Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts17 |
T |
C |
7: 66,909,376 |
F305L |
probably damaging |
Het |
Ankrd12 |
T |
C |
17: 65,984,403 |
H1345R |
probably benign |
Het |
Bloc1s5 |
A |
T |
13: 38,603,883 |
M175K |
probably damaging |
Het |
C9 |
T |
A |
15: 6,497,132 |
M549K |
probably benign |
Het |
Cfap52 |
A |
G |
11: 67,954,181 |
|
probably benign |
Het |
Cntnap2 |
A |
T |
6: 47,021,736 |
K907N |
possibly damaging |
Het |
Cox8c |
T |
A |
12: 102,899,493 |
|
probably null |
Het |
Csgalnact1 |
C |
A |
8: 68,401,492 |
G219V |
probably damaging |
Het |
Cyp26b1 |
A |
T |
6: 84,574,312 |
N307K |
possibly damaging |
Het |
Cyp2s1 |
T |
C |
7: 25,816,424 |
|
probably benign |
Het |
Dpysl2 |
G |
A |
14: 66,824,398 |
T253I |
probably damaging |
Het |
Efr3b |
C |
T |
12: 3,983,391 |
V139I |
probably benign |
Het |
Egflam |
T |
A |
15: 7,222,812 |
I835F |
probably damaging |
Het |
Eif5a |
A |
T |
11: 69,919,163 |
H51Q |
possibly damaging |
Het |
Fancd2 |
T |
A |
6: 113,562,461 |
I637N |
probably damaging |
Het |
Gpr173 |
T |
A |
X: 152,347,096 |
H127L |
probably damaging |
Het |
Klc3 |
T |
C |
7: 19,397,044 |
I203V |
probably benign |
Het |
Lsg1 |
T |
C |
16: 30,571,242 |
K352E |
probably benign |
Het |
Man2a2 |
G |
A |
7: 80,359,640 |
A822V |
probably damaging |
Het |
Med12l |
G |
T |
3: 59,077,089 |
D483Y |
probably damaging |
Het |
Mlh1 |
A |
G |
9: 111,229,875 |
Y694H |
probably benign |
Het |
Mmrn1 |
A |
G |
6: 60,958,176 |
R219G |
possibly damaging |
Het |
Nsd1 |
T |
C |
13: 55,302,833 |
|
probably benign |
Het |
Olfr1080 |
C |
T |
2: 86,553,880 |
M81I |
possibly damaging |
Het |
Olfr1392 |
A |
T |
11: 49,293,728 |
M136L |
possibly damaging |
Het |
Pax3 |
A |
T |
1: 78,121,787 |
S322T |
possibly damaging |
Het |
Pkhd1 |
T |
A |
1: 20,117,720 |
I3455F |
probably damaging |
Het |
Plekhb2 |
T |
C |
1: 34,876,941 |
V187A |
possibly damaging |
Het |
Pot1a |
A |
T |
6: 25,794,593 |
F31I |
probably damaging |
Het |
Rpap1 |
A |
T |
2: 119,783,239 |
|
probably benign |
Het |
Scmh1 |
T |
A |
4: 120,528,146 |
|
probably benign |
Het |
Scn2a |
A |
G |
2: 65,730,178 |
T1251A |
probably damaging |
Het |
Siglecf |
T |
C |
7: 43,352,210 |
V148A |
probably benign |
Het |
Slit3 |
A |
G |
11: 35,708,142 |
*1524W |
probably null |
Het |
Son |
C |
A |
16: 91,658,471 |
P1369T |
possibly damaging |
Het |
Spp2 |
T |
A |
1: 88,411,146 |
L25* |
probably null |
Het |
Sptbn4 |
T |
C |
7: 27,391,551 |
Q1405R |
probably damaging |
Het |
Traf3ip2 |
G |
T |
10: 39,646,906 |
A463S |
possibly damaging |
Het |
Trappc11 |
T |
C |
8: 47,507,582 |
E27G |
probably damaging |
Het |
Vmn2r12 |
C |
T |
5: 109,085,992 |
V785I |
probably damaging |
Het |
Zfp57 |
T |
A |
17: 37,006,164 |
S45T |
probably damaging |
Het |
|