Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
T |
G |
5: 146,185,219 |
S18R |
probably benign |
Het |
2010315B03Rik |
A |
C |
9: 124,293,766 |
V176G |
probably benign |
Het |
Abcb1a |
T |
A |
5: 8,715,732 |
|
probably null |
Het |
Acad11 |
C |
A |
9: 104,075,877 |
P102T |
probably damaging |
Het |
Aggf1 |
T |
A |
13: 95,364,713 |
D387V |
probably damaging |
Het |
Akr1c13 |
G |
A |
13: 4,198,497 |
V234I |
probably benign |
Het |
Alg5 |
A |
G |
3: 54,746,473 |
Y210C |
possibly damaging |
Het |
Arl8a |
C |
A |
1: 135,147,099 |
A41E |
probably benign |
Het |
Axin1 |
C |
A |
17: 26,173,756 |
T337K |
possibly damaging |
Het |
Bdp1 |
A |
G |
13: 100,056,267 |
L1353P |
probably damaging |
Het |
Bptf |
A |
T |
11: 107,043,694 |
V2851E |
probably damaging |
Het |
C9 |
A |
T |
15: 6,459,643 |
E160D |
probably damaging |
Het |
Cbx6 |
T |
C |
15: 79,828,680 |
D182G |
probably damaging |
Het |
Ccdc144b |
T |
G |
3: 36,010,660 |
*521C |
probably null |
Het |
Cep57l1 |
T |
C |
10: 41,721,682 |
R242G |
possibly damaging |
Het |
Chst8 |
T |
C |
7: 34,675,724 |
D230G |
probably damaging |
Het |
Col3a1 |
A |
C |
1: 45,346,110 |
D129A |
probably damaging |
Het |
Cst12 |
A |
G |
2: 148,789,473 |
E38G |
possibly damaging |
Het |
Disp1 |
G |
T |
1: 183,088,096 |
A920E |
probably damaging |
Het |
Dtna |
T |
G |
18: 23,535,149 |
|
probably null |
Het |
Elp3 |
T |
A |
14: 65,582,929 |
H97L |
probably damaging |
Het |
Exoc8 |
A |
G |
8: 124,897,575 |
F18L |
possibly damaging |
Het |
Extl3 |
T |
C |
14: 65,077,320 |
T138A |
probably benign |
Het |
Foxi2 |
G |
T |
7: 135,410,667 |
G95C |
probably damaging |
Het |
Foxj2 |
G |
T |
6: 122,833,271 |
Q196H |
probably benign |
Het |
Frem1 |
A |
T |
4: 82,989,189 |
D811E |
probably damaging |
Het |
Frmd4a |
A |
T |
2: 4,603,448 |
E709V |
probably damaging |
Het |
Galc |
C |
T |
12: 98,242,744 |
G217D |
possibly damaging |
Het |
Gm5592 |
G |
T |
7: 41,216,118 |
|
probably benign |
Het |
Hnrnpul1 |
A |
G |
7: 25,743,011 |
S269P |
probably benign |
Het |
Hrh1 |
T |
C |
6: 114,480,535 |
V259A |
probably benign |
Het |
Lef1 |
T |
C |
3: 131,184,733 |
S167P |
probably benign |
Het |
Mtf2 |
T |
C |
5: 108,093,352 |
I248T |
probably benign |
Het |
Muc2 |
C |
T |
7: 141,745,608 |
T130M |
possibly damaging |
Het |
Myo16 |
T |
C |
8: 10,435,880 |
F653S |
probably damaging |
Het |
Myo1e |
T |
C |
9: 70,343,135 |
|
probably null |
Het |
Myo5a |
G |
T |
9: 75,116,336 |
|
probably benign |
Het |
Nlrp1b |
T |
A |
11: 71,182,663 |
D118V |
probably damaging |
Het |
Npat |
T |
C |
9: 53,572,620 |
F1412S |
probably damaging |
Het |
Olfr1377 |
G |
A |
11: 50,984,775 |
E25K |
probably benign |
Het |
Olfr884 |
T |
G |
9: 38,048,140 |
L306R |
probably benign |
Het |
Onecut3 |
G |
T |
10: 80,495,707 |
A234S |
unknown |
Het |
Osbpl6 |
T |
A |
2: 76,546,000 |
I73K |
probably damaging |
Het |
Otog |
C |
T |
7: 46,288,519 |
T1884I |
probably benign |
Het |
Pax6 |
C |
A |
2: 105,696,502 |
P251Q |
probably benign |
Het |
Pias4 |
A |
G |
10: 81,164,034 |
Y62H |
possibly damaging |
Het |
Pknox1 |
T |
A |
17: 31,590,713 |
V97D |
possibly damaging |
Het |
Plekhf1 |
A |
G |
7: 38,221,598 |
V182A |
probably damaging |
Het |
Plscr4 |
T |
C |
9: 92,484,780 |
V149A |
probably damaging |
Het |
Polr2l |
A |
T |
7: 141,473,396 |
L35Q |
probably damaging |
Het |
Ppp3ca |
T |
C |
3: 136,890,489 |
I305T |
probably damaging |
Het |
Ptprg |
G |
A |
14: 12,122,068 |
A311T |
probably benign |
Het |
Raet1e |
T |
G |
10: 22,181,332 |
I185R |
probably damaging |
Het |
Rims1 |
A |
C |
1: 22,479,462 |
V520G |
probably damaging |
Het |
Rp1 |
A |
T |
1: 4,345,878 |
D1670E |
probably damaging |
Het |
Rps6ka1 |
A |
T |
4: 133,860,557 |
I352N |
probably damaging |
Het |
Rtp3 |
T |
C |
9: 110,987,350 |
|
probably benign |
Het |
Ryr3 |
T |
A |
2: 112,733,031 |
|
probably null |
Het |
Sall3 |
A |
G |
18: 80,974,476 |
V79A |
probably damaging |
Het |
Sdsl |
C |
T |
5: 120,462,054 |
V93M |
probably damaging |
Het |
Slc7a13 |
A |
G |
4: 19,819,390 |
N197D |
probably benign |
Het |
Slit1 |
T |
A |
19: 41,721,044 |
R137* |
probably null |
Het |
Stxbp5 |
C |
A |
10: 9,770,623 |
R115L |
probably damaging |
Het |
Tcea1 |
G |
A |
1: 4,894,944 |
R290H |
probably damaging |
Het |
Tmem132e |
A |
T |
11: 82,434,512 |
T113S |
probably damaging |
Het |
Tpp1 |
A |
T |
7: 105,749,251 |
I286N |
probably damaging |
Het |
Trio |
G |
A |
15: 27,732,538 |
R3086* |
probably null |
Het |
Usp22 |
T |
A |
11: 61,160,636 |
N294Y |
probably damaging |
Het |
Usp44 |
T |
A |
10: 93,846,071 |
S128T |
probably benign |
Het |
Zc3h7b |
T |
C |
15: 81,769,183 |
|
probably null |
Het |
Zfhx2 |
T |
C |
14: 55,066,915 |
Y1204C |
possibly damaging |
Het |
|