Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
C |
6: 128,568,712 |
F484C |
probably damaging |
Het |
Cdsn |
A |
G |
17: 35,554,906 |
S111G |
unknown |
Het |
Ctnnal1 |
T |
C |
4: 56,812,349 |
T726A |
probably benign |
Het |
Ddx60 |
T |
A |
8: 62,023,241 |
M1541K |
probably null |
Het |
Dnah14 |
C |
T |
1: 181,709,051 |
P2420S |
probably damaging |
Het |
Doxl2 |
A |
C |
6: 48,976,601 |
I487L |
probably benign |
Het |
Fhit |
T |
C |
14: 9,573,435 |
E205G |
probably benign |
Het |
Glipr1l1 |
C |
T |
10: 112,076,170 |
T203M |
probably benign |
Het |
Gm4353 |
T |
A |
7: 116,084,269 |
D97V |
probably benign |
Het |
Gprc6a |
A |
T |
10: 51,615,811 |
I543K |
probably damaging |
Het |
Ifi205 |
T |
C |
1: 174,027,264 |
T110A |
possibly damaging |
Het |
Med27 |
T |
A |
2: 29,509,441 |
S95T |
probably damaging |
Het |
Mocs1 |
T |
C |
17: 49,450,313 |
S308P |
probably damaging |
Het |
Mrpl11 |
C |
T |
19: 4,963,369 |
S88F |
possibly damaging |
Het |
Nav3 |
A |
T |
10: 109,866,984 |
Y229* |
probably null |
Het |
Olfr138 |
A |
G |
17: 38,274,881 |
M37V |
probably benign |
Het |
Olfr38 |
A |
T |
6: 42,762,965 |
L304F |
probably damaging |
Het |
Olfr569 |
C |
A |
7: 102,887,951 |
L67F |
probably benign |
Het |
Olfr668 |
C |
T |
7: 104,925,392 |
R124H |
probably benign |
Het |
Olfr996 |
T |
A |
2: 85,579,542 |
M101K |
possibly damaging |
Het |
Pear1 |
A |
G |
3: 87,755,931 |
I460T |
probably benign |
Het |
Phc3 |
T |
A |
3: 30,914,529 |
K816N |
probably damaging |
Het |
Phf19 |
T |
A |
2: 34,897,117 |
D445V |
probably damaging |
Het |
Pkd2l2 |
T |
C |
18: 34,430,689 |
F486L |
probably damaging |
Het |
Plagl1 |
G |
T |
10: 13,127,895 |
|
probably benign |
Het |
Prkca |
A |
G |
11: 108,057,845 |
I106T |
probably benign |
Het |
Ptpn3 |
C |
T |
4: 57,248,681 |
G218R |
probably damaging |
Het |
Ptx3 |
A |
G |
3: 66,224,709 |
D217G |
possibly damaging |
Het |
Rab3d |
T |
C |
9: 21,910,519 |
T209A |
probably benign |
Het |
Rfx2 |
A |
G |
17: 56,777,473 |
F642S |
possibly damaging |
Het |
Rhpn2 |
T |
A |
7: 35,376,211 |
M271K |
possibly damaging |
Het |
Serpinb6b |
A |
G |
13: 32,977,994 |
T259A |
probably damaging |
Het |
Speer3 |
G |
A |
5: 13,794,691 |
V123M |
possibly damaging |
Het |
Svil |
T |
G |
18: 5,106,724 |
V1855G |
probably damaging |
Het |
Thbs4 |
A |
G |
13: 92,751,795 |
F950L |
probably benign |
Het |
Tiparp |
T |
C |
3: 65,553,243 |
V551A |
probably damaging |
Het |
Vmn2r71 |
T |
A |
7: 85,619,274 |
D228E |
probably benign |
Het |
Vmn2r85 |
T |
C |
10: 130,425,662 |
I269V |
probably benign |
Het |
Vps9d1 |
A |
T |
8: 123,245,671 |
M497K |
probably damaging |
Het |
Wnt5b |
A |
G |
6: 119,433,642 |
V241A |
probably damaging |
Het |
Xdh |
T |
C |
17: 73,921,347 |
N353S |
probably damaging |
Het |
Zfp526 |
C |
T |
7: 25,226,332 |
T672M |
probably damaging |
Het |
|