Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4430402I18Rik |
G |
T |
19: 28,927,639 |
|
probably benign |
Het |
Abca12 |
G |
T |
1: 71,309,800 |
H851N |
probably benign |
Het |
Adamtsl4 |
T |
C |
3: 95,680,784 |
Y631C |
probably damaging |
Het |
Ankhd1 |
A |
G |
18: 36,625,159 |
I969V |
probably benign |
Het |
Apob |
A |
G |
12: 8,009,715 |
I2699M |
probably damaging |
Het |
Aqr |
A |
T |
2: 114,150,409 |
L297Q |
probably damaging |
Het |
BC067074 |
G |
A |
13: 113,368,492 |
V510I |
possibly damaging |
Het |
Camsap1 |
A |
G |
2: 25,945,178 |
Y301H |
probably damaging |
Het |
Ccdc88c |
A |
G |
12: 100,939,166 |
|
probably benign |
Het |
Cd209b |
T |
A |
8: 3,923,367 |
I106F |
possibly damaging |
Het |
Cdkn1b |
T |
A |
6: 134,921,097 |
W60R |
probably damaging |
Het |
Coasy |
A |
G |
11: 101,084,996 |
|
probably benign |
Het |
Col2a1 |
T |
A |
15: 97,979,651 |
Q1017L |
probably damaging |
Het |
Ctnnal1 |
T |
A |
4: 56,847,971 |
N56I |
probably damaging |
Het |
Cyb561d2 |
T |
A |
9: 107,541,643 |
|
probably benign |
Het |
Dcst1 |
G |
T |
3: 89,352,519 |
T632N |
probably damaging |
Het |
Ddx1 |
C |
T |
12: 13,237,231 |
V267I |
probably benign |
Het |
Dnah10 |
A |
T |
5: 124,774,986 |
M1736L |
probably benign |
Het |
Eln |
G |
A |
5: 134,729,437 |
|
probably benign |
Het |
Enpp2 |
A |
T |
15: 54,862,681 |
D566E |
probably damaging |
Het |
Ezh1 |
T |
C |
11: 101,194,917 |
K638R |
probably damaging |
Het |
Fam172a |
A |
T |
13: 77,761,922 |
Y98F |
probably damaging |
Het |
Fdx1l |
C |
A |
9: 21,073,398 |
G37W |
probably benign |
Het |
Grin2b |
T |
C |
6: 135,843,195 |
I340V |
probably benign |
Het |
Ikbkap |
T |
A |
4: 56,781,193 |
E493D |
probably benign |
Het |
Il16 |
T |
C |
7: 83,655,312 |
T671A |
probably benign |
Het |
Kcnd2 |
T |
A |
6: 21,216,357 |
M20K |
probably damaging |
Het |
Kndc1 |
C |
T |
7: 139,922,684 |
S962F |
probably damaging |
Het |
L1td1 |
A |
G |
4: 98,737,817 |
S750G |
possibly damaging |
Het |
Lama2 |
A |
G |
10: 27,208,370 |
C935R |
probably damaging |
Het |
Lgalsl |
T |
C |
11: 20,826,418 |
D158G |
possibly damaging |
Het |
Lman1 |
A |
T |
18: 65,993,073 |
|
probably null |
Het |
Lmtk2 |
A |
G |
5: 144,174,589 |
E709G |
probably damaging |
Het |
Lrfn3 |
T |
C |
7: 30,355,927 |
H531R |
possibly damaging |
Het |
Mark3 |
A |
G |
12: 111,623,325 |
|
probably benign |
Het |
Mov10 |
T |
C |
3: 104,795,174 |
E997G |
probably damaging |
Het |
Myo15 |
T |
A |
11: 60,504,331 |
W2484R |
probably benign |
Het |
Myo1g |
G |
T |
11: 6,509,372 |
Q833K |
probably benign |
Het |
Ncoa3 |
T |
A |
2: 166,055,510 |
D740E |
probably benign |
Het |
Nol12 |
A |
G |
15: 78,937,953 |
|
probably benign |
Het |
Nrxn2 |
T |
A |
19: 6,443,612 |
|
probably null |
Het |
Nsfl1c |
A |
C |
2: 151,500,746 |
I79L |
probably benign |
Het |
Olfr1462 |
A |
G |
19: 13,191,298 |
I210M |
probably benign |
Het |
Olfr173 |
G |
T |
16: 58,797,448 |
H133N |
probably benign |
Het |
Olfr691 |
T |
C |
7: 105,337,261 |
I152V |
probably benign |
Het |
Osbpl8 |
A |
C |
10: 111,291,581 |
E842A |
probably benign |
Het |
Pdxk |
G |
T |
10: 78,440,811 |
T310K |
probably benign |
Het |
Phip |
T |
G |
9: 82,959,605 |
K54Q |
probably damaging |
Het |
Pklr |
A |
T |
3: 89,143,035 |
D366V |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,751,540 |
|
probably benign |
Het |
Ppp4r3a |
A |
T |
12: 101,043,524 |
V618E |
probably damaging |
Het |
Prdm12 |
A |
T |
2: 31,640,307 |
Q70L |
possibly damaging |
Het |
Ptpn21 |
A |
T |
12: 98,688,590 |
M706K |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,586,714 |
F1606I |
probably damaging |
Het |
Rasgrp4 |
T |
C |
7: 29,137,727 |
|
probably null |
Het |
Rlbp1 |
C |
A |
7: 79,379,913 |
|
probably null |
Het |
Rtp2 |
T |
C |
16: 23,927,443 |
D166G |
probably benign |
Het |
Ryr3 |
A |
C |
2: 112,645,259 |
F4481V |
probably damaging |
Het |
Scn2a |
A |
G |
2: 65,701,991 |
D649G |
possibly damaging |
Het |
Slc30a5 |
T |
A |
13: 100,803,442 |
D655V |
probably damaging |
Het |
Slco5a1 |
G |
A |
1: 12,871,908 |
A838V |
probably benign |
Het |
Srprb |
A |
G |
9: 103,190,302 |
V239A |
probably damaging |
Het |
Tceanc2 |
T |
C |
4: 107,147,640 |
T104A |
probably benign |
Het |
Tcp1 |
T |
C |
17: 12,922,606 |
|
probably null |
Het |
Unc13b |
C |
T |
4: 43,239,385 |
R1056* |
probably null |
Het |
Wdr19 |
G |
A |
5: 65,223,504 |
|
probably benign |
Het |
Zadh2 |
A |
G |
18: 84,094,471 |
K91E |
probably benign |
Het |
Zfhx4 |
T |
A |
3: 5,241,859 |
H48Q |
probably benign |
Het |
Zfp787 |
T |
A |
7: 6,132,235 |
H339L |
probably damaging |
Het |
|