Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9030624J02Rik |
G |
A |
7: 118,797,047 |
|
probably null |
Het |
Axin1 |
A |
T |
17: 26,142,805 |
D41V |
possibly damaging |
Het |
BC034090 |
C |
A |
1: 155,225,451 |
E718* |
probably null |
Het |
Cdc123 |
G |
T |
2: 5,804,935 |
Q222K |
probably benign |
Het |
Clip1 |
A |
C |
5: 123,603,654 |
V1053G |
possibly damaging |
Het |
Dock7 |
T |
A |
4: 99,063,985 |
E416V |
probably damaging |
Het |
Dydc1 |
T |
C |
14: 41,087,413 |
L143P |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,158,839 |
V732A |
probably benign |
Het |
Dzip1l |
T |
A |
9: 99,637,777 |
L119Q |
probably damaging |
Het |
Erp27 |
T |
A |
6: 136,909,502 |
S178C |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,397,873 |
V298A |
probably benign |
Het |
Fbxo34 |
A |
G |
14: 47,529,474 |
H97R |
probably damaging |
Het |
Gm20521 |
C |
T |
14: 54,884,622 |
Q81* |
probably null |
Het |
Gspt1 |
T |
C |
16: 11,222,612 |
M610V |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,437,682 |
Q1919R |
possibly damaging |
Het |
Il19 |
A |
G |
1: 130,935,055 |
|
probably benign |
Het |
Kif14 |
G |
A |
1: 136,469,018 |
S354N |
probably benign |
Het |
Lrrk2 |
A |
G |
15: 91,747,799 |
K1309E |
possibly damaging |
Het |
Lurap1 |
T |
C |
4: 116,137,690 |
T115A |
probably damaging |
Het |
Myo18b |
G |
T |
5: 112,874,131 |
T465K |
probably benign |
Het |
Nwd1 |
A |
T |
8: 72,671,077 |
D648V |
probably damaging |
Het |
Olfr272 |
T |
G |
4: 52,911,618 |
M59L |
possibly damaging |
Het |
Olfr520 |
G |
A |
7: 99,735,317 |
R58H |
probably benign |
Het |
Otof |
T |
C |
5: 30,375,904 |
Y1527C |
probably damaging |
Het |
Otop3 |
G |
A |
11: 115,344,397 |
C285Y |
probably damaging |
Het |
Parp3 |
A |
G |
9: 106,471,387 |
I478T |
probably benign |
Het |
Pdzd2 |
C |
T |
15: 12,457,983 |
E265K |
possibly damaging |
Het |
Pik3c2g |
T |
C |
6: 139,896,125 |
L634P |
probably damaging |
Het |
Prkg1 |
C |
A |
19: 31,302,340 |
V165L |
probably benign |
Het |
Riok3 |
A |
G |
18: 12,148,891 |
I306V |
possibly damaging |
Het |
Ror2 |
T |
C |
13: 53,113,082 |
D439G |
probably benign |
Het |
Scn2a |
T |
A |
2: 65,743,090 |
I1428N |
probably damaging |
Het |
Sgcg |
C |
T |
14: 61,232,475 |
D146N |
probably benign |
Het |
Slc16a9 |
A |
G |
10: 70,282,699 |
R283G |
probably benign |
Het |
Sptb |
T |
C |
12: 76,621,331 |
D664G |
probably benign |
Het |
Tmprss3 |
T |
A |
17: 31,195,008 |
D54V |
probably damaging |
Het |
Ttc37 |
T |
C |
13: 76,143,278 |
|
probably null |
Het |
Tubd1 |
G |
T |
11: 86,565,729 |
V374F |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,945,999 |
E2458G |
probably benign |
Het |
Zhx2 |
A |
T |
15: 57,822,870 |
E545V |
probably damaging |
Het |
|
Other mutations in Vmn2r57 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01108:Vmn2r57
|
APN |
7 |
41,427,584 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01112:Vmn2r57
|
APN |
7 |
41,425,043 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01516:Vmn2r57
|
APN |
7 |
41,399,946 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01880:Vmn2r57
|
APN |
7 |
41,400,195 (GRCm38) |
missense |
possibly damaging |
0.73 |
IGL02117:Vmn2r57
|
APN |
7 |
41,400,450 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02500:Vmn2r57
|
APN |
7 |
41,428,226 (GRCm38) |
missense |
probably benign |
|
IGL02801:Vmn2r57
|
APN |
7 |
41,448,632 (GRCm38) |
missense |
probably benign |
0.13 |
IGL02993:Vmn2r57
|
APN |
7 |
41,428,074 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02996:Vmn2r57
|
APN |
7 |
41,399,741 (GRCm38) |
missense |
probably benign |
0.02 |
R0008:Vmn2r57
|
UTSW |
7 |
41,400,652 (GRCm38) |
missense |
probably damaging |
1.00 |
R0032:Vmn2r57
|
UTSW |
7 |
41,399,733 (GRCm38) |
splice site |
probably null |
|
R0305:Vmn2r57
|
UTSW |
7 |
41,427,543 (GRCm38) |
missense |
probably benign |
0.00 |
R0469:Vmn2r57
|
UTSW |
7 |
41,427,792 (GRCm38) |
missense |
possibly damaging |
0.58 |
R0510:Vmn2r57
|
UTSW |
7 |
41,427,792 (GRCm38) |
missense |
possibly damaging |
0.58 |
R0847:Vmn2r57
|
UTSW |
7 |
41,428,801 (GRCm38) |
missense |
probably benign |
0.00 |
R1025:Vmn2r57
|
UTSW |
7 |
41,427,804 (GRCm38) |
missense |
probably benign |
0.24 |
R1081:Vmn2r57
|
UTSW |
7 |
41,428,211 (GRCm38) |
missense |
possibly damaging |
0.47 |
R1479:Vmn2r57
|
UTSW |
7 |
41,427,830 (GRCm38) |
missense |
possibly damaging |
0.45 |
R1579:Vmn2r57
|
UTSW |
7 |
41,400,124 (GRCm38) |
missense |
probably benign |
0.38 |
R1764:Vmn2r57
|
UTSW |
7 |
41,400,643 (GRCm38) |
missense |
probably damaging |
1.00 |
R1848:Vmn2r57
|
UTSW |
7 |
41,428,107 (GRCm38) |
missense |
probably damaging |
1.00 |
R2006:Vmn2r57
|
UTSW |
7 |
41,448,577 (GRCm38) |
missense |
probably benign |
0.00 |
R2197:Vmn2r57
|
UTSW |
7 |
41,428,825 (GRCm38) |
critical splice acceptor site |
probably null |
|
R2242:Vmn2r57
|
UTSW |
7 |
41,428,074 (GRCm38) |
missense |
probably benign |
0.00 |
R2394:Vmn2r57
|
UTSW |
7 |
41,400,195 (GRCm38) |
missense |
possibly damaging |
0.73 |
R3937:Vmn2r57
|
UTSW |
7 |
41,428,130 (GRCm38) |
missense |
probably damaging |
0.97 |
R4193:Vmn2r57
|
UTSW |
7 |
41,428,239 (GRCm38) |
missense |
probably benign |
|
R4423:Vmn2r57
|
UTSW |
7 |
41,426,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R4865:Vmn2r57
|
UTSW |
7 |
41,400,468 (GRCm38) |
missense |
probably damaging |
1.00 |
R4947:Vmn2r57
|
UTSW |
7 |
41,400,495 (GRCm38) |
missense |
probably damaging |
1.00 |
R5042:Vmn2r57
|
UTSW |
7 |
41,428,662 (GRCm38) |
missense |
probably benign |
0.06 |
R5084:Vmn2r57
|
UTSW |
7 |
41,426,550 (GRCm38) |
critical splice donor site |
probably null |
|
R5177:Vmn2r57
|
UTSW |
7 |
41,400,240 (GRCm38) |
missense |
probably benign |
0.31 |
R5192:Vmn2r57
|
UTSW |
7 |
41,427,939 (GRCm38) |
missense |
probably damaging |
0.96 |
R5289:Vmn2r57
|
UTSW |
7 |
41,399,974 (GRCm38) |
missense |
probably damaging |
0.99 |
R5745:Vmn2r57
|
UTSW |
7 |
41,448,471 (GRCm38) |
missense |
possibly damaging |
0.51 |
R6051:Vmn2r57
|
UTSW |
7 |
41,448,472 (GRCm38) |
missense |
probably benign |
0.00 |
R6155:Vmn2r57
|
UTSW |
7 |
41,428,690 (GRCm38) |
missense |
probably benign |
0.14 |
R6248:Vmn2r57
|
UTSW |
7 |
41,399,860 (GRCm38) |
missense |
probably benign |
|
R6381:Vmn2r57
|
UTSW |
7 |
41,428,818 (GRCm38) |
missense |
probably benign |
0.08 |
R7019:Vmn2r57
|
UTSW |
7 |
41,428,665 (GRCm38) |
missense |
probably damaging |
1.00 |
R7126:Vmn2r57
|
UTSW |
7 |
41,399,794 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7146:Vmn2r57
|
UTSW |
7 |
41,448,471 (GRCm38) |
missense |
possibly damaging |
0.51 |
R7215:Vmn2r57
|
UTSW |
7 |
41,400,286 (GRCm38) |
missense |
probably benign |
0.00 |
R7432:Vmn2r57
|
UTSW |
7 |
41,426,724 (GRCm38) |
missense |
probably benign |
0.01 |
R7633:Vmn2r57
|
UTSW |
7 |
41,425,089 (GRCm38) |
missense |
possibly damaging |
0.76 |
R7811:Vmn2r57
|
UTSW |
7 |
41,425,015 (GRCm38) |
nonsense |
probably null |
|
R8025:Vmn2r57
|
UTSW |
7 |
41,426,759 (GRCm38) |
missense |
probably benign |
0.00 |
R8332:Vmn2r57
|
UTSW |
7 |
41,400,253 (GRCm38) |
missense |
probably benign |
0.01 |
R8345:Vmn2r57
|
UTSW |
7 |
41,427,544 (GRCm38) |
missense |
possibly damaging |
0.81 |
R8360:Vmn2r57
|
UTSW |
7 |
41,400,216 (GRCm38) |
missense |
probably damaging |
1.00 |
R8738:Vmn2r57
|
UTSW |
7 |
41,427,596 (GRCm38) |
missense |
probably benign |
0.00 |
R8758:Vmn2r57
|
UTSW |
7 |
41,428,739 (GRCm38) |
missense |
probably damaging |
1.00 |
R8955:Vmn2r57
|
UTSW |
7 |
41,400,147 (GRCm38) |
missense |
possibly damaging |
0.64 |
R8985:Vmn2r57
|
UTSW |
7 |
41,399,835 (GRCm38) |
missense |
probably benign |
|
R9108:Vmn2r57
|
UTSW |
7 |
41,428,768 (GRCm38) |
missense |
possibly damaging |
0.87 |
R9160:Vmn2r57
|
UTSW |
7 |
41,426,735 (GRCm38) |
missense |
possibly damaging |
0.48 |
R9354:Vmn2r57
|
UTSW |
7 |
41,400,239 (GRCm38) |
missense |
probably benign |
0.01 |
R9566:Vmn2r57
|
UTSW |
7 |
41,427,665 (GRCm38) |
missense |
probably benign |
0.32 |
R9633:Vmn2r57
|
UTSW |
7 |
41,426,582 (GRCm38) |
missense |
probably benign |
0.00 |
X0026:Vmn2r57
|
UTSW |
7 |
41,428,561 (GRCm38) |
missense |
possibly damaging |
0.91 |
X0026:Vmn2r57
|
UTSW |
7 |
41,428,125 (GRCm38) |
missense |
probably benign |
0.03 |
X0065:Vmn2r57
|
UTSW |
7 |
41,427,971 (GRCm38) |
missense |
probably benign |
0.09 |
Z1176:Vmn2r57
|
UTSW |
7 |
41,400,498 (GRCm38) |
missense |
probably damaging |
0.99 |
|