Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afg1l |
A |
T |
10: 42,425,249 |
Y193N |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,780,802 |
V70E |
|
Het |
Aimp1 |
T |
C |
3: 132,677,011 |
K44E |
probably damaging |
Het |
Arid1b |
T |
A |
17: 4,996,043 |
Y369N |
unknown |
Het |
Art5 |
A |
T |
7: 102,097,873 |
V233D |
probably damaging |
Het |
Baz2b |
T |
A |
2: 59,962,492 |
N431Y |
possibly damaging |
Het |
Bik |
T |
A |
15: 83,544,163 |
F131I |
possibly damaging |
Het |
Bmpr1a |
A |
G |
14: 34,441,125 |
Y103H |
probably damaging |
Het |
Cabp7 |
C |
T |
11: 4,746,676 |
V18M |
possibly damaging |
Het |
Cacna1a |
C |
A |
8: 84,571,237 |
T1240N |
probably damaging |
Het |
Cacna1h |
A |
G |
17: 25,384,765 |
V1311A |
probably damaging |
Het |
Cbarp |
A |
C |
10: 80,137,317 |
S16A |
possibly damaging |
Het |
Ccng2 |
C |
G |
5: 93,273,343 |
S237R |
probably benign |
Het |
Ces2b |
A |
T |
8: 104,837,840 |
H494L |
possibly damaging |
Het |
Cfap43 |
T |
A |
19: 47,739,785 |
H1511L |
possibly damaging |
Het |
Cfap54 |
A |
G |
10: 92,839,458 |
V2867A |
probably benign |
Het |
Col5a1 |
C |
T |
2: 27,997,585 |
P956L |
unknown |
Het |
Dcakd |
T |
G |
11: 103,000,206 |
Q19P |
possibly damaging |
Het |
Ddx47 |
T |
A |
6: 135,023,338 |
D432E |
probably benign |
Het |
Dhrs7b |
T |
C |
11: 60,844,229 |
F29L |
probably benign |
Het |
Dis3l2 |
A |
T |
1: 86,990,303 |
D558V |
possibly damaging |
Het |
Dtx3l |
T |
A |
16: 35,933,657 |
D193V |
probably damaging |
Het |
Epha4 |
G |
A |
1: 77,399,785 |
R486C |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,944,152 |
T1404A |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,037,438 |
T3796A |
probably damaging |
Het |
Ffar2 |
A |
T |
7: 30,819,504 |
W204R |
probably benign |
Het |
Ftmt |
A |
G |
18: 52,332,019 |
I136V |
probably benign |
Het |
Gm10300 |
T |
C |
4: 132,074,856 |
W54R |
unknown |
Het |
Gm10518 |
C |
T |
1: 179,803,384 |
P3L |
unknown |
Het |
Gm5788 |
T |
C |
12: 87,494,893 |
L58P |
probably damaging |
Het |
Gm9733 |
A |
T |
3: 15,320,644 |
I66N |
probably benign |
Het |
Grm2 |
G |
A |
9: 106,651,058 |
T209M |
probably damaging |
Het |
Gtdc1 |
C |
T |
2: 44,635,310 |
M176I |
probably benign |
Het |
Insrr |
T |
C |
3: 87,803,133 |
L382P |
probably damaging |
Het |
Jade2 |
A |
G |
11: 51,817,184 |
V734A |
possibly damaging |
Het |
Kcnh4 |
C |
T |
11: 100,747,646 |
R586H |
probably benign |
Het |
Kdm1a |
A |
T |
4: 136,552,527 |
D721E |
probably damaging |
Het |
Knl1 |
G |
A |
2: 119,102,522 |
C2054Y |
possibly damaging |
Het |
Lrrk2 |
C |
T |
15: 91,700,441 |
P354S |
probably benign |
Het |
Luzp2 |
A |
G |
7: 55,075,026 |
I112V |
probably damaging |
Het |
Mgl2 |
T |
C |
11: 70,135,680 |
S105P |
probably damaging |
Het |
Mocs1 |
T |
A |
17: 49,449,115 |
M200K |
possibly damaging |
Het |
Oat |
T |
A |
7: 132,567,198 |
I98L |
probably benign |
Het |
Obscn |
T |
C |
11: 59,029,486 |
Y8C |
|
Het |
Olfr1462 |
G |
A |
19: 13,191,404 |
V246I |
possibly damaging |
Het |
Olfr786 |
T |
G |
10: 129,437,450 |
F213V |
probably benign |
Het |
Pde1b |
T |
A |
15: 103,521,655 |
M137K |
possibly damaging |
Het |
Phf21a |
T |
C |
2: 92,327,139 |
I204T |
probably damaging |
Het |
Plcd4 |
A |
G |
1: 74,554,679 |
E321G |
possibly damaging |
Het |
Plpp7 |
C |
T |
2: 32,095,650 |
|
probably benign |
Het |
Prdm1 |
A |
G |
10: 44,441,570 |
I419T |
probably benign |
Het |
Sec16b |
A |
T |
1: 157,564,462 |
R855W |
probably damaging |
Het |
Sec16b |
G |
T |
1: 157,564,463 |
R855M |
probably damaging |
Het |
Sec31b |
T |
C |
19: 44,523,043 |
T640A |
probably benign |
Het |
Siglec1 |
T |
C |
2: 131,081,551 |
T425A |
possibly damaging |
Het |
Skil |
T |
C |
3: 31,097,175 |
|
probably benign |
Het |
Slc1a5 |
G |
A |
7: 16,785,698 |
V200M |
probably damaging |
Het |
Slc25a12 |
T |
C |
2: 71,324,025 |
H139R |
probably benign |
Het |
Slc25a32 |
A |
T |
15: 39,098,235 |
V187D |
probably damaging |
Het |
Slc35a3 |
G |
A |
3: 116,711,806 |
|
probably benign |
Het |
Smap2 |
C |
A |
4: 120,972,067 |
M328I |
probably benign |
Het |
Spef2 |
C |
T |
15: 9,599,980 |
|
probably null |
Het |
Srarp |
A |
G |
4: 141,433,078 |
V148A |
possibly damaging |
Het |
Tars |
A |
G |
15: 11,392,019 |
C236R |
probably benign |
Het |
Tchh |
G |
C |
3: 93,444,530 |
D426H |
unknown |
Het |
Tnks2 |
T |
C |
19: 36,859,145 |
F17S |
|
Het |
Ube2g1 |
T |
C |
11: 72,663,113 |
I30T |
possibly damaging |
Het |
Ube2o |
C |
T |
11: 116,543,935 |
D567N |
possibly damaging |
Het |
Unc5b |
A |
T |
10: 60,772,223 |
Y710* |
probably null |
Het |
Vmn1r215 |
T |
C |
13: 23,075,919 |
V43A |
possibly damaging |
Het |
Xkr8 |
A |
G |
4: 132,728,337 |
F242L |
probably benign |
Het |
Zfp526 |
T |
A |
7: 25,225,920 |
C535S |
probably damaging |
Het |
|