Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
C |
T |
5: 36,030,563 (GRCm39) |
T544M |
probably benign |
Het |
Adamts12 |
A |
G |
15: 11,270,697 (GRCm39) |
R651G |
probably benign |
Het |
Adck1 |
G |
A |
12: 88,335,203 (GRCm39) |
D30N |
possibly damaging |
Het |
Alcam |
T |
A |
16: 52,089,186 (GRCm39) |
I505F |
probably benign |
Het |
Alms1 |
T |
C |
6: 85,597,394 (GRCm39) |
L740P |
probably damaging |
Het |
Ankib1 |
C |
T |
5: 3,797,021 (GRCm39) |
D264N |
probably null |
Het |
Arid2 |
T |
G |
15: 96,299,849 (GRCm39) |
H1787Q |
probably damaging |
Het |
Asf1a |
C |
T |
10: 53,482,283 (GRCm39) |
R102* |
probably null |
Het |
Atp2b1 |
C |
A |
10: 98,858,667 (GRCm39) |
|
probably null |
Het |
Bdp1 |
T |
C |
13: 100,162,049 (GRCm39) |
D2291G |
probably benign |
Het |
Bnip5 |
T |
C |
17: 29,128,778 (GRCm39) |
D45G |
probably benign |
Het |
Brinp3 |
C |
G |
1: 146,777,748 (GRCm39) |
L732V |
possibly damaging |
Het |
Catsperg2 |
A |
G |
7: 29,397,144 (GRCm39) |
F1120L |
probably benign |
Het |
Ccdc80 |
C |
T |
16: 44,943,266 (GRCm39) |
A792V |
probably damaging |
Het |
Cdcp3 |
T |
A |
7: 130,904,426 (GRCm39) |
D2381E |
unknown |
Het |
Cenpe |
C |
T |
3: 134,954,395 (GRCm39) |
R1751W |
probably damaging |
Het |
Cenpm |
T |
C |
15: 82,125,562 (GRCm39) |
I66V |
probably benign |
Het |
Clcn4 |
A |
G |
7: 7,298,081 (GRCm39) |
W103R |
possibly damaging |
Het |
Cntn2 |
T |
C |
1: 132,454,055 (GRCm39) |
D317G |
possibly damaging |
Het |
Cwf19l1 |
G |
A |
19: 44,117,680 (GRCm39) |
T154M |
probably damaging |
Het |
Cyp2a4 |
T |
A |
7: 26,012,321 (GRCm39) |
M368K |
possibly damaging |
Het |
Dars1 |
A |
G |
1: 128,294,763 (GRCm39) |
S413P |
possibly damaging |
Het |
Dscc1 |
A |
G |
15: 54,947,581 (GRCm39) |
Y200H |
probably benign |
Het |
Dsn1 |
A |
T |
2: 156,842,792 (GRCm39) |
D183E |
probably damaging |
Het |
Etfdh |
T |
C |
3: 79,530,886 (GRCm39) |
Y45C |
probably damaging |
Het |
Fancc |
A |
T |
13: 63,550,867 (GRCm39) |
|
probably null |
Het |
Fbxo34 |
T |
A |
14: 47,767,135 (GRCm39) |
M216K |
probably benign |
Het |
Fer1l6 |
T |
G |
15: 58,432,331 (GRCm39) |
S293A |
probably benign |
Het |
Foxn1 |
T |
A |
11: 78,261,958 (GRCm39) |
E137V |
probably damaging |
Het |
Fshr |
A |
C |
17: 89,295,925 (GRCm39) |
F261V |
probably damaging |
Het |
Gabrb3 |
C |
T |
7: 57,461,926 (GRCm39) |
R153* |
probably null |
Het |
Garin1b |
T |
C |
6: 29,323,833 (GRCm39) |
V186A |
probably damaging |
Het |
Gps2 |
C |
A |
11: 69,807,308 (GRCm39) |
N321K |
probably benign |
Het |
Hdgf |
T |
C |
3: 87,813,993 (GRCm39) |
M20T |
possibly damaging |
Het |
Igdcc4 |
G |
T |
9: 65,031,306 (GRCm39) |
A415S |
probably damaging |
Het |
Kif26b |
A |
G |
1: 178,742,541 (GRCm39) |
E879G |
probably damaging |
Het |
Krt13 |
T |
C |
11: 100,010,162 (GRCm39) |
Y273C |
probably damaging |
Het |
Mab21l4 |
C |
A |
1: 93,087,689 (GRCm39) |
V55F |
probably damaging |
Het |
Mag |
A |
G |
7: 30,608,559 (GRCm39) |
V185A |
possibly damaging |
Het |
Map3k21 |
C |
T |
8: 126,665,539 (GRCm39) |
T576M |
probably damaging |
Het |
Mtcl2 |
A |
C |
2: 156,895,509 (GRCm39) |
L332R |
probably damaging |
Het |
Mtrr |
A |
G |
13: 68,714,336 (GRCm39) |
F468L |
probably damaging |
Het |
Myb |
C |
T |
10: 21,017,653 (GRCm39) |
|
probably null |
Het |
Naip5 |
T |
C |
13: 100,356,204 (GRCm39) |
Q1137R |
probably benign |
Het |
Naip5 |
G |
T |
13: 100,356,205 (GRCm39) |
Q1137K |
not run |
Het |
Nckap5l |
A |
T |
15: 99,321,166 (GRCm39) |
|
probably null |
Het |
Nop9 |
C |
T |
14: 55,986,809 (GRCm39) |
R240W |
probably benign |
Het |
Notch2 |
T |
C |
3: 98,020,430 (GRCm39) |
L775P |
probably damaging |
Het |
Or13a27 |
T |
C |
7: 139,925,143 (GRCm39) |
Y253C |
probably damaging |
Het |
Or4c116 |
C |
T |
2: 88,942,629 (GRCm39) |
V76I |
probably benign |
Het |
Or55b10 |
T |
A |
7: 102,143,227 (GRCm39) |
I252F |
possibly damaging |
Het |
Or7a40 |
T |
C |
16: 16,491,579 (GRCm39) |
N89D |
probably benign |
Het |
Or8c9 |
A |
G |
9: 38,241,239 (GRCm39) |
T116A |
probably damaging |
Het |
Oxa1l |
T |
A |
14: 54,600,934 (GRCm39) |
W136R |
probably damaging |
Het |
Palm3 |
T |
A |
8: 84,748,136 (GRCm39) |
V7E |
possibly damaging |
Het |
Pkhd1l1 |
C |
G |
15: 44,378,326 (GRCm39) |
R1027G |
possibly damaging |
Het |
Prickle2 |
A |
T |
6: 92,352,929 (GRCm39) |
*902K |
probably null |
Het |
Rassf7 |
C |
T |
7: 140,797,101 (GRCm39) |
R105* |
probably null |
Het |
Septin9 |
T |
C |
11: 117,217,337 (GRCm39) |
|
probably null |
Het |
Sorbs3 |
T |
C |
14: 70,444,976 (GRCm39) |
N34S |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,682,412 (GRCm39) |
T269A |
probably benign |
Het |
Spata20 |
T |
G |
11: 94,373,379 (GRCm39) |
K497N |
probably benign |
Het |
Speg |
A |
G |
1: 75,407,923 (GRCm39) |
D3206G |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,538,021 (GRCm39) |
T1865A |
probably damaging |
Het |
Tmc5 |
A |
T |
7: 118,222,549 (GRCm39) |
Y83F |
probably benign |
Het |
Tmem175 |
T |
A |
5: 108,789,715 (GRCm39) |
D103E |
probably damaging |
Het |
Vmn2r6 |
T |
C |
3: 64,463,941 (GRCm39) |
I298V |
probably benign |
Het |
Vmn2r69 |
T |
C |
7: 85,056,420 (GRCm39) |
I573V |
probably benign |
Het |
Vmn2r93 |
A |
G |
17: 18,518,731 (GRCm39) |
I63M |
probably benign |
Het |
Zfp568 |
G |
A |
7: 29,722,681 (GRCm39) |
R542H |
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 |
|
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 |
|
|