Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 138,066,126 |
T359A |
probably damaging |
Het |
Abcd4 |
A |
C |
12: 84,606,129 |
V433G |
probably damaging |
Het |
Acot5 |
C |
A |
12: 84,069,581 |
R39S |
probably damaging |
Het |
Actl9 |
T |
C |
17: 33,433,469 |
S168P |
probably damaging |
Het |
Adam15 |
A |
G |
3: 89,345,806 |
L237P |
probably damaging |
Het |
Ahctf1 |
T |
C |
1: 179,790,314 |
Q289R |
possibly damaging |
Het |
Arid5b |
C |
T |
10: 68,098,587 |
G495E |
probably benign |
Het |
Armh1 |
C |
A |
4: 117,213,741 |
A396S |
probably benign |
Het |
Asah1 |
C |
T |
8: 41,341,627 |
R385Q |
probably damaging |
Het |
AW549877 |
T |
C |
15: 3,988,683 |
Y170C |
probably damaging |
Het |
Bicc1 |
T |
C |
10: 70,946,590 |
T607A |
probably benign |
Het |
Ccdc88a |
T |
C |
11: 29,498,614 |
|
probably null |
Het |
Cdhr4 |
A |
T |
9: 107,998,772 |
R750* |
probably null |
Het |
Cep290 |
T |
A |
10: 100,554,536 |
|
probably null |
Het |
Clca3a1 |
T |
A |
3: 144,737,036 |
D749V |
probably benign |
Het |
Clcn1 |
C |
T |
6: 42,310,063 |
P685S |
possibly damaging |
Het |
Clk1 |
A |
G |
1: 58,421,160 |
S104P |
probably damaging |
Het |
Commd10 |
T |
C |
18: 47,086,256 |
V172A |
probably benign |
Het |
Cyp2c69 |
A |
T |
19: 39,877,509 |
C213* |
probably null |
Het |
Dnah14 |
A |
T |
1: 181,752,155 |
|
probably null |
Het |
Dock2 |
C |
T |
11: 34,721,027 |
G170R |
probably damaging |
Het |
Fam186a |
T |
G |
15: 99,945,069 |
H1098P |
probably benign |
Het |
Flt1 |
T |
C |
5: 147,655,120 |
T511A |
probably benign |
Het |
Fmo1 |
A |
C |
1: 162,836,297 |
I221S |
possibly damaging |
Het |
Fthl17b |
C |
T |
X: 8,962,804 |
R9Q |
possibly damaging |
Het |
Fthl17b |
C |
T |
X: 8,962,808 |
V8M |
possibly damaging |
Het |
Ginm1 |
A |
T |
10: 7,775,362 |
S93R |
possibly damaging |
Het |
Gm10251 |
A |
C |
14: 6,675,701 |
|
probably null |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 142,240,713 |
|
probably benign |
Het |
Gys2 |
C |
T |
6: 142,459,485 |
R192H |
probably damaging |
Het |
H2bfm |
G |
A |
X: 136,927,722 |
R120K |
unknown |
Het |
Hectd4 |
C |
A |
5: 121,324,031 |
A987E |
probably benign |
Het |
Herc2 |
G |
A |
7: 56,136,685 |
V1593I |
probably benign |
Het |
Ighv14-3 |
T |
C |
12: 114,059,934 |
T88A |
probably benign |
Het |
Jag2 |
T |
C |
12: 112,913,666 |
D695G |
probably damaging |
Het |
Kazn |
A |
T |
4: 142,104,898 |
D663E |
|
Het |
Krt79 |
T |
C |
15: 101,931,843 |
D306G |
probably damaging |
Het |
Lama1 |
T |
A |
17: 67,780,880 |
C1498S |
|
Het |
Ldb1 |
T |
C |
19: 46,035,524 |
Y141C |
probably damaging |
Het |
Lmnb2 |
T |
A |
10: 80,904,739 |
E336V |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 42,653,035 |
|
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,191,609 |
Y2377F |
probably damaging |
Het |
Neb |
T |
A |
2: 52,230,047 |
Y721F |
|
Het |
Ntf3 |
A |
G |
6: 126,101,815 |
S243P |
probably damaging |
Het |
Olfr1195 |
G |
C |
2: 88,683,352 |
P127A |
probably damaging |
Het |
Olfr1480 |
G |
T |
19: 13,530,445 |
M301I |
probably damaging |
Het |
Olfr593 |
T |
C |
7: 103,212,445 |
M195T |
possibly damaging |
Het |
Pdk1 |
G |
A |
2: 71,875,398 |
|
probably null |
Het |
Pdzd2 |
A |
G |
15: 12,373,203 |
V2282A |
probably damaging |
Het |
Piwil1 |
T |
C |
5: 128,747,433 |
F517L |
probably benign |
Het |
Plch2 |
T |
A |
4: 154,991,162 |
T738S |
probably damaging |
Het |
Plekhm3 |
G |
A |
1: 64,883,208 |
R603W |
probably damaging |
Het |
Pltp |
A |
T |
2: 164,857,006 |
|
probably null |
Het |
Prdm4 |
A |
G |
10: 85,899,281 |
S666P |
probably damaging |
Het |
Psmb3 |
G |
T |
11: 97,712,492 |
R177L |
probably damaging |
Het |
Ralgapa2 |
A |
G |
2: 146,418,415 |
V764A |
probably benign |
Het |
Rel |
T |
C |
11: 23,742,713 |
D440G |
probably benign |
Het |
Rims2 |
T |
A |
15: 39,507,026 |
V952E |
probably damaging |
Het |
Samd4b |
G |
T |
7: 28,423,500 |
C44* |
probably null |
Het |
Slamf8 |
C |
A |
1: 172,588,038 |
V78F |
possibly damaging |
Het |
Slc35a1 |
A |
T |
4: 34,675,493 |
N111K |
possibly damaging |
Het |
Slc7a5 |
A |
T |
8: 121,887,535 |
Y264* |
probably null |
Het |
Srsf2 |
T |
C |
11: 116,852,294 |
S134G |
unknown |
Het |
Stag1 |
T |
A |
9: 100,738,138 |
M98K |
probably damaging |
Het |
Trib1 |
T |
C |
15: 59,651,713 |
S199P |
probably damaging |
Het |
Txnip |
T |
C |
3: 96,559,837 |
S276P |
possibly damaging |
Het |
Vmn1r194 |
C |
T |
13: 22,244,741 |
T176I |
not run |
Het |
Vmn1r222 |
A |
G |
13: 23,232,431 |
L204P |
possibly damaging |
Het |
Vmn2r63 |
T |
A |
7: 42,927,042 |
H449L |
probably benign |
Het |
Vmn2r83 |
T |
A |
10: 79,479,122 |
N401K |
probably damaging |
Het |
Vmn2r87 |
T |
A |
10: 130,472,185 |
H728L |
probably damaging |
Het |
Zfp69 |
G |
A |
4: 120,935,126 |
A151V |
probably benign |
Het |
Zfp738 |
A |
G |
13: 67,683,401 |
|
probably null |
Het |
Zfp974 |
T |
C |
7: 27,911,685 |
E205G |
possibly damaging |
Het |
|