Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace3 |
T |
C |
11: 105,888,924 (GRCm39) |
|
probably null |
Het |
Arhgdib |
A |
G |
6: 136,901,274 (GRCm39) |
Y152H |
probably benign |
Het |
Atxn10 |
T |
G |
15: 85,277,594 (GRCm39) |
S354A |
probably benign |
Het |
Cacng6 |
T |
C |
7: 3,473,401 (GRCm39) |
V75A |
possibly damaging |
Het |
Cdc23 |
A |
G |
18: 34,784,741 (GRCm39) |
V7A |
unknown |
Het |
Cdc40 |
T |
A |
10: 40,728,512 (GRCm39) |
E157D |
probably benign |
Het |
Defa25 |
T |
A |
8: 21,575,253 (GRCm39) |
N77K |
probably benign |
Het |
Dsc2 |
C |
T |
18: 20,165,331 (GRCm39) |
G881R |
possibly damaging |
Het |
Efcab3 |
T |
C |
11: 104,772,295 (GRCm39) |
V2659A |
possibly damaging |
Het |
Efcab6 |
T |
C |
15: 83,867,699 (GRCm39) |
K260E |
possibly damaging |
Het |
Eif4a3 |
T |
C |
11: 119,179,731 (GRCm39) |
Y352C |
probably damaging |
Het |
Erc2 |
A |
T |
14: 27,733,649 (GRCm39) |
K566N |
probably damaging |
Het |
Fam3b |
A |
C |
16: 97,283,052 (GRCm39) |
Y74* |
probably null |
Het |
Flg2 |
T |
A |
3: 93,127,521 (GRCm39) |
S2144R |
unknown |
Het |
Fmo4 |
G |
T |
1: 162,626,421 (GRCm39) |
S375* |
probably null |
Het |
Fsip2 |
A |
G |
2: 82,817,235 (GRCm39) |
T4323A |
probably benign |
Het |
Gm16503 |
A |
T |
4: 147,625,767 (GRCm39) |
H87L |
unknown |
Het |
Hes7 |
C |
T |
11: 69,013,591 (GRCm39) |
A150V |
probably damaging |
Het |
Hk1 |
T |
A |
10: 62,132,478 (GRCm39) |
N190I |
probably benign |
Het |
Il17rc |
A |
G |
6: 113,459,782 (GRCm39) |
D576G |
probably damaging |
Het |
Inhba |
T |
A |
13: 16,200,860 (GRCm39) |
S141T |
possibly damaging |
Het |
Itga8 |
G |
T |
2: 12,160,297 (GRCm39) |
D840E |
probably benign |
Het |
Kazn |
T |
C |
4: 141,881,862 (GRCm39) |
E126G |
|
Het |
Kcnk13 |
A |
G |
12: 99,932,438 (GRCm39) |
Y78C |
probably damaging |
Het |
Kcnt1 |
C |
A |
2: 25,798,054 (GRCm39) |
|
probably benign |
Het |
Krt42 |
G |
C |
11: 100,155,865 (GRCm39) |
R294G |
possibly damaging |
Het |
Myo9a |
A |
G |
9: 59,687,374 (GRCm39) |
K160E |
probably benign |
Het |
Nlrp1b |
T |
C |
11: 71,107,747 (GRCm39) |
R585G |
probably benign |
Het |
Ntrk2 |
T |
C |
13: 59,022,193 (GRCm39) |
I416T |
probably benign |
Het |
Or4c112 |
A |
T |
2: 88,853,972 (GRCm39) |
I125N |
probably damaging |
Het |
Or52h7 |
T |
A |
7: 104,214,316 (GRCm39) |
I296N |
probably damaging |
Het |
Or5k14 |
T |
C |
16: 58,693,054 (GRCm39) |
N153S |
probably benign |
Het |
Or8k33 |
G |
A |
2: 86,384,447 (GRCm39) |
T7I |
probably damaging |
Het |
P4ha3 |
A |
G |
7: 99,941,905 (GRCm39) |
E106G |
probably damaging |
Het |
Pcif1 |
A |
G |
2: 164,728,442 (GRCm39) |
N233S |
probably damaging |
Het |
Pgm2l1 |
C |
A |
7: 99,921,625 (GRCm39) |
R619S |
probably damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,376,230 (GRCm39) |
Q964R |
probably damaging |
Het |
Pla2g4a |
T |
A |
1: 149,776,964 (GRCm39) |
I89F |
possibly damaging |
Het |
Ppp1cc |
G |
A |
5: 122,312,151 (GRCm39) |
A306T |
probably benign |
Het |
Psmd4 |
T |
C |
3: 94,943,203 (GRCm39) |
D67G |
probably damaging |
Het |
Ptprt |
G |
A |
2: 161,977,377 (GRCm39) |
T307I |
probably damaging |
Het |
Rnf213 |
C |
A |
11: 119,321,107 (GRCm39) |
C1188* |
probably null |
Het |
Ror2 |
C |
T |
13: 53,267,193 (GRCm39) |
C426Y |
probably damaging |
Het |
Sacs |
C |
T |
14: 61,441,640 (GRCm39) |
H1229Y |
probably damaging |
Het |
Slc25a25 |
A |
T |
2: 32,311,517 (GRCm39) |
L118Q |
probably damaging |
Het |
Slc38a6 |
G |
A |
12: 73,397,377 (GRCm39) |
A340T |
probably benign |
Het |
Smarca5 |
A |
T |
8: 81,431,311 (GRCm39) |
Y969N |
probably damaging |
Het |
Sorbs1 |
C |
A |
19: 40,314,933 (GRCm39) |
M626I |
probably benign |
Het |
Spink5 |
T |
A |
18: 44,143,303 (GRCm39) |
D753E |
probably benign |
Het |
Taf1d |
T |
G |
9: 15,221,695 (GRCm39) |
I226S |
probably damaging |
Het |
Tmem225 |
A |
G |
9: 40,060,689 (GRCm39) |
I83V |
possibly damaging |
Het |
Traf3ip1 |
A |
G |
1: 91,429,141 (GRCm39) |
K303E |
probably damaging |
Het |
Ube2n |
C |
T |
10: 95,377,244 (GRCm39) |
R70C |
probably benign |
Het |
Ubl7 |
C |
T |
9: 57,830,489 (GRCm39) |
P312S |
probably damaging |
Het |
Vmn1r34 |
A |
T |
6: 66,614,165 (GRCm39) |
M191K |
probably damaging |
Het |
Vmn2r103 |
C |
T |
17: 20,013,759 (GRCm39) |
H184Y |
probably benign |
Het |
Vmn2r104 |
T |
C |
17: 20,263,048 (GRCm39) |
I138V |
probably benign |
Het |
Vmn2r49 |
T |
C |
7: 9,720,408 (GRCm39) |
E361G |
possibly damaging |
Het |
Vmn2r78 |
T |
C |
7: 86,604,075 (GRCm39) |
L751P |
probably damaging |
Het |
Zc3h13 |
T |
A |
14: 75,568,070 (GRCm39) |
I1121N |
not run |
Het |
Zfp235 |
T |
A |
7: 23,841,114 (GRCm39) |
V511E |
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 |
IGL02886:Top2b
|
APN |
14 |
16,365,688 (GRCm38) |
missense |
possibly damaging |
0.73 |
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 |
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 |
|
|