Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
C |
A |
7: 40,643,968 (GRCm39) |
P546T |
possibly damaging |
Het |
Abca13 |
T |
C |
11: 9,241,599 (GRCm39) |
I1154T |
possibly damaging |
Het |
Abca8a |
A |
G |
11: 109,969,641 (GRCm39) |
|
probably benign |
Het |
Acsm5 |
A |
T |
7: 119,136,509 (GRCm39) |
Q360L |
probably benign |
Het |
Adamtsl5 |
T |
C |
10: 80,177,612 (GRCm39) |
E350G |
probably benign |
Het |
Adgrl2 |
A |
T |
3: 148,534,125 (GRCm39) |
L1017* |
probably null |
Het |
Aqr |
T |
C |
2: 113,940,417 (GRCm39) |
D1243G |
probably damaging |
Het |
Arhgef17 |
G |
T |
7: 100,578,650 (GRCm39) |
P766Q |
possibly damaging |
Het |
Bclaf1 |
T |
C |
10: 20,201,113 (GRCm39) |
V413A |
possibly damaging |
Het |
Bcr |
A |
G |
10: 75,011,131 (GRCm39) |
D14G |
probably benign |
Het |
Cadps2 |
C |
T |
6: 23,287,731 (GRCm39) |
V1190I |
probably benign |
Het |
Cdh9 |
A |
G |
15: 16,856,086 (GRCm39) |
I709V |
possibly damaging |
Het |
Cnbd1 |
C |
A |
4: 18,887,748 (GRCm39) |
|
probably null |
Het |
Cnbd1 |
T |
A |
4: 18,887,749 (GRCm39) |
|
probably null |
Het |
Col4a3 |
T |
C |
1: 82,650,509 (GRCm39) |
|
probably benign |
Het |
Coro1a |
T |
A |
7: 126,302,288 (GRCm39) |
K20* |
probably null |
Het |
Crb2 |
T |
A |
2: 37,673,447 (GRCm39) |
D114E |
probably damaging |
Het |
Dnah6 |
C |
A |
6: 73,053,623 (GRCm39) |
K2870N |
probably benign |
Het |
Gk5 |
T |
G |
9: 96,032,533 (GRCm39) |
S248A |
possibly damaging |
Het |
Grm4 |
T |
A |
17: 27,653,635 (GRCm39) |
I772F |
probably damaging |
Het |
Gstt4 |
A |
G |
10: 75,653,073 (GRCm39) |
I163T |
possibly damaging |
Het |
Hr |
A |
G |
14: 70,795,201 (GRCm39) |
R278G |
probably damaging |
Het |
Igfbp5 |
T |
A |
1: 72,903,108 (GRCm39) |
R156* |
probably null |
Het |
Ighv1-4 |
G |
A |
12: 114,450,753 (GRCm39) |
|
probably benign |
Het |
Insyn2a |
A |
T |
7: 134,500,873 (GRCm39) |
|
probably null |
Het |
Kcna2 |
A |
C |
3: 107,012,274 (GRCm39) |
Q285P |
probably benign |
Het |
Klf5 |
A |
T |
14: 99,538,894 (GRCm39) |
R102S |
possibly damaging |
Het |
Ldb1 |
A |
T |
19: 46,022,929 (GRCm39) |
M252K |
possibly damaging |
Het |
Lrrc66 |
T |
C |
5: 73,787,009 (GRCm39) |
I114V |
possibly damaging |
Het |
Map1b |
A |
T |
13: 99,567,651 (GRCm39) |
I1690N |
unknown |
Het |
Myo1a |
A |
G |
10: 127,550,354 (GRCm39) |
T565A |
probably benign |
Het |
Nt5c |
T |
C |
11: 115,382,127 (GRCm39) |
D84G |
possibly damaging |
Het |
Pde1b |
A |
G |
15: 103,428,417 (GRCm39) |
N51S |
possibly damaging |
Het |
Pikfyve |
T |
A |
1: 65,295,180 (GRCm39) |
L1437Q |
probably damaging |
Het |
Pld5 |
C |
T |
1: 175,967,610 (GRCm39) |
V82I |
probably damaging |
Het |
Psmb6 |
T |
A |
11: 70,416,737 (GRCm39) |
N42K |
probably benign |
Het |
Slco3a1 |
G |
A |
7: 74,204,238 (GRCm39) |
S34F |
probably damaging |
Het |
Slfn9 |
A |
G |
11: 82,872,046 (GRCm39) |
Y897H |
probably benign |
Het |
Spag6l |
T |
C |
16: 16,581,033 (GRCm39) |
|
probably null |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Tmem215 |
A |
T |
4: 40,474,534 (GRCm39) |
I204F |
probably benign |
Het |
Txnl1 |
A |
G |
18: 63,807,114 (GRCm39) |
|
probably null |
Het |
Ube2q2 |
T |
A |
9: 55,070,296 (GRCm39) |
D79E |
probably benign |
Het |
Ugt2a3 |
T |
C |
5: 87,484,658 (GRCm39) |
D122G |
probably benign |
Het |
Vmn2r73 |
A |
T |
7: 85,507,383 (GRCm39) |
I643K |
probably benign |
Het |
Xkrx |
T |
A |
X: 133,051,388 (GRCm39) |
H421L |
probably benign |
Het |
|
Other mutations in Fpr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01067:Fpr3
|
APN |
17 |
18,190,828 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01520:Fpr3
|
APN |
17 |
18,191,325 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02166:Fpr3
|
APN |
17 |
18,190,726 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02587:Fpr3
|
APN |
17 |
18,190,953 (GRCm39) |
missense |
probably benign |
0.12 |
R1521:Fpr3
|
UTSW |
17 |
18,191,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Fpr3
|
UTSW |
17 |
18,190,922 (GRCm39) |
nonsense |
probably null |
|
R1913:Fpr3
|
UTSW |
17 |
18,191,670 (GRCm39) |
missense |
probably damaging |
0.96 |
R2099:Fpr3
|
UTSW |
17 |
18,191,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Fpr3
|
UTSW |
17 |
18,190,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Fpr3
|
UTSW |
17 |
18,190,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2219:Fpr3
|
UTSW |
17 |
18,191,644 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2224:Fpr3
|
UTSW |
17 |
18,191,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R2244:Fpr3
|
UTSW |
17 |
18,191,449 (GRCm39) |
missense |
probably benign |
0.03 |
R2994:Fpr3
|
UTSW |
17 |
18,191,130 (GRCm39) |
nonsense |
probably null |
|
R5364:Fpr3
|
UTSW |
17 |
18,190,806 (GRCm39) |
missense |
probably benign |
0.00 |
R6179:Fpr3
|
UTSW |
17 |
18,190,919 (GRCm39) |
nonsense |
probably null |
|
R6781:Fpr3
|
UTSW |
17 |
18,190,978 (GRCm39) |
missense |
probably benign |
0.09 |
R6909:Fpr3
|
UTSW |
17 |
18,191,429 (GRCm39) |
missense |
probably benign |
0.00 |
R7565:Fpr3
|
UTSW |
17 |
18,191,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R8008:Fpr3
|
UTSW |
17 |
18,191,715 (GRCm39) |
missense |
probably benign |
0.03 |
R8097:Fpr3
|
UTSW |
17 |
18,191,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R8351:Fpr3
|
UTSW |
17 |
18,191,436 (GRCm39) |
missense |
probably benign |
0.27 |
R8732:Fpr3
|
UTSW |
17 |
18,191,223 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8994:Fpr3
|
UTSW |
17 |
18,191,341 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9076:Fpr3
|
UTSW |
17 |
18,191,725 (GRCm39) |
missense |
probably benign |
|
R9206:Fpr3
|
UTSW |
17 |
18,191,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Fpr3
|
UTSW |
17 |
18,191,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9327:Fpr3
|
UTSW |
17 |
18,191,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9553:Fpr3
|
UTSW |
17 |
18,191,612 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Fpr3
|
UTSW |
17 |
18,191,500 (GRCm39) |
missense |
probably benign |
0.06 |
Z1176:Fpr3
|
UTSW |
17 |
18,191,255 (GRCm39) |
missense |
possibly damaging |
0.55 |
|