Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts7 |
A |
G |
9: 90,089,838 (GRCm39) |
I897T |
possibly damaging |
Het |
Aqp2 |
G |
A |
15: 99,477,301 (GRCm39) |
V90M |
possibly damaging |
Het |
Atf6 |
T |
C |
1: 170,680,571 (GRCm39) |
|
probably benign |
Het |
Cdh3 |
T |
C |
8: 107,274,301 (GRCm39) |
Y607H |
probably damaging |
Het |
Cer1 |
T |
A |
4: 82,801,068 (GRCm39) |
E198D |
probably benign |
Het |
Dscam |
A |
G |
16: 96,453,278 (GRCm39) |
|
probably null |
Het |
Ecel1 |
C |
T |
1: 87,079,226 (GRCm39) |
R484H |
probably damaging |
Het |
Entpd7 |
C |
A |
19: 43,718,278 (GRCm39) |
H575Q |
probably benign |
Het |
F11r |
T |
C |
1: 171,290,477 (GRCm39) |
V279A |
probably damaging |
Het |
Gm17093 |
T |
A |
14: 44,759,122 (GRCm39) |
|
probably benign |
Het |
Got1 |
T |
A |
19: 43,491,488 (GRCm39) |
K321* |
probably null |
Het |
Gpn1 |
T |
C |
5: 31,664,882 (GRCm39) |
V302A |
probably benign |
Het |
Hivep1 |
G |
T |
13: 42,311,493 (GRCm39) |
K1244N |
probably damaging |
Het |
Idh3b |
T |
C |
2: 130,123,817 (GRCm39) |
T116A |
possibly damaging |
Het |
Itgb4 |
C |
A |
11: 115,897,283 (GRCm39) |
|
probably benign |
Het |
Mybl1 |
G |
T |
1: 9,742,872 (GRCm39) |
L579I |
probably damaging |
Het |
Myh14 |
T |
A |
7: 44,263,782 (GRCm39) |
T1694S |
probably null |
Het |
Mylk3 |
T |
C |
8: 86,063,030 (GRCm39) |
D537G |
probably damaging |
Het |
Myo1d |
A |
C |
11: 80,565,665 (GRCm39) |
F387V |
probably damaging |
Het |
Nek9 |
T |
C |
12: 85,361,361 (GRCm39) |
Y448C |
probably benign |
Het |
Or8k40 |
A |
T |
2: 86,584,508 (GRCm39) |
H191Q |
probably benign |
Het |
Paxbp1 |
T |
C |
16: 90,832,804 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
A |
T |
2: 111,055,740 (GRCm39) |
|
probably benign |
Het |
Retreg2 |
T |
A |
1: 75,121,749 (GRCm39) |
|
probably null |
Het |
Ripply3 |
G |
A |
16: 94,129,402 (GRCm39) |
C16Y |
possibly damaging |
Het |
Robo3 |
G |
A |
9: 37,330,407 (GRCm39) |
|
probably benign |
Het |
Rrm1 |
C |
A |
7: 102,106,759 (GRCm39) |
|
probably benign |
Het |
Rsad2 |
T |
A |
12: 26,498,666 (GRCm39) |
R269S |
probably benign |
Het |
Sbp |
A |
T |
17: 24,164,322 (GRCm39) |
|
probably benign |
Het |
Schip1 |
A |
T |
3: 68,525,110 (GRCm39) |
Q162L |
probably damaging |
Het |
Senp1 |
T |
C |
15: 97,980,144 (GRCm39) |
Y67C |
probably damaging |
Het |
Slc25a25 |
C |
T |
2: 32,309,103 (GRCm39) |
R233K |
probably damaging |
Het |
Smoc1 |
C |
A |
12: 81,199,525 (GRCm39) |
S220* |
probably null |
Het |
Stab1 |
C |
A |
14: 30,870,952 (GRCm39) |
R1299I |
probably benign |
Het |
Stk17b |
A |
G |
1: 53,805,074 (GRCm39) |
|
probably benign |
Het |
Tmc7 |
T |
G |
7: 118,151,985 (GRCm39) |
D312A |
probably damaging |
Het |
Zfc3h1 |
C |
A |
10: 115,259,128 (GRCm39) |
T1591K |
possibly damaging |
Het |
|
Other mutations in Vmn1r79 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00592:Vmn1r79
|
APN |
7 |
11,910,934 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01953:Vmn1r79
|
APN |
7 |
11,910,382 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4418001:Vmn1r79
|
UTSW |
7 |
11,910,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R0831:Vmn1r79
|
UTSW |
7 |
11,910,990 (GRCm39) |
missense |
probably damaging |
0.98 |
R1791:Vmn1r79
|
UTSW |
7 |
11,910,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1869:Vmn1r79
|
UTSW |
7 |
11,910,574 (GRCm39) |
missense |
probably benign |
0.00 |
R3713:Vmn1r79
|
UTSW |
7 |
11,910,139 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4210:Vmn1r79
|
UTSW |
7 |
11,910,415 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4243:Vmn1r79
|
UTSW |
7 |
11,910,971 (GRCm39) |
nonsense |
probably null |
|
R4244:Vmn1r79
|
UTSW |
7 |
11,910,971 (GRCm39) |
nonsense |
probably null |
|
R4839:Vmn1r79
|
UTSW |
7 |
11,910,361 (GRCm39) |
missense |
probably benign |
0.30 |
R5677:Vmn1r79
|
UTSW |
7 |
11,910,928 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6048:Vmn1r79
|
UTSW |
7 |
11,910,448 (GRCm39) |
missense |
probably damaging |
0.99 |
R7388:Vmn1r79
|
UTSW |
7 |
11,910,668 (GRCm39) |
nonsense |
probably null |
|
R7751:Vmn1r79
|
UTSW |
7 |
11,910,762 (GRCm39) |
nonsense |
probably null |
|
R8207:Vmn1r79
|
UTSW |
7 |
11,910,415 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9462:Vmn1r79
|
UTSW |
7 |
11,910,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Vmn1r79
|
UTSW |
7 |
11,910,582 (GRCm39) |
missense |
probably benign |
0.00 |
R9749:Vmn1r79
|
UTSW |
7 |
11,910,450 (GRCm39) |
missense |
probably damaging |
1.00 |
|