Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3300002I08Rik |
A |
G |
2: 150,152,980 (GRCm39) |
V135A |
unknown |
Het |
Cnot4 |
A |
T |
6: 35,047,183 (GRCm39) |
I143N |
probably damaging |
Het |
Cnot6l |
A |
T |
5: 96,234,105 (GRCm39) |
M302K |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,322,759 (GRCm39) |
T1542A |
probably damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,633,766 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,363,116 (GRCm39) |
S3893P |
probably benign |
Het |
Duox2 |
A |
T |
2: 122,117,683 (GRCm39) |
|
probably benign |
Het |
Dusp1 |
T |
C |
17: 26,725,295 (GRCm39) |
N355D |
probably benign |
Het |
Fam76b |
T |
C |
9: 13,741,046 (GRCm39) |
C60R |
probably damaging |
Het |
Gnptab |
G |
A |
10: 88,272,041 (GRCm39) |
V944I |
possibly damaging |
Het |
Gys1 |
A |
G |
7: 45,091,961 (GRCm39) |
Y249C |
probably damaging |
Het |
Ift88 |
A |
T |
14: 57,681,862 (GRCm39) |
E215D |
probably damaging |
Het |
Kcnu1 |
T |
C |
8: 26,424,551 (GRCm39) |
|
probably benign |
Het |
Lmln |
C |
A |
16: 32,937,490 (GRCm39) |
N618K |
probably benign |
Het |
Lrrc75a |
T |
C |
11: 62,496,813 (GRCm39) |
T250A |
probably damaging |
Het |
Mpp4 |
A |
G |
1: 59,164,719 (GRCm39) |
S435P |
probably damaging |
Het |
Myo1c |
T |
A |
11: 75,563,076 (GRCm39) |
V1036E |
probably damaging |
Het |
Nlrp12 |
T |
G |
7: 3,289,316 (GRCm39) |
T399P |
probably damaging |
Het |
Or2y16 |
A |
G |
11: 49,335,595 (GRCm39) |
R306G |
probably benign |
Het |
Or4c118 |
A |
G |
2: 88,974,575 (GRCm39) |
F264S |
possibly damaging |
Het |
Parp8 |
A |
T |
13: 117,031,600 (GRCm39) |
C332S |
possibly damaging |
Het |
Pdcd11 |
G |
A |
19: 47,098,053 (GRCm39) |
V780I |
probably benign |
Het |
Plekha5 |
A |
G |
6: 140,480,292 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
T |
A |
4: 122,737,848 (GRCm39) |
I62K |
probably damaging |
Het |
Proser3 |
T |
C |
7: 30,249,071 (GRCm39) |
N7S |
probably benign |
Het |
Ptk2b |
A |
G |
14: 66,414,567 (GRCm39) |
L311P |
possibly damaging |
Het |
Rasal2 |
T |
C |
1: 156,988,786 (GRCm39) |
N706S |
probably benign |
Het |
Ripk2 |
A |
G |
4: 16,132,775 (GRCm39) |
|
probably null |
Het |
Setx |
T |
A |
2: 29,034,821 (GRCm39) |
H435Q |
probably damaging |
Het |
Smurf2 |
T |
A |
11: 106,721,741 (GRCm39) |
|
probably benign |
Het |
Snx32 |
A |
G |
19: 5,547,764 (GRCm39) |
L182P |
possibly damaging |
Het |
Stpg2 |
A |
G |
3: 139,125,635 (GRCm39) |
|
probably benign |
Het |
Taar2 |
A |
G |
10: 23,816,997 (GRCm39) |
Y179C |
probably damaging |
Het |
Tenm2 |
G |
A |
11: 35,918,232 (GRCm39) |
R1843* |
probably null |
Het |
Tmco4 |
T |
C |
4: 138,748,260 (GRCm39) |
I280T |
probably damaging |
Het |
Tuba4a |
C |
A |
1: 75,193,921 (GRCm39) |
C46F |
probably damaging |
Het |
Ubr1 |
A |
G |
2: 120,703,603 (GRCm39) |
|
probably null |
Het |
Vldlr |
A |
T |
19: 27,217,081 (GRCm39) |
I45L |
possibly damaging |
Het |
Vmn2r120 |
C |
A |
17: 57,852,232 (GRCm39) |
G28V |
probably benign |
Het |
Vmn2r67 |
A |
G |
7: 84,786,127 (GRCm39) |
L626P |
probably damaging |
Het |
Wdr19 |
C |
T |
5: 65,379,082 (GRCm39) |
|
probably benign |
Het |
Zfp595 |
T |
A |
13: 67,464,749 (GRCm39) |
K505* |
probably null |
Het |
|
Other mutations in Vmn2r37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01909:Vmn2r37
|
APN |
7 |
9,219,032 (GRCm39) |
nonsense |
probably null |
|
IGL02281:Vmn2r37
|
APN |
7 |
9,220,881 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02282:Vmn2r37
|
APN |
7 |
9,209,761 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02513:Vmn2r37
|
APN |
7 |
9,220,934 (GRCm39) |
missense |
probably benign |
0.14 |
R0136:Vmn2r37
|
UTSW |
7 |
9,220,782 (GRCm39) |
nonsense |
probably null |
|
R2051:Vmn2r37
|
UTSW |
7 |
9,220,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R2262:Vmn2r37
|
UTSW |
7 |
9,220,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R3158:Vmn2r37
|
UTSW |
7 |
9,220,713 (GRCm39) |
missense |
probably benign |
0.03 |
R4084:Vmn2r37
|
UTSW |
7 |
9,218,984 (GRCm39) |
missense |
probably benign |
|
R4114:Vmn2r37
|
UTSW |
7 |
9,213,092 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5231:Vmn2r37
|
UTSW |
7 |
9,209,594 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5462:Vmn2r37
|
UTSW |
7 |
9,220,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R6437:Vmn2r37
|
UTSW |
7 |
9,220,850 (GRCm39) |
missense |
probably damaging |
0.98 |
R7104:Vmn2r37
|
UTSW |
7 |
9,219,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Vmn2r37
|
UTSW |
7 |
9,220,898 (GRCm39) |
missense |
probably benign |
0.00 |
R7381:Vmn2r37
|
UTSW |
7 |
9,213,032 (GRCm39) |
missense |
probably benign |
0.21 |
R8775:Vmn2r37
|
UTSW |
7 |
9,218,991 (GRCm39) |
nonsense |
probably null |
|
R8775-TAIL:Vmn2r37
|
UTSW |
7 |
9,218,991 (GRCm39) |
nonsense |
probably null |
|
R8869:Vmn2r37
|
UTSW |
7 |
9,209,854 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8884:Vmn2r37
|
UTSW |
7 |
9,218,916 (GRCm39) |
missense |
probably benign |
|
RF004:Vmn2r37
|
UTSW |
7 |
9,220,686 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Vmn2r37
|
UTSW |
7 |
9,212,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|