Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd5 |
T |
C |
9: 122,197,290 (GRCm39) |
F116S |
probably damaging |
Het |
Accsl |
A |
G |
2: 93,693,129 (GRCm39) |
|
probably benign |
Het |
Adgrl2 |
T |
A |
3: 148,523,036 (GRCm39) |
E165V |
probably damaging |
Het |
Alb |
T |
C |
5: 90,609,573 (GRCm39) |
|
probably benign |
Het |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Arhgef10 |
T |
C |
8: 14,978,847 (GRCm39) |
V38A |
probably benign |
Het |
Astn2 |
A |
G |
4: 65,664,530 (GRCm39) |
|
probably benign |
Het |
Bahcc1 |
G |
A |
11: 120,159,235 (GRCm39) |
R154H |
probably damaging |
Het |
Cep120 |
A |
G |
18: 53,868,844 (GRCm39) |
Y112H |
probably benign |
Het |
Chrna5 |
C |
T |
9: 54,911,923 (GRCm39) |
T241I |
probably damaging |
Het |
Clasp1 |
A |
G |
1: 118,530,206 (GRCm39) |
S1215G |
probably benign |
Het |
Ddx21 |
C |
T |
10: 62,427,769 (GRCm39) |
R378Q |
possibly damaging |
Het |
Dnah1 |
A |
T |
14: 30,991,846 (GRCm39) |
L3052Q |
probably damaging |
Het |
Dyrk4 |
G |
T |
6: 126,861,016 (GRCm39) |
T445K |
probably benign |
Het |
Ercc4 |
T |
C |
16: 12,945,457 (GRCm39) |
W291R |
probably damaging |
Het |
Flvcr1 |
A |
G |
1: 190,757,939 (GRCm39) |
W76R |
probably damaging |
Het |
Frmd3 |
A |
G |
4: 74,046,455 (GRCm39) |
I132V |
possibly damaging |
Het |
Gnb4 |
T |
C |
3: 32,639,324 (GRCm39) |
D323G |
probably damaging |
Het |
Hnrnpc |
G |
A |
14: 52,312,896 (GRCm39) |
|
probably benign |
Het |
Hnrnpl |
T |
C |
7: 28,513,505 (GRCm39) |
S202P |
probably benign |
Het |
Hydin |
T |
A |
8: 111,321,921 (GRCm39) |
F4524L |
probably damaging |
Het |
Iars2 |
A |
G |
1: 185,023,629 (GRCm39) |
|
probably benign |
Het |
Ino80d |
A |
G |
1: 63,107,341 (GRCm39) |
|
probably null |
Het |
Itga8 |
C |
A |
2: 12,137,327 (GRCm39) |
A13S |
probably benign |
Het |
Man2a1 |
T |
C |
17: 65,020,606 (GRCm39) |
F794S |
probably damaging |
Het |
Mpp7 |
T |
C |
18: 7,403,269 (GRCm39) |
D347G |
probably benign |
Het |
Nup93 |
T |
C |
8: 95,032,716 (GRCm39) |
L411P |
probably damaging |
Het |
Or51f23 |
C |
T |
7: 102,452,846 (GRCm39) |
Q54* |
probably null |
Het |
Plin1 |
C |
T |
7: 79,372,382 (GRCm39) |
V86I |
probably damaging |
Het |
Rgs6 |
A |
G |
12: 83,099,324 (GRCm39) |
|
probably benign |
Het |
Shroom3 |
C |
T |
5: 93,100,399 (GRCm39) |
P1473S |
probably benign |
Het |
Slc12a8 |
A |
G |
16: 33,371,397 (GRCm39) |
I178V |
probably damaging |
Het |
Slc20a2 |
T |
A |
8: 23,048,999 (GRCm39) |
S219T |
probably benign |
Het |
Tasor |
C |
T |
14: 27,198,649 (GRCm39) |
T1327I |
probably damaging |
Het |
Tfeb |
T |
C |
17: 48,097,920 (GRCm39) |
M36T |
probably benign |
Het |
Trim33 |
G |
A |
3: 103,218,289 (GRCm39) |
|
probably benign |
Het |
Trnau1ap |
A |
G |
4: 132,049,114 (GRCm39) |
Y30H |
probably damaging |
Het |
Tulp1 |
T |
C |
17: 28,578,298 (GRCm39) |
K276E |
possibly damaging |
Het |
Uvssa |
T |
A |
5: 33,549,160 (GRCm39) |
I340N |
probably damaging |
Het |
Xpc |
T |
C |
6: 91,481,565 (GRCm39) |
N250S |
probably damaging |
Het |
Ybey |
T |
C |
10: 76,304,161 (GRCm39) |
I14V |
probably benign |
Het |
Zfhx3 |
T |
C |
8: 109,673,182 (GRCm39) |
Y1411H |
probably damaging |
Het |
|
Other mutations in Vmn1r32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01449:Vmn1r32
|
APN |
6 |
66,529,916 (GRCm39) |
missense |
probably benign |
|
IGL02399:Vmn1r32
|
APN |
6 |
66,529,913 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02964:Vmn1r32
|
APN |
6 |
66,529,922 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03161:Vmn1r32
|
APN |
6 |
66,530,204 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03244:Vmn1r32
|
APN |
6 |
66,530,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R0668:Vmn1r32
|
UTSW |
6 |
66,530,644 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0732:Vmn1r32
|
UTSW |
6 |
66,530,690 (GRCm39) |
missense |
probably benign |
0.01 |
R1205:Vmn1r32
|
UTSW |
6 |
66,530,539 (GRCm39) |
missense |
probably benign |
0.01 |
R1638:Vmn1r32
|
UTSW |
6 |
66,529,939 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1732:Vmn1r32
|
UTSW |
6 |
66,530,285 (GRCm39) |
missense |
probably benign |
0.19 |
R2049:Vmn1r32
|
UTSW |
6 |
66,530,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Vmn1r32
|
UTSW |
6 |
66,530,533 (GRCm39) |
missense |
probably benign |
0.09 |
R3773:Vmn1r32
|
UTSW |
6 |
66,530,351 (GRCm39) |
missense |
probably benign |
0.01 |
R3834:Vmn1r32
|
UTSW |
6 |
66,530,647 (GRCm39) |
missense |
probably benign |
0.02 |
R3980:Vmn1r32
|
UTSW |
6 |
66,530,698 (GRCm39) |
missense |
probably damaging |
0.98 |
R4737:Vmn1r32
|
UTSW |
6 |
66,530,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Vmn1r32
|
UTSW |
6 |
66,530,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R6382:Vmn1r32
|
UTSW |
6 |
66,530,345 (GRCm39) |
missense |
probably benign |
0.07 |
R6894:Vmn1r32
|
UTSW |
6 |
66,530,345 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7394:Vmn1r32
|
UTSW |
6 |
66,530,173 (GRCm39) |
missense |
probably benign |
0.06 |
R7980:Vmn1r32
|
UTSW |
6 |
66,530,305 (GRCm39) |
nonsense |
probably null |
|
R8833:Vmn1r32
|
UTSW |
6 |
66,530,623 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8867:Vmn1r32
|
UTSW |
6 |
66,530,651 (GRCm39) |
missense |
probably damaging |
0.98 |
R8975:Vmn1r32
|
UTSW |
6 |
66,530,189 (GRCm39) |
missense |
probably benign |
0.03 |
R9131:Vmn1r32
|
UTSW |
6 |
66,530,020 (GRCm39) |
missense |
probably benign |
0.30 |
R9135:Vmn1r32
|
UTSW |
6 |
66,530,120 (GRCm39) |
nonsense |
probably null |
|
R9429:Vmn1r32
|
UTSW |
6 |
66,530,237 (GRCm39) |
missense |
probably benign |
0.03 |
|