Incidental Mutation 'R5055:Ipo9'
| ID |
390745 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ipo9
|
| Ensembl Gene |
ENSMUSG00000041879 |
| Gene Name |
importin 9 |
| Synonyms |
0710008K06Rik, Imp9 |
| MMRRC Submission |
042645-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R5055 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
135310050-135358237 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to A
at 135330097 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Stop codon
at position 448
(E448*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124779
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041023]
[ENSMUST00000161032]
[ENSMUST00000161189]
[ENSMUST00000161838]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably null
Transcript: ENSMUST00000041023
AA Change: E448*
|
| SMART Domains |
Protein: ENSMUSP00000036093
Gene: ENSMUSG00000041879
AA Change: E448*
| 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 null
Transcript: ENSMUST00000161032
AA Change: E448*
|
| SMART Domains |
Protein: ENSMUSP00000124779
Gene: ENSMUSG00000041879
AA Change: E448*
| 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 |
noncoding transcript
Transcript: ENSMUST00000161258
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161704
|
| 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 |
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 92.9%
|
| Validation Efficiency |
98% (84/86) |
| 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: 77 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam19 |
G |
A |
11: 46,013,996 (GRCm39) |
V329I |
probably damaging |
Het |
| Adgrl3 |
C |
A |
5: 81,794,398 (GRCm39) |
A541E |
possibly damaging |
Het |
| Agbl1 |
A |
T |
7: 76,063,325 (GRCm39) |
I263F |
probably damaging |
Het |
| Ash1l |
T |
C |
3: 88,930,519 (GRCm39) |
|
probably null |
Het |
| Bccip |
A |
G |
7: 133,316,652 (GRCm39) |
T91A |
probably benign |
Het |
| Bnc1 |
A |
T |
7: 81,624,163 (GRCm39) |
F355I |
probably damaging |
Het |
| Bpifa2 |
A |
T |
2: 153,855,630 (GRCm39) |
D185V |
probably damaging |
Het |
| Capn8 |
T |
A |
1: 182,399,526 (GRCm39) |
V89D |
probably damaging |
Het |
| Cfap46 |
A |
T |
7: 139,241,106 (GRCm39) |
M421K |
probably damaging |
Het |
| Chd2 |
A |
T |
7: 73,130,256 (GRCm39) |
L800M |
probably damaging |
Het |
| Chd4 |
A |
G |
6: 125,077,949 (GRCm39) |
D137G |
possibly damaging |
Het |
| Crtap |
A |
G |
9: 114,219,208 (GRCm39) |
Y154H |
probably benign |
Het |
| Ctdp1 |
T |
A |
18: 80,499,303 (GRCm39) |
Q213L |
probably damaging |
Het |
| Cts6 |
T |
C |
13: 61,344,164 (GRCm39) |
Y296C |
probably damaging |
Het |
| Daxx |
G |
T |
17: 34,131,134 (GRCm39) |
V354F |
probably benign |
Het |
| Dnah2 |
A |
G |
11: 69,411,599 (GRCm39) |
I341T |
possibly damaging |
Het |
| Epha2 |
A |
G |
4: 141,036,380 (GRCm39) |
D272G |
probably benign |
Het |
| Etfa |
A |
G |
9: 55,407,417 (GRCm39) |
V24A |
probably damaging |
Het |
| Fbxl7 |
C |
A |
15: 26,553,022 (GRCm39) |
G82W |
probably damaging |
Het |
| Fcamr |
G |
A |
1: 130,739,174 (GRCm39) |
C158Y |
probably damaging |
Het |
| Fyb1 |
A |
C |
15: 6,614,630 (GRCm39) |
|
probably benign |
Het |
| Gars1 |
G |
A |
6: 55,045,077 (GRCm39) |
R454H |
probably damaging |
Het |
| Ghsr |
T |
C |
3: 27,426,421 (GRCm39) |
V159A |
probably benign |
Het |
| Glp1r |
A |
T |
17: 31,137,861 (GRCm39) |
Q97H |
probably benign |
Het |
| Gm27047 |
T |
C |
6: 130,606,909 (GRCm39) |
|
noncoding transcript |
Het |
| Igkv3-3 |
A |
C |
6: 70,664,223 (GRCm39) |
I22L |
probably benign |
Het |
| Inpp5b |
G |
T |
4: 124,636,824 (GRCm39) |
|
probably null |
Het |
| Itgb2l |
A |
T |
16: 96,229,003 (GRCm39) |
I400N |
probably damaging |
Het |
| Kat6b |
T |
A |
14: 21,567,062 (GRCm39) |
H40Q |
probably damaging |
Het |
| Kcna7 |
G |
A |
7: 45,056,015 (GRCm39) |
R77H |
probably damaging |
Het |
| Kcnq2 |
G |
T |
2: 180,728,554 (GRCm39) |
|
probably benign |
Het |
| Klf7 |
T |
C |
1: 64,118,439 (GRCm39) |
T53A |
probably benign |
Het |
| Kmt2a |
A |
G |
9: 44,729,649 (GRCm39) |
|
probably benign |
Het |
| Lrp10 |
C |
T |
14: 54,705,802 (GRCm39) |
R331C |
probably benign |
Het |
| Map4k5 |
A |
T |
12: 69,878,332 (GRCm39) |
D289E |
probably benign |
Het |
| Mfsd4b2 |
A |
T |
10: 39,799,773 (GRCm39) |
M43K |
possibly damaging |
Het |
| Msr1 |
T |
G |
8: 40,076,997 (GRCm39) |
R138S |
possibly damaging |
Het |
| Myh7b |
G |
C |
2: 155,474,293 (GRCm39) |
R1669S |
possibly damaging |
Het |
| Myh9 |
G |
A |
15: 77,648,723 (GRCm39) |
A1711V |
probably benign |
Het |
| Myo18b |
A |
G |
5: 113,023,083 (GRCm39) |
|
probably benign |
Het |
| Nampt |
A |
T |
12: 32,883,120 (GRCm39) |
N102Y |
possibly damaging |
Het |
| Nell2 |
T |
C |
15: 95,371,460 (GRCm39) |
I92V |
probably benign |
Het |
| Nes |
A |
G |
3: 87,884,521 (GRCm39) |
N883D |
probably benign |
Het |
| Neurl3 |
T |
A |
1: 36,312,463 (GRCm39) |
|
probably benign |
Het |
| Ocln |
T |
A |
13: 100,675,930 (GRCm39) |
T188S |
probably benign |
Het |
| Or2ag20 |
T |
A |
7: 106,464,937 (GRCm39) |
M250K |
probably damaging |
Het |
| Or5m10 |
T |
C |
2: 85,717,585 (GRCm39) |
F147S |
probably benign |
Het |
| Parp14 |
T |
A |
16: 35,664,733 (GRCm39) |
Q1305L |
probably benign |
Het |
| Pde3a |
C |
T |
6: 141,433,682 (GRCm39) |
Q855* |
probably null |
Het |
| Pde4b |
T |
C |
4: 102,052,311 (GRCm39) |
|
probably benign |
Het |
| Pdk2 |
T |
C |
11: 94,930,242 (GRCm39) |
M65V |
probably benign |
Het |
| Phf21a |
T |
C |
2: 92,182,201 (GRCm39) |
S377P |
probably damaging |
Het |
| Plcb2 |
T |
A |
2: 118,548,703 (GRCm39) |
T408S |
probably benign |
Het |
| Ppp1r12b |
G |
T |
1: 134,883,471 (GRCm39) |
A17E |
probably benign |
Het |
| Ppp6r2 |
A |
G |
15: 89,167,152 (GRCm39) |
D789G |
probably benign |
Het |
| Prdm16 |
T |
C |
4: 154,419,719 (GRCm39) |
M897V |
possibly damaging |
Het |
| Prss57 |
A |
G |
10: 79,620,178 (GRCm39) |
|
probably null |
Het |
| Psd |
G |
T |
19: 46,310,907 (GRCm39) |
L381I |
probably benign |
Het |
| Ptprq |
A |
T |
10: 107,370,540 (GRCm39) |
D2050E |
probably benign |
Het |
| Rfc1 |
G |
T |
5: 65,423,505 (GRCm39) |
N1034K |
probably damaging |
Het |
| Ryr3 |
C |
T |
2: 112,661,504 (GRCm39) |
G1829S |
probably benign |
Het |
| Scaper |
T |
C |
9: 55,767,003 (GRCm39) |
|
probably null |
Het |
| Scn5a |
A |
G |
9: 119,351,632 (GRCm39) |
I783T |
probably damaging |
Het |
| Slc28a1 |
A |
G |
7: 80,818,796 (GRCm39) |
N583S |
possibly damaging |
Het |
| Slc35e3 |
C |
T |
10: 117,580,884 (GRCm39) |
G140D |
probably damaging |
Het |
| Slc6a9 |
G |
A |
4: 117,725,347 (GRCm39) |
|
probably null |
Het |
| Sptlc1 |
A |
G |
13: 53,496,218 (GRCm39) |
S376P |
probably benign |
Het |
| Sspo |
G |
A |
6: 48,441,729 (GRCm39) |
C1913Y |
probably damaging |
Het |
| Taar7b |
A |
T |
10: 23,876,845 (GRCm39) |
I337F |
possibly damaging |
Het |
| Tdpoz2 |
T |
A |
3: 93,559,235 (GRCm39) |
I246F |
probably damaging |
Het |
| Trpa1 |
C |
T |
1: 14,946,183 (GRCm39) |
V983M |
probably damaging |
Het |
| Trpm5 |
A |
T |
7: 142,626,521 (GRCm39) |
M1112K |
probably benign |
Het |
| Tsbp1 |
G |
A |
17: 34,667,770 (GRCm39) |
C154Y |
possibly damaging |
Het |
| Uso1 |
A |
T |
5: 92,340,594 (GRCm39) |
K670I |
probably benign |
Het |
| Washc4 |
A |
G |
10: 83,392,771 (GRCm39) |
D257G |
probably damaging |
Het |
| Wdr41 |
T |
A |
13: 95,151,725 (GRCm39) |
|
probably null |
Het |
| Zbtb17 |
A |
G |
4: 141,193,860 (GRCm39) |
Q668R |
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 |
|
|
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'- CTGGCTTATGATGTGCATAAATCAC -3'
(R):5'- AGTGCTCCCACATGATAGATGATTG -3'
Sequencing Primer
(F):5'- AGTGAGTTAACATCAGGTCCC -3'
(R):5'- GGAATACTCTGAGGGATCTTAC -3'
|
| Posted On |
2016-06-06 |
Incidental Mutation