Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002L01Rik |
C |
A |
12: 3,476,688 (GRCm39) |
|
probably benign |
Het |
2210408I21Rik |
T |
C |
13: 77,408,150 (GRCm39) |
I159T |
possibly damaging |
Het |
Agpat3 |
T |
A |
10: 78,120,900 (GRCm39) |
I93F |
probably damaging |
Het |
Armc8 |
T |
C |
9: 99,409,122 (GRCm39) |
|
probably benign |
Het |
Atr |
G |
A |
9: 95,790,453 (GRCm39) |
A1598T |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,095,633 (GRCm39) |
|
probably benign |
Het |
Clk1 |
T |
C |
1: 58,453,614 (GRCm39) |
D324G |
probably damaging |
Het |
Cntnap4 |
A |
T |
8: 113,537,355 (GRCm39) |
D742V |
probably damaging |
Het |
Esrrb |
A |
G |
12: 86,468,735 (GRCm39) |
N16S |
probably benign |
Het |
Grm1 |
A |
T |
10: 10,564,755 (GRCm39) |
Y1184* |
probably null |
Het |
Hint1 |
G |
T |
11: 54,761,011 (GRCm39) |
|
probably benign |
Het |
Itch |
A |
T |
2: 155,014,504 (GRCm39) |
|
probably null |
Het |
Lmod3 |
T |
C |
6: 97,215,796 (GRCm39) |
|
probably benign |
Het |
Map3k4 |
C |
A |
17: 12,482,900 (GRCm39) |
A606S |
probably damaging |
Het |
Mapk4 |
A |
T |
18: 74,103,346 (GRCm39) |
S54R |
probably damaging |
Het |
Megf11 |
A |
G |
9: 64,601,214 (GRCm39) |
D807G |
probably benign |
Het |
Mgat5 |
A |
G |
1: 127,325,326 (GRCm39) |
T398A |
possibly damaging |
Het |
Nme8 |
T |
G |
13: 19,859,818 (GRCm39) |
K28N |
probably damaging |
Het |
Pamr1 |
A |
G |
2: 102,464,688 (GRCm39) |
N279S |
probably benign |
Het |
Pcca |
A |
T |
14: 122,922,391 (GRCm39) |
D384V |
probably damaging |
Het |
Prkag1 |
A |
T |
15: 98,711,909 (GRCm39) |
I239N |
probably damaging |
Het |
Psme4 |
A |
G |
11: 30,798,131 (GRCm39) |
T1375A |
probably benign |
Het |
Ptk2 |
A |
C |
15: 73,077,994 (GRCm39) |
L1024R |
probably damaging |
Het |
Rere |
G |
A |
4: 150,698,269 (GRCm39) |
|
probably benign |
Het |
Scn2a |
A |
G |
2: 65,579,223 (GRCm39) |
|
probably benign |
Het |
Sema5a |
T |
A |
15: 32,538,802 (GRCm39) |
|
probably benign |
Het |
Shoc1 |
A |
T |
4: 59,062,668 (GRCm39) |
W863R |
probably damaging |
Het |
Slc9a1 |
T |
A |
4: 133,097,879 (GRCm39) |
W9R |
probably benign |
Het |
Slco1a5 |
T |
A |
6: 142,187,741 (GRCm39) |
M533L |
probably benign |
Het |
Ttll4 |
T |
A |
1: 74,726,643 (GRCm39) |
S720T |
probably damaging |
Het |
Vmn2r114 |
T |
C |
17: 23,529,494 (GRCm39) |
I203V |
probably damaging |
Het |
Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
|
Other mutations in Vmn1r168 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Vmn1r168
|
APN |
7 |
23,241,070 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02650:Vmn1r168
|
APN |
7 |
23,240,916 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4466001:Vmn1r168
|
UTSW |
7 |
23,240,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R0320:Vmn1r168
|
UTSW |
7 |
23,240,767 (GRCm39) |
missense |
probably benign |
0.12 |
R1595:Vmn1r168
|
UTSW |
7 |
23,240,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Vmn1r168
|
UTSW |
7 |
23,240,725 (GRCm39) |
missense |
probably benign |
0.02 |
R1808:Vmn1r168
|
UTSW |
7 |
23,240,184 (GRCm39) |
missense |
probably benign |
0.05 |
R2418:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R2419:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R4846:Vmn1r168
|
UTSW |
7 |
23,240,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Vmn1r168
|
UTSW |
7 |
23,240,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R5269:Vmn1r168
|
UTSW |
7 |
23,240,839 (GRCm39) |
missense |
probably benign |
0.40 |
R6265:Vmn1r168
|
UTSW |
7 |
23,240,961 (GRCm39) |
missense |
probably benign |
|
R6353:Vmn1r168
|
UTSW |
7 |
23,240,944 (GRCm39) |
missense |
probably benign |
0.02 |
R6768:Vmn1r168
|
UTSW |
7 |
23,240,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R6921:Vmn1r168
|
UTSW |
7 |
23,240,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Vmn1r168
|
UTSW |
7 |
23,240,487 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8749:Vmn1r168
|
UTSW |
7 |
23,240,428 (GRCm39) |
missense |
probably benign |
0.10 |
R9749:Vmn1r168
|
UTSW |
7 |
23,240,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R9768:Vmn1r168
|
UTSW |
7 |
23,240,509 (GRCm39) |
missense |
probably benign |
0.02 |
|