Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,429,234 (GRCm39) |
I774F |
probably benign |
Het |
Alpi |
A |
G |
1: 87,026,384 (GRCm39) |
S536P |
unknown |
Het |
Ankar |
A |
G |
1: 72,705,643 (GRCm39) |
V789A |
possibly damaging |
Het |
Atp5f1b |
C |
A |
10: 127,919,277 (GRCm39) |
Q28K |
unknown |
Het |
Brpf1 |
T |
C |
6: 113,296,050 (GRCm39) |
V781A |
probably benign |
Het |
Cd177 |
G |
A |
7: 24,451,774 (GRCm39) |
S414L |
not run |
Het |
Cimip3 |
T |
A |
17: 47,747,661 (GRCm39) |
E28V |
probably damaging |
Het |
Clca3b |
T |
A |
3: 144,550,370 (GRCm39) |
T192S |
probably benign |
Het |
Coro2a |
A |
T |
4: 46,551,349 (GRCm39) |
S119T |
probably damaging |
Het |
Cpped1 |
T |
C |
16: 11,646,260 (GRCm39) |
N164S |
probably damaging |
Het |
Crybg2 |
T |
A |
4: 133,818,415 (GRCm39) |
N1390K |
probably damaging |
Het |
Epn2 |
C |
T |
11: 61,437,492 (GRCm39) |
A27T |
probably damaging |
Het |
Esp34 |
T |
C |
17: 38,870,490 (GRCm39) |
F128S |
possibly damaging |
Het |
Evpl |
T |
A |
11: 116,121,298 (GRCm39) |
N410Y |
probably null |
Het |
Flnb |
A |
G |
14: 7,892,155 (GRCm38) |
Y608C |
probably damaging |
Het |
Frem2 |
T |
A |
3: 53,560,331 (GRCm39) |
N1392I |
probably damaging |
Het |
Garin2 |
T |
A |
12: 78,761,817 (GRCm39) |
D160E |
probably benign |
Het |
Gpi1 |
G |
T |
7: 33,917,726 (GRCm39) |
N249K |
probably damaging |
Het |
Gpr87 |
T |
C |
3: 59,087,466 (GRCm39) |
N13S |
probably benign |
Het |
Gys2 |
T |
C |
6: 142,400,243 (GRCm39) |
T323A |
probably damaging |
Het |
Iqgap3 |
T |
C |
3: 88,016,770 (GRCm39) |
I1084T |
probably damaging |
Het |
Lrfn4 |
C |
G |
19: 4,663,565 (GRCm39) |
G323A |
probably benign |
Het |
Lrrc4c |
A |
T |
2: 97,460,594 (GRCm39) |
S407C |
possibly damaging |
Het |
Map3k20 |
A |
T |
2: 72,268,613 (GRCm39) |
Q540L |
probably benign |
Het |
Myom1 |
T |
C |
17: 71,407,057 (GRCm39) |
V1158A |
probably benign |
Het |
Ncor2 |
T |
C |
5: 125,144,983 (GRCm39) |
D378G |
unknown |
Het |
Nhsl1 |
T |
A |
10: 18,284,186 (GRCm39) |
D42E |
probably damaging |
Het |
Nr0b2 |
C |
A |
4: 133,283,339 (GRCm39) |
A192E |
probably benign |
Het |
Nt5c1b |
A |
G |
12: 10,425,000 (GRCm39) |
D182G |
possibly damaging |
Het |
Or12d14-ps1 |
T |
C |
17: 37,673,265 (GRCm39) |
S86P |
probably damaging |
Het |
Or4c115 |
A |
T |
2: 88,928,059 (GRCm39) |
C71S |
probably benign |
Het |
Or5b119 |
T |
C |
19: 13,457,170 (GRCm39) |
T131A |
probably benign |
Het |
Or5k15 |
T |
C |
16: 58,710,251 (GRCm39) |
T111A |
probably benign |
Het |
Or8b12 |
A |
T |
9: 37,658,089 (GRCm39) |
I220F |
probably damaging |
Het |
Pepd |
A |
G |
7: 34,721,126 (GRCm39) |
N250S |
probably benign |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Pmp22 |
C |
T |
11: 63,049,233 (GRCm39) |
R159C |
probably damaging |
Het |
Pou3f1 |
C |
T |
4: 124,552,764 (GRCm39) |
A422V |
unknown |
Het |
Rab11fip3 |
A |
G |
17: 26,286,956 (GRCm39) |
L399P |
probably damaging |
Het |
Rragc |
A |
G |
4: 123,829,340 (GRCm39) |
D352G |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,671,980 (GRCm39) |
V3420A |
probably benign |
Het |
Sez6 |
T |
A |
11: 77,864,082 (GRCm39) |
Y521* |
probably null |
Het |
Smc4 |
T |
C |
3: 68,914,645 (GRCm39) |
V86A |
probably damaging |
Het |
Stap2 |
T |
A |
17: 56,304,790 (GRCm39) |
M331L |
probably benign |
Het |
Syt8 |
G |
A |
7: 141,992,259 (GRCm39) |
R89H |
probably benign |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Trim21 |
G |
T |
7: 102,209,183 (GRCm39) |
T280K |
probably benign |
Het |
Trim36 |
C |
A |
18: 46,305,556 (GRCm39) |
V476F |
probably benign |
Het |
Troap |
G |
T |
15: 98,973,511 (GRCm39) |
R56L |
probably benign |
Het |
Ttn |
A |
T |
2: 76,667,130 (GRCm39) |
I11492K |
unknown |
Het |
Tuft1 |
T |
C |
3: 94,521,440 (GRCm39) |
T390A |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 84,020,640 (GRCm39) |
I150T |
probably benign |
Het |
Usp17lb |
A |
T |
7: 104,490,481 (GRCm39) |
C149S |
possibly damaging |
Het |
Vmn1r159 |
A |
T |
7: 22,542,665 (GRCm39) |
N122K |
possibly damaging |
Het |
Vmn1r237 |
T |
C |
17: 21,534,456 (GRCm39) |
C60R |
probably damaging |
Het |
Wdr12 |
A |
T |
1: 60,128,494 (GRCm39) |
Y85* |
probably null |
Het |
Wdr3 |
T |
C |
3: 100,062,252 (GRCm39) |
D221G |
probably benign |
Het |
Wdr97 |
G |
A |
15: 76,244,832 (GRCm39) |
E1125K |
|
Het |
Zan |
T |
C |
5: 137,403,624 (GRCm39) |
E3974G |
unknown |
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 |
|
IGL02380:Fpr3
|
APN |
17 |
18,191,254 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|