Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd16a |
A |
G |
17: 35,315,459 (GRCm39) |
K169E |
probably benign |
Het |
Ago4 |
A |
G |
4: 126,410,988 (GRCm39) |
V167A |
probably damaging |
Het |
Bcam |
C |
T |
7: 19,499,423 (GRCm39) |
R200H |
probably damaging |
Het |
Cblb |
G |
A |
16: 51,959,996 (GRCm39) |
|
probably null |
Het |
Cdc37 |
T |
C |
9: 21,054,409 (GRCm39) |
E72G |
probably benign |
Het |
Chek2 |
T |
A |
5: 110,989,093 (GRCm39) |
|
probably benign |
Het |
Col6a1 |
A |
T |
10: 76,554,957 (GRCm39) |
|
probably null |
Het |
Col7a1 |
A |
G |
9: 108,813,084 (GRCm39) |
|
probably null |
Het |
Ecpas |
A |
G |
4: 58,849,937 (GRCm39) |
F429L |
possibly damaging |
Het |
Fmo3 |
C |
T |
1: 162,794,575 (GRCm39) |
R165H |
probably benign |
Het |
Gm2663 |
C |
T |
6: 40,973,010 (GRCm39) |
G199D |
probably damaging |
Het |
Gm8108 |
T |
C |
14: 4,127,217 (GRCm38) |
S134P |
probably damaging |
Het |
Kif1b |
A |
T |
4: 149,299,362 (GRCm39) |
|
probably null |
Het |
Krt76 |
T |
A |
15: 101,797,480 (GRCm39) |
D293V |
probably null |
Het |
Lifr |
T |
A |
15: 7,217,630 (GRCm39) |
C853S |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,415,234 (GRCm39) |
I2727F |
possibly damaging |
Het |
Myo7a |
T |
C |
7: 97,714,854 (GRCm39) |
K1606R |
possibly damaging |
Het |
Noxred1 |
G |
T |
12: 87,269,955 (GRCm39) |
Q259K |
probably benign |
Het |
Obox3 |
C |
T |
7: 15,360,777 (GRCm39) |
E121K |
probably benign |
Het |
Or14j1 |
G |
A |
17: 38,145,944 (GRCm39) |
R18H |
probably benign |
Het |
Or1j19 |
T |
C |
2: 36,677,095 (GRCm39) |
I186T |
probably benign |
Het |
Or2y16 |
T |
A |
11: 49,335,015 (GRCm39) |
C112* |
probably null |
Het |
Or5b24 |
T |
C |
19: 12,913,038 (GRCm39) |
L312S |
probably benign |
Het |
Phf11 |
A |
T |
14: 59,488,611 (GRCm39) |
V62E |
probably damaging |
Het |
Pkd2l2 |
T |
C |
18: 34,550,089 (GRCm39) |
F245L |
probably damaging |
Het |
Pla2g6 |
T |
C |
15: 79,197,316 (GRCm39) |
Q86R |
probably null |
Het |
Polq |
T |
A |
16: 36,881,805 (GRCm39) |
I1044K |
possibly damaging |
Het |
Pomgnt2 |
G |
T |
9: 121,811,536 (GRCm39) |
T415N |
probably benign |
Het |
Pprc1 |
T |
A |
19: 46,052,983 (GRCm39) |
|
probably benign |
Het |
Prol1 |
T |
A |
5: 88,475,820 (GRCm39) |
M70K |
probably benign |
Het |
Ptpn22 |
T |
A |
3: 103,793,652 (GRCm39) |
V601E |
probably benign |
Het |
Slc16a3 |
T |
C |
11: 120,847,709 (GRCm39) |
|
probably null |
Het |
Slco1b2 |
A |
G |
6: 141,622,012 (GRCm39) |
D489G |
possibly damaging |
Het |
Sphk2 |
T |
C |
7: 45,360,148 (GRCm39) |
|
probably benign |
Het |
Stat4 |
C |
T |
1: 52,136,014 (GRCm39) |
T441I |
possibly damaging |
Het |
Tle1 |
A |
T |
4: 72,040,639 (GRCm39) |
V647E |
probably damaging |
Het |
Tnrc6b |
C |
A |
15: 80,811,896 (GRCm39) |
Y814* |
probably null |
Het |
Tubgcp3 |
A |
G |
8: 12,704,301 (GRCm39) |
F256S |
probably damaging |
Het |
Uqcrb |
A |
T |
13: 67,050,827 (GRCm39) |
|
probably null |
Het |
Zfp324 |
C |
T |
7: 12,702,713 (GRCm39) |
|
probably benign |
Het |
Zxdc |
T |
C |
6: 90,349,520 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn1r200 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00970:Vmn1r200
|
APN |
13 |
22,579,893 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01123:Vmn1r200
|
APN |
13 |
22,579,571 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02691:Vmn1r200
|
APN |
13 |
22,579,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Vmn1r200
|
UTSW |
13 |
22,579,361 (GRCm39) |
missense |
probably benign |
0.00 |
R0507:Vmn1r200
|
UTSW |
13 |
22,579,718 (GRCm39) |
missense |
probably benign |
0.00 |
R0530:Vmn1r200
|
UTSW |
13 |
22,579,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1033:Vmn1r200
|
UTSW |
13 |
22,580,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Vmn1r200
|
UTSW |
13 |
22,579,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1714:Vmn1r200
|
UTSW |
13 |
22,579,640 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1920:Vmn1r200
|
UTSW |
13 |
22,579,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Vmn1r200
|
UTSW |
13 |
22,579,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Vmn1r200
|
UTSW |
13 |
22,580,025 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4827:Vmn1r200
|
UTSW |
13 |
22,579,265 (GRCm39) |
missense |
probably benign |
0.00 |
R5285:Vmn1r200
|
UTSW |
13 |
22,579,457 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5299:Vmn1r200
|
UTSW |
13 |
22,579,945 (GRCm39) |
nonsense |
probably null |
|
R6127:Vmn1r200
|
UTSW |
13 |
22,579,373 (GRCm39) |
missense |
probably benign |
0.07 |
R7167:Vmn1r200
|
UTSW |
13 |
22,579,487 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7854:Vmn1r200
|
UTSW |
13 |
22,580,009 (GRCm39) |
missense |
probably benign |
0.08 |
R7977:Vmn1r200
|
UTSW |
13 |
22,580,025 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7987:Vmn1r200
|
UTSW |
13 |
22,580,025 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8061:Vmn1r200
|
UTSW |
13 |
22,579,453 (GRCm39) |
nonsense |
probably null |
|
R8208:Vmn1r200
|
UTSW |
13 |
22,579,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R9481:Vmn1r200
|
UTSW |
13 |
22,579,911 (GRCm39) |
missense |
probably damaging |
1.00 |
|