Incidental Mutation 'R8906:Ipo9'
| ID |
680073 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ipo9
|
| Ensembl Gene |
ENSMUSG00000041879 |
| Gene Name |
importin 9 |
| Synonyms |
0710008K06Rik, Imp9 |
| MMRRC Submission |
068699-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R8906 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
135310050-135358237 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 135321951 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glycine
at position 593
(V593G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124779
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041023]
[ENSMUST00000161032]
[ENSMUST00000161189]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000041023
AA Change: V593G
PolyPhen 2
Score 0.950 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000036093
Gene: ENSMUSG00000041879
AA Change: V593G
| 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 damaging
Transcript: ENSMUST00000161032
AA Change: V593G
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000124779
Gene: ENSMUSG00000041879
AA Change: V593G
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.4%
|
| Validation Efficiency |
100% (88/88) |
| 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: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1810055G02Rik |
A |
C |
19: 3,766,686 (GRCm39) |
N91T |
possibly damaging |
Het |
| 2510009E07Rik |
CCGGAAGGGGAGGAGCAGTGACCCAGTTTCGGA |
CCGGA |
16: 21,472,148 (GRCm39) |
|
probably null |
Het |
| 4932414N04Rik |
A |
G |
2: 68,562,498 (GRCm39) |
D375G |
possibly damaging |
Het |
| Adad2 |
C |
A |
8: 120,339,725 (GRCm39) |
P69Q |
probably benign |
Het |
| Adamts3 |
G |
A |
5: 89,825,575 (GRCm39) |
T1088I |
probably damaging |
Het |
| Ank2 |
A |
G |
3: 126,726,720 (GRCm39) |
V858A |
probably benign |
Het |
| Ankrd13a |
A |
G |
5: 114,939,798 (GRCm39) |
N475S |
probably benign |
Het |
| Barhl2 |
G |
A |
5: 106,603,352 (GRCm39) |
T269I |
probably benign |
Het |
| Boc |
G |
A |
16: 44,323,931 (GRCm39) |
R157W |
|
Het |
| Bsn |
G |
T |
9: 107,984,752 (GRCm39) |
P3101T |
unknown |
Het |
| Catsperb |
C |
A |
12: 101,486,904 (GRCm39) |
A477E |
possibly damaging |
Het |
| Ccser1 |
T |
A |
6: 61,787,842 (GRCm39) |
I220K |
probably benign |
Het |
| Cd200r3 |
A |
T |
16: 44,778,102 (GRCm39) |
I242F |
possibly damaging |
Het |
| Cdc34b |
A |
C |
11: 94,632,911 (GRCm39) |
D37A |
probably damaging |
Het |
| Chek2 |
A |
G |
5: 111,013,458 (GRCm39) |
|
probably benign |
Het |
| Cngb1 |
A |
T |
8: 95,989,736 (GRCm39) |
V792D |
probably damaging |
Het |
| Cops7a |
T |
C |
6: 124,939,371 (GRCm39) |
K93E |
possibly damaging |
Het |
| Crispld1 |
T |
C |
1: 17,820,995 (GRCm39) |
I345T |
possibly damaging |
Het |
| Dgkd |
A |
G |
1: 87,869,157 (GRCm39) |
D1170G |
probably damaging |
Het |
| Dhx35 |
A |
G |
2: 158,648,918 (GRCm39) |
T115A |
possibly damaging |
Het |
| Dnai1 |
G |
A |
4: 41,625,125 (GRCm39) |
R363H |
probably benign |
Het |
| Dnmbp |
T |
A |
19: 43,878,681 (GRCm39) |
Q130L |
probably benign |
Het |
| Egfr |
A |
G |
11: 16,861,635 (GRCm39) |
Y1138C |
probably damaging |
Het |
| Elf3 |
A |
T |
1: 135,182,678 (GRCm39) |
L329Q |
probably damaging |
Het |
| Enkur |
A |
G |
2: 21,201,568 (GRCm39) |
M39T |
probably benign |
Het |
| Epha7 |
T |
C |
4: 28,821,615 (GRCm39) |
I260T |
probably damaging |
Het |
| Fbxo28 |
A |
T |
1: 182,144,634 (GRCm39) |
I310K |
probably damaging |
Het |
| Fga |
C |
A |
3: 82,939,111 (GRCm39) |
N495K |
probably benign |
Het |
| Galnt6 |
T |
C |
15: 100,601,247 (GRCm39) |
D344G |
probably damaging |
Het |
| Gm572 |
A |
G |
4: 148,751,290 (GRCm39) |
Q221R |
probably benign |
Het |
| Gpa33 |
G |
A |
1: 165,974,216 (GRCm39) |
A18T |
probably benign |
Het |
| Gpatch11 |
C |
T |
17: 79,145,289 (GRCm39) |
T6I |
probably benign |
Het |
| Gpr84 |
T |
A |
15: 103,217,625 (GRCm39) |
S151C |
probably damaging |
Het |
| H2-M11 |
T |
A |
17: 36,859,851 (GRCm39) |
Y281* |
probably null |
Het |
| Hadh |
T |
C |
3: 131,038,891 (GRCm39) |
N155S |
probably benign |
Het |
| Hoxd13 |
A |
G |
2: 74,500,266 (GRCm39) |
Y269C |
|
Het |
| Iars1 |
T |
A |
13: 49,882,177 (GRCm39) |
C1074S |
probably benign |
Het |
| Ibtk |
G |
T |
9: 85,625,457 (GRCm39) |
H98N |
possibly damaging |
Het |
| Igsf10 |
C |
T |
3: 59,233,739 (GRCm39) |
G1665R |
probably benign |
Het |
| Inpp5d |
A |
G |
1: 87,625,337 (GRCm39) |
|
probably benign |
Het |
| Irx3 |
T |
C |
8: 92,526,915 (GRCm39) |
D263G |
possibly damaging |
Het |
| Kif13a |
A |
G |
13: 46,927,154 (GRCm39) |
V1179A |
probably benign |
Het |
| Lrrc4c |
T |
C |
2: 97,460,393 (GRCm39) |
Y340H |
probably benign |
Het |
| Lysmd1 |
A |
G |
3: 95,045,219 (GRCm39) |
D155G |
probably damaging |
Het |
| Mical2 |
T |
A |
7: 111,980,671 (GRCm39) |
I105N |
probably damaging |
Het |
| Mob2 |
A |
T |
7: 141,563,261 (GRCm39) |
L66Q |
probably damaging |
Het |
| Myh1 |
A |
G |
11: 67,096,739 (GRCm39) |
S337G |
probably benign |
Het |
| Neb |
T |
C |
2: 52,096,259 (GRCm39) |
D1002G |
probably benign |
Het |
| Nebl |
A |
T |
2: 17,382,928 (GRCm39) |
N116K |
probably benign |
Het |
| Nkx2-6 |
T |
C |
14: 69,412,623 (GRCm39) |
S264P |
probably benign |
Het |
| Nlgn3 |
T |
C |
X: 100,352,390 (GRCm39) |
V179A |
probably damaging |
Het |
| Nlrp4e |
A |
G |
7: 23,020,556 (GRCm39) |
T348A |
possibly damaging |
Het |
| Nomo1 |
A |
T |
7: 45,722,004 (GRCm39) |
I982F |
probably benign |
Het |
| Or10j5 |
A |
G |
1: 172,784,186 (GRCm39) |
|
probably benign |
Het |
| Or11g24 |
T |
G |
14: 50,662,291 (GRCm39) |
F105C |
probably damaging |
Het |
| Or1j19 |
A |
T |
2: 36,676,621 (GRCm39) |
Y28F |
probably benign |
Het |
| Or8g22 |
A |
G |
9: 38,958,077 (GRCm39) |
F213L |
possibly damaging |
Het |
| Palld |
A |
G |
8: 62,003,198 (GRCm39) |
|
probably null |
Het |
| Pcdh7 |
A |
G |
5: 57,879,154 (GRCm39) |
Y903C |
probably damaging |
Het |
| Pknox2 |
G |
A |
9: 36,804,167 (GRCm39) |
T460M |
possibly damaging |
Het |
| Ppm1h |
C |
T |
10: 122,714,451 (GRCm39) |
T330I |
probably damaging |
Het |
| Ppp2r2b |
C |
T |
18: 42,821,399 (GRCm39) |
R253H |
probably damaging |
Het |
| Pramel58 |
G |
T |
5: 94,831,413 (GRCm39) |
R140L |
possibly damaging |
Het |
| Prr18 |
G |
A |
17: 8,560,476 (GRCm39) |
A211T |
probably benign |
Het |
| Ptgs2 |
A |
G |
1: 149,979,859 (GRCm39) |
I321M |
|
Het |
| Rara |
G |
T |
11: 98,860,989 (GRCm39) |
R159L |
probably damaging |
Het |
| Rasa4 |
T |
A |
5: 136,133,446 (GRCm39) |
I635N |
probably benign |
Het |
| Rxfp2 |
A |
T |
5: 149,989,888 (GRCm39) |
H423L |
possibly damaging |
Het |
| Scn4b |
A |
G |
9: 45,059,169 (GRCm39) |
I147V |
possibly damaging |
Het |
| Scrn3 |
G |
A |
2: 73,161,352 (GRCm39) |
V313I |
probably benign |
Het |
| Scrn3 |
C |
A |
2: 73,161,355 (GRCm39) |
P314T |
possibly damaging |
Het |
| Sh2b1 |
A |
G |
7: 126,070,292 (GRCm39) |
|
probably null |
Het |
| Slc26a10 |
T |
C |
10: 127,016,459 (GRCm39) |
Q3R |
probably benign |
Het |
| Slitrk1 |
A |
G |
14: 109,149,139 (GRCm39) |
I524T |
probably damaging |
Het |
| Smcp |
T |
A |
3: 92,491,530 (GRCm39) |
N106Y |
unknown |
Het |
| Spata31h1 |
T |
C |
10: 82,122,379 (GRCm39) |
T3544A |
probably benign |
Het |
| St8sia5 |
G |
A |
18: 77,336,172 (GRCm39) |
V202M |
probably damaging |
Het |
| Stxbp5l |
A |
T |
16: 37,028,526 (GRCm39) |
D512E |
probably damaging |
Het |
| Tas1r2 |
A |
G |
4: 139,397,046 (GRCm39) |
E795G |
probably damaging |
Het |
| Tdrd1 |
T |
A |
19: 56,831,145 (GRCm39) |
V320D |
probably damaging |
Het |
| Tmem71 |
T |
A |
15: 66,404,606 (GRCm39) |
I261L |
probably benign |
Het |
| Tns2 |
T |
C |
15: 102,020,039 (GRCm39) |
L643P |
probably damaging |
Het |
| Upf1 |
G |
A |
8: 70,786,815 (GRCm39) |
Q890* |
probably null |
Het |
| Usp43 |
A |
T |
11: 67,782,307 (GRCm39) |
H370Q |
possibly damaging |
Het |
| Vmn1r236 |
T |
A |
17: 21,507,356 (GRCm39) |
I158N |
possibly damaging |
Het |
| Vmn2r98 |
T |
A |
17: 19,286,532 (GRCm39) |
N343K |
probably benign |
Het |
| Vwa8 |
T |
C |
14: 79,329,815 (GRCm39) |
S1216P |
probably benign |
Het |
| Yars1 |
A |
C |
4: 129,090,747 (GRCm39) |
D97A |
probably damaging |
Het |
| Zer1 |
G |
A |
2: 30,001,035 (GRCm39) |
H129Y |
probably benign |
Het |
| Zfat |
C |
T |
15: 67,956,404 (GRCm39) |
D1143N |
possibly 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 |
|
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 |
|
|
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 |
|
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'- CCATGTCTATAGGAGAACGGG -3'
(R):5'- ACTGTAGTCTGAGAACTCATAAGAC -3'
Sequencing Primer
(F):5'- AGAACGGGGTAGCTCCTAACC -3'
(R):5'- GCACCTGCTTGAACATGTAG -3'
|
| Posted On |
2021-08-31 |
Incidental Mutation