Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak2 |
G |
T |
12: 112,783,119 |
A1036E |
|
Het |
Baz2b |
A |
T |
2: 59,962,184 |
H533Q |
possibly damaging |
Het |
Bcl2l11 |
T |
A |
2: 128,158,315 |
W193R |
probably damaging |
Het |
Bcl2l12 |
C |
T |
7: 44,996,914 |
G24D |
probably damaging |
Het |
Cacna1b |
A |
G |
2: 24,690,761 |
V691A |
probably damaging |
Het |
Cdh8 |
T |
C |
8: 99,196,352 |
D304G |
probably damaging |
Het |
Ces3a |
A |
T |
8: 105,057,962 |
Q525H |
probably damaging |
Het |
Csmd1 |
C |
A |
8: 16,101,128 |
C1391F |
probably damaging |
Het |
Cul7 |
G |
T |
17: 46,651,698 |
G85V |
probably damaging |
Het |
Dnah8 |
G |
A |
17: 30,871,392 |
V4623I |
possibly damaging |
Het |
Dnhd1 |
T |
A |
7: 105,713,985 |
L3918Q |
probably damaging |
Het |
Exoc4 |
A |
T |
6: 33,921,488 |
N881Y |
probably damaging |
Het |
Flt1 |
G |
C |
5: 147,603,569 |
A770G |
probably damaging |
Het |
Fndc5 |
A |
G |
4: 129,142,122 |
N184S |
probably benign |
Het |
Folh1 |
A |
G |
7: 86,775,637 |
|
probably null |
Het |
Frem3 |
A |
T |
8: 80,612,031 |
T318S |
probably damaging |
Het |
Gba2 |
A |
G |
4: 43,568,453 |
V671A |
probably benign |
Het |
Gm7102 |
T |
G |
19: 61,175,559 |
D146A |
probably damaging |
Het |
Gpt2 |
G |
A |
8: 85,518,052 |
E325K |
probably benign |
Het |
Jph2 |
G |
A |
2: 163,375,784 |
T324M |
probably damaging |
Het |
Kank4 |
A |
G |
4: 98,761,521 |
V937A |
probably damaging |
Het |
Kdm3a |
T |
A |
6: 71,632,170 |
E24D |
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,004,019 |
L464Q |
probably damaging |
Het |
Loxhd1 |
T |
A |
18: 77,388,514 |
V1159E |
probably damaging |
Het |
Malrd1 |
A |
G |
2: 15,925,176 |
N1498D |
unknown |
Het |
Mrgprb5 |
C |
T |
7: 48,168,907 |
V27I |
probably benign |
Het |
Mtfr2 |
A |
G |
10: 20,357,566 |
N294D |
probably damaging |
Het |
Muc6 |
A |
T |
7: 141,649,277 |
L498H |
probably damaging |
Het |
N4bp2 |
A |
G |
5: 65,790,707 |
T227A |
possibly damaging |
Het |
Nin |
C |
T |
12: 70,102,799 |
R12Q |
|
Het |
Obscn |
G |
C |
11: 59,029,325 |
A27G |
|
Het |
Olfr284 |
T |
A |
15: 98,340,540 |
M150L |
possibly damaging |
Het |
Olfr582 |
G |
A |
7: 103,041,655 |
D54N |
probably damaging |
Het |
Olfr729 |
T |
G |
14: 50,147,935 |
E313A |
probably benign |
Het |
Olfr746 |
T |
A |
14: 50,654,126 |
D296E |
probably benign |
Het |
Olfr912 |
T |
A |
9: 38,582,034 |
Y252* |
probably null |
Het |
Polr2a |
A |
G |
11: 69,735,309 |
S1672P |
unknown |
Het |
Qprt |
A |
G |
7: 127,108,189 |
V245A |
probably damaging |
Het |
Rab11fip5 |
T |
A |
6: 85,348,194 |
E377V |
probably damaging |
Het |
Rere |
A |
G |
4: 150,406,604 |
T71A |
probably benign |
Het |
Ret |
A |
T |
6: 118,197,102 |
L11Q |
possibly damaging |
Het |
Rp1 |
C |
T |
1: 4,349,018 |
V624I |
probably benign |
Het |
Scaf8 |
T |
A |
17: 3,163,029 |
L131H |
unknown |
Het |
Scgb2a2 |
A |
G |
19: 9,851,657 |
R58G |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,754,809 |
I1580T |
probably damaging |
Het |
Slco4c1 |
T |
G |
1: 96,841,141 |
K332T |
probably damaging |
Het |
Sntg1 |
T |
G |
1: 8,448,065 |
Y368S |
possibly damaging |
Het |
Stim1 |
A |
G |
7: 102,408,408 |
T143A |
probably benign |
Het |
Tbr1 |
A |
G |
2: 61,811,816 |
D475G |
probably benign |
Het |
Tcp1 |
A |
G |
17: 12,917,873 |
D47G |
probably damaging |
Het |
Tpgs2 |
T |
C |
18: 25,149,137 |
D119G |
probably damaging |
Het |
Trim40 |
C |
A |
17: 36,882,642 |
R225M |
probably null |
Het |
Tro |
GCAGTGCTTGGTCCTCCGAAGCCACCTCCAGTGCTTGGTCCTCCGAAGCCACCTCCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTATTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCC |
GCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTATTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCC |
X: 150,645,856 |
|
probably benign |
Het |
Trpm1 |
A |
T |
7: 64,235,845 |
N870Y |
probably damaging |
Het |
Tsr3 |
A |
G |
17: 25,240,471 |
D47G |
probably benign |
Het |
Vil1 |
G |
A |
1: 74,416,002 |
G38R |
probably damaging |
Het |
Wdr33 |
C |
T |
18: 31,893,003 |
T919I |
unknown |
Het |
Wdr36 |
T |
C |
18: 32,839,451 |
V64A |
probably benign |
Het |
Xpnpep1 |
T |
C |
19: 53,010,107 |
I237V |
probably benign |
Het |
Zfp780b |
A |
T |
7: 27,963,141 |
I663N |
probably damaging |
Het |
Zfyve9 |
G |
A |
4: 108,650,322 |
A513V |
probably benign |
Het |
|