Incidental Mutation 'R2141:Ipo9'
| ID |
236207 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ipo9
|
| Ensembl Gene |
ENSMUSG00000041879 |
| Gene Name |
importin 9 |
| Synonyms |
0710008K06Rik, Imp9 |
| MMRRC Submission |
040144-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R2141 (G1)
|
| Quality Score |
217 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
135310050-135358237 bp(-) (GRCm39) |
| Type of Mutation |
small insertion (1 aa in frame mutation) |
| DNA Base Change (assembly) |
ATCCTCCTCCTCCTCCTC to ATCCTCCTCCTCCTCCTCCTC
at 135314006 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041023]
[ENSMUST00000161032]
[ENSMUST00000161189]
|
| 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: ENSMUST00000159089
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159487
|
| 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 |
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 |
noncoding transcript
Transcript: ENSMUST00000161258
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161750
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000161934
|
| SMART Domains |
Protein: ENSMUSP00000124210
Gene: ENSMUSG00000041879
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
81 |
92 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162858
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.1%
|
| Validation Efficiency |
97% (107/110) |
| 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: 102 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1810065E05Rik |
G |
T |
11: 58,314,752 (GRCm39) |
C150F |
probably damaging |
Het |
| Aagab |
T |
A |
9: 63,523,957 (GRCm39) |
|
probably null |
Het |
| Abca15 |
A |
C |
7: 120,006,697 (GRCm39) |
T1654P |
probably damaging |
Het |
| Abca17 |
T |
A |
17: 24,553,240 (GRCm39) |
Y157F |
probably benign |
Het |
| Aftph |
A |
T |
11: 20,648,318 (GRCm39) |
L813* |
probably null |
Het |
| Agap1 |
T |
C |
1: 89,765,477 (GRCm39) |
I615T |
probably damaging |
Het |
| Ak3 |
T |
G |
19: 29,000,247 (GRCm39) |
Q221H |
probably benign |
Het |
| Aldoa |
A |
G |
7: 126,396,814 (GRCm39) |
|
probably null |
Het |
| Anxa8 |
T |
C |
14: 33,813,873 (GRCm39) |
|
probably null |
Het |
| Atpsckmt |
T |
C |
15: 31,609,718 (GRCm39) |
F146L |
probably benign |
Het |
| Baz2a |
A |
G |
10: 127,959,481 (GRCm39) |
D1329G |
probably damaging |
Het |
| Calhm6 |
G |
T |
10: 34,003,691 (GRCm39) |
A72E |
probably damaging |
Het |
| Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
| Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
| Cep70 |
A |
G |
9: 99,178,438 (GRCm39) |
Y512C |
probably damaging |
Het |
| Cfhr2 |
T |
G |
1: 139,758,893 (GRCm39) |
R52S |
probably benign |
Het |
| Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
| Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
| Diablo |
A |
G |
5: 123,661,424 (GRCm39) |
V24A |
probably benign |
Het |
| Dnah7b |
T |
A |
1: 46,307,830 (GRCm39) |
M3048K |
probably damaging |
Het |
| Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
| Efnb1 |
A |
G |
X: 98,191,123 (GRCm39) |
Y343C |
probably damaging |
Het |
| Esco1 |
A |
G |
18: 10,574,873 (GRCm39) |
|
probably null |
Het |
| Fancd2 |
A |
G |
6: 113,526,282 (GRCm39) |
N335S |
probably benign |
Het |
| Flnc |
A |
G |
6: 29,448,674 (GRCm39) |
Y1304C |
probably damaging |
Het |
| Fubp3 |
A |
G |
2: 31,490,569 (GRCm39) |
|
probably benign |
Het |
| Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
| Gjc3 |
A |
C |
5: 137,955,808 (GRCm39) |
L159R |
probably damaging |
Het |
| Gli1 |
A |
G |
10: 127,172,596 (GRCm39) |
L182P |
probably damaging |
Het |
| Gm21957 |
G |
T |
7: 124,818,625 (GRCm39) |
|
noncoding transcript |
Het |
| Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
| Gm5885 |
A |
G |
6: 133,506,238 (GRCm39) |
|
noncoding transcript |
Het |
| Gon4l |
A |
T |
3: 88,794,902 (GRCm39) |
T402S |
possibly damaging |
Het |
| Gprasp1 |
G |
A |
X: 134,702,791 (GRCm39) |
E995K |
possibly damaging |
Het |
| Gvin-ps5 |
T |
A |
7: 105,929,163 (GRCm39) |
T245S |
probably damaging |
Het |
| Helb |
A |
T |
10: 119,941,926 (GRCm39) |
M254K |
possibly damaging |
Het |
| Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
| Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
| Impdh2 |
A |
G |
9: 108,442,546 (GRCm39) |
E305G |
possibly damaging |
Het |
| Ints7 |
T |
A |
1: 191,336,972 (GRCm39) |
C351S |
possibly damaging |
Het |
| Kcnq3 |
T |
C |
15: 65,867,700 (GRCm39) |
M648V |
probably benign |
Het |
| Kctd16 |
A |
G |
18: 40,392,231 (GRCm39) |
E273G |
possibly damaging |
Het |
| Kif18a |
T |
A |
2: 109,163,848 (GRCm39) |
N732K |
probably benign |
Het |
| Kif21b |
C |
T |
1: 136,080,002 (GRCm39) |
R513W |
probably damaging |
Het |
| Klhl36 |
T |
C |
8: 120,603,511 (GRCm39) |
C589R |
possibly damaging |
Het |
| Lck |
A |
G |
4: 129,442,713 (GRCm39) |
Y481H |
probably damaging |
Het |
| Lmtk2 |
A |
G |
5: 144,084,433 (GRCm39) |
Y156C |
probably damaging |
Het |
| Mical3 |
A |
T |
6: 121,008,095 (GRCm39) |
|
probably null |
Het |
| Mki67 |
A |
G |
7: 135,297,321 (GRCm39) |
I2571T |
possibly damaging |
Het |
| Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
| Myo10 |
A |
G |
15: 25,714,194 (GRCm39) |
E87G |
probably benign |
Het |
| Myo18b |
T |
C |
5: 113,021,892 (GRCm39) |
K500R |
probably benign |
Het |
| N4bp2l2 |
A |
T |
5: 150,571,001 (GRCm39) |
I458N |
probably damaging |
Het |
| Nat10 |
T |
C |
2: 103,561,648 (GRCm39) |
|
probably null |
Het |
| Nfasc |
G |
A |
1: 132,524,383 (GRCm39) |
P932L |
probably damaging |
Het |
| Nipa1 |
C |
A |
7: 55,647,259 (GRCm39) |
|
probably null |
Het |
| Nkpd1 |
A |
G |
7: 19,258,162 (GRCm39) |
Q647R |
probably damaging |
Het |
| Nlrc4 |
T |
A |
17: 74,754,946 (GRCm39) |
|
probably benign |
Het |
| Nmbr |
C |
A |
10: 14,646,186 (GRCm39) |
Y353* |
probably null |
Het |
| Nos1ap |
T |
A |
1: 170,156,735 (GRCm39) |
D241V |
probably damaging |
Het |
| Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
| Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
| Or4f4b |
A |
T |
2: 111,313,975 (GRCm39) |
T95S |
probably benign |
Het |
| Or5d43 |
A |
G |
2: 88,105,354 (GRCm39) |
V13A |
probably benign |
Het |
| Or5m13 |
A |
G |
2: 85,749,171 (GRCm39) |
I301V |
probably null |
Het |
| Or6c201 |
A |
G |
10: 128,968,875 (GRCm39) |
I254T |
probably benign |
Het |
| Pank1 |
G |
A |
19: 34,856,380 (GRCm39) |
R33C |
possibly damaging |
Het |
| Pcmtd1 |
C |
T |
1: 7,239,789 (GRCm39) |
R77C |
probably damaging |
Het |
| Phkg2 |
G |
A |
7: 127,181,386 (GRCm39) |
|
probably null |
Het |
| Plcb4 |
G |
A |
2: 135,818,019 (GRCm39) |
V762M |
probably damaging |
Het |
| Pramel7 |
T |
A |
2: 87,320,321 (GRCm39) |
H324L |
probably damaging |
Het |
| Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
| Ptgr3 |
T |
C |
18: 84,112,668 (GRCm39) |
Y115H |
probably benign |
Het |
| Rai1 |
C |
A |
11: 60,080,293 (GRCm39) |
S1452R |
possibly damaging |
Het |
| Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
| Rev3l |
T |
C |
10: 39,724,045 (GRCm39) |
V785A |
probably benign |
Het |
| Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
| Rufy2 |
G |
T |
10: 62,826,773 (GRCm39) |
R104L |
probably damaging |
Het |
| Senp6 |
T |
A |
9: 80,031,102 (GRCm39) |
N8K |
probably damaging |
Het |
| Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
| Sipa1l2 |
G |
A |
8: 126,218,230 (GRCm39) |
P369L |
probably benign |
Het |
| Slc43a1 |
T |
C |
2: 84,671,305 (GRCm39) |
L37P |
probably damaging |
Het |
| Slf1 |
T |
A |
13: 77,197,338 (GRCm39) |
|
probably null |
Het |
| Ssr2 |
T |
A |
3: 88,483,949 (GRCm39) |
|
probably benign |
Het |
| Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,674,479 (GRCm39) |
|
probably benign |
Het |
| Tas2r115 |
T |
C |
6: 132,714,321 (GRCm39) |
K210R |
probably benign |
Het |
| Tbx18 |
A |
G |
9: 87,597,706 (GRCm39) |
V276A |
probably damaging |
Het |
| Tesl1 |
T |
A |
X: 23,773,549 (GRCm39) |
V350E |
probably benign |
Het |
| Tie1 |
G |
A |
4: 118,330,008 (GRCm39) |
R1072* |
probably null |
Het |
| Tm2d2 |
C |
A |
8: 25,512,674 (GRCm39) |
T174K |
probably damaging |
Het |
| Tmem98 |
A |
G |
11: 80,705,158 (GRCm39) |
D82G |
possibly damaging |
Het |
| Tmub2 |
A |
G |
11: 102,178,379 (GRCm39) |
E94G |
possibly damaging |
Het |
| Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
| Tonsl |
A |
T |
15: 76,516,861 (GRCm39) |
I923N |
probably damaging |
Het |
| Ttc21a |
G |
A |
9: 119,793,361 (GRCm39) |
V977M |
probably damaging |
Het |
| Ube2ql1 |
T |
C |
13: 69,886,783 (GRCm39) |
D226G |
probably damaging |
Het |
| Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
| Wdr87-ps |
T |
C |
7: 29,230,935 (GRCm39) |
|
noncoding transcript |
Het |
| Zfp408 |
A |
G |
2: 91,478,194 (GRCm39) |
|
probably benign |
Het |
| Zfp473 |
T |
C |
7: 44,382,501 (GRCm39) |
T610A |
possibly damaging |
Het |
| Zfp804b |
A |
G |
5: 6,822,583 (GRCm39) |
V160A |
probably benign |
Het |
| Zfp960 |
A |
G |
17: 17,308,146 (GRCm39) |
T287A |
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 |
|
|
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 |
|
|
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'- AGATGCGTTTACTGCATGGC -3'
(R):5'- CTAGGGCATCCTTGGTGCTATC -3'
Sequencing Primer
(F):5'- TTACTGCATGGCTGAGGC -3'
(R):5'- CATCCTTGGTGCTATCACGTTTGG -3'
|
| Posted On |
2014-10-01 |
Incidental Mutation