Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts10 |
T |
A |
17: 33,531,739 |
M251K |
possibly damaging |
Het |
Adcy2 |
A |
T |
13: 68,727,843 |
H513Q |
possibly damaging |
Het |
Ahctf1 |
A |
G |
1: 179,753,054 |
L1861P |
possibly damaging |
Het |
Apc2 |
C |
A |
10: 80,311,043 |
R615S |
probably damaging |
Het |
Arhgap45 |
A |
C |
10: 80,025,530 |
D509A |
probably damaging |
Het |
Atp6v1c2 |
T |
C |
12: 17,301,207 |
T108A |
probably benign |
Het |
Blm |
T |
A |
7: 80,494,228 |
D821V |
probably damaging |
Het |
C3 |
T |
A |
17: 57,221,057 |
I721L |
probably benign |
Het |
Ccdc13 |
A |
T |
9: 121,820,760 |
V207E |
probably damaging |
Het |
Ccndbp1 |
C |
T |
2: 121,014,727 |
|
probably benign |
Het |
Cd180 |
A |
C |
13: 102,705,760 |
Q438P |
probably benign |
Het |
Cd248 |
C |
T |
19: 5,068,445 |
T107M |
probably damaging |
Het |
Cdan1 |
G |
A |
2: 120,728,383 |
R445C |
probably damaging |
Het |
Cic |
C |
A |
7: 25,273,588 |
H915N |
possibly damaging |
Het |
Cox8c |
T |
C |
12: 102,899,483 |
S40P |
possibly damaging |
Het |
Cyp2d34 |
A |
T |
15: 82,616,891 |
C347S |
probably benign |
Het |
Dhx30 |
A |
T |
9: 110,085,288 |
F974I |
probably damaging |
Het |
Dlec1 |
A |
T |
9: 119,143,153 |
T1414S |
probably benign |
Het |
Dlg2 |
C |
A |
7: 92,437,962 |
|
probably null |
Het |
Dzip1l |
T |
A |
9: 99,647,205 |
M329K |
probably benign |
Het |
Dzip3 |
A |
T |
16: 48,951,561 |
L582I |
probably damaging |
Het |
Emilin2 |
T |
C |
17: 71,252,778 |
Y1068C |
probably damaging |
Het |
Fam221b |
T |
A |
4: 43,659,622 |
|
probably null |
Het |
Fbxw22 |
A |
G |
9: 109,378,871 |
I444T |
probably damaging |
Het |
Flnc |
T |
A |
6: 29,440,429 |
N245K |
probably damaging |
Het |
Fnip1 |
T |
A |
11: 54,499,419 |
I380N |
probably damaging |
Het |
Gbf1 |
C |
T |
19: 46,259,167 |
R181* |
probably null |
Het |
Igkv6-17 |
T |
A |
6: 70,371,502 |
F12I |
probably benign |
Het |
Itln1 |
C |
A |
1: 171,531,077 |
G174V |
probably damaging |
Het |
Lrrc52 |
A |
G |
1: 167,466,091 |
|
probably null |
Het |
Matn2 |
A |
G |
15: 34,402,925 |
Y432C |
probably damaging |
Het |
Metap1d |
A |
G |
2: 71,524,961 |
*336W |
probably null |
Het |
Mgam2-ps |
T |
A |
6: 40,802,555 |
|
noncoding transcript |
Het |
Mrps9 |
T |
A |
1: 42,862,515 |
V61D |
possibly damaging |
Het |
Myh9 |
T |
A |
15: 77,768,853 |
D1428V |
probably damaging |
Het |
N4bp3 |
A |
T |
11: 51,644,479 |
|
probably null |
Het |
Nat9 |
T |
A |
11: 115,184,590 |
Q75L |
probably benign |
Het |
Nop2 |
T |
C |
6: 125,144,556 |
V767A |
probably benign |
Het |
Ntrk2 |
A |
G |
13: 59,126,493 |
K728E |
probably damaging |
Het |
Olfr497 |
G |
A |
7: 108,422,989 |
M139I |
probably benign |
Het |
Olfr558 |
T |
G |
7: 102,709,557 |
C99W |
probably damaging |
Het |
Olfr836 |
T |
A |
9: 19,121,010 |
H15Q |
probably null |
Het |
Oraov1 |
T |
C |
7: 144,928,978 |
|
probably null |
Het |
Pcdhgb2 |
A |
G |
18: 37,692,322 |
T789A |
probably benign |
Het |
Pcyt2 |
T |
C |
11: 120,611,174 |
D321G |
probably benign |
Het |
Rad9a |
G |
A |
19: 4,200,561 |
R85C |
probably damaging |
Het |
Rbbp8 |
A |
T |
18: 11,721,782 |
K355* |
probably null |
Het |
Rhag |
T |
C |
17: 40,836,467 |
Y407H |
probably damaging |
Het |
Robo4 |
G |
A |
9: 37,403,199 |
V161M |
probably damaging |
Het |
Rpl27-ps3 |
C |
A |
18: 6,332,922 |
N97K |
probably benign |
Het |
Slc45a4 |
A |
G |
15: 73,582,075 |
I691T |
possibly damaging |
Het |
Slc9a9 |
A |
T |
9: 94,936,449 |
|
probably benign |
Het |
Spata5 |
T |
G |
3: 37,458,325 |
F713C |
probably damaging |
Het |
Stard13 |
A |
G |
5: 151,060,815 |
F619L |
probably benign |
Het |
Stt3b |
A |
T |
9: 115,254,794 |
V438E |
probably damaging |
Het |
Tacr3 |
C |
T |
3: 134,829,421 |
T50I |
probably benign |
Het |
Tacr3 |
G |
T |
3: 134,929,929 |
C298F |
probably damaging |
Het |
Taok3 |
C |
T |
5: 117,228,066 |
T394M |
probably benign |
Het |
Tctex1d1 |
T |
A |
4: 103,004,229 |
I136K |
probably damaging |
Het |
Tgfb1i1 |
A |
G |
7: 128,249,176 |
D128G |
probably damaging |
Het |
Tgfbr3l |
G |
T |
8: 4,250,574 |
V251L |
probably benign |
Het |
Tom1l2 |
C |
G |
11: 60,270,433 |
R84P |
probably damaging |
Het |
Top3a |
A |
G |
11: 60,742,412 |
S953P |
probably benign |
Het |
Trappc10 |
T |
C |
10: 78,197,863 |
K957E |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,735,324 |
E28228V |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,754,824 |
I22042F |
probably damaging |
Het |
Vdr |
A |
T |
15: 97,858,920 |
|
probably null |
Het |
Zfp42 |
A |
T |
8: 43,296,131 |
L111Q |
probably damaging |
Het |
|