Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
T |
C |
5: 113,183,355 |
T998A |
probably damaging |
Het |
AI314180 |
A |
G |
4: 58,847,038 |
I508T |
possibly damaging |
Het |
Akap9 |
C |
G |
5: 3,968,745 |
H1109D |
probably benign |
Het |
Akt3 |
T |
A |
1: 177,020,107 |
K465* |
probably null |
Het |
Ankar |
T |
C |
1: 72,688,641 |
D371G |
probably benign |
Het |
Ankib1 |
T |
G |
5: 3,755,734 |
N178H |
possibly damaging |
Het |
Arhgap10 |
A |
G |
8: 77,420,070 |
|
probably null |
Het |
Arhgef4 |
A |
G |
1: 34,809,704 |
D286G |
probably damaging |
Het |
Bsdc1 |
A |
T |
4: 129,461,684 |
|
probably benign |
Het |
Camk4 |
T |
C |
18: 33,185,032 |
V414A |
probably benign |
Het |
Cyp2d9 |
T |
A |
15: 82,454,092 |
V139E |
possibly damaging |
Het |
Dhrs13 |
C |
A |
11: 78,032,434 |
N21K |
unknown |
Het |
Dopey1 |
C |
T |
9: 86,506,290 |
A439V |
probably damaging |
Het |
Dpy19l4 |
G |
A |
4: 11,317,160 |
Q13* |
probably null |
Het |
Eif2ak1 |
T |
C |
5: 143,886,898 |
S388P |
probably damaging |
Het |
Emilin2 |
T |
C |
17: 71,274,979 |
S251G |
probably benign |
Het |
Eml4 |
T |
A |
17: 83,445,950 |
L350Q |
probably damaging |
Het |
Fblim1 |
A |
T |
4: 141,590,080 |
L98H |
probably damaging |
Het |
Fcrl6 |
T |
A |
1: 172,597,672 |
N264I |
probably benign |
Het |
Gm13124 |
A |
G |
4: 144,565,010 |
F42S |
probably damaging |
Het |
Gzme |
A |
C |
14: 56,119,333 |
D57E |
probably benign |
Het |
H2-D1 |
A |
G |
17: 35,265,933 |
T257A |
probably damaging |
Het |
Hrc |
A |
G |
7: 45,336,379 |
E318G |
probably benign |
Het |
Hspbp1 |
A |
G |
7: 4,663,436 |
L315P |
probably damaging |
Het |
Insr |
A |
T |
8: 3,192,642 |
Y591N |
probably damaging |
Het |
Lrch4 |
T |
A |
5: 137,639,465 |
I582N |
probably damaging |
Het |
Lrit2 |
A |
G |
14: 37,072,493 |
K505E |
possibly damaging |
Het |
Lrp1b |
A |
T |
2: 40,657,416 |
N4251K |
|
Het |
Mfsd13a |
T |
C |
19: 46,369,277 |
F290S |
probably damaging |
Het |
Mgam |
T |
G |
6: 40,766,020 |
N1791K |
probably benign |
Het |
Mroh7 |
A |
T |
4: 106,709,702 |
I450N |
probably benign |
Het |
Mylk |
G |
A |
16: 34,988,987 |
M1771I |
probably benign |
Het |
Olfr1335 |
A |
T |
4: 118,809,494 |
F123L |
probably damaging |
Het |
Olfr26 |
A |
T |
9: 38,855,238 |
M59L |
possibly damaging |
Het |
Olfr612 |
A |
T |
7: 103,539,131 |
C34* |
probably null |
Het |
Olfr972 |
T |
A |
9: 39,874,139 |
L288* |
probably null |
Het |
Parp14 |
A |
T |
16: 35,857,491 |
H702Q |
probably benign |
Het |
Pcdhga1 |
T |
C |
18: 37,662,228 |
L95P |
probably damaging |
Het |
Pcsk5 |
T |
C |
19: 17,642,590 |
T373A |
probably damaging |
Het |
Pdzph1 |
A |
G |
17: 58,967,341 |
V836A |
possibly damaging |
Het |
Pgap1 |
T |
A |
1: 54,530,922 |
N322I |
probably benign |
Het |
Pikfyve |
C |
T |
1: 65,244,426 |
R741* |
probably null |
Het |
Pip4k2c |
A |
G |
10: 127,208,904 |
S80P |
probably damaging |
Het |
Plekhh3 |
A |
G |
11: 101,166,619 |
F271L |
probably damaging |
Het |
Prkdc |
A |
T |
16: 15,672,327 |
Y565F |
probably damaging |
Het |
Prom2 |
T |
C |
2: 127,532,781 |
R612G |
probably benign |
Het |
Psap |
T |
C |
10: 60,299,474 |
V303A |
probably benign |
Het |
Ptch1 |
C |
T |
13: 63,511,714 |
R1375H |
probably benign |
Het |
Slc24a3 |
A |
C |
2: 145,613,530 |
K446N |
probably benign |
Het |
Slc39a12 |
T |
A |
2: 14,494,461 |
M661K |
probably benign |
Het |
Slc6a16 |
T |
C |
7: 45,259,113 |
L39P |
probably benign |
Het |
Syne1 |
T |
G |
10: 5,185,559 |
|
probably null |
Het |
Taar8c |
T |
C |
10: 24,101,866 |
N16S |
probably benign |
Het |
Tmem98 |
A |
G |
11: 80,817,518 |
T105A |
probably damaging |
Het |
Tmub1 |
T |
A |
5: 24,446,013 |
Y216F |
probably damaging |
Het |
Trim16 |
T |
G |
11: 62,820,754 |
C84G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,731,229 |
K28978* |
probably null |
Het |
Usp38 |
A |
G |
8: 81,014,246 |
V64A |
probably damaging |
Het |
Vmn2r63 |
A |
T |
7: 42,926,982 |
F469Y |
possibly damaging |
Het |
Vmn2r74 |
A |
G |
7: 85,961,302 |
W61R |
probably benign |
Het |
Whamm |
G |
T |
7: 81,593,850 |
G607C |
probably damaging |
Het |
Xkr6 |
G |
T |
14: 63,819,161 |
V430F |
probably benign |
Het |
Zfp398 |
A |
G |
6: 47,865,818 |
D268G |
probably benign |
Het |
|