Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adtrp |
A |
T |
13: 41,981,622 (GRCm39) |
N82K |
probably damaging |
Het |
Ankrd36 |
T |
A |
11: 5,578,906 (GRCm39) |
S57T |
possibly damaging |
Het |
Aoc3 |
A |
G |
11: 101,222,643 (GRCm39) |
N293S |
probably benign |
Het |
Aup1 |
A |
T |
6: 83,033,602 (GRCm39) |
H302L |
probably damaging |
Het |
Bptf |
G |
A |
11: 106,931,206 (GRCm39) |
R277W |
probably damaging |
Het |
Cald1 |
A |
G |
6: 34,734,946 (GRCm39) |
I346V |
unknown |
Het |
Cd44 |
T |
C |
2: 102,664,645 (GRCm39) |
T519A |
possibly damaging |
Het |
Cela1 |
A |
G |
15: 100,580,766 (GRCm39) |
|
probably null |
Het |
Ces2g |
T |
C |
8: 105,689,195 (GRCm39) |
V57A |
possibly damaging |
Het |
Cpt1b |
G |
C |
15: 89,308,628 (GRCm39) |
T100S |
probably benign |
Het |
D6Wsu163e |
A |
T |
6: 126,932,859 (GRCm39) |
I361F |
possibly damaging |
Het |
Dock5 |
A |
T |
14: 68,083,449 (GRCm39) |
D153E |
possibly damaging |
Het |
Dync2h1 |
G |
T |
9: 7,168,326 (GRCm39) |
R430S |
probably damaging |
Het |
Dync2i2 |
T |
A |
2: 29,922,220 (GRCm39) |
T414S |
possibly damaging |
Het |
Efcab3 |
T |
A |
11: 104,695,100 (GRCm39) |
F1730L |
probably benign |
Het |
Eml5 |
C |
T |
12: 98,782,218 (GRCm39) |
G1405R |
probably damaging |
Het |
Ergic2 |
G |
A |
6: 148,102,975 (GRCm39) |
A91V |
probably damaging |
Het |
Fancl |
A |
T |
11: 26,419,754 (GRCm39) |
I336L |
probably benign |
Het |
Gon4l |
A |
G |
3: 88,807,291 (GRCm39) |
I1662V |
possibly damaging |
Het |
Gpr153 |
C |
T |
4: 152,363,558 (GRCm39) |
|
probably benign |
Het |
Hdac4 |
C |
A |
1: 91,875,239 (GRCm39) |
A911S |
probably damaging |
Het |
Ighd |
T |
C |
12: 113,378,183 (GRCm39) |
N139D |
|
Het |
Klhl22 |
T |
A |
16: 17,589,690 (GRCm39) |
L117Q |
probably damaging |
Het |
Kntc1 |
A |
G |
5: 123,928,180 (GRCm39) |
S1226G |
probably benign |
Het |
Lama5 |
A |
T |
2: 179,828,481 (GRCm39) |
C2126S |
probably damaging |
Het |
Ldlr |
A |
G |
9: 21,650,985 (GRCm39) |
I468V |
probably benign |
Het |
Lmtk3 |
G |
A |
7: 45,447,712 (GRCm39) |
A1253T |
unknown |
Het |
Lta |
T |
A |
17: 35,423,045 (GRCm39) |
N93Y |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,403,563 (GRCm39) |
|
probably null |
Het |
Mink1 |
A |
G |
11: 70,500,902 (GRCm39) |
|
probably null |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Ntpcr |
A |
G |
8: 126,472,074 (GRCm39) |
M132V |
probably benign |
Het |
Or14a257 |
A |
G |
7: 86,138,061 (GRCm39) |
S233P |
probably damaging |
Het |
Or52n1 |
A |
G |
7: 104,383,115 (GRCm39) |
M152T |
probably benign |
Het |
Or7g32 |
T |
C |
9: 19,408,098 (GRCm39) |
I18T |
probably benign |
Het |
Padi2 |
A |
G |
4: 140,660,590 (GRCm39) |
I357V |
probably benign |
Het |
Pax7 |
G |
T |
4: 139,506,920 (GRCm39) |
H372Q |
probably benign |
Het |
Paxip1 |
A |
G |
5: 27,949,541 (GRCm39) |
Y966H |
probably damaging |
Het |
Pde4b |
A |
C |
4: 102,412,822 (GRCm39) |
D199A |
probably null |
Het |
Pkd1l2 |
T |
C |
8: 117,792,311 (GRCm39) |
N494D |
probably benign |
Het |
Prdm2 |
G |
T |
4: 142,862,580 (GRCm39) |
Q237K |
probably benign |
Het |
Prune2 |
T |
C |
19: 17,097,769 (GRCm39) |
L1091P |
probably damaging |
Het |
Rab9 |
C |
T |
X: 165,240,754 (GRCm39) |
D186N |
probably benign |
Het |
Rassf5 |
A |
G |
1: 131,106,264 (GRCm39) |
*414Q |
probably null |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Rrp9 |
C |
A |
9: 106,360,388 (GRCm39) |
T238K |
probably benign |
Het |
Slc44a2 |
A |
G |
9: 21,259,882 (GRCm39) |
D630G |
probably benign |
Het |
Slc7a9 |
A |
G |
7: 35,156,443 (GRCm39) |
D295G |
probably benign |
Het |
Slco3a1 |
A |
T |
7: 73,934,054 (GRCm39) |
M706K |
possibly damaging |
Het |
Spag9 |
T |
C |
11: 93,962,514 (GRCm39) |
|
probably null |
Het |
Stam2 |
A |
T |
2: 52,590,180 (GRCm39) |
Y394N |
probably damaging |
Het |
Stard9 |
T |
C |
2: 120,510,442 (GRCm39) |
L341P |
probably damaging |
Het |
Steap3 |
A |
T |
1: 120,171,624 (GRCm39) |
H160Q |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,061,809 (GRCm39) |
C334S |
probably benign |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Thap1 |
CAGCATCTGCTCGGAGCA |
CAGCA |
8: 26,650,884 (GRCm39) |
|
probably null |
Het |
Tmem74 |
A |
T |
15: 43,731,456 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,537,480 (GRCm39) |
K34816R |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,627,735 (GRCm39) |
N14736I |
probably damaging |
Het |
Vmn1r183 |
A |
G |
7: 23,754,890 (GRCm39) |
Q231R |
possibly damaging |
Het |
Vmn1r235 |
A |
G |
17: 21,482,439 (GRCm39) |
T255A |
probably damaging |
Het |
Wasl |
A |
T |
6: 24,619,209 (GRCm39) |
I437K |
unknown |
Het |
Ywhae |
A |
G |
11: 75,642,769 (GRCm39) |
N43D |
probably damaging |
Het |
Zfp583 |
A |
T |
7: 6,320,210 (GRCm39) |
Y267* |
probably null |
Het |
Zfp608 |
C |
T |
18: 55,121,072 (GRCm39) |
G172R |
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 |
|
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 |
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 |
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 |
|