Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
T |
C |
8: 24,884,455 |
E507G |
probably damaging |
Het |
Adam39 |
C |
T |
8: 40,824,731 |
T53I |
probably benign |
Het |
Adam4 |
A |
T |
12: 81,421,761 |
S29T |
possibly damaging |
Het |
Adamdec1 |
C |
A |
14: 68,577,904 |
E104* |
probably null |
Het |
Alas1 |
G |
T |
9: 106,236,477 |
P523Q |
probably damaging |
Het |
Aldh3a1 |
A |
G |
11: 61,213,494 |
D69G |
probably benign |
Het |
Arhgap29 |
T |
A |
3: 122,014,971 |
V1266E |
probably damaging |
Het |
Bcdin3d |
T |
C |
15: 99,470,838 |
D160G |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,978,372 |
F569I |
probably benign |
Het |
Cacna1b |
A |
G |
2: 24,631,944 |
L1718S |
probably damaging |
Het |
Casd1 |
A |
G |
6: 4,629,975 |
Y457C |
probably damaging |
Het |
Creb3 |
T |
C |
4: 43,563,192 |
V97A |
probably benign |
Het |
Cux2 |
G |
T |
5: 121,887,476 |
S43* |
probably null |
Het |
Fam160a1 |
A |
T |
3: 85,730,713 |
V93D |
probably damaging |
Het |
Fsbp |
T |
G |
4: 11,579,841 |
N36K |
probably benign |
Het |
Gm11565 |
A |
G |
11: 99,915,214 |
D144G |
probably benign |
Het |
Gm7534 |
G |
A |
4: 134,200,347 |
A365V |
probably benign |
Het |
Gpn3 |
A |
G |
5: 122,373,918 |
Y19C |
probably damaging |
Het |
Gstz1 |
A |
T |
12: 87,162,063 |
T148S |
probably benign |
Het |
Gtf3c5 |
A |
G |
2: 28,572,224 |
I282T |
probably benign |
Het |
Hspa2 |
T |
A |
12: 76,405,740 |
S403T |
possibly damaging |
Het |
Il27 |
G |
A |
7: 126,591,079 |
T121I |
possibly damaging |
Het |
Itpr2 |
A |
G |
6: 146,373,173 |
F837S |
probably damaging |
Het |
Kctd1 |
T |
A |
18: 15,063,227 |
|
probably benign |
Het |
Kynu |
A |
G |
2: 43,679,803 |
T366A |
probably damaging |
Het |
Lama5 |
G |
A |
2: 180,199,266 |
T507I |
probably damaging |
Het |
Myh11 |
C |
T |
16: 14,269,241 |
V124M |
probably damaging |
Het |
Myh14 |
T |
A |
7: 44,624,330 |
H1331L |
probably damaging |
Het |
Myh2 |
T |
A |
11: 67,188,477 |
L957Q |
probably damaging |
Het |
Myh4 |
T |
C |
11: 67,246,401 |
F483L |
probably benign |
Het |
Nbeal1 |
A |
C |
1: 60,329,390 |
K2631N |
probably damaging |
Het |
Ofcc1 |
G |
A |
13: 40,015,388 |
T841I |
probably damaging |
Het |
Ogg1 |
T |
C |
6: 113,327,307 |
C28R |
probably damaging |
Het |
Olfr1449 |
G |
A |
19: 12,935,097 |
A120T |
probably damaging |
Het |
Olfr157 |
T |
C |
4: 43,836,430 |
H20R |
probably benign |
Het |
Olfr181 |
C |
T |
16: 58,925,690 |
V294I |
possibly damaging |
Het |
Olfr49 |
C |
T |
14: 54,282,332 |
A188T |
possibly damaging |
Het |
Olfr855 |
A |
G |
9: 19,585,430 |
K298E |
possibly damaging |
Het |
Parp6 |
G |
C |
9: 59,640,110 |
R460P |
probably damaging |
Het |
Phf14 |
A |
G |
6: 11,992,057 |
H744R |
probably damaging |
Het |
Pibf1 |
A |
G |
14: 99,133,351 |
N263S |
possibly damaging |
Het |
Plcb4 |
A |
G |
2: 135,932,271 |
T158A |
possibly damaging |
Het |
Plce1 |
T |
C |
19: 38,749,396 |
S1615P |
possibly damaging |
Het |
Plxna3 |
T |
G |
X: 74,338,948 |
|
probably null |
Het |
Rad54b |
T |
A |
4: 11,609,449 |
H633Q |
probably benign |
Het |
Rgs22 |
T |
A |
15: 36,099,933 |
Y212F |
probably benign |
Het |
Rnd3 |
G |
A |
2: 51,132,541 |
A163V |
probably benign |
Het |
Rnf10 |
A |
T |
5: 115,251,089 |
V315E |
probably damaging |
Het |
Robo2 |
C |
T |
16: 73,904,378 |
|
probably null |
Het |
Rp1l1 |
T |
G |
14: 64,031,270 |
V1435G |
probably damaging |
Het |
Scaf8 |
T |
A |
17: 3,197,985 |
D1194E |
probably benign |
Het |
Sept12 |
T |
C |
16: 4,991,943 |
T198A |
probably damaging |
Het |
Shisa2 |
A |
G |
14: 59,630,180 |
T294A |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,191,062 |
|
probably null |
Het |
Strbp |
A |
T |
2: 37,645,679 |
S6T |
probably damaging |
Het |
Syf2 |
A |
G |
4: 134,934,493 |
E56G |
probably damaging |
Het |
Thap4 |
T |
C |
1: 93,714,866 |
|
probably benign |
Het |
Tnfaip3 |
T |
C |
10: 19,011,832 |
|
probably benign |
Het |
Tnxb |
A |
G |
17: 34,672,540 |
E619G |
probably damaging |
Het |
Tpr |
G |
A |
1: 150,423,567 |
A1173T |
probably benign |
Het |
Tspan3 |
G |
A |
9: 56,136,696 |
R240W |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,410,716 |
S1128L |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 83,295,247 |
V236A |
probably damaging |
Het |
Zcchc6 |
G |
T |
13: 59,796,845 |
T658K |
probably damaging |
Het |
Zfp940 |
T |
C |
7: 29,845,438 |
D348G |
probably benign |
Het |
|