Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,921,863 (GRCm39) |
C1140S |
probably damaging |
Het |
Abhd12b |
T |
C |
12: 70,229,740 (GRCm39) |
I238T |
possibly damaging |
Het |
Adgrb3 |
T |
C |
1: 25,543,991 (GRCm39) |
|
probably null |
Het |
Baz2b |
A |
T |
2: 59,788,087 (GRCm39) |
|
probably null |
Het |
Brwd3 |
T |
C |
X: 107,794,454 (GRCm39) |
Y1410C |
probably damaging |
Het |
Casp7 |
T |
A |
19: 56,421,775 (GRCm39) |
I71N |
probably damaging |
Het |
Cspg4 |
A |
T |
9: 56,804,672 (GRCm39) |
I1828F |
probably damaging |
Het |
Cul2 |
T |
C |
18: 3,426,920 (GRCm39) |
|
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,986,700 (GRCm39) |
D5409G |
possibly damaging |
Het |
Fam187a |
A |
T |
11: 102,777,380 (GRCm39) |
T395S |
probably benign |
Het |
Fcgr2b |
A |
G |
1: 170,793,297 (GRCm39) |
V244A |
possibly damaging |
Het |
Fubp1 |
A |
G |
3: 151,926,392 (GRCm39) |
E333G |
possibly damaging |
Het |
Ganab |
G |
T |
19: 8,888,391 (GRCm39) |
|
probably benign |
Het |
Hpdl |
A |
G |
4: 116,677,952 (GRCm39) |
S170P |
probably benign |
Het |
Hsd17b7 |
C |
T |
1: 169,780,649 (GRCm39) |
E320K |
probably damaging |
Het |
Klhl11 |
T |
C |
11: 100,363,047 (GRCm39) |
S170G |
possibly damaging |
Het |
Lrrc56 |
A |
G |
7: 140,777,090 (GRCm39) |
|
probably benign |
Het |
Lrrd1 |
T |
C |
5: 3,901,534 (GRCm39) |
V613A |
probably benign |
Het |
Myo1e |
T |
C |
9: 70,276,055 (GRCm39) |
F757L |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,059,169 (GRCm39) |
|
probably benign |
Het |
Myocd |
T |
A |
11: 65,069,569 (GRCm39) |
D837V |
probably damaging |
Het |
Naip6 |
T |
C |
13: 100,436,984 (GRCm39) |
Q513R |
possibly damaging |
Het |
Nol4l |
A |
G |
2: 153,371,457 (GRCm39) |
F76L |
probably benign |
Het |
Or10ak7 |
T |
C |
4: 118,792,027 (GRCm39) |
E6G |
probably benign |
Het |
Or2b2b |
T |
A |
13: 21,859,122 (GRCm39) |
|
probably benign |
Het |
Or5b98 |
T |
A |
19: 12,931,882 (GRCm39) |
S310T |
probably benign |
Het |
Pck1 |
G |
A |
2: 172,996,649 (GRCm39) |
E188K |
probably benign |
Het |
Pdcd11 |
T |
C |
19: 47,102,064 (GRCm39) |
V1083A |
possibly damaging |
Het |
Primpol |
G |
A |
8: 47,046,619 (GRCm39) |
Q226* |
probably null |
Het |
Rbm15 |
A |
C |
3: 107,233,611 (GRCm39) |
V959G |
probably benign |
Het |
Rorb |
A |
G |
19: 18,954,943 (GRCm39) |
|
probably null |
Het |
Spata9 |
T |
C |
13: 76,125,853 (GRCm39) |
L112P |
probably damaging |
Het |
Stk24 |
A |
T |
14: 121,529,527 (GRCm39) |
L375Q |
probably null |
Het |
Svip |
A |
G |
7: 51,655,509 (GRCm39) |
S11P |
possibly damaging |
Het |
Taf13 |
T |
C |
3: 108,488,500 (GRCm39) |
|
probably benign |
Het |
Tex30 |
T |
C |
1: 44,127,683 (GRCm39) |
Y7C |
probably damaging |
Het |
Tmem68 |
T |
C |
4: 3,569,361 (GRCm39) |
|
probably benign |
Het |
Tnc |
T |
C |
4: 63,918,344 (GRCm39) |
E1189G |
probably damaging |
Het |
Trav3-3 |
C |
A |
14: 53,903,822 (GRCm39) |
L47I |
probably benign |
Het |
Ttn |
G |
A |
2: 76,733,557 (GRCm39) |
|
probably benign |
Het |
Uroc1 |
A |
G |
6: 90,323,811 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Top2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00430:Top2b
|
APN |
14 |
16,422,692 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00730:Top2b
|
APN |
14 |
16,389,831 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00917:Top2b
|
APN |
14 |
16,407,354 (GRCm38) |
missense |
probably benign |
0.05 |
IGL01959:Top2b
|
APN |
14 |
16,422,695 (GRCm38) |
missense |
probably benign |
0.19 |
IGL02019:Top2b
|
APN |
14 |
16,409,965 (GRCm38) |
missense |
probably benign |
0.44 |
IGL02119:Top2b
|
APN |
14 |
16,406,733 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02136:Top2b
|
APN |
14 |
16,407,103 (GRCm38) |
unclassified |
probably benign |
|
IGL02148:Top2b
|
APN |
14 |
16,400,488 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02496:Top2b
|
APN |
14 |
16,387,335 (GRCm38) |
missense |
probably benign |
|
IGL02503:Top2b
|
APN |
14 |
16,407,163 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL02672:Top2b
|
APN |
14 |
16,409,166 (GRCm38) |
unclassified |
probably benign |
|
IGL02721:Top2b
|
APN |
14 |
16,409,236 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03252:Top2b
|
APN |
14 |
16,393,163 (GRCm38) |
missense |
possibly damaging |
0.60 |
PIT4434001:Top2b
|
UTSW |
14 |
16,423,780 (GRCm38) |
critical splice donor site |
probably null |
|
R0092:Top2b
|
UTSW |
14 |
16,409,263 (GRCm38) |
missense |
probably damaging |
1.00 |
R0201:Top2b
|
UTSW |
14 |
16,383,174 (GRCm38) |
missense |
probably damaging |
1.00 |
R0390:Top2b
|
UTSW |
14 |
16,418,442 (GRCm38) |
missense |
probably benign |
0.00 |
R0394:Top2b
|
UTSW |
14 |
16,413,556 (GRCm38) |
splice site |
probably null |
|
R1159:Top2b
|
UTSW |
14 |
16,430,329 (GRCm38) |
missense |
possibly damaging |
0.81 |
R1424:Top2b
|
UTSW |
14 |
16,383,177 (GRCm38) |
missense |
probably damaging |
1.00 |
R1519:Top2b
|
UTSW |
14 |
16,408,953 (GRCm38) |
splice site |
probably null |
|
R1561:Top2b
|
UTSW |
14 |
16,398,993 (GRCm38) |
missense |
possibly damaging |
0.80 |
R1713:Top2b
|
UTSW |
14 |
16,409,823 (GRCm38) |
missense |
probably benign |
0.05 |
R1987:Top2b
|
UTSW |
14 |
16,398,916 (GRCm38) |
missense |
probably damaging |
0.99 |
R2219:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R2287:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R2422:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R2679:Top2b
|
UTSW |
14 |
16,413,947 (GRCm38) |
missense |
probably damaging |
1.00 |
R3687:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3707:Top2b
|
UTSW |
14 |
16,388,447 (GRCm38) |
missense |
probably damaging |
1.00 |
R3810:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3812:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3815:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3816:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3818:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4023:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4025:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4026:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4133:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4157:Top2b
|
UTSW |
14 |
16,384,491 (GRCm38) |
missense |
probably benign |
0.42 |
R4179:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4180:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4300:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4376:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4377:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4492:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4549:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4550:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4581:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4582:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4628:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4630:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4667:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4668:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4669:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4698:Top2b
|
UTSW |
14 |
16,387,331 (GRCm38) |
nonsense |
probably null |
|
R4769:Top2b
|
UTSW |
14 |
16,398,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R4809:Top2b
|
UTSW |
14 |
16,383,125 (GRCm38) |
missense |
probably benign |
0.06 |
R4899:Top2b
|
UTSW |
14 |
16,387,313 (GRCm38) |
missense |
probably damaging |
1.00 |
R5035:Top2b
|
UTSW |
14 |
16,409,966 (GRCm38) |
missense |
probably benign |
0.01 |
R5621:Top2b
|
UTSW |
14 |
16,387,280 (GRCm38) |
missense |
probably damaging |
1.00 |
R5631:Top2b
|
UTSW |
14 |
16,409,882 (GRCm38) |
missense |
probably damaging |
1.00 |
R5685:Top2b
|
UTSW |
14 |
16,413,666 (GRCm38) |
missense |
probably damaging |
1.00 |
R5732:Top2b
|
UTSW |
14 |
16,400,106 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5939:Top2b
|
UTSW |
14 |
16,422,786 (GRCm38) |
missense |
probably damaging |
0.96 |
R6007:Top2b
|
UTSW |
14 |
16,423,779 (GRCm38) |
critical splice donor site |
probably null |
|
R6087:Top2b
|
UTSW |
14 |
16,409,864 (GRCm38) |
missense |
probably benign |
0.14 |
R6144:Top2b
|
UTSW |
14 |
16,423,740 (GRCm38) |
missense |
possibly damaging |
0.48 |
R6196:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R6218:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R6229:Top2b
|
UTSW |
14 |
16,409,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R6249:Top2b
|
UTSW |
14 |
16,399,006 (GRCm38) |
missense |
probably damaging |
1.00 |
R6337:Top2b
|
UTSW |
14 |
16,399,026 (GRCm38) |
missense |
possibly damaging |
0.77 |
R6353:Top2b
|
UTSW |
14 |
16,416,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R6512:Top2b
|
UTSW |
14 |
16,409,854 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6573:Top2b
|
UTSW |
14 |
16,398,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R6614:Top2b
|
UTSW |
14 |
16,407,142 (GRCm38) |
nonsense |
probably null |
|
R6844:Top2b
|
UTSW |
14 |
16,429,383 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6848:Top2b
|
UTSW |
14 |
16,409,958 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6871:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R6895:Top2b
|
UTSW |
14 |
16,413,604 (GRCm38) |
missense |
probably benign |
0.06 |
R7162:Top2b
|
UTSW |
14 |
16,416,653 (GRCm38) |
missense |
probably benign |
0.00 |
R7247:Top2b
|
UTSW |
14 |
16,416,962 (GRCm38) |
missense |
probably benign |
0.08 |
R7250:Top2b
|
UTSW |
14 |
16,420,411 (GRCm38) |
missense |
probably benign |
|
R7359:Top2b
|
UTSW |
14 |
16,407,376 (GRCm38) |
missense |
probably null |
1.00 |
R7365:Top2b
|
UTSW |
14 |
16,416,649 (GRCm38) |
missense |
probably benign |
0.04 |
R7493:Top2b
|
UTSW |
14 |
16,416,605 (GRCm38) |
missense |
probably benign |
0.00 |
R7528:Top2b
|
UTSW |
14 |
16,395,427 (GRCm38) |
nonsense |
probably null |
|
R7562:Top2b
|
UTSW |
14 |
16,412,946 (GRCm38) |
missense |
probably benign |
0.04 |
R7594:Top2b
|
UTSW |
14 |
16,428,587 (GRCm38) |
missense |
probably benign |
|
R7670:Top2b
|
UTSW |
14 |
16,416,620 (GRCm38) |
missense |
possibly damaging |
0.61 |
R7894:Top2b
|
UTSW |
14 |
16,413,081 (GRCm38) |
missense |
possibly damaging |
0.68 |
R8031:Top2b
|
UTSW |
14 |
16,412,986 (GRCm38) |
missense |
probably damaging |
0.98 |
R8150:Top2b
|
UTSW |
14 |
16,393,291 (GRCm38) |
missense |
probably damaging |
0.99 |
R8214:Top2b
|
UTSW |
14 |
16,383,177 (GRCm38) |
missense |
probably damaging |
1.00 |
R8299:Top2b
|
UTSW |
14 |
16,386,123 (GRCm38) |
missense |
possibly damaging |
0.68 |
R8977:Top2b
|
UTSW |
14 |
16,393,239 (GRCm38) |
missense |
probably benign |
0.36 |
R9562:Top2b
|
UTSW |
14 |
16,365,718 (GRCm38) |
missense |
probably benign |
0.09 |
R9565:Top2b
|
UTSW |
14 |
16,365,718 (GRCm38) |
missense |
probably benign |
0.09 |
R9798:Top2b
|
UTSW |
14 |
16,389,845 (GRCm38) |
missense |
probably damaging |
1.00 |
X0028:Top2b
|
UTSW |
14 |
16,384,499 (GRCm38) |
nonsense |
probably null |
|
Z1176:Top2b
|
UTSW |
14 |
16,395,434 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Top2b
|
UTSW |
14 |
16,416,953 (GRCm38) |
missense |
probably benign |
|
|