Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
C |
T |
6: 92,885,527 (GRCm39) |
R416Q |
possibly damaging |
Het |
Adgre1 |
C |
A |
17: 57,713,859 (GRCm39) |
D181E |
probably benign |
Het |
Arhgap24 |
T |
C |
5: 103,028,652 (GRCm39) |
S183P |
probably damaging |
Het |
Asb1 |
T |
C |
1: 91,474,748 (GRCm39) |
L90P |
probably damaging |
Het |
Bmp3 |
T |
C |
5: 99,020,209 (GRCm39) |
F211L |
probably benign |
Het |
C8a |
A |
G |
4: 104,703,139 (GRCm39) |
I306T |
probably benign |
Het |
Cdkn3 |
G |
A |
14: 47,007,373 (GRCm39) |
G177R |
probably damaging |
Het |
Chat |
A |
G |
14: 32,170,984 (GRCm39) |
S172P |
probably damaging |
Het |
Chd5 |
CAAGAAGAAGAAGAAGAA |
CAAGAAGAAGAAGAA |
4: 152,438,078 (GRCm39) |
|
probably benign |
Het |
Cyp4a12a |
T |
C |
4: 115,184,420 (GRCm39) |
I265T |
probably damaging |
Het |
Dlst |
T |
A |
12: 85,165,664 (GRCm39) |
|
probably null |
Het |
Dnmt1 |
A |
T |
9: 20,837,716 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
C |
T |
2: 125,205,800 (GRCm39) |
E1066K |
probably damaging |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Fstl1 |
T |
A |
16: 37,641,538 (GRCm39) |
S105T |
probably benign |
Het |
Gm19410 |
C |
G |
8: 36,276,518 (GRCm39) |
A1725G |
probably benign |
Het |
Hspb7 |
A |
G |
4: 141,151,215 (GRCm39) |
N119S |
probably damaging |
Het |
Il20 |
T |
A |
1: 130,838,478 (GRCm39) |
D73V |
possibly damaging |
Het |
Insrr |
T |
C |
3: 87,716,608 (GRCm39) |
I612T |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 23,359,105 (GRCm39) |
Y1107C |
probably benign |
Het |
Klhl32 |
A |
G |
4: 24,792,615 (GRCm39) |
|
probably null |
Het |
Krt77 |
C |
A |
15: 101,769,351 (GRCm39) |
R470L |
possibly damaging |
Het |
Muc1 |
T |
C |
3: 89,139,336 (GRCm39) |
Y579H |
probably damaging |
Het |
Myof |
T |
C |
19: 37,966,132 (GRCm39) |
D396G |
probably damaging |
Het |
Myom1 |
T |
G |
17: 71,417,746 (GRCm39) |
D1316E |
probably damaging |
Het |
Nbea |
T |
C |
3: 55,912,538 (GRCm39) |
E1083G |
probably benign |
Het |
Nek9 |
G |
A |
12: 85,359,859 (GRCm39) |
A531V |
probably benign |
Het |
Nlrp12 |
A |
T |
7: 3,290,002 (GRCm39) |
I170N |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,784,002 (GRCm39) |
I1093T |
probably benign |
Het |
Ovch2 |
G |
A |
7: 107,388,318 (GRCm39) |
L421F |
probably damaging |
Het |
Paqr4 |
T |
C |
17: 23,958,968 (GRCm39) |
D11G |
probably damaging |
Het |
Parp8 |
A |
G |
13: 117,014,134 (GRCm39) |
S561P |
probably damaging |
Het |
Pcgf5 |
T |
A |
19: 36,420,306 (GRCm39) |
F179L |
probably damaging |
Het |
Pde4d |
A |
T |
13: 110,084,876 (GRCm39) |
Q422L |
probably damaging |
Het |
Pigs |
T |
A |
11: 78,232,651 (GRCm39) |
V495E |
probably damaging |
Het |
Polh |
C |
T |
17: 46,498,959 (GRCm39) |
R252H |
probably benign |
Het |
Psg28 |
T |
C |
7: 18,160,107 (GRCm39) |
D363G |
possibly damaging |
Het |
Ptgir |
A |
T |
7: 16,640,815 (GRCm39) |
I36F |
possibly damaging |
Het |
Ptprr |
G |
A |
10: 116,072,668 (GRCm39) |
|
probably null |
Het |
Rax |
C |
T |
18: 66,068,418 (GRCm39) |
G229D |
unknown |
Het |
Secisbp2l |
T |
A |
2: 125,615,136 (GRCm39) |
H163L |
probably benign |
Het |
Sf3a2 |
A |
G |
10: 80,637,297 (GRCm39) |
Y45C |
probably damaging |
Het |
Sgo2a |
C |
T |
1: 58,055,775 (GRCm39) |
T653I |
possibly damaging |
Het |
Slc38a9 |
A |
T |
13: 112,806,231 (GRCm39) |
I26F |
probably damaging |
Het |
Slc5a8 |
A |
G |
10: 88,722,436 (GRCm39) |
I90V |
probably benign |
Het |
Slx4 |
G |
A |
16: 3,803,911 (GRCm39) |
H968Y |
possibly damaging |
Het |
Stam2 |
T |
C |
2: 52,599,611 (GRCm39) |
T233A |
probably benign |
Het |
Tln1 |
G |
C |
4: 43,555,052 (GRCm39) |
F259L |
probably damaging |
Het |
Trav4-2 |
G |
A |
14: 53,655,866 (GRCm39) |
V8M |
possibly damaging |
Het |
Ttll5 |
T |
A |
12: 85,878,729 (GRCm39) |
H45Q |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,714,762 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
A |
1: 188,051,217 (GRCm39) |
F234L |
possibly damaging |
Het |
Vmn2r74 |
T |
A |
7: 85,607,526 (GRCm39) |
|
probably null |
Het |
Wdr6 |
CTG |
C |
9: 108,450,994 (GRCm39) |
|
probably null |
Het |
Zfp644 |
A |
G |
5: 106,783,291 (GRCm39) |
S997P |
possibly damaging |
Het |
|
Other mutations in Zfp853 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1656:Zfp853
|
UTSW |
5 |
143,274,840 (GRCm39) |
splice site |
probably benign |
|
R2072:Zfp853
|
UTSW |
5 |
143,275,137 (GRCm39) |
missense |
unknown |
|
R2915:Zfp853
|
UTSW |
5 |
143,275,332 (GRCm39) |
missense |
unknown |
|
R4862:Zfp853
|
UTSW |
5 |
143,275,416 (GRCm39) |
missense |
unknown |
|
R4869:Zfp853
|
UTSW |
5 |
143,274,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R4945:Zfp853
|
UTSW |
5 |
143,274,584 (GRCm39) |
missense |
unknown |
|
R5139:Zfp853
|
UTSW |
5 |
143,274,570 (GRCm39) |
missense |
unknown |
|
R5335:Zfp853
|
UTSW |
5 |
143,274,318 (GRCm39) |
missense |
unknown |
|
R5426:Zfp853
|
UTSW |
5 |
143,274,624 (GRCm39) |
missense |
unknown |
|
R5844:Zfp853
|
UTSW |
5 |
143,274,424 (GRCm39) |
missense |
unknown |
|
R5845:Zfp853
|
UTSW |
5 |
143,274,424 (GRCm39) |
missense |
unknown |
|
R5847:Zfp853
|
UTSW |
5 |
143,274,424 (GRCm39) |
missense |
unknown |
|
R6039:Zfp853
|
UTSW |
5 |
143,274,529 (GRCm39) |
nonsense |
probably null |
|
R7124:Zfp853
|
UTSW |
5 |
143,275,362 (GRCm39) |
missense |
unknown |
|
R7283:Zfp853
|
UTSW |
5 |
143,273,493 (GRCm39) |
missense |
unknown |
|
R7323:Zfp853
|
UTSW |
5 |
143,275,110 (GRCm39) |
missense |
unknown |
|
R8026:Zfp853
|
UTSW |
5 |
143,274,280 (GRCm39) |
missense |
unknown |
|
R8121:Zfp853
|
UTSW |
5 |
143,274,018 (GRCm39) |
missense |
probably damaging |
0.99 |
R8290:Zfp853
|
UTSW |
5 |
143,274,826 (GRCm39) |
nonsense |
probably null |
|
R8347:Zfp853
|
UTSW |
5 |
143,274,702 (GRCm39) |
missense |
unknown |
|
R9017:Zfp853
|
UTSW |
5 |
143,274,243 (GRCm39) |
missense |
unknown |
|
R9110:Zfp853
|
UTSW |
5 |
143,275,320 (GRCm39) |
missense |
unknown |
|
R9123:Zfp853
|
UTSW |
5 |
143,274,496 (GRCm39) |
nonsense |
probably null |
|
R9560:Zfp853
|
UTSW |
5 |
143,275,080 (GRCm39) |
missense |
unknown |
|
|