Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cacna1h |
A |
G |
17: 25,599,601 (GRCm39) |
V1588A |
probably damaging |
Het |
Card6 |
T |
A |
15: 5,130,536 (GRCm39) |
M287L |
probably damaging |
Het |
Fam227b |
T |
A |
2: 125,958,045 (GRCm39) |
Y240F |
possibly damaging |
Het |
Fbln1 |
T |
A |
15: 85,115,757 (GRCm39) |
|
probably null |
Het |
Fndc5 |
A |
G |
4: 129,036,322 (GRCm39) |
|
probably null |
Het |
Gm10799 |
C |
A |
2: 103,898,409 (GRCm39) |
A99S |
possibly damaging |
Het |
Gm27013 |
A |
T |
6: 130,654,728 (GRCm39) |
S245T |
possibly damaging |
Het |
Gm5592 |
A |
G |
7: 40,935,872 (GRCm39) |
T125A |
probably benign |
Het |
Gml2 |
T |
C |
15: 74,696,188 (GRCm39) |
|
probably benign |
Het |
Gpbp1 |
A |
T |
13: 111,585,498 (GRCm39) |
N149K |
possibly damaging |
Het |
Gprc6a |
T |
C |
10: 51,504,639 (GRCm39) |
I68M |
probably benign |
Het |
Hnrnpu |
T |
C |
1: 178,158,368 (GRCm39) |
|
probably benign |
Het |
Irf5 |
A |
G |
6: 29,534,000 (GRCm39) |
|
probably null |
Het |
Lrp2 |
T |
A |
2: 69,297,513 (GRCm39) |
K3149N |
probably benign |
Het |
Lrrn3 |
A |
G |
12: 41,504,041 (GRCm39) |
V92A |
probably benign |
Het |
Map3k12 |
T |
C |
15: 102,413,837 (GRCm39) |
T45A |
probably damaging |
Het |
Myof |
A |
G |
19: 37,911,426 (GRCm39) |
S1502P |
probably damaging |
Het |
Or4k77 |
T |
A |
2: 111,199,625 (GRCm39) |
I216K |
possibly damaging |
Het |
Or9s18 |
A |
G |
13: 65,300,514 (GRCm39) |
T159A |
probably benign |
Het |
Osr2 |
T |
C |
15: 35,300,617 (GRCm39) |
Y58H |
possibly damaging |
Het |
Pop5 |
C |
T |
5: 115,378,836 (GRCm39) |
|
probably benign |
Het |
Ror2 |
A |
G |
13: 53,272,997 (GRCm39) |
C211R |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Sgsm2 |
C |
A |
11: 74,742,592 (GRCm39) |
R957L |
probably damaging |
Het |
Slc16a11 |
A |
G |
11: 70,106,560 (GRCm39) |
|
probably null |
Het |
Spag17 |
T |
A |
3: 100,010,694 (GRCm39) |
Y2063N |
probably benign |
Het |
Usp25 |
A |
C |
16: 76,912,341 (GRCm39) |
K1020T |
probably damaging |
Het |
Vmn1r23 |
T |
C |
6: 57,903,353 (GRCm39) |
I142V |
probably benign |
Het |
Vmn1r235 |
A |
G |
17: 21,481,854 (GRCm39) |
K60E |
probably damaging |
Het |
Vps13b |
C |
T |
15: 35,709,440 (GRCm39) |
P1796S |
probably damaging |
Het |
Vwa3a |
G |
A |
7: 120,378,149 (GRCm39) |
V480I |
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 |
R6571:Vmn2r33
|
UTSW |
7 |
7,566,668 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|