Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot2 |
C |
T |
12: 84,039,630 (GRCm39) |
R380C |
possibly damaging |
Het |
Allc |
A |
T |
12: 28,603,993 (GRCm39) |
D363E |
probably damaging |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
App |
C |
A |
16: 84,876,837 (GRCm39) |
V185L |
probably damaging |
Het |
Atp5if1 |
T |
C |
4: 132,258,078 (GRCm39) |
D47G |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Cbr4 |
T |
A |
8: 61,956,192 (GRCm39) |
Y220N |
probably damaging |
Het |
Ccdc6 |
C |
A |
10: 70,002,877 (GRCm39) |
Q203K |
probably damaging |
Het |
Cntnap2 |
T |
C |
6: 45,992,264 (GRCm39) |
V397A |
probably benign |
Het |
Dmxl2 |
A |
G |
9: 54,316,547 (GRCm39) |
I1613T |
possibly damaging |
Het |
Dnah14 |
T |
C |
1: 181,577,742 (GRCm39) |
S3020P |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,392,126 (GRCm39) |
L3829P |
probably damaging |
Het |
Fbxw25 |
C |
T |
9: 109,492,578 (GRCm39) |
C53Y |
probably benign |
Het |
Fndc1 |
G |
T |
17: 7,991,598 (GRCm39) |
H699Q |
unknown |
Het |
Gnaq |
G |
A |
19: 16,360,618 (GRCm39) |
V314M |
possibly damaging |
Het |
Gpr158 |
A |
G |
2: 21,788,104 (GRCm39) |
T582A |
possibly damaging |
Het |
Mapk1 |
T |
C |
16: 16,856,170 (GRCm39) |
|
probably benign |
Het |
Med1 |
T |
A |
11: 98,051,996 (GRCm39) |
H456L |
possibly damaging |
Het |
Myo6 |
G |
A |
9: 80,195,499 (GRCm39) |
|
probably null |
Het |
Nipbl |
A |
G |
15: 8,396,148 (GRCm39) |
Y142H |
probably damaging |
Het |
Or4c113 |
A |
T |
2: 88,885,688 (GRCm39) |
F27L |
probably benign |
Het |
Or8k24 |
A |
G |
2: 86,215,838 (GRCm39) |
I308T |
probably benign |
Het |
Or8k33 |
A |
C |
2: 86,383,949 (GRCm39) |
V173G |
probably damaging |
Het |
Pgbd5 |
T |
C |
8: 125,160,750 (GRCm39) |
D39G |
probably benign |
Het |
Pnisr |
G |
T |
4: 21,871,440 (GRCm39) |
G387* |
probably null |
Het |
Pnpla6 |
T |
C |
8: 3,567,135 (GRCm39) |
L61P |
probably damaging |
Het |
Prkra |
A |
T |
2: 76,463,936 (GRCm39) |
I242N |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,419,424 (GRCm39) |
S563P |
probably damaging |
Het |
Rtp3 |
A |
G |
9: 110,815,085 (GRCm39) |
|
probably benign |
Het |
Sema3d |
A |
G |
5: 12,591,023 (GRCm39) |
T301A |
probably damaging |
Het |
Setmar |
A |
G |
6: 108,053,076 (GRCm39) |
D190G |
probably benign |
Het |
Sf3b2 |
A |
G |
19: 5,345,061 (GRCm39) |
|
probably benign |
Het |
Taf4b |
A |
G |
18: 14,968,938 (GRCm39) |
K692E |
probably damaging |
Het |
Tktl2 |
A |
G |
8: 66,965,504 (GRCm39) |
E354G |
probably benign |
Het |
Tspan4 |
A |
G |
7: 141,071,557 (GRCm39) |
T135A |
probably damaging |
Het |
Vmn1r22 |
G |
T |
6: 57,877,733 (GRCm39) |
Y81* |
probably null |
Het |
Xrn1 |
A |
T |
9: 95,856,946 (GRCm39) |
K389N |
probably benign |
Het |
Zfp277 |
A |
T |
12: 40,378,719 (GRCm39) |
N379K |
probably damaging |
Het |
|
Other mutations in Vmn2r31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01104:Vmn2r31
|
APN |
7 |
7,399,565 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01536:Vmn2r31
|
APN |
7 |
7,387,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Vmn2r31
|
APN |
7 |
7,397,510 (GRCm39) |
missense |
probably benign |
|
IGL02116:Vmn2r31
|
APN |
7 |
7,397,548 (GRCm39) |
missense |
probably damaging |
0.97 |
FR4304:Vmn2r31
|
UTSW |
7 |
7,387,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Vmn2r31
|
UTSW |
7 |
7,387,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Vmn2r31
|
UTSW |
7 |
7,387,757 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4824:Vmn2r31
|
UTSW |
7 |
7,390,062 (GRCm39) |
critical splice donor site |
probably null |
|
R5619:Vmn2r31
|
UTSW |
7 |
7,387,529 (GRCm39) |
nonsense |
probably null |
|
R6225:Vmn2r31
|
UTSW |
7 |
7,397,638 (GRCm39) |
missense |
probably benign |
0.19 |
R6610:Vmn2r31
|
UTSW |
7 |
7,387,588 (GRCm39) |
missense |
probably damaging |
0.97 |
R6956:Vmn2r31
|
UTSW |
7 |
7,397,505 (GRCm39) |
missense |
probably benign |
|
R7111:Vmn2r31
|
UTSW |
7 |
7,399,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R7219:Vmn2r31
|
UTSW |
7 |
7,397,397 (GRCm39) |
missense |
probably damaging |
0.97 |
R7219:Vmn2r31
|
UTSW |
7 |
7,390,105 (GRCm39) |
missense |
probably benign |
|
R7300:Vmn2r31
|
UTSW |
7 |
7,387,775 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7395:Vmn2r31
|
UTSW |
7 |
7,387,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Vmn2r31
|
UTSW |
7 |
7,387,579 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8015:Vmn2r31
|
UTSW |
7 |
7,387,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8434:Vmn2r31
|
UTSW |
7 |
7,387,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R8781:Vmn2r31
|
UTSW |
7 |
7,387,400 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8972:Vmn2r31
|
UTSW |
7 |
7,399,654 (GRCm39) |
missense |
probably benign |
0.00 |
R9034:Vmn2r31
|
UTSW |
7 |
7,397,680 (GRCm39) |
missense |
probably benign |
0.08 |
R9596:Vmn2r31
|
UTSW |
7 |
7,397,292 (GRCm39) |
missense |
probably benign |
0.01 |
R9711:Vmn2r31
|
UTSW |
7 |
7,387,085 (GRCm39) |
missense |
probably damaging |
0.99 |
R9714:Vmn2r31
|
UTSW |
7 |
7,387,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|