Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
G |
1: 71,327,712 (GRCm39) |
H1456P |
possibly damaging |
Het |
Abcg1 |
C |
A |
17: 31,324,578 (GRCm39) |
H274Q |
probably damaging |
Het |
Adamts4 |
G |
A |
1: 171,078,512 (GRCm39) |
R44Q |
probably benign |
Het |
Amigo2 |
A |
T |
15: 97,143,494 (GRCm39) |
C309* |
probably null |
Het |
Ccdc88c |
A |
C |
12: 100,919,552 (GRCm39) |
S446A |
probably benign |
Het |
Cd9 |
A |
T |
6: 125,449,458 (GRCm39) |
V28E |
probably damaging |
Het |
Cops2 |
A |
T |
2: 125,678,163 (GRCm39) |
|
probably benign |
Het |
Csn1s1 |
C |
T |
5: 87,825,453 (GRCm39) |
|
probably benign |
Het |
Cul9 |
G |
T |
17: 46,851,302 (GRCm39) |
R373S |
possibly damaging |
Het |
D630045J12Rik |
G |
T |
6: 38,126,640 (GRCm39) |
H1457N |
probably damaging |
Het |
Dennd2b |
C |
A |
7: 109,155,442 (GRCm39) |
R436L |
possibly damaging |
Het |
Dnah9 |
A |
G |
11: 65,920,189 (GRCm39) |
S2235P |
probably damaging |
Het |
Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
Fbxo10 |
A |
T |
4: 45,043,883 (GRCm39) |
W647R |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,930,919 (GRCm38) |
|
probably benign |
Het |
Flnc |
G |
T |
6: 29,440,684 (GRCm39) |
V301L |
probably damaging |
Het |
Hfm1 |
T |
C |
5: 107,049,627 (GRCm39) |
S445G |
probably benign |
Het |
Hif3a |
A |
G |
7: 16,773,603 (GRCm39) |
|
probably benign |
Het |
Hsd17b4 |
T |
C |
18: 50,288,220 (GRCm39) |
Y217H |
probably damaging |
Het |
Iba57 |
T |
C |
11: 59,049,772 (GRCm39) |
T192A |
probably benign |
Het |
Igkv5-48 |
A |
T |
6: 69,703,671 (GRCm39) |
I78N |
probably damaging |
Het |
Inhbe |
A |
T |
10: 127,186,797 (GRCm39) |
W128R |
probably damaging |
Het |
Ism1 |
T |
C |
2: 139,599,121 (GRCm39) |
C365R |
probably damaging |
Het |
Kif19a |
A |
T |
11: 114,670,470 (GRCm39) |
T127S |
probably damaging |
Het |
Kmt2d |
C |
A |
15: 98,755,439 (GRCm39) |
|
probably benign |
Het |
Mmp20 |
A |
G |
9: 7,654,042 (GRCm39) |
R321G |
probably damaging |
Het |
Msl2 |
T |
C |
9: 100,977,854 (GRCm39) |
M76T |
possibly damaging |
Het |
Nme9 |
T |
C |
9: 99,351,684 (GRCm39) |
C223R |
probably damaging |
Het |
Nucb1 |
G |
T |
7: 45,144,467 (GRCm39) |
|
probably benign |
Het |
Ocrl |
G |
A |
X: 47,022,315 (GRCm39) |
D262N |
probably benign |
Het |
Or13a18 |
A |
C |
7: 140,190,081 (GRCm39) |
M1L |
probably benign |
Het |
Or5b98 |
T |
A |
19: 12,931,556 (GRCm39) |
I201N |
possibly damaging |
Het |
Or6b1 |
A |
C |
6: 42,815,738 (GRCm39) |
I308L |
probably benign |
Het |
P4ha1 |
A |
G |
10: 59,206,824 (GRCm39) |
|
probably null |
Het |
Parp8 |
T |
C |
13: 116,998,838 (GRCm39) |
|
probably benign |
Het |
Pcdhb6 |
A |
G |
18: 37,468,507 (GRCm39) |
D476G |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,303,535 (GRCm39) |
E1685G |
possibly damaging |
Het |
Plod2 |
T |
A |
9: 92,489,147 (GRCm39) |
L714Q |
probably damaging |
Het |
Plscr2 |
A |
G |
9: 92,171,716 (GRCm39) |
I103V |
probably benign |
Het |
Plscr3 |
C |
A |
11: 69,738,209 (GRCm39) |
|
probably benign |
Het |
Pmaip1 |
A |
G |
18: 66,596,370 (GRCm39) |
R80G |
probably damaging |
Het |
Ppm1d |
C |
T |
11: 85,230,492 (GRCm39) |
P370L |
possibly damaging |
Het |
Prr36 |
C |
A |
8: 4,266,407 (GRCm39) |
E48* |
probably null |
Het |
Ptgir |
G |
A |
7: 16,641,409 (GRCm39) |
V234I |
possibly damaging |
Het |
Ptk7 |
A |
T |
17: 46,901,070 (GRCm39) |
V219E |
probably benign |
Het |
Rab39b |
T |
A |
X: 74,618,609 (GRCm39) |
I74F |
probably damaging |
Het |
Rasal2 |
A |
T |
1: 156,977,449 (GRCm39) |
M1075K |
possibly damaging |
Het |
Rpl37a |
G |
A |
1: 72,750,885 (GRCm39) |
A20T |
probably null |
Het |
Serpinb10 |
A |
C |
1: 107,466,155 (GRCm39) |
|
probably null |
Het |
Sipa1l1 |
T |
A |
12: 82,471,868 (GRCm39) |
Y1283N |
probably damaging |
Het |
Slc22a23 |
T |
A |
13: 34,528,468 (GRCm39) |
I105F |
possibly damaging |
Het |
Slc25a20 |
T |
A |
9: 108,559,599 (GRCm39) |
I221N |
probably damaging |
Het |
Smarcal1 |
A |
T |
1: 72,659,247 (GRCm39) |
H691L |
probably damaging |
Het |
Smo |
A |
C |
6: 29,758,480 (GRCm39) |
T542P |
probably damaging |
Het |
Spats2 |
T |
A |
15: 99,071,329 (GRCm39) |
I51N |
probably damaging |
Het |
Spon1 |
G |
T |
7: 113,635,897 (GRCm39) |
V704L |
probably benign |
Het |
Tex9 |
T |
A |
9: 72,389,774 (GRCm39) |
Q112L |
probably benign |
Het |
Tgfbr2 |
T |
C |
9: 115,919,486 (GRCm39) |
E580G |
probably benign |
Het |
Top2b |
T |
A |
14: 16,387,335 (GRCm38) |
V141E |
probably benign |
Het |
Trhde |
A |
T |
10: 114,636,466 (GRCm39) |
L247* |
probably null |
Het |
Umodl1 |
G |
T |
17: 31,217,628 (GRCm39) |
V1145F |
probably damaging |
Het |
Vasp |
C |
A |
7: 18,992,748 (GRCm39) |
|
probably benign |
Het |
Vmn1r8 |
G |
T |
6: 57,013,556 (GRCm39) |
L202F |
probably damaging |
Het |
Wdr27 |
A |
G |
17: 15,112,693 (GRCm39) |
|
probably benign |
Het |
Wfdc1 |
T |
G |
8: 120,406,909 (GRCm39) |
V109G |
probably damaging |
Het |
Zan |
C |
A |
5: 137,463,056 (GRCm39) |
E708* |
probably null |
Het |
Zbtb1 |
T |
A |
12: 76,432,169 (GRCm39) |
F52I |
possibly damaging |
Het |
Zfp236 |
A |
G |
18: 82,648,117 (GRCm39) |
S1015P |
probably damaging |
Het |
Zfp532 |
T |
C |
18: 65,757,113 (GRCm39) |
S349P |
probably damaging |
Het |
Znfx1 |
A |
T |
2: 166,889,550 (GRCm39) |
C731S |
possibly damaging |
Het |
|
Other mutations in Vmn2r111 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00932:Vmn2r111
|
APN |
17 |
22,767,734 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01306:Vmn2r111
|
APN |
17 |
22,787,965 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01309:Vmn2r111
|
APN |
17 |
22,787,997 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01457:Vmn2r111
|
APN |
17 |
22,790,966 (GRCm39) |
nonsense |
probably null |
|
IGL01465:Vmn2r111
|
APN |
17 |
22,767,718 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01505:Vmn2r111
|
APN |
17 |
22,767,553 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01571:Vmn2r111
|
APN |
17 |
22,790,373 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01715:Vmn2r111
|
APN |
17 |
22,788,054 (GRCm39) |
splice site |
probably benign |
|
IGL01962:Vmn2r111
|
APN |
17 |
22,767,265 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02190:Vmn2r111
|
APN |
17 |
22,789,754 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02519:Vmn2r111
|
APN |
17 |
22,767,320 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02616:Vmn2r111
|
APN |
17 |
22,790,031 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02641:Vmn2r111
|
APN |
17 |
22,792,205 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02690:Vmn2r111
|
APN |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02698:Vmn2r111
|
APN |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03017:Vmn2r111
|
APN |
17 |
22,789,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Vmn2r111
|
UTSW |
17 |
22,766,990 (GRCm39) |
missense |
probably benign |
|
R0064:Vmn2r111
|
UTSW |
17 |
22,791,053 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Vmn2r111
|
UTSW |
17 |
22,792,102 (GRCm39) |
missense |
probably benign |
0.02 |
R1439:Vmn2r111
|
UTSW |
17 |
22,790,097 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Vmn2r111
|
UTSW |
17 |
22,790,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Vmn2r111
|
UTSW |
17 |
22,790,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R1636:Vmn2r111
|
UTSW |
17 |
22,790,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
R1648:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
R1697:Vmn2r111
|
UTSW |
17 |
22,767,041 (GRCm39) |
missense |
probably benign |
0.26 |
R1996:Vmn2r111
|
UTSW |
17 |
22,767,062 (GRCm39) |
missense |
probably benign |
0.21 |
R2040:Vmn2r111
|
UTSW |
17 |
22,767,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Vmn2r111
|
UTSW |
17 |
22,778,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Vmn2r111
|
UTSW |
17 |
22,792,085 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2357:Vmn2r111
|
UTSW |
17 |
22,778,151 (GRCm39) |
splice site |
probably benign |
|
R3700:Vmn2r111
|
UTSW |
17 |
22,790,142 (GRCm39) |
nonsense |
probably null |
|
R3782:Vmn2r111
|
UTSW |
17 |
22,790,301 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4085:Vmn2r111
|
UTSW |
17 |
22,778,096 (GRCm39) |
missense |
probably benign |
0.00 |
R4323:Vmn2r111
|
UTSW |
17 |
22,792,159 (GRCm39) |
missense |
probably benign |
0.02 |
R4900:Vmn2r111
|
UTSW |
17 |
22,767,637 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5072:Vmn2r111
|
UTSW |
17 |
22,767,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R5123:Vmn2r111
|
UTSW |
17 |
22,790,124 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5181:Vmn2r111
|
UTSW |
17 |
22,790,001 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5357:Vmn2r111
|
UTSW |
17 |
22,767,083 (GRCm39) |
nonsense |
probably null |
|
R5398:Vmn2r111
|
UTSW |
17 |
22,792,252 (GRCm39) |
start codon destroyed |
probably null |
0.88 |
R5434:Vmn2r111
|
UTSW |
17 |
22,767,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R5462:Vmn2r111
|
UTSW |
17 |
22,767,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R6149:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6149:Vmn2r111
|
UTSW |
17 |
22,767,796 (GRCm39) |
missense |
probably benign |
0.00 |
R6207:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6281:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6282:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6283:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6307:Vmn2r111
|
UTSW |
17 |
22,792,070 (GRCm39) |
missense |
probably benign |
0.00 |
R6323:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6325:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6367:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6368:Vmn2r111
|
UTSW |
17 |
22,790,889 (GRCm39) |
missense |
probably benign |
0.38 |
R6369:Vmn2r111
|
UTSW |
17 |
22,767,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6490:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6546:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6547:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6557:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6654:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6655:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6657:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6659:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6660:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6664:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6798:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6799:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6801:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6893:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6895:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6897:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6922:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6923:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6944:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6945:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7017:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7018:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7024:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7031:Vmn2r111
|
UTSW |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Vmn2r111
|
UTSW |
17 |
22,767,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R7053:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7054:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7055:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7056:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7145:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7146:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7246:Vmn2r111
|
UTSW |
17 |
22,767,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R7259:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7260:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7327:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7401:Vmn2r111
|
UTSW |
17 |
22,790,067 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7514:Vmn2r111
|
UTSW |
17 |
22,767,380 (GRCm39) |
missense |
probably benign |
0.05 |
R7651:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7781:Vmn2r111
|
UTSW |
17 |
22,789,714 (GRCm39) |
missense |
probably benign |
0.17 |
R7816:Vmn2r111
|
UTSW |
17 |
22,792,083 (GRCm39) |
missense |
probably damaging |
0.97 |
R7821:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7838:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8078:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8080:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8117:Vmn2r111
|
UTSW |
17 |
22,790,469 (GRCm39) |
missense |
probably benign |
0.12 |
R8171:Vmn2r111
|
UTSW |
17 |
22,792,073 (GRCm39) |
missense |
probably benign |
0.10 |
R8195:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8197:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8411:Vmn2r111
|
UTSW |
17 |
22,767,562 (GRCm39) |
missense |
probably benign |
0.03 |
R8539:Vmn2r111
|
UTSW |
17 |
22,790,274 (GRCm39) |
missense |
probably benign |
0.23 |
R8540:Vmn2r111
|
UTSW |
17 |
22,778,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8540:Vmn2r111
|
UTSW |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
R8557:Vmn2r111
|
UTSW |
17 |
22,790,910 (GRCm39) |
nonsense |
probably null |
|
R8720:Vmn2r111
|
UTSW |
17 |
22,792,194 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8729:Vmn2r111
|
UTSW |
17 |
22,767,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R8843:Vmn2r111
|
UTSW |
17 |
22,767,011 (GRCm39) |
missense |
probably benign |
0.00 |
R9184:Vmn2r111
|
UTSW |
17 |
22,790,822 (GRCm39) |
missense |
probably benign |
|
R9374:Vmn2r111
|
UTSW |
17 |
22,787,859 (GRCm39) |
missense |
probably benign |
0.17 |
R9452:Vmn2r111
|
UTSW |
17 |
22,778,132 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Vmn2r111
|
UTSW |
17 |
22,767,676 (GRCm39) |
missense |
probably damaging |
0.98 |
|