Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
C |
T |
6: 121,624,972 (GRCm39) |
A450V |
probably benign |
Het |
Abca8a |
T |
C |
11: 109,954,048 (GRCm39) |
|
probably null |
Het |
Adgrl3 |
A |
T |
5: 81,660,173 (GRCm39) |
N246I |
probably damaging |
Het |
Bmal2 |
T |
A |
6: 146,731,194 (GRCm39) |
S500T |
possibly damaging |
Het |
Cdipt |
A |
T |
7: 126,576,131 (GRCm39) |
M29L |
possibly damaging |
Het |
Chml |
G |
T |
1: 175,514,624 (GRCm39) |
Y432* |
probably null |
Het |
Clasp2 |
G |
T |
9: 113,681,803 (GRCm39) |
V320L |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,599,675 (GRCm39) |
T826M |
probably damaging |
Het |
Cpsf3 |
A |
G |
12: 21,345,194 (GRCm39) |
I169V |
probably damaging |
Het |
Dhx36 |
G |
A |
3: 62,404,241 (GRCm39) |
T234M |
probably damaging |
Het |
Dhx57 |
A |
G |
17: 80,571,375 (GRCm39) |
|
probably null |
Het |
Dnah1 |
A |
T |
14: 30,991,382 (GRCm39) |
I3132N |
possibly damaging |
Het |
Fbxw20 |
G |
T |
9: 109,052,431 (GRCm39) |
Q231K |
probably benign |
Het |
Glg1 |
T |
A |
8: 111,907,667 (GRCm39) |
I510F |
probably damaging |
Het |
Gm10801 |
TC |
TCGGC |
2: 98,494,151 (GRCm39) |
|
probably benign |
Het |
Gse1 |
C |
A |
8: 121,297,908 (GRCm39) |
|
probably benign |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Klrd1 |
T |
C |
6: 129,572,499 (GRCm39) |
L97P |
probably damaging |
Het |
Lgmn |
A |
T |
12: 102,366,413 (GRCm39) |
M240K |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 41,075,880 (GRCm39) |
|
probably null |
Het |
Notch2 |
A |
T |
3: 98,042,693 (GRCm39) |
R1353* |
probably null |
Het |
Or2d2b |
A |
G |
7: 106,705,456 (GRCm39) |
V204A |
possibly damaging |
Het |
Or5t18 |
A |
C |
2: 86,636,701 (GRCm39) |
V214G |
possibly damaging |
Het |
Pcdhb14 |
G |
A |
18: 37,581,659 (GRCm39) |
S255N |
probably benign |
Het |
Pcgf2 |
C |
T |
11: 97,581,817 (GRCm39) |
M25I |
possibly damaging |
Het |
Poll |
G |
T |
19: 45,544,436 (GRCm39) |
D328E |
probably benign |
Het |
Pomgnt2 |
A |
T |
9: 121,811,863 (GRCm39) |
L306Q |
probably damaging |
Het |
Proser1 |
A |
T |
3: 53,386,088 (GRCm39) |
M657L |
probably benign |
Het |
Rbm47 |
G |
C |
5: 66,183,626 (GRCm39) |
R326G |
probably damaging |
Het |
Rdh11 |
G |
T |
12: 79,235,838 (GRCm39) |
P37T |
probably benign |
Het |
Rsph10b |
A |
T |
5: 143,913,946 (GRCm39) |
I286L |
probably benign |
Het |
Septin4 |
G |
A |
11: 87,480,343 (GRCm39) |
R238K |
possibly damaging |
Het |
Sptan1 |
C |
T |
2: 29,883,899 (GRCm39) |
R580C |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,524,135 (GRCm39) |
W777R |
probably damaging |
Het |
Timd2 |
T |
C |
11: 46,578,063 (GRCm39) |
T23A |
probably benign |
Het |
Tmc4 |
A |
G |
7: 3,674,052 (GRCm39) |
Y376H |
probably damaging |
Het |
Tmem143 |
A |
G |
7: 45,558,950 (GRCm39) |
I297M |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,014,575 (GRCm39) |
T609A |
probably benign |
Het |
Tyw3 |
T |
C |
3: 154,302,704 (GRCm39) |
H10R |
probably benign |
Het |
Unc13b |
C |
A |
4: 43,239,306 (GRCm39) |
H3456Q |
probably damaging |
Het |
Zfp131 |
A |
T |
13: 120,237,532 (GRCm39) |
H275Q |
probably damaging |
Het |
|
Other mutations in Gfod1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02402:Gfod1
|
APN |
13 |
43,354,211 (GRCm39) |
missense |
probably benign |
|
R0483:Gfod1
|
UTSW |
13 |
43,354,012 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0959:Gfod1
|
UTSW |
13 |
43,456,905 (GRCm39) |
missense |
probably benign |
|
R1913:Gfod1
|
UTSW |
13 |
43,456,921 (GRCm39) |
missense |
probably damaging |
0.98 |
R1927:Gfod1
|
UTSW |
13 |
43,354,336 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2061:Gfod1
|
UTSW |
13 |
43,456,719 (GRCm39) |
critical splice donor site |
probably null |
|
R2154:Gfod1
|
UTSW |
13 |
43,456,946 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2370:Gfod1
|
UTSW |
13 |
43,354,621 (GRCm39) |
missense |
probably benign |
0.04 |
R3956:Gfod1
|
UTSW |
13 |
43,354,538 (GRCm39) |
missense |
probably damaging |
0.98 |
R5061:Gfod1
|
UTSW |
13 |
43,353,992 (GRCm39) |
missense |
probably benign |
0.01 |
R6156:Gfod1
|
UTSW |
13 |
43,354,514 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6573:Gfod1
|
UTSW |
13 |
43,353,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R7692:Gfod1
|
UTSW |
13 |
43,354,528 (GRCm39) |
missense |
probably benign |
0.00 |
R8353:Gfod1
|
UTSW |
13 |
43,354,366 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9063:Gfod1
|
UTSW |
13 |
43,354,280 (GRCm39) |
missense |
probably benign |
0.35 |
R9087:Gfod1
|
UTSW |
13 |
43,353,838 (GRCm39) |
missense |
probably damaging |
0.96 |
R9090:Gfod1
|
UTSW |
13 |
43,456,861 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9271:Gfod1
|
UTSW |
13 |
43,456,861 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9380:Gfod1
|
UTSW |
13 |
43,354,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|