Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Angpt4 |
G |
T |
2: 151,771,517 (GRCm39) |
V278L |
probably benign |
Het |
Dmbt1 |
A |
G |
7: 130,633,827 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,321,304 (GRCm39) |
N3921K |
probably benign |
Het |
Duxf4 |
G |
A |
10: 58,071,356 (GRCm39) |
T286I |
possibly damaging |
Het |
Fam193a |
A |
T |
5: 34,623,016 (GRCm39) |
E1201D |
probably benign |
Het |
Gm10220 |
G |
C |
5: 26,322,826 (GRCm39) |
D195E |
probably damaging |
Het |
Gmps |
A |
G |
3: 63,922,857 (GRCm39) |
K607E |
possibly damaging |
Het |
Gprin1 |
T |
A |
13: 54,886,288 (GRCm39) |
D662V |
probably benign |
Het |
Gria4 |
A |
G |
9: 4,464,294 (GRCm39) |
I556T |
probably damaging |
Het |
Hcar2 |
A |
T |
5: 124,002,768 (GRCm39) |
V245E |
probably damaging |
Het |
Hmces |
T |
G |
6: 87,894,823 (GRCm39) |
D62E |
probably benign |
Het |
Ighv1-4 |
T |
A |
12: 114,450,769 (GRCm39) |
Y113F |
possibly damaging |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Kng1 |
C |
T |
16: 22,898,120 (GRCm39) |
H507Y |
possibly damaging |
Het |
Lypd10 |
A |
G |
7: 24,412,821 (GRCm39) |
I76M |
possibly damaging |
Het |
Map3k5 |
A |
T |
10: 19,970,175 (GRCm39) |
Y694F |
probably damaging |
Het |
Myo1a |
T |
G |
10: 127,552,214 (GRCm39) |
F778V |
probably damaging |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Or1ad1 |
A |
G |
11: 50,875,534 (GRCm39) |
D2G |
probably benign |
Het |
Or4l1 |
G |
A |
14: 50,166,489 (GRCm39) |
H171Y |
probably benign |
Het |
Or6aa1 |
A |
G |
7: 86,043,884 (GRCm39) |
V274A |
probably benign |
Het |
Or6z6 |
A |
T |
7: 6,491,470 (GRCm39) |
Y134* |
probably null |
Het |
Parp3 |
C |
A |
9: 106,348,514 (GRCm39) |
S507I |
possibly damaging |
Het |
Ppip5k2 |
T |
A |
1: 97,671,800 (GRCm39) |
T491S |
probably damaging |
Het |
Psmg1 |
T |
A |
16: 95,781,248 (GRCm39) |
I266F |
probably damaging |
Het |
Ptpn23 |
T |
C |
9: 110,218,763 (GRCm39) |
T476A |
probably benign |
Het |
Rttn |
G |
C |
18: 89,032,744 (GRCm39) |
V671L |
probably damaging |
Het |
Srsf7 |
T |
C |
17: 80,508,990 (GRCm39) |
E235G |
unknown |
Het |
Sv2a |
G |
A |
3: 96,096,751 (GRCm39) |
W416* |
probably null |
Het |
Tas2r107 |
A |
G |
6: 131,636,972 (GRCm39) |
Y26H |
probably benign |
Het |
Tenm2 |
T |
C |
11: 35,914,800 (GRCm39) |
T2245A |
probably damaging |
Het |
Vmn2r13 |
T |
A |
5: 109,319,627 (GRCm39) |
H451L |
possibly damaging |
Het |
Xkr6 |
T |
C |
14: 64,056,793 (GRCm39) |
Y235H |
unknown |
Het |
|
Other mutations in Grm7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01729:Grm7
|
APN |
6 |
111,223,145 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02058:Grm7
|
APN |
6 |
111,335,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Grm7
|
APN |
6 |
111,335,919 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Grm7
|
APN |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03074:Grm7
|
APN |
6 |
111,472,604 (GRCm39) |
splice site |
probably null |
|
IGL03185:Grm7
|
APN |
6 |
110,623,183 (GRCm39) |
missense |
possibly damaging |
0.84 |
Appropriated
|
UTSW |
6 |
111,472,642 (GRCm39) |
missense |
possibly damaging |
0.64 |
Consumed
|
UTSW |
6 |
111,335,836 (GRCm39) |
missense |
probably damaging |
1.00 |
Devoured
|
UTSW |
6 |
111,335,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Ravaged
|
UTSW |
6 |
111,335,874 (GRCm39) |
missense |
probably damaging |
1.00 |
shaky
|
UTSW |
6 |
111,472,752 (GRCm39) |
nonsense |
probably null |
|
PIT4651001:Grm7
|
UTSW |
6 |
110,623,050 (GRCm39) |
missense |
probably benign |
|
R0539:Grm7
|
UTSW |
6 |
111,336,055 (GRCm39) |
splice site |
probably benign |
|
R0622:Grm7
|
UTSW |
6 |
111,335,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Grm7
|
UTSW |
6 |
111,335,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Grm7
|
UTSW |
6 |
111,472,752 (GRCm39) |
nonsense |
probably null |
|
R1823:Grm7
|
UTSW |
6 |
111,184,730 (GRCm39) |
missense |
probably benign |
0.17 |
R1864:Grm7
|
UTSW |
6 |
111,057,384 (GRCm39) |
missense |
probably benign |
0.03 |
R1894:Grm7
|
UTSW |
6 |
111,335,568 (GRCm39) |
missense |
probably benign |
|
R1987:Grm7
|
UTSW |
6 |
110,891,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Grm7
|
UTSW |
6 |
111,184,769 (GRCm39) |
missense |
probably benign |
0.13 |
R2138:Grm7
|
UTSW |
6 |
110,623,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Grm7
|
UTSW |
6 |
111,335,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2289:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2296:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2339:Grm7
|
UTSW |
6 |
111,472,642 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2847:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2879:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2921:Grm7
|
UTSW |
6 |
111,472,866 (GRCm39) |
splice site |
probably null |
|
R2923:Grm7
|
UTSW |
6 |
111,472,866 (GRCm39) |
splice site |
probably null |
|
R3015:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3703:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4009:Grm7
|
UTSW |
6 |
111,472,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Grm7
|
UTSW |
6 |
110,891,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R4131:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4132:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4161:Grm7
|
UTSW |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R4329:Grm7
|
UTSW |
6 |
110,891,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4357:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4359:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Grm7
|
UTSW |
6 |
111,223,335 (GRCm39) |
missense |
probably benign |
0.05 |
R4380:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Grm7
|
UTSW |
6 |
111,335,265 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4518:Grm7
|
UTSW |
6 |
110,891,507 (GRCm39) |
splice site |
probably null |
|
R4647:Grm7
|
UTSW |
6 |
110,891,344 (GRCm39) |
nonsense |
probably null |
|
R4714:Grm7
|
UTSW |
6 |
111,057,383 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4775:Grm7
|
UTSW |
6 |
110,891,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Grm7
|
UTSW |
6 |
111,335,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:Grm7
|
UTSW |
6 |
111,057,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R5062:Grm7
|
UTSW |
6 |
110,623,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Grm7
|
UTSW |
6 |
111,335,182 (GRCm39) |
missense |
probably benign |
0.01 |
R5431:Grm7
|
UTSW |
6 |
111,335,387 (GRCm39) |
missense |
probably benign |
|
R6026:Grm7
|
UTSW |
6 |
111,478,500 (GRCm39) |
nonsense |
probably null |
|
R6174:Grm7
|
UTSW |
6 |
111,223,258 (GRCm39) |
missense |
probably benign |
|
R6305:Grm7
|
UTSW |
6 |
111,335,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Grm7
|
UTSW |
6 |
111,335,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6440:Grm7
|
UTSW |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R6519:Grm7
|
UTSW |
6 |
111,184,713 (GRCm39) |
missense |
probably benign |
0.00 |
R6531:Grm7
|
UTSW |
6 |
111,335,386 (GRCm39) |
missense |
probably benign |
0.29 |
R6888:Grm7
|
UTSW |
6 |
111,335,314 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6949:Grm7
|
UTSW |
6 |
111,472,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Grm7
|
UTSW |
6 |
110,623,265 (GRCm39) |
missense |
probably benign |
0.03 |
R6989:Grm7
|
UTSW |
6 |
111,184,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:Grm7
|
UTSW |
6 |
111,335,113 (GRCm39) |
missense |
probably benign |
0.04 |
R7203:Grm7
|
UTSW |
6 |
111,335,530 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7208:Grm7
|
UTSW |
6 |
111,335,530 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7217:Grm7
|
UTSW |
6 |
111,335,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Grm7
|
UTSW |
6 |
110,623,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R7297:Grm7
|
UTSW |
6 |
110,622,974 (GRCm39) |
missense |
probably benign |
0.16 |
R7470:Grm7
|
UTSW |
6 |
111,478,476 (GRCm39) |
missense |
|
|
R7567:Grm7
|
UTSW |
6 |
111,335,722 (GRCm39) |
missense |
probably damaging |
0.96 |
R7806:Grm7
|
UTSW |
6 |
111,223,314 (GRCm39) |
nonsense |
probably null |
|
R8018:Grm7
|
UTSW |
6 |
111,184,737 (GRCm39) |
missense |
probably benign |
0.01 |
R8076:Grm7
|
UTSW |
6 |
111,543,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R8409:Grm7
|
UTSW |
6 |
110,891,297 (GRCm39) |
missense |
probably benign |
0.02 |
R8420:Grm7
|
UTSW |
6 |
111,057,315 (GRCm39) |
missense |
probably benign |
|
R8523:Grm7
|
UTSW |
6 |
111,223,280 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8816:Grm7
|
UTSW |
6 |
111,230,966 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8958:Grm7
|
UTSW |
6 |
111,472,783 (GRCm39) |
missense |
probably damaging |
0.96 |
R9135:Grm7
|
UTSW |
6 |
111,472,729 (GRCm39) |
missense |
probably benign |
0.39 |
R9207:Grm7
|
UTSW |
6 |
111,335,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Grm7
|
UTSW |
6 |
110,622,869 (GRCm39) |
missense |
probably benign |
0.01 |
R9438:Grm7
|
UTSW |
6 |
111,231,077 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9448:Grm7
|
UTSW |
6 |
111,335,193 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Grm7
|
UTSW |
6 |
111,335,451 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Grm7
|
UTSW |
6 |
111,335,110 (GRCm39) |
missense |
probably benign |
0.01 |
|