Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110008L16Rik |
G |
T |
12: 55,304,613 |
V236F |
possibly damaging |
Het |
Aass |
A |
T |
6: 23,109,498 |
D324E |
possibly damaging |
Het |
Adam7 |
T |
C |
14: 68,520,539 |
T245A |
probably benign |
Het |
Aim2 |
T |
C |
1: 173,459,851 |
|
probably null |
Het |
Arhgef1 |
G |
T |
7: 24,925,846 |
D850Y |
probably damaging |
Het |
Aspm |
C |
A |
1: 139,470,755 |
Q1024K |
probably damaging |
Het |
C7 |
T |
C |
15: 4,990,464 |
S734G |
probably benign |
Het |
Ccdc158 |
A |
T |
5: 92,623,396 |
S987T |
probably benign |
Het |
Chrna2 |
G |
T |
14: 66,143,417 |
G45V |
probably benign |
Het |
Chrna2 |
C |
A |
14: 66,143,424 |
Y47* |
probably null |
Het |
Clec2g |
C |
A |
6: 128,981,324 |
Q117K |
probably damaging |
Het |
Cntnap5a |
A |
G |
1: 116,101,574 |
S253G |
probably benign |
Het |
Cttn |
T |
A |
7: 144,457,724 |
D116V |
probably damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,802,529 |
V286A |
probably benign |
Het |
Dcbld2 |
T |
A |
16: 58,465,373 |
S632T |
probably damaging |
Het |
Dscam |
A |
T |
16: 96,683,772 |
N1118K |
probably benign |
Het |
Eif2a |
C |
T |
3: 58,539,629 |
T92M |
possibly damaging |
Het |
Frmpd1 |
T |
A |
4: 45,284,382 |
C1068S |
probably benign |
Het |
Fstl1 |
G |
A |
16: 37,822,603 |
V110I |
probably benign |
Het |
Gpat2 |
T |
C |
2: 127,433,622 |
I465T |
probably damaging |
Het |
Gpr137 |
C |
T |
19: 6,940,423 |
|
probably benign |
Het |
Hgsnat |
A |
G |
8: 25,946,343 |
I561T |
probably benign |
Het |
Ift74 |
T |
A |
4: 94,652,912 |
|
probably null |
Het |
Ilf3 |
A |
G |
9: 21,403,134 |
|
probably null |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 52,725,906 |
|
probably benign |
Het |
Klk14 |
G |
A |
7: 43,692,077 |
C51Y |
probably damaging |
Het |
Lrrc41 |
C |
A |
4: 116,080,546 |
|
probably null |
Het |
Myh11 |
C |
A |
16: 14,224,059 |
R700L |
possibly damaging |
Het |
Myo16 |
A |
G |
8: 10,562,240 |
D1295G |
probably damaging |
Het |
Myo5b |
A |
G |
18: 74,740,488 |
M1488V |
probably benign |
Het |
Naip6 |
A |
T |
13: 100,299,307 |
Y903N |
probably damaging |
Het |
Nek6 |
A |
G |
2: 38,550,637 |
H19R |
probably damaging |
Het |
Nktr |
A |
C |
9: 121,741,126 |
T127P |
probably damaging |
Het |
Noc4l |
A |
T |
5: 110,649,872 |
D335E |
probably benign |
Het |
Nsd1 |
A |
G |
13: 55,301,809 |
D1993G |
probably damaging |
Het |
Olfr1377 |
G |
A |
11: 50,984,856 |
D52N |
probably damaging |
Het |
Olfr190 |
A |
T |
16: 59,074,256 |
F275I |
probably damaging |
Het |
Pabpc2 |
A |
T |
18: 39,775,530 |
Q616L |
possibly damaging |
Het |
Pcdhga4 |
A |
T |
18: 37,685,779 |
D127V |
probably damaging |
Het |
Phrf1 |
T |
C |
7: 141,259,720 |
|
probably benign |
Het |
Phtf2 |
T |
A |
5: 20,813,296 |
I16F |
probably damaging |
Het |
Plekhg3 |
G |
T |
12: 76,577,981 |
R1200L |
probably benign |
Het |
Plod3 |
G |
C |
5: 136,988,146 |
A50P |
probably benign |
Het |
Prss12 |
A |
G |
3: 123,485,485 |
N404D |
probably benign |
Het |
Ptch2 |
C |
G |
4: 117,111,206 |
A926G |
probably damaging |
Het |
Ptpa |
T |
C |
2: 30,443,305 |
F6L |
probably damaging |
Het |
Reck |
T |
C |
4: 43,942,293 |
I853T |
possibly damaging |
Het |
Reep6 |
G |
A |
10: 80,330,162 |
|
probably benign |
Het |
Rex2 |
T |
A |
4: 147,058,697 |
S547R |
probably benign |
Het |
Rgs22 |
C |
T |
15: 36,107,076 |
E55K |
probably damaging |
Het |
Rtl6 |
T |
C |
15: 84,557,001 |
T65A |
possibly damaging |
Het |
Scarb1 |
G |
T |
5: 125,277,795 |
P491Q |
probably damaging |
Het |
Scfd1 |
A |
G |
12: 51,431,519 |
S505G |
probably benign |
Het |
Scube1 |
T |
G |
15: 83,608,747 |
Q904P |
probably damaging |
Het |
Sis |
T |
C |
3: 72,921,184 |
Y1186C |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,214,066 |
D1334G |
probably benign |
Het |
Spty2d1 |
T |
C |
7: 46,998,581 |
E200G |
probably damaging |
Het |
Stard13 |
C |
A |
5: 151,092,829 |
|
probably null |
Het |
Sybu |
T |
C |
15: 44,718,943 |
K95R |
probably damaging |
Het |
Trappc9 |
T |
A |
15: 72,941,947 |
D488V |
probably damaging |
Het |
Txk |
G |
A |
5: 72,700,663 |
P381S |
probably damaging |
Het |
Ubr2 |
A |
T |
17: 46,988,722 |
M198K |
probably benign |
Het |
Unc5a |
A |
T |
13: 55,004,481 |
T786S |
possibly damaging |
Het |
Unc93b1 |
G |
A |
19: 3,941,959 |
R231Q |
probably damaging |
Het |
Wfdc1 |
T |
A |
8: 119,683,793 |
|
probably null |
Het |
Zfp667 |
T |
G |
7: 6,305,106 |
C258G |
possibly damaging |
Het |
Zfr |
G |
A |
15: 12,162,233 |
R823H |
probably benign |
Het |
|