Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
A |
12: 71,195,034 (GRCm39) |
V144I |
probably benign |
Het |
B3gat1 |
A |
G |
9: 26,669,043 (GRCm39) |
K325E |
possibly damaging |
Het |
Cd36 |
T |
A |
5: 18,033,766 (GRCm39) |
|
probably benign |
Het |
Ces3a |
A |
G |
8: 105,782,263 (GRCm39) |
E325G |
probably benign |
Het |
Col1a2 |
G |
A |
6: 4,515,639 (GRCm39) |
G136D |
unknown |
Het |
Cyp3a25 |
T |
G |
5: 145,946,273 (GRCm39) |
|
probably benign |
Het |
Cyp3a59 |
T |
C |
5: 146,039,690 (GRCm39) |
L321P |
probably damaging |
Het |
Dag1 |
A |
G |
9: 108,095,391 (GRCm39) |
S34P |
probably damaging |
Het |
Defa27 |
A |
T |
8: 21,805,674 (GRCm39) |
K13* |
probably null |
Het |
Disp2 |
T |
C |
2: 118,621,350 (GRCm39) |
F694S |
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,437,732 (GRCm39) |
A454S |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,147,791 (GRCm39) |
D946E |
probably benign |
Het |
Fcgbp |
A |
G |
7: 27,791,379 (GRCm39) |
E880G |
probably damaging |
Het |
Fgfr4 |
T |
C |
13: 55,308,992 (GRCm39) |
V371A |
probably benign |
Het |
Frem3 |
G |
T |
8: 81,340,736 (GRCm39) |
V1010F |
possibly damaging |
Het |
Gm13283 |
G |
A |
4: 88,679,272 (GRCm39) |
V88I |
probably benign |
Het |
Gm5134 |
G |
A |
10: 75,821,945 (GRCm39) |
V260I |
probably benign |
Het |
Grhl2 |
A |
G |
15: 37,270,830 (GRCm39) |
|
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,820,920 (GRCm39) |
W1090R |
probably damaging |
Het |
Hydin |
G |
A |
8: 111,293,570 (GRCm39) |
V3506I |
probably benign |
Het |
Igkc |
C |
T |
6: 70,703,559 (GRCm39) |
R47* |
probably null |
Het |
Iglv3 |
T |
A |
16: 19,060,160 (GRCm39) |
Q56L |
probably damaging |
Het |
Impg2 |
T |
A |
16: 56,079,831 (GRCm39) |
M436K |
probably benign |
Het |
Kcnma1 |
T |
A |
14: 23,359,113 (GRCm39) |
K1110N |
probably damaging |
Het |
Marf1 |
T |
C |
16: 13,959,776 (GRCm39) |
E694G |
probably damaging |
Het |
Nup37 |
A |
C |
10: 87,994,791 (GRCm39) |
K118T |
probably benign |
Het |
Or10al7 |
A |
G |
17: 38,366,481 (GRCm39) |
M1T |
probably null |
Het |
Or4a73 |
T |
C |
2: 89,420,586 (GRCm39) |
E291G |
probably damaging |
Het |
P3h1 |
A |
G |
4: 119,095,062 (GRCm39) |
D273G |
probably damaging |
Het |
Pcsk9 |
T |
C |
4: 106,311,843 (GRCm39) |
D178G |
probably benign |
Het |
Phyhipl |
T |
C |
10: 70,406,660 (GRCm39) |
K53R |
probably damaging |
Het |
Pkp3 |
T |
G |
7: 140,669,249 (GRCm39) |
L697R |
probably damaging |
Het |
Rab11fip3 |
A |
G |
17: 26,286,866 (GRCm39) |
V429A |
probably benign |
Het |
Rgl2 |
A |
G |
17: 34,152,098 (GRCm39) |
N295S |
probably damaging |
Het |
Spag5 |
A |
T |
11: 78,206,459 (GRCm39) |
D817V |
possibly damaging |
Het |
Tas2r117 |
C |
A |
6: 132,780,558 (GRCm39) |
T232K |
probably benign |
Het |
Thumpd1 |
A |
G |
7: 119,316,232 (GRCm39) |
V239A |
possibly damaging |
Het |
Timd4 |
T |
A |
11: 46,710,841 (GRCm39) |
S248T |
possibly damaging |
Het |
Tmem207 |
A |
T |
16: 26,335,490 (GRCm39) |
N82K |
probably benign |
Het |
Ttn |
T |
A |
2: 76,538,557 (GRCm39) |
T34714S |
possibly damaging |
Het |
Vmn2r24 |
T |
A |
6: 123,757,631 (GRCm39) |
S166R |
probably damaging |
Het |
Vmn2r32 |
A |
G |
7: 7,479,696 (GRCm39) |
F159S |
probably damaging |
Het |
Wdr72 |
A |
T |
9: 74,117,505 (GRCm39) |
Q739L |
probably benign |
Het |
|
Other mutations in Vmn1r194 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01890:Vmn1r194
|
APN |
13 |
22,428,776 (GRCm39) |
missense |
probably benign |
0.01 |
R0066:Vmn1r194
|
UTSW |
13 |
22,428,641 (GRCm39) |
missense |
probably benign |
0.33 |
R0066:Vmn1r194
|
UTSW |
13 |
22,428,641 (GRCm39) |
missense |
probably benign |
0.33 |
R0109:Vmn1r194
|
UTSW |
13 |
22,429,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Vmn1r194
|
UTSW |
13 |
22,429,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1276:Vmn1r194
|
UTSW |
13 |
22,429,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Vmn1r194
|
UTSW |
13 |
22,429,236 (GRCm39) |
missense |
probably damaging |
0.99 |
R1620:Vmn1r194
|
UTSW |
13 |
22,429,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R4593:Vmn1r194
|
UTSW |
13 |
22,428,461 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4844:Vmn1r194
|
UTSW |
13 |
22,429,223 (GRCm39) |
missense |
probably benign |
0.02 |
R5011:Vmn1r194
|
UTSW |
13 |
22,429,058 (GRCm39) |
missense |
probably benign |
0.00 |
R5110:Vmn1r194
|
UTSW |
13 |
22,429,170 (GRCm39) |
missense |
probably benign |
0.07 |
R5588:Vmn1r194
|
UTSW |
13 |
22,428,512 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5810:Vmn1r194
|
UTSW |
13 |
22,428,597 (GRCm39) |
nonsense |
probably null |
|
R6648:Vmn1r194
|
UTSW |
13 |
22,428,694 (GRCm39) |
missense |
probably benign |
0.11 |
R7660:Vmn1r194
|
UTSW |
13 |
22,428,767 (GRCm39) |
missense |
not run |
|
R7663:Vmn1r194
|
UTSW |
13 |
22,428,911 (GRCm39) |
missense |
not run |
|
R7879:Vmn1r194
|
UTSW |
13 |
22,428,772 (GRCm39) |
missense |
probably benign |
0.06 |
R8344:Vmn1r194
|
UTSW |
13 |
22,429,247 (GRCm39) |
missense |
probably benign |
0.01 |
R8830:Vmn1r194
|
UTSW |
13 |
22,429,006 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9245:Vmn1r194
|
UTSW |
13 |
22,428,731 (GRCm39) |
missense |
probably benign |
0.44 |
R9291:Vmn1r194
|
UTSW |
13 |
22,428,875 (GRCm39) |
missense |
probably benign |
0.20 |
R9624:Vmn1r194
|
UTSW |
13 |
22,428,671 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn1r194
|
UTSW |
13 |
22,428,596 (GRCm39) |
missense |
probably benign |
0.08 |
|