Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
G |
A |
11: 110,165,170 (GRCm39) |
Q1581* |
probably null |
Het |
Abcc10 |
A |
T |
17: 46,635,085 (GRCm39) |
|
probably null |
Het |
Adam25 |
A |
G |
8: 41,208,423 (GRCm39) |
Y563C |
probably damaging |
Het |
Cnr2 |
T |
A |
4: 135,644,522 (GRCm39) |
I200N |
possibly damaging |
Het |
Col5a2 |
T |
C |
1: 45,422,747 (GRCm39) |
|
probably null |
Het |
Cpa2 |
T |
C |
6: 30,557,666 (GRCm39) |
|
probably benign |
Het |
Dis3l2 |
T |
C |
1: 86,917,953 (GRCm39) |
V534A |
probably damaging |
Het |
Dlg2 |
A |
T |
7: 92,093,746 (GRCm39) |
D845V |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,925,487 (GRCm39) |
|
probably null |
Het |
Ephb4 |
T |
A |
5: 137,352,763 (GRCm39) |
Y115* |
probably null |
Het |
Evc2 |
A |
G |
5: 37,535,681 (GRCm39) |
Y452C |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,163,530 (GRCm39) |
|
probably benign |
Het |
Gm5134 |
A |
T |
10: 75,844,334 (GRCm39) |
|
probably null |
Het |
Hoxc6 |
A |
G |
15: 102,918,308 (GRCm39) |
T91A |
probably benign |
Het |
Lin9 |
C |
A |
1: 180,516,865 (GRCm39) |
A535E |
probably damaging |
Het |
Muc1 |
G |
A |
3: 89,138,935 (GRCm39) |
V515I |
probably benign |
Het |
Mup3 |
A |
G |
4: 62,003,016 (GRCm39) |
I170T |
probably damaging |
Het |
Myo1e |
T |
C |
9: 70,291,081 (GRCm39) |
|
probably benign |
Het |
Or3a1d |
A |
G |
11: 74,238,254 (GRCm39) |
V52A |
possibly damaging |
Het |
Or8b50 |
A |
G |
9: 38,518,538 (GRCm39) |
Y259C |
probably damaging |
Het |
Pde4d |
T |
C |
13: 109,877,084 (GRCm39) |
S202P |
probably damaging |
Het |
Pomt2 |
A |
G |
12: 87,158,185 (GRCm39) |
V676A |
probably benign |
Het |
Rasl10a |
C |
A |
11: 5,008,333 (GRCm39) |
L10M |
probably damaging |
Het |
Rilp |
T |
C |
11: 75,403,538 (GRCm39) |
Y327H |
probably damaging |
Het |
Sec23ip |
A |
G |
7: 128,380,903 (GRCm39) |
S957G |
probably damaging |
Het |
Srbd1 |
T |
C |
17: 86,406,050 (GRCm39) |
|
probably null |
Het |
Thsd7a |
T |
C |
6: 12,555,257 (GRCm39) |
H209R |
probably benign |
Het |
Trav14-3 |
T |
C |
14: 54,000,643 (GRCm39) |
|
probably benign |
Het |
Vipr2 |
A |
G |
12: 116,058,356 (GRCm39) |
N91S |
probably damaging |
Het |
Zfp318 |
C |
T |
17: 46,707,736 (GRCm39) |
R265* |
probably null |
Het |
|
Other mutations in Gpr157 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01611:Gpr157
|
APN |
4 |
150,186,094 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2912:Gpr157
|
UTSW |
4 |
150,183,222 (GRCm39) |
missense |
probably benign |
0.08 |
R2913:Gpr157
|
UTSW |
4 |
150,183,222 (GRCm39) |
missense |
probably benign |
0.08 |
R4721:Gpr157
|
UTSW |
4 |
150,183,420 (GRCm39) |
missense |
probably benign |
0.01 |
R4840:Gpr157
|
UTSW |
4 |
150,186,823 (GRCm39) |
missense |
probably benign |
0.00 |
R5089:Gpr157
|
UTSW |
4 |
150,186,750 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5322:Gpr157
|
UTSW |
4 |
150,183,309 (GRCm39) |
missense |
probably benign |
|
R5445:Gpr157
|
UTSW |
4 |
150,186,825 (GRCm39) |
missense |
probably benign |
0.00 |
R6210:Gpr157
|
UTSW |
4 |
150,186,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R7252:Gpr157
|
UTSW |
4 |
150,183,331 (GRCm39) |
missense |
probably benign |
0.01 |
R8246:Gpr157
|
UTSW |
4 |
150,186,753 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8274:Gpr157
|
UTSW |
4 |
150,172,500 (GRCm39) |
missense |
probably damaging |
1.00 |
|