C61S |
probably benign |
Het |
Myorg |
A |
T |
4: 41,498,912 (GRCm39) |
N239K |
probably benign |
Het |
Nbn |
T |
C |
4: 15,986,672 (GRCm39) |
|
probably benign |
Het |
Ndufa4 |
C |
T |
6: 11,906,023 (GRCm39) |
V10I |
probably benign |
Het |
Nf1 |
A |
T |
11: 79,309,400 (GRCm39) |
K438M |
possibly damaging |
Het |
Nlrp9c |
A |
G |
7: 26,077,437 (GRCm39) |
S727P |
possibly damaging |
Het |
Nmbr |
C |
T |
10: 14,646,139 (GRCm39) |
Q338* |
probably null |
Het |
Nt5e |
A |
G |
9: 88,249,385 (GRCm39) |
S440G |
possibly damaging |
Het |
Nubp2 |
T |
C |
17: 25,103,445 (GRCm39) |
E144G |
probably damaging |
Het |
Or12e7 |
T |
C |
2: 87,288,381 (GRCm39) |
F291L |
probably benign |
Het |
Or2ag1b |
A |
G |
7: 106,288,462 (GRCm39) |
Y159H |
probably benign |
Het |
Or52s1 |
G |
A |
7: 102,861,933 (GRCm39) |
V289M |
possibly damaging |
Het |
Otogl |
T |
A |
10: 107,642,557 (GRCm39) |
N1291I |
probably damaging |
Het |
Pa2g4 |
T |
C |
10: 128,399,511 (GRCm39) |
K51R |
probably benign |
Het |
Pah |
C |
T |
10: 87,403,143 (GRCm39) |
P173S |
possibly damaging |
Het |
Pcdhb12 |
A |
G |
18: 37,569,780 (GRCm39) |
I309V |
probably benign |
Het |
Pck1 |
T |
G |
2: 172,998,861 (GRCm39) |
I373S |
possibly damaging |
Het |
Pga5 |
A |
G |
19: 10,646,817 (GRCm39) |
Y305H |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,945,754 (GRCm39) |
D906E |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,256,927 (GRCm39) |
E98G |
possibly damaging |
Het |
Pzp |
C |
T |
6: 128,466,119 (GRCm39) |
|
probably benign |
Het |
Rab39 |
G |
A |
9: 53,617,330 (GRCm39) |
T29I |
probably damaging |
Het |
Raet1e |
C |
A |
10: 22,056,761 (GRCm39) |
H112Q |
possibly damaging |
Het |
Rars2 |
T |
C |
4: 34,645,838 (GRCm39) |
Y252H |
probably damaging |
Het |
Rars2 |
A |
C |
4: 34,656,030 (GRCm39) |
Q421P |
probably benign |
Het |
Rasa2 |
A |
T |
9: 96,450,460 (GRCm39) |
D479E |
probably damaging |
Het |
Rbl2 |
A |
T |
8: 91,833,135 (GRCm39) |
T689S |
probably damaging |
Het |
Rims4 |
C |
T |
2: 163,705,945 (GRCm39) |
V230M |
probably benign |
Het |
Scgb1b27 |
G |
A |
7: 33,721,377 (GRCm39) |
|
probably benign |
Het |
Sec31b |
G |
A |
19: 44,513,908 (GRCm39) |
|
probably benign |
Het |
Six3 |
G |
A |
17: 85,928,818 (GRCm39) |
G51R |
probably damaging |
Het |
Skp2 |
A |
C |
15: 9,127,971 (GRCm39) |
|
probably null |
Het |
Slc35f4 |
A |
T |
14: 49,541,713 (GRCm39) |
I347N |
possibly damaging |
Het |
Slc4a2 |
A |
T |
5: 24,641,272 (GRCm39) |
|
probably null |
Het |
Slc52a3 |
T |
C |
2: 151,850,076 (GRCm39) |
*461Q |
probably null |
Het |
Slc6a1 |
G |
A |
6: 114,279,761 (GRCm39) |
V142I |
probably benign |
Het |
Susd5 |
A |
G |
9: 113,925,977 (GRCm39) |
*620W |
probably null |
Het |
Timm21 |
T |
C |
18: 84,965,791 (GRCm39) |
N239S |
probably damaging |
Het |
Tmem131 |
T |
C |
1: 36,867,131 (GRCm39) |
|
probably benign |
Het |
Tmem63c |
T |
C |
12: 87,122,413 (GRCm39) |
W404R |
probably damaging |
Het |
Tnrc6b |
A |
G |
15: 80,772,065 (GRCm39) |
D1118G |
probably damaging |
Het |
Traf2 |
G |
C |
2: 25,427,138 (GRCm39) |
A71G |
possibly damaging |
Het |
Trim54 |
A |
G |
5: 31,291,463 (GRCm39) |
M195V |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,850,987 (GRCm39) |
E741K |
probably damaging |
Het |
Trp73 |
AGCTGCTGCTGCTGCTGCTG |
AGCTGCTGCTGCTGCTG |
4: 154,146,981 (GRCm39) |
|
probably benign |
Het |
Trpm5 |
G |
T |
7: 142,636,695 (GRCm39) |
T414N |
probably damaging |
Het |
Vps51 |
G |
T |
19: 6,121,467 (GRCm39) |
S185* |
probably null |
Het |
Zfp329 |
G |
T |
7: 12,544,756 (GRCm39) |
T256K |
probably damaging |
Het |
Zfp729b |
A |
G |
13: 67,740,022 (GRCm39) |
Y748H |
probably damaging |
Het |
Zfp777 |
T |
C |
6: 48,001,903 (GRCm39) |
E773G |
probably damaging |
Het |
Zfp866 |
T |
C |
8: 70,219,365 (GRCm39) |
Y53C |
probably damaging |
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 |
R0239:Ipo9
|
UTSW |
1 |
135,332,074 (GRCm39) |
splice site |
probably benign |
|
R0279:Ipo9
|
UTSW |
1 |
135,348,101 (GRCm39) |
intron |
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'- GTTCTGGACTCAATGAGCCAGGTG -3'
(R):5'- TTTATCAGAGTAGCAAGCTGATGGCAG -3'
Sequencing Primer
(F):5'- TGAGGTGACGCTGTCCAAC -3'
(R):5'- TACTGCTACAGATATATAGTCAGCCC -3'
|
Posted On |
2013-07-11 |