Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
T |
6: 121,622,212 (GRCm39) |
V372F |
probably benign |
Het |
Adcy10 |
G |
A |
1: 165,347,464 (GRCm39) |
C393Y |
probably damaging |
Het |
Adgrg7 |
A |
C |
16: 56,550,669 (GRCm39) |
I681S |
possibly damaging |
Het |
Akap8l |
T |
C |
17: 32,540,485 (GRCm39) |
|
probably benign |
Het |
Akr1a1 |
A |
T |
4: 116,497,092 (GRCm39) |
V156E |
probably damaging |
Het |
Alk |
T |
G |
17: 72,202,734 (GRCm39) |
D1167A |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,620,453 (GRCm39) |
|
probably null |
Het |
Aspm |
T |
A |
1: 139,385,221 (GRCm39) |
N288K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,398,133 (GRCm39) |
|
probably null |
Het |
Asxl2 |
G |
A |
12: 3,524,618 (GRCm39) |
|
probably null |
Het |
Atp6v0a1 |
A |
G |
11: 100,946,413 (GRCm39) |
H802R |
probably damaging |
Het |
B4galnt1 |
A |
G |
10: 127,007,691 (GRCm39) |
T531A |
possibly damaging |
Het |
Cecr2 |
A |
G |
6: 120,733,530 (GRCm39) |
N506D |
possibly damaging |
Het |
Crebrf |
T |
C |
17: 26,978,839 (GRCm39) |
V509A |
probably damaging |
Het |
Cyp4f40 |
A |
T |
17: 32,894,590 (GRCm39) |
I413F |
probably null |
Het |
Defb12 |
C |
A |
8: 19,164,342 (GRCm39) |
|
probably null |
Het |
Dnah2 |
T |
C |
11: 69,312,674 (GRCm39) |
E4297G |
probably damaging |
Het |
Dpysl5 |
A |
T |
5: 30,948,857 (GRCm39) |
N371Y |
probably damaging |
Het |
Eef1d |
G |
T |
15: 75,775,038 (GRCm39) |
T207N |
probably benign |
Het |
Esrrb |
C |
T |
12: 86,565,783 (GRCm39) |
Q416* |
probably null |
Het |
Exd2 |
T |
C |
12: 80,536,222 (GRCm39) |
L284P |
probably damaging |
Het |
Fat3 |
T |
A |
9: 16,287,739 (GRCm39) |
I595F |
probably benign |
Het |
Gm9920 |
A |
G |
15: 54,972,371 (GRCm39) |
|
probably benign |
Het |
Hephl1 |
T |
C |
9: 14,981,084 (GRCm39) |
K783E |
probably damaging |
Het |
Irs2 |
A |
G |
8: 11,055,277 (GRCm39) |
S1052P |
probably benign |
Het |
Kctd18 |
T |
C |
1: 58,002,252 (GRCm39) |
I192V |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,586,803 (GRCm39) |
D722G |
probably damaging |
Het |
Lepr |
T |
C |
4: 101,672,216 (GRCm39) |
V1080A |
possibly damaging |
Het |
Lpin1 |
C |
T |
12: 16,613,656 (GRCm39) |
G504S |
probably damaging |
Het |
Lrit2 |
A |
C |
14: 36,791,140 (GRCm39) |
Q273P |
possibly damaging |
Het |
Mlkl |
T |
A |
8: 112,054,569 (GRCm39) |
E189D |
probably benign |
Het |
Mttp |
C |
T |
3: 137,810,790 (GRCm39) |
R608H |
probably benign |
Het |
Nav2 |
T |
C |
7: 49,238,908 (GRCm39) |
V2011A |
probably benign |
Het |
Nos2 |
A |
T |
11: 78,848,317 (GRCm39) |
I1075F |
probably benign |
Het |
Npat |
A |
G |
9: 53,461,336 (GRCm39) |
|
probably null |
Het |
Nucks1 |
T |
C |
1: 131,846,771 (GRCm39) |
F16L |
probably damaging |
Het |
Nus1 |
T |
C |
10: 52,305,309 (GRCm39) |
S150P |
possibly damaging |
Het |
Odad1 |
C |
T |
7: 45,591,506 (GRCm39) |
R257* |
probably null |
Het |
Oga |
A |
T |
19: 45,746,461 (GRCm39) |
Y779* |
probably null |
Het |
Or4c123 |
G |
T |
2: 89,127,506 (GRCm39) |
T36K |
probably damaging |
Het |
Or8b35 |
A |
T |
9: 37,903,908 (GRCm39) |
Y40F |
probably benign |
Het |
Pclo |
A |
G |
5: 14,731,367 (GRCm39) |
T3290A |
unknown |
Het |
Pign |
A |
T |
1: 105,585,537 (GRCm39) |
F4Y |
probably benign |
Het |
Rfx4 |
A |
G |
10: 84,696,406 (GRCm39) |
N233D |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,397,652 (GRCm39) |
M1325L |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Scaf11 |
T |
A |
15: 96,315,001 (GRCm39) |
H1227L |
possibly damaging |
Het |
Sec31b |
G |
T |
19: 44,507,076 (GRCm39) |
P840T |
probably damaging |
Het |
Slc16a9 |
T |
A |
10: 70,118,958 (GRCm39) |
L426I |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc34a1 |
T |
C |
13: 23,996,575 (GRCm39) |
S27P |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,299 (GRCm39) |
S310P |
possibly damaging |
Het |
Tmem245 |
G |
A |
4: 56,947,084 (GRCm39) |
R110C |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,735,152 (GRCm39) |
Y953C |
probably damaging |
Het |
Trpm7 |
C |
A |
2: 126,684,775 (GRCm39) |
|
probably null |
Het |
Ush2a |
G |
A |
1: 188,644,320 (GRCm39) |
V4561I |
probably benign |
Het |
Vmn2r66 |
A |
T |
7: 84,656,026 (GRCm39) |
I330N |
probably damaging |
Het |
Vmn2r99 |
T |
C |
17: 19,599,531 (GRCm39) |
V405A |
probably damaging |
Het |
Wdhd1 |
A |
C |
14: 47,509,678 (GRCm39) |
V172G |
probably benign |
Het |
Zfhx3 |
C |
T |
8: 109,677,817 (GRCm39) |
R2956C |
possibly damaging |
Het |
Zfp446 |
T |
C |
7: 12,716,178 (GRCm39) |
L283P |
possibly damaging |
Het |
Zfp82 |
T |
C |
7: 29,756,591 (GRCm39) |
K164E |
probably damaging |
Het |
|
Other mutations in Vmn1r192 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01410:Vmn1r192
|
APN |
13 |
22,372,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01869:Vmn1r192
|
APN |
13 |
22,371,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R0975:Vmn1r192
|
UTSW |
13 |
22,371,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Vmn1r192
|
UTSW |
13 |
22,371,441 (GRCm39) |
missense |
probably benign |
0.08 |
R1767:Vmn1r192
|
UTSW |
13 |
22,371,441 (GRCm39) |
missense |
probably benign |
0.08 |
R1880:Vmn1r192
|
UTSW |
13 |
22,371,764 (GRCm39) |
missense |
probably benign |
0.12 |
R1881:Vmn1r192
|
UTSW |
13 |
22,371,764 (GRCm39) |
missense |
probably benign |
0.12 |
R2113:Vmn1r192
|
UTSW |
13 |
22,371,800 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4290:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4292:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4294:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4295:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Vmn1r192
|
UTSW |
13 |
22,371,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Vmn1r192
|
UTSW |
13 |
22,371,384 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6181:Vmn1r192
|
UTSW |
13 |
22,371,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Vmn1r192
|
UTSW |
13 |
22,372,000 (GRCm39) |
missense |
probably benign |
0.08 |
R6860:Vmn1r192
|
UTSW |
13 |
22,372,122 (GRCm39) |
missense |
probably benign |
|
R7246:Vmn1r192
|
UTSW |
13 |
22,371,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Vmn1r192
|
UTSW |
13 |
22,371,845 (GRCm39) |
missense |
probably damaging |
0.97 |
R8066:Vmn1r192
|
UTSW |
13 |
22,371,565 (GRCm39) |
nonsense |
probably null |
|
R8378:Vmn1r192
|
UTSW |
13 |
22,372,029 (GRCm39) |
nonsense |
probably null |
|
R9075:Vmn1r192
|
UTSW |
13 |
22,371,333 (GRCm39) |
missense |
probably benign |
|
R9206:Vmn1r192
|
UTSW |
13 |
22,371,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Vmn1r192
|
UTSW |
13 |
22,371,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Vmn1r192
|
UTSW |
13 |
22,372,191 (GRCm39) |
missense |
probably benign |
0.38 |
R9367:Vmn1r192
|
UTSW |
13 |
22,371,800 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9694:Vmn1r192
|
UTSW |
13 |
22,372,119 (GRCm39) |
missense |
probably benign |
|
R9760:Vmn1r192
|
UTSW |
13 |
22,372,010 (GRCm39) |
missense |
probably damaging |
1.00 |
|