Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim3 |
A |
T |
18: 61,839,701 |
M249K |
possibly damaging |
Het |
Adamtsl1 |
T |
C |
4: 86,342,189 |
F879S |
possibly damaging |
Het |
Afap1l2 |
T |
C |
19: 56,930,261 |
E30G |
probably damaging |
Het |
Aqp9 |
A |
G |
9: 71,130,549 |
|
probably benign |
Het |
Arhgap17 |
A |
T |
7: 123,286,568 |
|
probably benign |
Het |
Arhgef10 |
T |
C |
8: 14,979,977 |
S921P |
probably damaging |
Het |
Atp6v0e2 |
T |
C |
6: 48,537,815 |
I22T |
probably damaging |
Het |
AY074887 |
C |
T |
9: 54,950,679 |
|
probably benign |
Het |
Bcl2l15 |
T |
A |
3: 103,833,414 |
D65E |
probably damaging |
Het |
C2cd6 |
A |
T |
1: 58,997,348 |
|
probably benign |
Het |
Ccdc138 |
G |
A |
10: 58,540,915 |
|
probably null |
Het |
Ccdc7b |
A |
G |
8: 129,178,357 |
T159A |
possibly damaging |
Het |
Ccser1 |
A |
G |
6: 61,638,490 |
T659A |
probably benign |
Het |
Cd300ld2 |
T |
A |
11: 115,012,297 |
I241F |
probably benign |
Het |
Cep192 |
T |
A |
18: 67,812,406 |
N192K |
possibly damaging |
Het |
Csmd1 |
T |
C |
8: 15,917,341 |
K3174R |
probably benign |
Het |
Dpy30 |
A |
T |
17: 74,307,754 |
L65I |
probably damaging |
Het |
Eci2 |
A |
T |
13: 34,990,329 |
L83* |
probably null |
Het |
F7 |
A |
T |
8: 13,033,409 |
E183V |
probably damaging |
Het |
Fam192a |
G |
A |
8: 94,587,362 |
R104W |
probably damaging |
Het |
Gabrg1 |
T |
C |
5: 70,778,169 |
K214R |
probably benign |
Het |
Galr2 |
A |
T |
11: 116,283,170 |
T209S |
probably damaging |
Het |
Gimap9 |
T |
C |
6: 48,677,917 |
|
probably null |
Het |
Gip |
C |
A |
11: 96,025,459 |
F28L |
probably benign |
Het |
Gpd2 |
A |
G |
2: 57,364,530 |
N662S |
probably benign |
Het |
Grik2 |
T |
G |
10: 49,272,956 |
D511A |
probably damaging |
Het |
Ift122 |
T |
A |
6: 115,899,491 |
Y563N |
probably damaging |
Het |
Ipo8 |
A |
G |
6: 148,789,063 |
|
probably benign |
Het |
Islr |
T |
C |
9: 58,157,228 |
E332G |
probably damaging |
Het |
Itgb7 |
G |
A |
15: 102,227,585 |
S5L |
probably benign |
Het |
Itpr2 |
G |
A |
6: 146,345,161 |
R1087W |
probably damaging |
Het |
Katnal2 |
C |
A |
18: 77,017,554 |
V66F |
probably damaging |
Het |
Krt81 |
T |
C |
15: 101,461,019 |
D284G |
probably benign |
Het |
Krtap4-8 |
T |
A |
11: 99,780,005 |
|
probably benign |
Het |
Map1s |
C |
A |
8: 70,913,910 |
N486K |
probably benign |
Het |
Med13l |
G |
A |
5: 118,734,028 |
D842N |
probably damaging |
Het |
Mef2c |
T |
A |
13: 83,655,595 |
M306K |
probably damaging |
Het |
Myb |
C |
T |
10: 21,146,260 |
V377I |
probably benign |
Het |
Myocd |
C |
T |
11: 65,184,625 |
G558R |
possibly damaging |
Het |
Nars |
G |
T |
18: 64,504,968 |
A305E |
probably damaging |
Het |
Neb |
A |
T |
2: 52,196,361 |
N5233K |
probably benign |
Het |
Nipsnap2 |
T |
C |
5: 129,746,439 |
I181T |
possibly damaging |
Het |
Olfr1496 |
T |
C |
19: 13,781,573 |
|
probably benign |
Het |
Olfr960 |
A |
T |
9: 39,623,365 |
M81L |
probably benign |
Het |
P3h2 |
A |
C |
16: 25,987,248 |
C282G |
probably damaging |
Het |
Pcgf5 |
T |
A |
19: 36,442,868 |
C167S |
probably damaging |
Het |
Pck2 |
T |
C |
14: 55,544,069 |
|
probably benign |
Het |
Peli2 |
C |
T |
14: 48,252,730 |
R169* |
probably null |
Het |
Pramef25 |
T |
A |
4: 143,950,214 |
|
probably benign |
Het |
Ralgapa2 |
T |
A |
2: 146,421,739 |
Q686L |
possibly damaging |
Het |
Scap |
C |
A |
9: 110,362,420 |
P50H |
probably damaging |
Het |
Sh3rf2 |
T |
A |
18: 42,054,192 |
D125E |
possibly damaging |
Het |
Slc25a38 |
T |
C |
9: 120,116,494 |
|
probably benign |
Het |
Slc35a5 |
A |
G |
16: 45,143,832 |
V346A |
probably damaging |
Het |
Smad4 |
T |
A |
18: 73,675,809 |
N129I |
probably damaging |
Het |
Sod2 |
C |
T |
17: 13,013,577 |
A163V |
possibly damaging |
Het |
Spred3 |
T |
A |
7: 29,161,523 |
|
probably benign |
Het |
Stag1 |
C |
A |
9: 100,855,859 |
A423E |
possibly damaging |
Het |
Stk17b |
A |
T |
1: 53,761,037 |
S261T |
probably benign |
Het |
Stx3 |
T |
C |
19: 11,791,788 |
K58E |
probably damaging |
Het |
Timm10b |
C |
A |
7: 105,641,138 |
Y79* |
probably null |
Het |
Tmem204 |
T |
C |
17: 25,070,355 |
D97G |
probably damaging |
Het |
Tnfrsf25 |
T |
C |
4: 152,118,428 |
V181A |
probably benign |
Het |
Trim54 |
T |
G |
5: 31,136,958 |
S313A |
probably benign |
Het |
Unc79 |
T |
A |
12: 103,112,455 |
D1433E |
probably damaging |
Het |
Wdr27 |
T |
A |
17: 14,926,247 |
H162L |
probably damaging |
Het |
|