Other mutations in this stock |
Total: 12 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933411K16Rik |
A |
G |
19: 42,041,394 (GRCm39) |
N175S |
possibly damaging |
Het |
Adam20 |
A |
T |
8: 41,249,873 (GRCm39) |
N661I |
probably damaging |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or51f1 |
T |
A |
7: 102,506,031 (GRCm39) |
M153L |
probably benign |
Het |
Or6c1b |
T |
A |
10: 129,272,903 (GRCm39) |
V74D |
possibly damaging |
Het |
Pdlim2 |
T |
A |
14: 70,403,532 (GRCm39) |
|
probably benign |
Het |
Phtf2 |
T |
C |
5: 21,012,428 (GRCm39) |
D49G |
probably damaging |
Het |
Ppp1ca |
T |
A |
19: 4,244,481 (GRCm39) |
L180* |
probably null |
Het |
Prdm10 |
T |
C |
9: 31,273,664 (GRCm39) |
V1027A |
probably benign |
Het |
Slc38a10 |
T |
C |
11: 120,007,684 (GRCm39) |
|
probably benign |
Het |
Tlr1 |
A |
T |
5: 65,083,290 (GRCm39) |
L429* |
probably null |
Het |
Vps13a |
A |
G |
19: 16,692,406 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn1r172 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02407:Vmn1r172
|
APN |
7 |
23,359,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Vmn1r172
|
APN |
7 |
23,359,350 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03090:Vmn1r172
|
APN |
7 |
23,359,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R0396:Vmn1r172
|
UTSW |
7 |
23,359,957 (GRCm39) |
missense |
probably benign |
0.06 |
R1087:Vmn1r172
|
UTSW |
7 |
23,359,673 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1502:Vmn1r172
|
UTSW |
7 |
23,359,681 (GRCm39) |
nonsense |
probably null |
|
R1701:Vmn1r172
|
UTSW |
7 |
23,359,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R1882:Vmn1r172
|
UTSW |
7 |
23,359,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R2272:Vmn1r172
|
UTSW |
7 |
23,359,616 (GRCm39) |
missense |
probably damaging |
0.98 |
R4646:Vmn1r172
|
UTSW |
7 |
23,359,919 (GRCm39) |
missense |
probably benign |
0.03 |
R4653:Vmn1r172
|
UTSW |
7 |
23,359,997 (GRCm39) |
missense |
probably damaging |
0.96 |
R4709:Vmn1r172
|
UTSW |
7 |
23,359,606 (GRCm39) |
missense |
probably benign |
0.25 |
R4937:Vmn1r172
|
UTSW |
7 |
23,359,312 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4945:Vmn1r172
|
UTSW |
7 |
23,359,745 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5840:Vmn1r172
|
UTSW |
7 |
23,359,600 (GRCm39) |
missense |
probably benign |
0.03 |
R6154:Vmn1r172
|
UTSW |
7 |
23,359,583 (GRCm39) |
missense |
probably damaging |
0.96 |
R6317:Vmn1r172
|
UTSW |
7 |
23,359,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7206:Vmn1r172
|
UTSW |
7 |
23,359,582 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7290:Vmn1r172
|
UTSW |
7 |
23,360,048 (GRCm39) |
missense |
unknown |
|
R7362:Vmn1r172
|
UTSW |
7 |
23,359,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R7369:Vmn1r172
|
UTSW |
7 |
23,360,030 (GRCm39) |
missense |
unknown |
|
R7528:Vmn1r172
|
UTSW |
7 |
23,359,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7946:Vmn1r172
|
UTSW |
7 |
23,358,857 (GRCm39) |
splice site |
probably null |
|
R8193:Vmn1r172
|
UTSW |
7 |
23,359,752 (GRCm39) |
nonsense |
probably null |
|
R8540:Vmn1r172
|
UTSW |
7 |
23,359,498 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8863:Vmn1r172
|
UTSW |
7 |
23,359,210 (GRCm39) |
missense |
probably benign |
0.08 |
R8974:Vmn1r172
|
UTSW |
7 |
23,359,840 (GRCm39) |
missense |
probably benign |
0.06 |
R9006:Vmn1r172
|
UTSW |
7 |
23,359,402 (GRCm39) |
missense |
probably benign |
0.04 |
R9021:Vmn1r172
|
UTSW |
7 |
23,359,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Vmn1r172
|
UTSW |
7 |
23,359,593 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9604:Vmn1r172
|
UTSW |
7 |
23,359,193 (GRCm39) |
missense |
possibly damaging |
0.68 |
U24488:Vmn1r172
|
UTSW |
7 |
23,359,171 (GRCm39) |
missense |
probably benign |
0.02 |
|