Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
C |
10: 79,851,149 (GRCm39) |
Y2121H |
probably benign |
Het |
Adgrf2 |
A |
G |
17: 43,021,574 (GRCm39) |
Y417H |
probably damaging |
Het |
Ap5z1 |
A |
C |
5: 142,452,265 (GRCm39) |
D66A |
probably benign |
Het |
Cachd1 |
T |
A |
4: 100,821,688 (GRCm39) |
Y422N |
probably damaging |
Het |
Cfap54 |
C |
T |
10: 92,773,700 (GRCm39) |
G114D |
probably benign |
Het |
Cgref1 |
C |
T |
5: 31,091,049 (GRCm39) |
G255E |
probably benign |
Het |
Cyp2a22 |
A |
C |
7: 26,635,750 (GRCm39) |
L271R |
probably damaging |
Het |
Dcp2 |
G |
T |
18: 44,550,662 (GRCm39) |
E379* |
probably null |
Het |
Fhl3 |
T |
A |
4: 124,601,724 (GRCm39) |
D277E |
probably benign |
Het |
Gm19684 |
C |
T |
17: 36,439,411 (GRCm39) |
V190M |
probably damaging |
Het |
Hpse |
T |
C |
5: 100,867,375 (GRCm39) |
D29G |
probably benign |
Het |
Il31 |
T |
C |
5: 123,620,121 (GRCm39) |
|
probably benign |
Het |
Ilk |
T |
C |
7: 105,391,774 (GRCm39) |
C422R |
possibly damaging |
Het |
Itga1 |
T |
G |
13: 115,121,678 (GRCm39) |
D777A |
possibly damaging |
Het |
Kank3 |
A |
G |
17: 34,041,176 (GRCm39) |
D556G |
probably damaging |
Het |
Lrit3 |
A |
G |
3: 129,597,574 (GRCm39) |
S36P |
possibly damaging |
Het |
Magi1 |
C |
T |
6: 93,724,248 (GRCm39) |
E256K |
probably damaging |
Het |
Mroh9 |
C |
G |
1: 162,888,329 (GRCm39) |
G249R |
probably damaging |
Het |
Mymk |
C |
T |
2: 26,952,299 (GRCm39) |
M148I |
probably benign |
Het |
Nlrp12 |
T |
A |
7: 3,290,003 (GRCm39) |
I170F |
possibly damaging |
Het |
Odad3 |
T |
C |
9: 21,906,158 (GRCm39) |
E260G |
probably benign |
Het |
Or5al7 |
A |
T |
2: 85,992,378 (GRCm39) |
I305K |
possibly damaging |
Het |
Or5an11 |
T |
A |
19: 12,246,268 (GRCm39) |
S225T |
probably damaging |
Het |
Pkd1l1 |
G |
A |
11: 8,799,003 (GRCm39) |
T1803I |
possibly damaging |
Het |
Ppp2r2b |
C |
T |
18: 42,778,942 (GRCm39) |
V398I |
probably benign |
Het |
Ppp2r5e |
T |
A |
12: 75,516,544 (GRCm39) |
R214S |
probably damaging |
Het |
Prss16 |
T |
C |
13: 22,190,264 (GRCm39) |
D298G |
possibly damaging |
Het |
Qprt |
G |
A |
7: 126,707,622 (GRCm39) |
R189W |
probably damaging |
Het |
Rara |
C |
T |
11: 98,841,550 (GRCm39) |
S36F |
probably benign |
Het |
Rasal2 |
A |
G |
1: 157,003,264 (GRCm39) |
V465A |
probably damaging |
Het |
Slc22a1 |
C |
T |
17: 12,869,838 (GRCm39) |
G508R |
probably damaging |
Het |
Slco2a1 |
C |
A |
9: 102,927,468 (GRCm39) |
F120L |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,062,340 (GRCm39) |
L864* |
probably null |
Het |
Tssk4 |
A |
G |
14: 55,888,430 (GRCm39) |
I100V |
possibly damaging |
Het |
Vgll4 |
A |
G |
6: 114,867,576 (GRCm39) |
|
probably null |
Het |
Vps13b |
C |
T |
15: 35,456,824 (GRCm39) |
P757S |
probably benign |
Het |
Ythdc2 |
G |
A |
18: 44,977,359 (GRCm39) |
G385E |
probably damaging |
Het |
|
Other mutations in Vmn1r65 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01636:Vmn1r65
|
APN |
7 |
6,011,720 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02821:Vmn1r65
|
APN |
7 |
6,011,893 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0991:Vmn1r65
|
UTSW |
7 |
6,012,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R1457:Vmn1r65
|
UTSW |
7 |
6,012,156 (GRCm39) |
missense |
probably benign |
0.10 |
R1507:Vmn1r65
|
UTSW |
7 |
6,012,108 (GRCm39) |
missense |
probably benign |
0.13 |
R1856:Vmn1r65
|
UTSW |
7 |
6,011,265 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2914:Vmn1r65
|
UTSW |
7 |
6,012,040 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5279:Vmn1r65
|
UTSW |
7 |
6,011,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Vmn1r65
|
UTSW |
7 |
6,011,809 (GRCm39) |
nonsense |
probably null |
|
R5409:Vmn1r65
|
UTSW |
7 |
6,012,012 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5646:Vmn1r65
|
UTSW |
7 |
6,012,223 (GRCm39) |
missense |
probably benign |
0.01 |
R5963:Vmn1r65
|
UTSW |
7 |
6,011,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Vmn1r65
|
UTSW |
7 |
6,011,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Vmn1r65
|
UTSW |
7 |
6,011,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6327:Vmn1r65
|
UTSW |
7 |
6,011,651 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7958:Vmn1r65
|
UTSW |
7 |
6,011,254 (GRCm39) |
missense |
probably benign |
0.01 |
R8121:Vmn1r65
|
UTSW |
7 |
6,011,464 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8345:Vmn1r65
|
UTSW |
7 |
6,011,256 (GRCm39) |
missense |
probably benign |
|
R8725:Vmn1r65
|
UTSW |
7 |
6,011,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Vmn1r65
|
UTSW |
7 |
6,011,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Vmn1r65
|
UTSW |
7 |
6,011,769 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9279:Vmn1r65
|
UTSW |
7 |
6,011,988 (GRCm39) |
missense |
probably benign |
0.06 |
R9778:Vmn1r65
|
UTSW |
7 |
6,011,387 (GRCm39) |
nonsense |
probably null |
|
|