Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
C |
7: 120,423,770 |
I43T |
probably benign |
Het |
Aqr |
G |
A |
2: 114,104,062 |
A1366V |
possibly damaging |
Het |
Arhgap45 |
G |
A |
10: 80,026,558 |
|
probably null |
Het |
Atf7ip |
T |
A |
6: 136,565,089 |
M607K |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,888,136 |
|
probably benign |
Het |
BC028528 |
TCACTGGTTCTGTGGTCACTGGTTCTGTGG |
TCACTGGTTCTGTGGCCACTGGTTCTGTGGTCACTGGTTCTGTGG |
3: 95,888,152 |
|
probably benign |
Het |
BC028528 |
ACTGGTTCTGTGGTC |
ACTGGTTCTGTGGTCCCTGGTTCTGTGGTC |
3: 95,888,169 |
|
probably benign |
Het |
Bcar3 |
T |
A |
3: 122,508,493 |
V279E |
probably benign |
Het |
Cd96 |
C |
T |
16: 46,071,734 |
|
probably null |
Het |
Cdca2 |
G |
A |
14: 67,694,991 |
P488S |
probably benign |
Het |
Col4a2 |
T |
G |
8: 11,406,856 |
|
probably null |
Het |
Cyp4a12a |
A |
G |
4: 115,327,758 |
R379G |
possibly damaging |
Het |
Defb34 |
A |
G |
8: 19,126,379 |
S29G |
probably benign |
Het |
Dnah11 |
A |
G |
12: 117,995,275 |
S2958P |
probably damaging |
Het |
Dync1h1 |
A |
G |
12: 110,665,162 |
D4431G |
possibly damaging |
Het |
Egfem1 |
A |
T |
3: 29,151,866 |
H84L |
probably benign |
Het |
Enah |
A |
T |
1: 181,906,385 |
|
probably null |
Het |
Fam178b |
G |
T |
1: 36,659,407 |
Q78K |
probably benign |
Het |
Glb1 |
A |
G |
9: 114,473,863 |
N589S |
probably damaging |
Het |
Gm1527 |
C |
T |
3: 28,902,280 |
H132Y |
probably benign |
Het |
Gm4788 |
A |
G |
1: 139,754,303 |
V185A |
possibly damaging |
Het |
Gm4858 |
A |
G |
3: 93,074,565 |
T223A |
probably benign |
Het |
Gm5799 |
A |
G |
14: 43,543,707 |
R22G |
possibly damaging |
Het |
Grip2 |
T |
C |
6: 91,778,688 |
D617G |
possibly damaging |
Het |
Hax1 |
A |
T |
3: 89,998,566 |
D5E |
possibly damaging |
Het |
Hic1 |
A |
G |
11: 75,167,151 |
L304P |
probably damaging |
Het |
Hmox1 |
T |
A |
8: 75,097,019 |
I105N |
probably damaging |
Het |
Hormad1 |
T |
C |
3: 95,562,555 |
S38P |
probably damaging |
Het |
Hspa4 |
A |
G |
11: 53,267,103 |
S558P |
possibly damaging |
Het |
Kcnf1 |
T |
A |
12: 17,174,729 |
H497L |
probably benign |
Het |
Kcnma1 |
C |
T |
14: 23,330,935 |
D1022N |
probably damaging |
Het |
Kcnt1 |
T |
C |
2: 25,900,463 |
F479S |
possibly damaging |
Het |
Krba1 |
T |
C |
6: 48,406,339 |
V203A |
probably benign |
Het |
Lct |
G |
T |
1: 128,319,087 |
P233Q |
probably benign |
Het |
Ly75 |
T |
C |
2: 60,334,515 |
D773G |
probably benign |
Het |
Malt1 |
T |
C |
18: 65,449,609 |
|
probably null |
Het |
Man1a2 |
A |
T |
3: 100,620,105 |
L333Q |
probably damaging |
Het |
Mtus1 |
T |
C |
8: 41,082,928 |
T584A |
probably benign |
Het |
Myof |
A |
T |
19: 37,910,911 |
S1800R |
probably damaging |
Het |
Nbea |
A |
C |
3: 56,091,031 |
C118W |
probably damaging |
Het |
Nsd3 |
A |
T |
8: 25,640,724 |
D35V |
probably damaging |
Het |
Olfr1386 |
G |
A |
11: 49,469,927 |
|
probably benign |
Het |
Olfr739 |
G |
A |
14: 50,425,265 |
V249I |
possibly damaging |
Het |
Pcnx3 |
C |
T |
19: 5,686,147 |
R217H |
possibly damaging |
Het |
Pcsk4 |
G |
A |
10: 80,323,173 |
P462L |
probably benign |
Het |
Pdia5 |
T |
G |
16: 35,456,509 |
K96N |
probably damaging |
Het |
Pik3c2a |
T |
C |
7: 116,373,839 |
Y707C |
probably damaging |
Het |
Ppig |
A |
T |
2: 69,749,462 |
N447Y |
unknown |
Het |
Ppp1r9b |
T |
C |
11: 95,004,571 |
L695P |
possibly damaging |
Het |
Proser1 |
C |
T |
3: 53,478,704 |
A669V |
probably benign |
Het |
Rdx |
A |
T |
9: 52,068,870 |
K254N |
probably damaging |
Het |
Slc35f2 |
T |
C |
9: 53,798,010 |
S95P |
probably benign |
Het |
Slc4a3 |
T |
A |
1: 75,557,362 |
S1118T |
probably benign |
Het |
Slf1 |
G |
A |
13: 77,051,168 |
P698L |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,751,574 |
E2338G |
probably benign |
Het |
Taok3 |
T |
A |
5: 117,200,151 |
Y91* |
probably null |
Het |
Tbc1d31 |
C |
T |
15: 57,952,816 |
L649F |
probably damaging |
Het |
Tmem132b |
A |
T |
5: 125,787,646 |
I939F |
possibly damaging |
Het |
Trav17 |
T |
A |
14: 53,806,979 |
Y69N |
probably benign |
Het |
Trmt13 |
T |
C |
3: 116,594,739 |
D16G |
probably benign |
Het |
Upf2 |
T |
A |
2: 5,973,518 |
Y398N |
unknown |
Het |
Vmn1r238 |
T |
C |
18: 3,122,875 |
T180A |
probably benign |
Het |
Wdyhv1 |
T |
C |
15: 58,152,610 |
V85A |
possibly damaging |
Het |
Zfp738 |
A |
T |
13: 67,669,553 |
I773N |
probably benign |
Het |
Zscan4e |
A |
T |
7: 11,307,153 |
M264K |
probably benign |
Het |
|