Incidental Mutation 'R4679:Ipo9'
ID |
349880 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ipo9
|
Ensembl Gene |
ENSMUSG00000041879 |
Gene Name |
importin 9 |
Synonyms |
0710008K06Rik, Imp9 |
MMRRC Submission |
041932-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4679 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
135310050-135358237 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 135321907 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 608
(F608L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124779
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041023]
[ENSMUST00000161032]
[ENSMUST00000161189]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000041023
AA Change: F608L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000036093 Gene: ENSMUSG00000041879 AA Change: F608L
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 |
noncoding transcript
Transcript: ENSMUST00000159089
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161032
AA Change: F608L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000124779 Gene: ENSMUSG00000041879 AA Change: F608L
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
|
Meta Mutation Damage Score |
0.0676 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.7%
- 20x: 93.9%
|
Validation Efficiency |
98% (112/114) |
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: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
T |
A |
1: 130,670,140 (GRCm39) |
S121T |
possibly damaging |
Het |
Abcb9 |
A |
G |
5: 124,216,867 (GRCm39) |
V450A |
probably benign |
Het |
Abcg1 |
A |
T |
17: 31,333,235 (GRCm39) |
R659S |
probably benign |
Het |
Acad9 |
A |
T |
3: 36,142,989 (GRCm39) |
N508I |
possibly damaging |
Het |
Acrbp |
T |
A |
6: 125,037,881 (GRCm39) |
C393S |
probably damaging |
Het |
Adcy7 |
T |
C |
8: 89,044,565 (GRCm39) |
V486A |
probably benign |
Het |
Adgrf1 |
G |
T |
17: 43,621,384 (GRCm39) |
L540F |
probably damaging |
Het |
Ap5m1 |
T |
C |
14: 49,316,285 (GRCm39) |
I285T |
probably benign |
Het |
Arhgap27 |
G |
T |
11: 103,251,775 (GRCm39) |
|
probably benign |
Het |
Armc5 |
A |
T |
7: 127,839,276 (GRCm39) |
E198V |
possibly damaging |
Het |
Atp8b5 |
A |
T |
4: 43,365,955 (GRCm39) |
K742M |
probably benign |
Het |
Atp9a |
T |
G |
2: 168,503,884 (GRCm39) |
T603P |
possibly damaging |
Het |
Bsn |
A |
G |
9: 107,987,329 (GRCm39) |
S2808P |
unknown |
Het |
C9orf72 |
C |
T |
4: 35,226,033 (GRCm39) |
|
probably benign |
Het |
Catsper4 |
T |
C |
4: 133,953,916 (GRCm39) |
N81S |
probably damaging |
Het |
Ccl17 |
C |
G |
8: 95,537,128 (GRCm39) |
T10S |
probably benign |
Het |
Cdc123 |
A |
T |
2: 5,849,703 (GRCm39) |
V6D |
probably damaging |
Het |
Cdca2 |
T |
C |
14: 67,952,415 (GRCm39) |
K14E |
possibly damaging |
Het |
Cdh3 |
C |
A |
8: 107,266,488 (GRCm39) |
T302K |
probably damaging |
Het |
Cdh9 |
A |
G |
15: 16,851,045 (GRCm39) |
M605V |
probably benign |
Het |
Cdk4 |
A |
G |
10: 126,900,780 (GRCm39) |
E144G |
possibly damaging |
Het |
Clasp1 |
C |
T |
1: 118,471,001 (GRCm39) |
A879V |
probably damaging |
Het |
Cldn8 |
G |
A |
16: 88,359,296 (GRCm39) |
H210Y |
probably benign |
Het |
Cntn5 |
T |
C |
9: 9,970,536 (GRCm39) |
D518G |
probably benign |
Het |
Cog1 |
C |
T |
11: 113,543,116 (GRCm39) |
A208V |
probably damaging |
Het |
Col4a2 |
T |
A |
8: 11,481,337 (GRCm39) |
H836Q |
possibly damaging |
Het |
Copb1 |
T |
C |
7: 113,848,211 (GRCm39) |
D108G |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 48,024,479 (GRCm39) |
Y600* |
probably null |
Het |
Cyb5r1 |
T |
A |
1: 134,335,571 (GRCm39) |
H164Q |
probably benign |
Het |
Dkc1 |
A |
G |
X: 74,144,598 (GRCm39) |
I215V |
probably benign |
Het |
Enpep |
A |
G |
3: 129,097,362 (GRCm39) |
|
probably null |
Het |
Fam110d |
A |
G |
4: 133,978,747 (GRCm39) |
S244P |
probably damaging |
Het |
Fbln7 |
A |
G |
2: 128,736,806 (GRCm39) |
Y311C |
probably damaging |
Het |
Fign |
A |
C |
2: 63,809,605 (GRCm39) |
L555R |
probably damaging |
Het |
Fkbp7 |
A |
T |
2: 76,502,032 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
T |
C |
1: 174,330,728 (GRCm39) |
S373P |
unknown |
Het |
Frmd4b |
C |
T |
6: 97,272,627 (GRCm39) |
D868N |
possibly damaging |
Het |
Garin3 |
T |
A |
11: 46,295,640 (GRCm39) |
M4K |
possibly damaging |
Het |
Gfpt2 |
A |
G |
11: 49,714,564 (GRCm39) |
N321S |
probably benign |
Het |
Glmn |
G |
T |
5: 107,708,941 (GRCm39) |
T372K |
probably damaging |
Het |
Gm26602 |
C |
T |
10: 79,746,808 (GRCm39) |
|
probably benign |
Het |
Gm6797 |
A |
G |
X: 8,505,933 (GRCm39) |
|
noncoding transcript |
Het |
Gpat3 |
T |
A |
5: 101,041,322 (GRCm39) |
F383L |
probably damaging |
Het |
H2-M11 |
C |
T |
17: 36,859,042 (GRCm39) |
T194I |
possibly damaging |
Het |
Hcn1 |
C |
T |
13: 117,793,551 (GRCm39) |
H268Y |
probably benign |
Het |
Hectd4 |
G |
T |
5: 121,463,314 (GRCm39) |
C2345F |
possibly damaging |
Het |
Htt |
A |
G |
5: 34,977,424 (GRCm39) |
D770G |
probably benign |
Het |
Ints3 |
T |
C |
3: 90,315,817 (GRCm39) |
T316A |
possibly damaging |
Het |
Irak1 |
A |
C |
X: 73,065,995 (GRCm39) |
|
probably benign |
Het |
Jam2 |
G |
A |
16: 84,609,840 (GRCm39) |
V151M |
probably damaging |
Het |
Lag3 |
T |
A |
6: 124,881,508 (GRCm39) |
Q488L |
possibly damaging |
Het |
Large2 |
A |
T |
2: 92,197,903 (GRCm39) |
L266Q |
probably benign |
Het |
Lrp3 |
T |
G |
7: 34,903,365 (GRCm39) |
D327A |
probably damaging |
Het |
Mamstr |
C |
A |
7: 45,294,116 (GRCm39) |
|
probably benign |
Het |
Mettl14 |
G |
A |
3: 123,163,063 (GRCm39) |
|
probably benign |
Het |
Miga1 |
A |
G |
3: 152,028,112 (GRCm39) |
V139A |
probably damaging |
Het |
Mthfd2l |
A |
C |
5: 91,096,770 (GRCm39) |
R130S |
probably benign |
Het |
Myo1b |
A |
G |
1: 51,797,132 (GRCm39) |
I970T |
possibly damaging |
Het |
Nat10 |
C |
A |
2: 103,562,515 (GRCm39) |
W607L |
probably damaging |
Het |
Nop56 |
A |
G |
2: 130,120,193 (GRCm39) |
T183A |
probably benign |
Het |
Or10h1 |
A |
G |
17: 33,418,367 (GRCm39) |
H115R |
probably benign |
Het |
Or2d4 |
A |
T |
7: 106,544,152 (GRCm39) |
S19T |
probably benign |
Het |
Or4c10 |
A |
G |
2: 89,761,008 (GRCm39) |
Y285C |
possibly damaging |
Het |
Or4d1 |
T |
A |
11: 87,805,136 (GRCm39) |
M199L |
probably benign |
Het |
Or52j3 |
A |
G |
7: 102,836,309 (GRCm39) |
Y167C |
probably benign |
Het |
Or5ae2 |
T |
A |
7: 84,506,112 (GRCm39) |
Y178* |
probably null |
Het |
Pcdhb12 |
T |
C |
18: 37,570,002 (GRCm39) |
F383L |
probably damaging |
Het |
Pde4dip |
C |
A |
3: 97,602,321 (GRCm39) |
D2252Y |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Plscr2 |
T |
G |
9: 92,169,823 (GRCm39) |
L91R |
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,630,306 (GRCm39) |
Y1531F |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,521,043 (GRCm39) |
F710I |
probably benign |
Het |
Rad51ap2 |
A |
G |
12: 11,506,552 (GRCm39) |
E158G |
probably damaging |
Het |
Rasip1 |
T |
A |
7: 45,277,247 (GRCm39) |
H18Q |
possibly damaging |
Het |
Rcsd1 |
T |
A |
1: 165,483,493 (GRCm39) |
N166I |
probably damaging |
Het |
Ripor1 |
T |
A |
8: 106,344,417 (GRCm39) |
I517K |
possibly damaging |
Het |
Ryr2 |
T |
A |
13: 11,839,255 (GRCm39) |
H506L |
probably benign |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Septin14 |
T |
C |
5: 129,770,090 (GRCm39) |
D202G |
possibly damaging |
Het |
Siglec1 |
A |
T |
2: 130,915,331 (GRCm39) |
L1420Q |
possibly damaging |
Het |
Slc22a29 |
T |
A |
19: 8,138,948 (GRCm39) |
I505F |
possibly damaging |
Het |
Sorcs1 |
T |
A |
19: 50,171,107 (GRCm39) |
Y927F |
probably benign |
Het |
Spats2 |
T |
G |
15: 99,078,603 (GRCm39) |
M191R |
possibly damaging |
Het |
Sycp1 |
C |
T |
3: 102,829,778 (GRCm39) |
|
probably null |
Het |
T2 |
A |
G |
17: 8,609,848 (GRCm39) |
E99G |
possibly damaging |
Het |
Taf3 |
G |
A |
2: 10,053,375 (GRCm39) |
|
probably benign |
Het |
Tnfsf10 |
A |
T |
3: 27,389,728 (GRCm39) |
N263I |
probably damaging |
Het |
Treml2 |
A |
T |
17: 48,615,203 (GRCm39) |
R229S |
probably benign |
Het |
Trmt13 |
T |
C |
3: 116,383,404 (GRCm39) |
K125E |
probably damaging |
Het |
Ttc9 |
G |
T |
12: 81,678,375 (GRCm39) |
C66F |
probably damaging |
Het |
Vmn2r63 |
C |
T |
7: 42,577,544 (GRCm39) |
M331I |
probably benign |
Het |
Zfp353-ps |
T |
C |
8: 42,535,251 (GRCm39) |
|
noncoding transcript |
Het |
Zfp932 |
A |
T |
5: 110,157,760 (GRCm39) |
H486L |
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 |
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 |
|
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'- AAGAGCTTTAAGTGAGGCTGC -3'
(R):5'- GTCTCAGAGAGTACGCATGTG -3'
Sequencing Primer
(F):5'- AGCTTTAAGTGAGGCTGCTTTGC -3'
(R):5'- AGAGTACGCATGTGCTTCAGC -3'
|
Posted On |
2015-10-08 |