Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
A |
11: 110,201,101 (GRCm39) |
Y433F |
probably benign |
Het |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Anks4b |
A |
T |
7: 119,781,140 (GRCm39) |
D57V |
probably damaging |
Het |
Brwd1 |
A |
G |
16: 95,813,050 (GRCm39) |
V1486A |
probably benign |
Het |
Cd163 |
A |
G |
6: 124,294,945 (GRCm39) |
T670A |
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,174,435 (GRCm39) |
|
probably benign |
Het |
Dnajc22 |
T |
A |
15: 98,999,403 (GRCm39) |
L196Q |
probably damaging |
Het |
Dock9 |
A |
G |
14: 121,844,682 (GRCm39) |
L1097P |
possibly damaging |
Het |
Dtna |
T |
C |
18: 23,735,662 (GRCm39) |
V339A |
possibly damaging |
Het |
Dysf |
T |
A |
6: 84,165,208 (GRCm39) |
S1646T |
probably benign |
Het |
Ermp1 |
A |
T |
19: 29,589,935 (GRCm39) |
Y893N |
probably damaging |
Het |
Etv6 |
A |
T |
6: 134,199,888 (GRCm39) |
N76I |
probably damaging |
Het |
Farp2 |
T |
C |
1: 93,488,049 (GRCm39) |
V92A |
probably benign |
Het |
Fgf21 |
T |
C |
7: 45,263,605 (GRCm39) |
T158A |
probably benign |
Het |
Gcm1 |
T |
C |
9: 77,972,057 (GRCm39) |
S333P |
possibly damaging |
Het |
Itgae |
T |
C |
11: 73,016,136 (GRCm39) |
F782L |
probably benign |
Het |
Kbtbd8 |
A |
G |
6: 95,099,333 (GRCm39) |
T204A |
probably damaging |
Het |
Kcp |
A |
G |
6: 29,496,630 (GRCm39) |
C627R |
probably damaging |
Het |
Loxhd1 |
T |
C |
18: 77,529,480 (GRCm39) |
V2041A |
possibly damaging |
Het |
Mcm5 |
T |
C |
8: 75,845,929 (GRCm39) |
M379T |
possibly damaging |
Het |
Mcu |
A |
G |
10: 59,303,580 (GRCm39) |
S86P |
probably damaging |
Het |
Naa25 |
T |
C |
5: 121,546,400 (GRCm39) |
|
probably null |
Het |
Or10ag59 |
T |
A |
2: 87,405,680 (GRCm39) |
L84H |
possibly damaging |
Het |
Or5b117 |
A |
G |
19: 13,431,417 (GRCm39) |
S155P |
probably damaging |
Het |
Osbpl9 |
T |
C |
4: 108,929,158 (GRCm39) |
H400R |
probably damaging |
Het |
Pip5kl1 |
A |
G |
2: 32,470,353 (GRCm39) |
N278D |
probably damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,763,758 (GRCm39) |
T759A |
probably benign |
Het |
Psg27 |
T |
C |
7: 18,294,454 (GRCm39) |
T318A |
probably benign |
Het |
Rtkn2 |
T |
G |
10: 67,877,551 (GRCm39) |
L537R |
probably damaging |
Het |
Sdr39u1 |
C |
T |
14: 56,137,103 (GRCm39) |
|
probably null |
Het |
Slc38a1 |
A |
T |
15: 96,490,405 (GRCm39) |
I124N |
possibly damaging |
Het |
Sumf2 |
T |
A |
5: 129,888,674 (GRCm39) |
|
probably benign |
Het |
Thsd7a |
A |
G |
6: 12,324,680 (GRCm39) |
Y1464H |
probably damaging |
Het |
Unc80 |
C |
T |
1: 66,710,877 (GRCm39) |
|
probably benign |
Het |
Zfp366 |
A |
G |
13: 99,382,913 (GRCm39) |
D692G |
probably benign |
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 |
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 |
|
R3014:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|