Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bcar3 |
C |
T |
3: 122,306,417 (GRCm39) |
|
probably null |
Het |
Cyp3a59 |
T |
C |
5: 146,027,556 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
G |
A |
11: 69,343,759 (GRCm39) |
T2844M |
probably benign |
Het |
Ehbp1l1 |
T |
C |
19: 5,770,853 (GRCm39) |
I241M |
probably damaging |
Het |
Fancl |
G |
A |
11: 26,418,722 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
G |
16: 57,392,142 (GRCm39) |
Q910R |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,658,641 (GRCm39) |
V1139E |
probably damaging |
Het |
Gm4787 |
A |
G |
12: 81,425,543 (GRCm39) |
V205A |
possibly damaging |
Het |
Gpr158 |
T |
A |
2: 21,820,441 (GRCm39) |
L646Q |
probably damaging |
Het |
Il11ra1 |
T |
A |
4: 41,768,552 (GRCm39) |
M412K |
possibly damaging |
Het |
Klra10 |
T |
A |
6: 130,256,382 (GRCm39) |
M91L |
probably damaging |
Het |
Krba1 |
T |
A |
6: 48,381,052 (GRCm39) |
D129E |
probably damaging |
Het |
Mat1a |
T |
C |
14: 40,844,453 (GRCm39) |
|
probably benign |
Het |
Med24 |
T |
A |
11: 98,600,565 (GRCm39) |
K627* |
probably null |
Het |
Mpl |
A |
T |
4: 118,306,068 (GRCm39) |
|
probably benign |
Het |
Mynn |
T |
A |
3: 30,670,791 (GRCm39) |
D554E |
probably benign |
Het |
Niban2 |
A |
G |
2: 32,801,402 (GRCm39) |
Y122C |
probably benign |
Het |
Or1e23 |
T |
C |
11: 73,407,356 (GRCm39) |
Y223C |
probably benign |
Het |
Prkcd |
T |
C |
14: 30,323,190 (GRCm39) |
|
probably null |
Het |
Prrc2c |
T |
C |
1: 162,533,181 (GRCm39) |
|
probably benign |
Het |
Scp2d1 |
T |
C |
2: 144,665,804 (GRCm39) |
F48L |
probably benign |
Het |
Slc12a2 |
A |
G |
18: 58,012,471 (GRCm39) |
H198R |
probably benign |
Het |
Sulf2 |
A |
G |
2: 165,958,905 (GRCm39) |
V101A |
probably benign |
Het |
Synj2 |
T |
A |
17: 6,040,611 (GRCm39) |
V144E |
probably damaging |
Het |
Tas2r113 |
T |
G |
6: 132,870,330 (GRCm39) |
F119L |
probably damaging |
Het |
Tspan17 |
A |
G |
13: 54,937,442 (GRCm39) |
E12G |
probably damaging |
Het |
|
Other mutations in Ifna1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02630:Ifna1
|
APN |
4 |
88,768,496 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02675:Ifna1
|
APN |
4 |
88,768,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02680:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02709:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02710:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02712:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02721:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
R1630:Ifna1
|
UTSW |
4 |
88,768,566 (GRCm39) |
missense |
probably benign |
0.00 |
R2897:Ifna1
|
UTSW |
4 |
88,768,450 (GRCm39) |
missense |
probably benign |
|
R6150:Ifna1
|
UTSW |
4 |
88,768,349 (GRCm39) |
missense |
probably null |
0.34 |
R8233:Ifna1
|
UTSW |
4 |
88,768,628 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9181:Ifna1
|
UTSW |
4 |
88,768,453 (GRCm39) |
missense |
probably benign |
0.13 |
|