Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts1 |
A |
G |
16: 85,599,112 (GRCm39) |
F163L |
probably benign |
Het |
Ap2b1 |
A |
G |
11: 83,212,799 (GRCm39) |
T60A |
probably damaging |
Het |
Casp3 |
A |
G |
8: 47,082,776 (GRCm39) |
|
probably benign |
Het |
Ces1d |
T |
C |
8: 93,919,438 (GRCm39) |
Y118C |
probably damaging |
Het |
Chuk |
T |
C |
19: 44,087,015 (GRCm39) |
|
probably benign |
Het |
Clec4b2 |
A |
T |
6: 123,179,169 (GRCm39) |
Y157F |
possibly damaging |
Het |
Crppa |
C |
T |
12: 36,523,176 (GRCm39) |
L202F |
probably damaging |
Het |
Dlg4 |
T |
A |
11: 69,932,173 (GRCm39) |
F480I |
probably damaging |
Het |
Dock8 |
T |
A |
19: 25,038,656 (GRCm39) |
|
probably benign |
Het |
Dsg1b |
T |
C |
18: 20,530,906 (GRCm39) |
|
probably benign |
Het |
Dstyk |
T |
C |
1: 132,390,677 (GRCm39) |
Y830H |
probably damaging |
Het |
Hook2 |
T |
C |
8: 85,719,865 (GRCm39) |
|
probably null |
Het |
Ighv2-9-1 |
T |
C |
12: 113,733,548 (GRCm39) |
D91G |
probably damaging |
Het |
Igkv12-41 |
T |
C |
6: 69,835,510 (GRCm39) |
R81G |
probably damaging |
Het |
Jmjd1c |
T |
A |
10: 67,067,794 (GRCm39) |
S1766T |
probably damaging |
Het |
Mdn1 |
G |
A |
4: 32,708,483 (GRCm39) |
V1670I |
probably benign |
Het |
Naa15 |
T |
C |
3: 51,350,274 (GRCm39) |
F124L |
probably damaging |
Het |
Nek2 |
C |
T |
1: 191,557,598 (GRCm39) |
Q187* |
probably null |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or8b48 |
C |
T |
9: 38,492,809 (GRCm39) |
P79S |
probably damaging |
Het |
Pif1 |
G |
A |
9: 65,500,590 (GRCm39) |
G505D |
probably damaging |
Het |
Plxna4 |
T |
A |
6: 32,287,413 (GRCm39) |
I495F |
probably benign |
Het |
Ppp1r21 |
T |
C |
17: 88,869,530 (GRCm39) |
|
probably benign |
Het |
Prex1 |
T |
C |
2: 166,444,802 (GRCm39) |
I282V |
probably benign |
Het |
Pzp |
A |
T |
6: 128,479,146 (GRCm39) |
I669N |
possibly damaging |
Het |
Sipa1l2 |
T |
A |
8: 126,180,031 (GRCm39) |
|
probably benign |
Het |
Trerf1 |
T |
A |
17: 47,626,362 (GRCm39) |
|
noncoding transcript |
Het |
Uso1 |
T |
C |
5: 92,300,777 (GRCm39) |
|
probably null |
Het |
Vmn2r-ps158 |
T |
A |
7: 42,674,139 (GRCm39) |
V399E |
probably damaging |
Het |
Zcchc7 |
A |
G |
4: 44,929,217 (GRCm39) |
I390V |
probably benign |
Het |
Zfp90 |
C |
T |
8: 107,150,782 (GRCm39) |
T165I |
probably benign |
Het |
|
Other mutations in Top2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00518:Top2a
|
APN |
11 |
98,909,647 (GRCm39) |
nonsense |
probably null |
|
IGL01285:Top2a
|
APN |
11 |
98,896,985 (GRCm39) |
splice site |
probably benign |
|
IGL01445:Top2a
|
APN |
11 |
98,901,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01451:Top2a
|
APN |
11 |
98,901,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01456:Top2a
|
APN |
11 |
98,901,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01458:Top2a
|
APN |
11 |
98,901,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01481:Top2a
|
APN |
11 |
98,901,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01485:Top2a
|
APN |
11 |
98,901,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03029:Top2a
|
APN |
11 |
98,909,625 (GRCm39) |
missense |
probably benign |
0.03 |
PIT4581001:Top2a
|
UTSW |
11 |
98,893,790 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4585001:Top2a
|
UTSW |
11 |
98,892,199 (GRCm39) |
missense |
probably benign |
0.02 |
R0008:Top2a
|
UTSW |
11 |
98,893,729 (GRCm39) |
nonsense |
probably null |
|
R0047:Top2a
|
UTSW |
11 |
98,888,682 (GRCm39) |
missense |
probably benign |
|
R0047:Top2a
|
UTSW |
11 |
98,888,682 (GRCm39) |
missense |
probably benign |
|
R0070:Top2a
|
UTSW |
11 |
98,905,886 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0070:Top2a
|
UTSW |
11 |
98,905,886 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0116:Top2a
|
UTSW |
11 |
98,894,416 (GRCm39) |
missense |
probably benign |
0.00 |
R0245:Top2a
|
UTSW |
11 |
98,900,922 (GRCm39) |
missense |
probably benign |
0.37 |
R0276:Top2a
|
UTSW |
11 |
98,900,733 (GRCm39) |
splice site |
probably benign |
|
R0288:Top2a
|
UTSW |
11 |
98,907,249 (GRCm39) |
splice site |
probably benign |
|
R0335:Top2a
|
UTSW |
11 |
98,913,781 (GRCm39) |
missense |
probably benign |
0.08 |
R0422:Top2a
|
UTSW |
11 |
98,900,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Top2a
|
UTSW |
11 |
98,890,052 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0558:Top2a
|
UTSW |
11 |
98,887,665 (GRCm39) |
missense |
probably benign |
|
R0599:Top2a
|
UTSW |
11 |
98,892,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R0727:Top2a
|
UTSW |
11 |
98,902,974 (GRCm39) |
nonsense |
probably null |
|
R1565:Top2a
|
UTSW |
11 |
98,891,880 (GRCm39) |
missense |
probably damaging |
0.99 |
R1674:Top2a
|
UTSW |
11 |
98,900,099 (GRCm39) |
missense |
probably damaging |
0.96 |
R1844:Top2a
|
UTSW |
11 |
98,906,895 (GRCm39) |
missense |
probably benign |
0.06 |
R1959:Top2a
|
UTSW |
11 |
98,886,803 (GRCm39) |
splice site |
probably null |
|
R2124:Top2a
|
UTSW |
11 |
98,895,054 (GRCm39) |
missense |
probably benign |
0.00 |
R2128:Top2a
|
UTSW |
11 |
98,900,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R3707:Top2a
|
UTSW |
11 |
98,887,651 (GRCm39) |
missense |
probably benign |
0.13 |
R4110:Top2a
|
UTSW |
11 |
98,913,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4112:Top2a
|
UTSW |
11 |
98,913,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4423:Top2a
|
UTSW |
11 |
98,892,231 (GRCm39) |
missense |
probably benign |
0.00 |
R4425:Top2a
|
UTSW |
11 |
98,892,231 (GRCm39) |
missense |
probably benign |
0.00 |
R4914:Top2a
|
UTSW |
11 |
98,893,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4939:Top2a
|
UTSW |
11 |
98,900,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R4944:Top2a
|
UTSW |
11 |
98,888,676 (GRCm39) |
missense |
probably benign |
0.37 |
R4971:Top2a
|
UTSW |
11 |
98,884,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Top2a
|
UTSW |
11 |
98,909,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5477:Top2a
|
UTSW |
11 |
98,907,306 (GRCm39) |
nonsense |
probably null |
|
R5499:Top2a
|
UTSW |
11 |
98,913,202 (GRCm39) |
missense |
probably benign |
0.20 |
R5911:Top2a
|
UTSW |
11 |
98,907,291 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7126:Top2a
|
UTSW |
11 |
98,905,818 (GRCm39) |
missense |
probably benign |
0.09 |
R7131:Top2a
|
UTSW |
11 |
98,895,008 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7174:Top2a
|
UTSW |
11 |
98,914,922 (GRCm39) |
start gained |
probably benign |
|
R7329:Top2a
|
UTSW |
11 |
98,895,072 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7560:Top2a
|
UTSW |
11 |
98,891,663 (GRCm39) |
missense |
probably benign |
|
R7563:Top2a
|
UTSW |
11 |
98,907,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7740:Top2a
|
UTSW |
11 |
98,884,640 (GRCm39) |
missense |
probably benign |
0.34 |
R7841:Top2a
|
UTSW |
11 |
98,913,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Top2a
|
UTSW |
11 |
98,900,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Top2a
|
UTSW |
11 |
98,889,993 (GRCm39) |
missense |
probably benign |
|
R8260:Top2a
|
UTSW |
11 |
98,891,595 (GRCm39) |
missense |
probably null |
0.87 |
R8504:Top2a
|
UTSW |
11 |
98,905,567 (GRCm39) |
missense |
probably benign |
|
R8550:Top2a
|
UTSW |
11 |
98,886,744 (GRCm39) |
missense |
probably benign |
|
R8558:Top2a
|
UTSW |
11 |
98,912,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8693:Top2a
|
UTSW |
11 |
98,900,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R8851:Top2a
|
UTSW |
11 |
98,900,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R9143:Top2a
|
UTSW |
11 |
98,900,705 (GRCm39) |
missense |
probably benign |
0.14 |
R9240:Top2a
|
UTSW |
11 |
98,901,368 (GRCm39) |
nonsense |
probably null |
|
R9294:Top2a
|
UTSW |
11 |
98,891,904 (GRCm39) |
missense |
probably benign |
0.00 |
R9301:Top2a
|
UTSW |
11 |
98,897,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R9383:Top2a
|
UTSW |
11 |
98,901,884 (GRCm39) |
nonsense |
probably null |
|
R9450:Top2a
|
UTSW |
11 |
98,894,434 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9515:Top2a
|
UTSW |
11 |
98,902,970 (GRCm39) |
missense |
probably damaging |
0.99 |
R9655:Top2a
|
UTSW |
11 |
98,905,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R9683:Top2a
|
UTSW |
11 |
98,887,683 (GRCm39) |
missense |
probably benign |
0.21 |
R9689:Top2a
|
UTSW |
11 |
98,914,883 (GRCm39) |
missense |
probably benign |
0.01 |
U24488:Top2a
|
UTSW |
11 |
98,913,252 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Top2a
|
UTSW |
11 |
98,886,767 (GRCm39) |
missense |
probably benign |
0.32 |
|