Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
A |
G |
10: 79,094,452 |
Y43H |
probably damaging |
Het |
Aamp |
A |
T |
1: 74,281,126 |
L348Q |
probably damaging |
Het |
Abcb1b |
T |
A |
5: 8,813,722 |
L226M |
probably damaging |
Het |
Acap1 |
A |
G |
11: 69,883,685 |
S396P |
probably damaging |
Het |
Aif1l |
A |
T |
2: 31,962,239 |
S40C |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 25,000,930 |
D48G |
probably benign |
Het |
Bhmt-ps1 |
T |
A |
4: 26,369,352 |
|
noncoding transcript |
Het |
C130026I21Rik |
T |
C |
1: 85,112,557 |
D83G |
probably damaging |
Het |
Ccdc116 |
A |
G |
16: 17,146,945 |
|
probably benign |
Het |
Cmtm5 |
T |
A |
14: 54,937,919 |
C51S |
probably damaging |
Het |
Cyb5rl |
T |
C |
4: 107,080,988 |
V214A |
probably damaging |
Het |
Cyp4x1 |
A |
T |
4: 115,112,880 |
I350N |
probably damaging |
Het |
Efcab6 |
C |
A |
15: 83,867,108 |
D1498Y |
probably damaging |
Het |
Eif3c |
C |
G |
7: 126,566,299 |
|
probably benign |
Het |
Epha3 |
G |
A |
16: 63,583,539 |
S733L |
probably damaging |
Het |
Esyt1 |
T |
C |
10: 128,520,648 |
Y376C |
probably damaging |
Het |
Galnt1 |
T |
C |
18: 24,238,356 |
F4L |
probably benign |
Het |
Glis1 |
T |
C |
4: 107,567,845 |
S218P |
probably benign |
Het |
Gm15854 |
A |
T |
6: 129,972,463 |
|
noncoding transcript |
Het |
Gm29125 |
T |
C |
1: 80,383,519 |
|
noncoding transcript |
Het |
Inpp5a |
T |
C |
7: 139,558,905 |
V263A |
possibly damaging |
Het |
Itgb1 |
T |
G |
8: 128,714,143 |
I255S |
probably damaging |
Het |
Kcp |
A |
G |
6: 29,482,258 |
L1547P |
possibly damaging |
Het |
Kifc3 |
C |
A |
8: 95,109,982 |
L72F |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,450,403 |
C683R |
probably damaging |
Het |
Lrrc55 |
G |
A |
2: 85,196,116 |
A188V |
possibly damaging |
Het |
Ly6i |
A |
T |
15: 74,983,035 |
S9T |
probably benign |
Het |
Nipsnap3a |
T |
A |
4: 52,997,251 |
D172E |
probably benign |
Het |
Olfr1288 |
A |
T |
2: 111,479,144 |
Y120F |
probably benign |
Het |
Oxgr1 |
T |
C |
14: 120,022,613 |
K61E |
probably damaging |
Het |
Pak2 |
G |
T |
16: 32,052,210 |
N51K |
probably benign |
Het |
Pcdhgb7 |
T |
A |
18: 37,753,803 |
D675E |
probably benign |
Het |
Pcolce |
T |
A |
5: 137,605,127 |
|
probably benign |
Het |
Phc3 |
A |
T |
3: 30,936,819 |
S383R |
probably damaging |
Het |
Phf1 |
C |
T |
17: 26,937,500 |
R539* |
probably null |
Het |
Plch1 |
G |
A |
3: 63,701,900 |
T48I |
probably damaging |
Het |
Plekha2 |
A |
G |
8: 25,043,020 |
S312P |
probably damaging |
Het |
Pnpla7 |
T |
C |
2: 24,982,114 |
F69L |
possibly damaging |
Het |
Ppcdc |
T |
A |
9: 57,414,715 |
M181L |
possibly damaging |
Het |
Ptbp1 |
T |
C |
10: 79,859,213 |
I125T |
probably benign |
Het |
Rfc3 |
C |
A |
5: 151,651,172 |
|
probably benign |
Het |
Rpa2 |
T |
G |
4: 132,776,744 |
I69S |
probably damaging |
Het |
Rtn4 |
G |
A |
11: 29,706,856 |
V337I |
probably benign |
Het |
Rttn |
T |
C |
18: 89,095,584 |
L1709P |
probably damaging |
Het |
Sh2b2 |
G |
A |
5: 136,219,053 |
P548L |
possibly damaging |
Het |
Slc12a2 |
T |
A |
18: 57,910,256 |
S591T |
probably damaging |
Het |
Slc25a45 |
A |
T |
19: 5,880,118 |
I39F |
probably damaging |
Het |
Slc38a9 |
G |
A |
13: 112,714,248 |
|
probably null |
Het |
Slc9a4 |
T |
C |
1: 40,619,126 |
V603A |
probably damaging |
Het |
Snx19 |
T |
G |
9: 30,428,448 |
V294G |
possibly damaging |
Het |
Sspo |
G |
T |
6: 48,451,157 |
V313L |
possibly damaging |
Het |
Stard9 |
A |
G |
2: 120,664,991 |
T116A |
possibly damaging |
Het |
Strn3 |
C |
T |
12: 51,627,855 |
R382Q |
probably damaging |
Het |
Trim43b |
T |
A |
9: 89,090,639 |
Q154L |
probably benign |
Het |
Trps1 |
A |
G |
15: 50,846,648 |
V98A |
probably benign |
Het |
Vmn1r220 |
T |
A |
13: 23,183,978 |
M183L |
probably benign |
Het |
Vmn2r60 |
A |
T |
7: 42,116,528 |
T20S |
probably benign |
Het |
Wdr81 |
T |
C |
11: 75,448,002 |
T1444A |
probably benign |
Het |
Xirp2 |
A |
T |
2: 67,516,493 |
E3026V |
possibly damaging |
Het |
|