Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
G |
A |
6: 23,122,702 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,726,991 (GRCm39) |
S454P |
probably damaging |
Het |
Adh4 |
A |
T |
3: 138,124,981 (GRCm39) |
I51F |
possibly damaging |
Het |
Amigo2 |
A |
T |
15: 97,143,578 (GRCm39) |
C281* |
probably null |
Het |
Btn2a2 |
C |
T |
13: 23,664,637 (GRCm39) |
R307Q |
probably benign |
Het |
C2cd6 |
T |
C |
1: 59,090,307 (GRCm39) |
I483M |
probably damaging |
Het |
Capn9 |
T |
C |
8: 125,327,236 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
A |
G |
14: 55,744,867 (GRCm39) |
K1279E |
probably damaging |
Het |
Cdadc1 |
T |
C |
14: 59,823,496 (GRCm39) |
Y332C |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cep112 |
T |
G |
11: 108,750,177 (GRCm39) |
F893L |
probably damaging |
Het |
Cit |
A |
G |
5: 116,133,511 (GRCm39) |
S1867G |
probably benign |
Het |
Clptm1l |
T |
C |
13: 73,762,721 (GRCm39) |
|
probably benign |
Het |
Cyp4a12b |
A |
T |
4: 115,292,368 (GRCm39) |
|
probably benign |
Het |
Dlx3 |
G |
T |
11: 95,014,470 (GRCm39) |
W251L |
possibly damaging |
Het |
Dnah1 |
C |
T |
14: 30,984,177 (GRCm39) |
V3993M |
probably damaging |
Het |
Efs |
A |
T |
14: 55,157,172 (GRCm39) |
Y380N |
probably damaging |
Het |
Fam53c |
T |
A |
18: 34,903,720 (GRCm39) |
W331R |
probably damaging |
Het |
Gm5414 |
T |
C |
15: 101,533,990 (GRCm39) |
E331G |
probably damaging |
Het |
Gstcd |
A |
G |
3: 132,777,722 (GRCm39) |
V363A |
probably benign |
Het |
Jak1 |
A |
G |
4: 101,021,647 (GRCm39) |
|
probably benign |
Het |
Kifc3 |
A |
G |
8: 95,834,993 (GRCm39) |
V264A |
probably benign |
Het |
Mapk8ip2 |
A |
G |
15: 89,341,785 (GRCm39) |
D332G |
probably damaging |
Het |
Nbeal1 |
G |
A |
1: 60,323,146 (GRCm39) |
E2075K |
probably damaging |
Het |
Opn5 |
T |
G |
17: 42,907,517 (GRCm39) |
S120R |
probably damaging |
Het |
Or52m2 |
C |
T |
7: 102,264,046 (GRCm39) |
G50E |
probably damaging |
Het |
Paqr8 |
C |
T |
1: 21,005,733 (GRCm39) |
Q296* |
probably null |
Het |
Pcsk6 |
C |
T |
7: 65,629,995 (GRCm39) |
R374* |
probably null |
Het |
Pld1 |
A |
G |
3: 28,141,411 (GRCm39) |
H469R |
probably damaging |
Het |
Rbl1 |
A |
G |
2: 157,041,349 (GRCm39) |
S93P |
possibly damaging |
Het |
Reln |
C |
T |
5: 22,202,939 (GRCm39) |
R1287Q |
probably damaging |
Het |
Rev3l |
C |
T |
10: 39,698,391 (GRCm39) |
R963* |
probably null |
Het |
Serinc4 |
C |
T |
2: 121,282,908 (GRCm39) |
S418N |
probably benign |
Het |
Slc6a18 |
A |
G |
13: 73,818,087 (GRCm39) |
M310T |
probably benign |
Het |
Slitrk3 |
T |
A |
3: 72,958,101 (GRCm39) |
S224C |
probably damaging |
Het |
Slu7 |
T |
C |
11: 43,336,030 (GRCm39) |
I471T |
probably benign |
Het |
Stxbp5 |
A |
G |
10: 9,665,105 (GRCm39) |
|
probably null |
Het |
Tm7sf3 |
A |
T |
6: 146,514,872 (GRCm39) |
|
probably benign |
Het |
Trem1 |
C |
T |
17: 48,539,869 (GRCm39) |
S16L |
probably benign |
Het |
Trp53bp2 |
T |
A |
1: 182,281,289 (GRCm39) |
D963E |
probably benign |
Het |
Trp63 |
A |
T |
16: 25,682,491 (GRCm39) |
D184V |
probably damaging |
Het |
Ttll6 |
T |
C |
11: 96,042,899 (GRCm39) |
|
probably null |
Het |
Usp32 |
A |
G |
11: 84,897,817 (GRCm39) |
|
probably null |
Het |
Vmn2r76 |
T |
C |
7: 85,874,914 (GRCm39) |
R688G |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,525,296 (GRCm39) |
H318L |
probably damaging |
Het |
Vstm4 |
A |
G |
14: 32,585,574 (GRCm39) |
H47R |
probably damaging |
Het |
Wdr55 |
A |
G |
18: 36,896,435 (GRCm39) |
E375G |
probably benign |
Het |
Ybx2 |
T |
A |
11: 69,831,157 (GRCm39) |
S56T |
probably benign |
Het |
Ybx2 |
C |
A |
11: 69,831,158 (GRCm39) |
S251Y |
probably benign |
Het |
Zbtb3 |
T |
C |
19: 8,781,578 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vmn2r14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01472:Vmn2r14
|
APN |
5 |
109,364,180 (GRCm39) |
nonsense |
probably null |
|
IGL01504:Vmn2r14
|
APN |
5 |
109,369,285 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01828:Vmn2r14
|
APN |
5 |
109,372,443 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02093:Vmn2r14
|
APN |
5 |
109,368,275 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02103:Vmn2r14
|
APN |
5 |
109,372,349 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02123:Vmn2r14
|
APN |
5 |
109,367,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02145:Vmn2r14
|
APN |
5 |
109,368,454 (GRCm39) |
nonsense |
probably null |
|
IGL02676:Vmn2r14
|
APN |
5 |
109,367,882 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02877:Vmn2r14
|
APN |
5 |
109,368,054 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02974:Vmn2r14
|
APN |
5 |
109,369,292 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03151:Vmn2r14
|
APN |
5 |
109,364,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Vmn2r14
|
APN |
5 |
109,363,973 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03386:Vmn2r14
|
APN |
5 |
109,368,350 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03394:Vmn2r14
|
APN |
5 |
109,367,702 (GRCm39) |
missense |
probably null |
0.83 |
ANU74:Vmn2r14
|
UTSW |
5 |
109,366,910 (GRCm39) |
missense |
probably benign |
0.00 |
R0316:Vmn2r14
|
UTSW |
5 |
109,366,762 (GRCm39) |
missense |
probably benign |
0.07 |
R0755:Vmn2r14
|
UTSW |
5 |
109,364,226 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1219:Vmn2r14
|
UTSW |
5 |
109,372,440 (GRCm39) |
missense |
probably benign |
0.17 |
R1321:Vmn2r14
|
UTSW |
5 |
109,364,117 (GRCm39) |
missense |
probably benign |
0.08 |
R1465:Vmn2r14
|
UTSW |
5 |
109,368,195 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1465:Vmn2r14
|
UTSW |
5 |
109,368,195 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1509:Vmn2r14
|
UTSW |
5 |
109,363,862 (GRCm39) |
missense |
probably benign |
0.00 |
R1551:Vmn2r14
|
UTSW |
5 |
109,369,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1628:Vmn2r14
|
UTSW |
5 |
109,367,838 (GRCm39) |
missense |
probably benign |
0.00 |
R1668:Vmn2r14
|
UTSW |
5 |
109,366,913 (GRCm39) |
nonsense |
probably null |
|
R2013:Vmn2r14
|
UTSW |
5 |
109,369,109 (GRCm39) |
missense |
probably benign |
0.00 |
R2201:Vmn2r14
|
UTSW |
5 |
109,366,698 (GRCm39) |
splice site |
probably null |
|
R2417:Vmn2r14
|
UTSW |
5 |
109,372,329 (GRCm39) |
missense |
probably benign |
0.00 |
R3029:Vmn2r14
|
UTSW |
5 |
109,363,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R3120:Vmn2r14
|
UTSW |
5 |
109,372,431 (GRCm39) |
missense |
probably null |
0.00 |
R3729:Vmn2r14
|
UTSW |
5 |
109,364,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R3762:Vmn2r14
|
UTSW |
5 |
109,368,033 (GRCm39) |
missense |
probably benign |
0.02 |
R3943:Vmn2r14
|
UTSW |
5 |
109,363,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Vmn2r14
|
UTSW |
5 |
109,363,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R4222:Vmn2r14
|
UTSW |
5 |
109,364,149 (GRCm39) |
missense |
probably benign |
0.00 |
R4224:Vmn2r14
|
UTSW |
5 |
109,364,149 (GRCm39) |
missense |
probably benign |
0.00 |
R4239:Vmn2r14
|
UTSW |
5 |
109,364,277 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4240:Vmn2r14
|
UTSW |
5 |
109,364,277 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4782:Vmn2r14
|
UTSW |
5 |
109,369,370 (GRCm39) |
missense |
probably benign |
0.01 |
R4832:Vmn2r14
|
UTSW |
5 |
109,363,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Vmn2r14
|
UTSW |
5 |
109,369,384 (GRCm39) |
splice site |
probably null |
|
R4896:Vmn2r14
|
UTSW |
5 |
109,368,246 (GRCm39) |
missense |
probably benign |
0.19 |
R5004:Vmn2r14
|
UTSW |
5 |
109,368,246 (GRCm39) |
missense |
probably benign |
0.19 |
R5117:Vmn2r14
|
UTSW |
5 |
109,363,961 (GRCm39) |
missense |
probably benign |
0.16 |
R5285:Vmn2r14
|
UTSW |
5 |
109,365,442 (GRCm39) |
missense |
probably damaging |
0.98 |
R5413:Vmn2r14
|
UTSW |
5 |
109,369,154 (GRCm39) |
missense |
probably benign |
0.29 |
R5569:Vmn2r14
|
UTSW |
5 |
109,368,261 (GRCm39) |
missense |
probably benign |
0.44 |
R5701:Vmn2r14
|
UTSW |
5 |
109,367,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Vmn2r14
|
UTSW |
5 |
109,365,486 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5763:Vmn2r14
|
UTSW |
5 |
109,363,724 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5872:Vmn2r14
|
UTSW |
5 |
109,369,222 (GRCm39) |
missense |
probably benign |
|
R5985:Vmn2r14
|
UTSW |
5 |
109,368,082 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6268:Vmn2r14
|
UTSW |
5 |
109,369,283 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6273:Vmn2r14
|
UTSW |
5 |
109,369,133 (GRCm39) |
missense |
probably benign |
0.44 |
R6409:Vmn2r14
|
UTSW |
5 |
109,364,096 (GRCm39) |
missense |
probably benign |
0.09 |
R6944:Vmn2r14
|
UTSW |
5 |
109,364,140 (GRCm39) |
missense |
probably benign |
0.06 |
R6944:Vmn2r14
|
UTSW |
5 |
109,363,925 (GRCm39) |
missense |
probably benign |
0.22 |
R7608:Vmn2r14
|
UTSW |
5 |
109,369,276 (GRCm39) |
missense |
probably benign |
0.03 |
R7740:Vmn2r14
|
UTSW |
5 |
109,368,324 (GRCm39) |
missense |
probably benign |
0.41 |
R7768:Vmn2r14
|
UTSW |
5 |
109,368,086 (GRCm39) |
missense |
probably benign |
0.01 |
R7804:Vmn2r14
|
UTSW |
5 |
109,368,324 (GRCm39) |
missense |
probably benign |
0.41 |
R7872:Vmn2r14
|
UTSW |
5 |
109,369,219 (GRCm39) |
missense |
probably benign |
0.02 |
R7993:Vmn2r14
|
UTSW |
5 |
109,363,862 (GRCm39) |
missense |
probably benign |
0.00 |
R8006:Vmn2r14
|
UTSW |
5 |
109,368,324 (GRCm39) |
missense |
probably benign |
0.41 |
R8007:Vmn2r14
|
UTSW |
5 |
109,368,324 (GRCm39) |
missense |
probably benign |
0.41 |
R8187:Vmn2r14
|
UTSW |
5 |
109,368,420 (GRCm39) |
missense |
probably benign |
0.03 |
R8369:Vmn2r14
|
UTSW |
5 |
109,369,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R8463:Vmn2r14
|
UTSW |
5 |
109,369,340 (GRCm39) |
missense |
probably benign |
0.30 |
R8968:Vmn2r14
|
UTSW |
5 |
109,365,533 (GRCm39) |
missense |
probably benign |
0.01 |
R9008:Vmn2r14
|
UTSW |
5 |
109,367,893 (GRCm39) |
missense |
probably benign |
0.00 |
R9030:Vmn2r14
|
UTSW |
5 |
109,368,054 (GRCm39) |
missense |
probably damaging |
0.99 |
R9039:Vmn2r14
|
UTSW |
5 |
109,367,902 (GRCm39) |
nonsense |
probably null |
|
R9150:Vmn2r14
|
UTSW |
5 |
109,367,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R9164:Vmn2r14
|
UTSW |
5 |
109,364,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R9216:Vmn2r14
|
UTSW |
5 |
109,369,112 (GRCm39) |
missense |
probably benign |
0.01 |
R9225:Vmn2r14
|
UTSW |
5 |
109,369,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9245:Vmn2r14
|
UTSW |
5 |
109,368,176 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9342:Vmn2r14
|
UTSW |
5 |
109,368,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R9472:Vmn2r14
|
UTSW |
5 |
109,367,962 (GRCm39) |
missense |
probably benign |
0.00 |
R9678:Vmn2r14
|
UTSW |
5 |
109,364,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R9774:Vmn2r14
|
UTSW |
5 |
109,369,126 (GRCm39) |
missense |
probably benign |
0.07 |
Z1177:Vmn2r14
|
UTSW |
5 |
109,367,741 (GRCm39) |
missense |
probably benign |
0.33 |
|