Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 138,066,264 |
T405A |
probably damaging |
Het |
4932438A13Rik |
T |
A |
3: 36,908,192 |
L481M |
possibly damaging |
Het |
Acer1 |
A |
T |
17: 56,955,624 |
D175E |
possibly damaging |
Het |
Adamts9 |
G |
A |
6: 92,905,306 |
|
probably benign |
Het |
Amigo3 |
T |
C |
9: 108,054,658 |
S427P |
probably benign |
Het |
Arid4a |
T |
G |
12: 71,075,419 |
L858W |
probably damaging |
Het |
Bbox1 |
A |
G |
2: 110,268,302 |
F310S |
probably damaging |
Het |
Bmper |
T |
A |
9: 23,406,686 |
C534S |
probably damaging |
Het |
Cacna1d |
T |
G |
14: 30,346,790 |
|
probably benign |
Het |
Capn12 |
G |
A |
7: 28,890,387 |
|
probably null |
Het |
Chchd1 |
T |
C |
14: 20,704,163 |
S48P |
possibly damaging |
Het |
Cnot7 |
A |
G |
8: 40,495,921 |
|
probably benign |
Het |
Cux1 |
T |
C |
5: 136,363,253 |
|
probably benign |
Het |
Cyp2b19 |
T |
A |
7: 26,766,826 |
D351E |
probably benign |
Het |
Dctn1 |
G |
T |
6: 83,182,632 |
G31* |
probably null |
Het |
Duox1 |
T |
A |
2: 122,346,641 |
|
probably benign |
Het |
Egflam |
T |
G |
15: 7,253,430 |
E382A |
possibly damaging |
Het |
Ext1 |
T |
C |
15: 53,345,146 |
N73S |
probably benign |
Het |
Glg1 |
A |
T |
8: 111,165,582 |
M866K |
probably damaging |
Het |
Gm3333 |
A |
G |
13: 62,274,471 |
|
noncoding transcript |
Het |
Golm1 |
T |
A |
13: 59,645,100 |
H197L |
probably benign |
Het |
Gtse1 |
A |
G |
15: 85,862,378 |
K132E |
probably damaging |
Het |
Gxylt2 |
A |
T |
6: 100,733,378 |
|
probably benign |
Het |
Hrc |
T |
A |
7: 45,336,689 |
S421R |
probably benign |
Het |
Ighg2c |
T |
A |
12: 113,288,168 |
|
probably benign |
Het |
Ihh |
A |
G |
1: 74,946,591 |
I245T |
probably benign |
Het |
Ilf3 |
T |
A |
9: 21,388,714 |
M65K |
possibly damaging |
Het |
Kif9 |
A |
G |
9: 110,485,038 |
I33V |
probably benign |
Het |
Lama1 |
A |
T |
17: 67,795,186 |
|
probably benign |
Het |
Lamb1 |
T |
C |
12: 31,278,601 |
I188T |
possibly damaging |
Het |
Lpp |
T |
A |
16: 24,661,800 |
|
probably benign |
Het |
Mark2 |
A |
C |
19: 7,283,577 |
|
probably benign |
Het |
Mmp3 |
T |
C |
9: 7,451,910 |
|
probably benign |
Het |
Mthfd1l |
T |
A |
10: 3,978,727 |
|
probably benign |
Het |
Mtr |
A |
T |
13: 12,222,226 |
S569T |
probably damaging |
Het |
Myh13 |
T |
A |
11: 67,367,237 |
S1752T |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,156,207 |
L565H |
probably damaging |
Het |
Numa1 |
A |
G |
7: 102,009,453 |
K296E |
probably damaging |
Het |
Olfr1477 |
A |
G |
19: 13,502,589 |
E82G |
probably benign |
Het |
Olfr201 |
C |
T |
16: 59,269,211 |
G152D |
probably damaging |
Het |
Olfr613 |
A |
T |
7: 103,552,322 |
Y179F |
probably damaging |
Het |
Pla2g2c |
T |
C |
4: 138,743,590 |
|
probably benign |
Het |
Pnpla7 |
A |
T |
2: 25,011,606 |
E548V |
probably damaging |
Het |
Ppm1m |
C |
A |
9: 106,196,696 |
E273* |
probably null |
Het |
Ppp2r1b |
C |
T |
9: 50,861,573 |
R117* |
probably null |
Het |
Psg-ps1 |
A |
G |
7: 17,677,881 |
|
noncoding transcript |
Het |
Rabgap1l |
G |
A |
1: 160,231,789 |
|
probably benign |
Het |
Rapgef6 |
T |
A |
11: 54,546,378 |
M49K |
possibly damaging |
Het |
Rnf219 |
T |
A |
14: 104,503,344 |
|
probably null |
Het |
Rtel1 |
T |
G |
2: 181,323,405 |
I146M |
probably damaging |
Het |
Sdr9c7 |
A |
T |
10: 127,903,672 |
M219L |
probably benign |
Het |
Serpinb1a |
A |
T |
13: 32,850,276 |
L44Q |
probably damaging |
Het |
Slc13a4 |
A |
G |
6: 35,287,362 |
I190T |
possibly damaging |
Het |
Slc46a2 |
A |
G |
4: 59,914,392 |
L177P |
probably damaging |
Het |
Slc47a2 |
C |
T |
11: 61,336,242 |
V167M |
possibly damaging |
Het |
Snrnp200 |
C |
T |
2: 127,234,954 |
|
probably benign |
Het |
Snx13 |
C |
A |
12: 35,101,124 |
|
probably benign |
Het |
Snx25 |
C |
T |
8: 46,041,365 |
A828T |
probably damaging |
Het |
Spic |
A |
G |
10: 88,675,941 |
L151P |
probably damaging |
Het |
Sptb |
G |
T |
12: 76,622,950 |
Q535K |
probably damaging |
Het |
Ssu2 |
G |
A |
6: 112,374,820 |
H315Y |
probably damaging |
Het |
Stk32a |
T |
C |
18: 43,313,378 |
|
probably benign |
Het |
Tcaf2 |
A |
G |
6: 42,629,613 |
I469T |
probably benign |
Het |
Tln2 |
A |
G |
9: 67,240,672 |
|
probably benign |
Het |
Top2a |
T |
A |
11: 98,997,856 |
I1260L |
probably benign |
Het |
Treml1 |
C |
A |
17: 48,364,980 |
S91* |
probably null |
Het |
Trmt11 |
T |
C |
10: 30,535,243 |
N418S |
probably benign |
Het |
Ttf1 |
A |
G |
2: 29,084,655 |
Y801C |
probably damaging |
Het |
Vps4a |
T |
C |
8: 107,036,701 |
L29P |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 101,944,033 |
I480T |
probably damaging |
Het |
Ywhag |
A |
T |
5: 135,911,299 |
V147E |
probably damaging |
Het |
|