Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
C |
6: 121,647,971 |
V436A |
probably benign |
Het |
Abcc5 |
T |
C |
16: 20,405,501 |
T111A |
possibly damaging |
Het |
Acsbg2 |
T |
A |
17: 56,857,000 |
D203V |
probably benign |
Het |
Alpk2 |
G |
T |
18: 65,306,978 |
T448K |
probably benign |
Het |
Arhgef2 |
A |
G |
3: 88,643,872 |
N780S |
possibly damaging |
Het |
Atxn2l |
T |
C |
7: 126,499,222 |
N252S |
possibly damaging |
Het |
Bmpr1b |
A |
T |
3: 141,863,080 |
L163Q |
probably benign |
Het |
Clca2 |
T |
C |
3: 145,097,784 |
R100G |
probably benign |
Het |
Col2a1 |
A |
G |
15: 98,000,456 |
I79T |
unknown |
Het |
Csmd1 |
A |
G |
8: 15,926,524 |
V2898A |
probably benign |
Het |
Cux1 |
G |
A |
5: 136,310,041 |
|
probably null |
Het |
Cyp2u1 |
A |
G |
3: 131,303,124 |
S2P |
probably benign |
Het |
Daam1 |
C |
A |
12: 71,988,904 |
H958N |
probably damaging |
Het |
Dnah7a |
C |
T |
1: 53,503,776 |
V2412I |
probably benign |
Het |
Ergic2 |
T |
C |
6: 148,206,635 |
R2G |
probably damaging |
Het |
Fam159b |
A |
G |
13: 104,863,658 |
V19A |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,285,001 |
T1629A |
possibly damaging |
Het |
Ftl1 |
T |
A |
7: 45,459,778 |
|
probably benign |
Het |
Fut8 |
T |
C |
12: 77,448,632 |
V332A |
possibly damaging |
Het |
Gm28363 |
T |
C |
1: 117,727,389 |
S113P |
probably damaging |
Het |
Gm6502 |
G |
A |
5: 94,317,125 |
A457T |
possibly damaging |
Het |
Hfe |
A |
T |
13: 23,708,069 |
V104E |
probably damaging |
Het |
Ifih1 |
A |
T |
2: 62,598,896 |
N899K |
probably benign |
Het |
Krt75 |
A |
G |
15: 101,568,315 |
S380P |
possibly damaging |
Het |
Meiob |
T |
G |
17: 24,836,445 |
F409V |
probably damaging |
Het |
Mkrn2os |
A |
T |
6: 115,585,513 |
I163N |
probably damaging |
Het |
Nanos1 |
G |
T |
19: 60,756,608 |
G115W |
probably damaging |
Het |
Naprt |
C |
T |
15: 75,892,612 |
A276T |
probably damaging |
Het |
Oas1e |
G |
T |
5: 120,795,422 |
T26N |
probably benign |
Het |
Olfr1179 |
A |
G |
2: 88,402,208 |
V242A |
possibly damaging |
Het |
Olfr1279 |
T |
C |
2: 111,306,448 |
M81T |
probably benign |
Het |
Olfr355 |
T |
C |
2: 36,927,521 |
I198V |
probably benign |
Het |
Olfr53 |
T |
A |
7: 140,652,553 |
C191* |
probably null |
Het |
Olfr766-ps1 |
T |
G |
10: 129,063,272 |
Q245P |
probably damaging |
Het |
Olfr792 |
T |
C |
10: 129,540,738 |
L67P |
possibly damaging |
Het |
Olfr967 |
T |
C |
9: 39,750,569 |
F61S |
probably damaging |
Het |
Optn |
T |
C |
2: 5,042,483 |
N207S |
probably benign |
Het |
Oxnad1 |
G |
T |
14: 32,101,019 |
E236* |
probably null |
Het |
Pcdha3 |
G |
A |
18: 36,946,993 |
A263T |
probably damaging |
Het |
Pex13 |
A |
T |
11: 23,655,472 |
W253R |
possibly damaging |
Het |
Pip5k1b |
T |
A |
19: 24,397,069 |
E49D |
probably benign |
Het |
Plau |
C |
A |
14: 20,839,450 |
F194L |
possibly damaging |
Het |
Ppm1n |
A |
G |
7: 19,279,741 |
L95S |
probably damaging |
Het |
Radil |
G |
T |
5: 142,485,505 |
|
probably null |
Het |
Ralgapa2 |
C |
T |
2: 146,348,454 |
M1266I |
probably benign |
Het |
Reln |
A |
T |
5: 21,942,620 |
L2444Q |
probably damaging |
Het |
Rims2 |
T |
C |
15: 39,437,077 |
V260A |
probably benign |
Het |
Rnase2b |
T |
A |
14: 51,162,765 |
V101E |
probably damaging |
Het |
Rtp3 |
T |
A |
9: 110,986,704 |
T198S |
probably benign |
Het |
Smad3 |
T |
A |
9: 63,666,153 |
D201V |
probably benign |
Het |
Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,660,334 |
|
probably benign |
Het |
Spata7 |
T |
G |
12: 98,664,296 |
F371C |
probably damaging |
Het |
Stag1 |
T |
G |
9: 100,945,889 |
N990K |
probably benign |
Het |
Tbx18 |
C |
T |
9: 87,707,830 |
A352T |
probably damaging |
Het |
Thada |
C |
T |
17: 84,230,963 |
R1539Q |
probably benign |
Het |
Thrap3 |
A |
C |
4: 126,185,127 |
|
probably benign |
Het |
Tnks |
G |
A |
8: 34,849,304 |
T887M |
probably damaging |
Het |
Trap1 |
A |
C |
16: 4,052,928 |
V393G |
probably damaging |
Het |
Trpm4 |
A |
G |
7: 45,327,719 |
|
probably null |
Het |
Trrap |
G |
T |
5: 144,839,614 |
G3007C |
probably benign |
Het |
U2surp |
A |
T |
9: 95,481,673 |
N611K |
probably damaging |
Het |
Usp12 |
A |
G |
5: 146,768,935 |
|
probably null |
Het |
Vmn1r200 |
A |
G |
13: 22,395,317 |
T97A |
possibly damaging |
Het |
Vmn2r110 |
C |
T |
17: 20,574,179 |
V743I |
probably benign |
Het |
Vps50 |
C |
T |
6: 3,600,256 |
T905M |
probably damaging |
Het |
Wdr48 |
T |
A |
9: 119,907,789 |
|
probably null |
Het |
Zfp446 |
C |
T |
7: 12,978,122 |
|
probably benign |
Het |
Zfr |
T |
C |
15: 12,180,929 |
S1012P |
probably benign |
Het |
|