Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl6 |
A |
G |
11: 54,216,390 (GRCm39) |
I161V |
possibly damaging |
Het |
Adamts12 |
T |
C |
15: 11,065,187 (GRCm39) |
F24S |
probably benign |
Het |
Bche |
G |
T |
3: 73,608,824 (GRCm39) |
Q201K |
probably benign |
Het |
Camsap1 |
A |
T |
2: 25,829,512 (GRCm39) |
D757E |
possibly damaging |
Het |
Crebbp |
C |
T |
16: 3,937,670 (GRCm39) |
A698T |
possibly damaging |
Het |
Dab2ip |
T |
C |
2: 35,602,902 (GRCm39) |
S399P |
probably damaging |
Het |
Fbxo40 |
A |
T |
16: 36,789,668 (GRCm39) |
C481S |
probably damaging |
Het |
Fn1 |
T |
A |
1: 71,665,349 (GRCm39) |
T923S |
probably damaging |
Het |
Gm11437 |
T |
C |
11: 84,047,038 (GRCm39) |
D147G |
probably benign |
Het |
Gm5592 |
A |
G |
7: 40,937,999 (GRCm39) |
E427G |
probably damaging |
Het |
Gm6401 |
T |
A |
14: 41,787,452 (GRCm39) |
I125F |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,491,189 (GRCm39) |
|
probably null |
Het |
Inpp4a |
T |
C |
1: 37,426,839 (GRCm39) |
M600T |
probably damaging |
Het |
Itgb6 |
T |
C |
2: 60,458,800 (GRCm39) |
E374G |
probably damaging |
Het |
Lrba |
A |
C |
3: 86,267,367 (GRCm39) |
S1686R |
probably damaging |
Het |
Map3k4 |
T |
C |
17: 12,461,579 (GRCm39) |
D1200G |
possibly damaging |
Het |
Mmp25 |
T |
C |
17: 23,858,870 (GRCm39) |
H227R |
probably benign |
Het |
Or6c38 |
A |
C |
10: 128,928,990 (GRCm39) |
N284K |
probably damaging |
Het |
Papss2 |
G |
A |
19: 32,629,342 (GRCm39) |
|
probably null |
Het |
Rasal2 |
T |
A |
1: 156,988,749 (GRCm39) |
R718S |
possibly damaging |
Het |
Relch |
A |
G |
1: 105,620,707 (GRCm39) |
D394G |
probably benign |
Het |
Rngtt |
T |
A |
4: 33,379,413 (GRCm39) |
D438E |
probably damaging |
Het |
S1pr1 |
A |
G |
3: 115,505,452 (GRCm39) |
S381P |
possibly damaging |
Het |
Septin8 |
A |
G |
11: 53,427,990 (GRCm39) |
E268G |
probably damaging |
Het |
Slc6a21 |
A |
G |
7: 44,930,303 (GRCm39) |
K234R |
probably damaging |
Het |
Smg1 |
A |
G |
7: 117,783,737 (GRCm39) |
|
probably benign |
Het |
Sntg1 |
T |
C |
1: 8,433,752 (GRCm39) |
|
probably benign |
Het |
Spag5 |
G |
T |
11: 78,212,095 (GRCm39) |
R1041I |
probably damaging |
Het |
Spata31d1b |
A |
T |
13: 59,865,269 (GRCm39) |
M806L |
probably benign |
Het |
Tnfrsf18 |
T |
A |
4: 156,112,776 (GRCm39) |
L154* |
probably null |
Het |
Trib2 |
T |
C |
12: 15,844,060 (GRCm39) |
E194G |
probably damaging |
Het |
Wiz |
G |
A |
17: 32,578,298 (GRCm39) |
R405W |
probably damaging |
Het |
Zfp747l1 |
T |
C |
7: 126,984,310 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn2r33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01893:Vmn2r33
|
APN |
7 |
7,566,776 (GRCm39) |
missense |
probably benign |
|
R1147:Vmn2r33
|
UTSW |
7 |
7,557,144 (GRCm39) |
missense |
probably benign |
0.16 |
R1147:Vmn2r33
|
UTSW |
7 |
7,557,144 (GRCm39) |
missense |
probably benign |
0.16 |
R3966:Vmn2r33
|
UTSW |
7 |
7,557,168 (GRCm39) |
missense |
probably benign |
0.00 |
R4408:Vmn2r33
|
UTSW |
7 |
7,554,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Vmn2r33
|
UTSW |
7 |
7,566,797 (GRCm39) |
missense |
probably benign |
|
R7180:Vmn2r33
|
UTSW |
7 |
7,566,896 (GRCm39) |
missense |
probably benign |
0.00 |
R7984:Vmn2r33
|
UTSW |
7 |
7,566,862 (GRCm39) |
missense |
probably benign |
0.01 |
R8202:Vmn2r33
|
UTSW |
7 |
7,557,153 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8894:Vmn2r33
|
UTSW |
7 |
7,566,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8954:Vmn2r33
|
UTSW |
7 |
7,554,655 (GRCm39) |
missense |
probably benign |
0.02 |
R8995:Vmn2r33
|
UTSW |
7 |
7,554,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R9027:Vmn2r33
|
UTSW |
7 |
7,554,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Vmn2r33
|
UTSW |
7 |
7,557,081 (GRCm39) |
missense |
probably benign |
0.06 |
R9608:Vmn2r33
|
UTSW |
7 |
7,557,153 (GRCm39) |
missense |
possibly damaging |
0.87 |
|