Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310002L09Rik |
A |
T |
4: 73,943,053 |
D103E |
probably benign |
Het |
Abcc3 |
A |
T |
11: 94,375,555 |
S70T |
possibly damaging |
Het |
Atp6v0a1 |
A |
G |
11: 101,029,183 |
Y214C |
possibly damaging |
Het |
Azi2 |
A |
G |
9: 118,049,895 |
|
probably null |
Het |
Cacnb2 |
T |
A |
2: 14,986,015 |
V636E |
possibly damaging |
Het |
Cd8a |
A |
C |
6: 71,374,562 |
T169P |
probably damaging |
Het |
Cfap44 |
G |
A |
16: 44,404,132 |
V68I |
probably benign |
Het |
Eea1 |
G |
T |
10: 96,037,478 |
C1134F |
probably benign |
Het |
Ehmt2 |
T |
G |
17: 34,912,772 |
F1192V |
probably damaging |
Het |
Emc1 |
T |
C |
4: 139,365,350 |
F531L |
probably damaging |
Het |
Eme1 |
G |
A |
11: 94,650,477 |
T173I |
probably benign |
Het |
Gli2 |
A |
T |
1: 118,844,416 |
C520S |
probably damaging |
Het |
Gm43302 |
T |
C |
5: 105,280,138 |
K186E |
probably benign |
Het |
Gpr108 |
A |
T |
17: 57,236,990 |
N405K |
probably damaging |
Het |
Hmgcl |
C |
A |
4: 135,955,642 |
T135N |
probably benign |
Het |
Hydin |
G |
A |
8: 110,532,856 |
D2487N |
possibly damaging |
Het |
Igfl3 |
G |
T |
7: 18,179,800 |
R25L |
probably benign |
Het |
Igsf10 |
A |
C |
3: 59,331,933 |
S276A |
probably benign |
Het |
Kctd1 |
A |
G |
18: 14,973,988 |
S211P |
probably damaging |
Het |
Kctd7 |
A |
T |
5: 130,152,501 |
Q255L |
probably benign |
Het |
Lrig1 |
A |
G |
6: 94,625,063 |
Y270H |
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,809,744 |
|
probably benign |
Het |
Myh15 |
A |
G |
16: 49,153,111 |
N1248S |
possibly damaging |
Het |
Nod1 |
A |
G |
6: 54,944,109 |
F408S |
probably benign |
Het |
Nrp1 |
T |
C |
8: 128,493,057 |
F652S |
probably damaging |
Het |
Olfr1338 |
G |
A |
4: 118,754,307 |
T79I |
probably damaging |
Het |
Olfr487 |
A |
T |
7: 108,211,918 |
F204I |
probably benign |
Het |
Olfr574 |
A |
T |
7: 102,948,768 |
H91L |
possibly damaging |
Het |
Olfr821 |
T |
C |
10: 130,034,532 |
M302T |
probably benign |
Het |
Opa1 |
G |
T |
16: 29,620,868 |
R792L |
probably benign |
Het |
Pcdha6 |
G |
T |
18: 36,968,343 |
L196F |
probably damaging |
Het |
Pdia2 |
A |
T |
17: 26,196,970 |
Y347* |
probably null |
Het |
Pdpr |
G |
T |
8: 111,124,613 |
|
probably null |
Het |
Pigt |
T |
A |
2: 164,507,331 |
L518Q |
probably damaging |
Het |
Ppfibp2 |
A |
C |
7: 107,737,981 |
D591A |
possibly damaging |
Het |
Prrg2 |
G |
A |
7: 45,059,989 |
T97M |
possibly damaging |
Het |
Qars |
A |
G |
9: 108,513,183 |
T428A |
probably damaging |
Het |
Rai1 |
T |
C |
11: 60,185,715 |
F202L |
probably damaging |
Het |
Rars |
A |
T |
11: 35,808,486 |
M660K |
probably damaging |
Het |
Rsf1 |
GCGGCGGCG |
GCGGCGGCGTCGGCGGCG |
7: 97,579,925 |
|
probably benign |
Het |
Slc16a6 |
A |
C |
11: 109,455,040 |
F382V |
probably damaging |
Het |
Slc30a7 |
T |
C |
3: 115,954,153 |
T330A |
probably damaging |
Het |
Smc1b |
A |
T |
15: 85,067,759 |
L1157Q |
probably damaging |
Het |
Snx4 |
G |
T |
16: 33,251,470 |
A4S |
possibly damaging |
Het |
Sv2b |
A |
C |
7: 75,125,767 |
|
probably null |
Het |
Syt9 |
A |
T |
7: 107,425,286 |
I129L |
probably damaging |
Het |
Ttbk2 |
T |
C |
2: 120,773,353 |
E198G |
probably damaging |
Het |
Ubr3 |
A |
T |
2: 69,944,300 |
D488V |
possibly damaging |
Het |
Ush2a |
T |
A |
1: 188,797,871 |
C3286S |
probably damaging |
Het |
Vill |
A |
G |
9: 119,065,882 |
D56G |
possibly damaging |
Het |
Vmn1r41 |
A |
T |
6: 89,747,370 |
I298F |
probably damaging |
Het |
Vmn2r2 |
A |
T |
3: 64,117,267 |
V631D |
probably damaging |
Het |
Vmn2r32 |
A |
G |
7: 7,472,574 |
S437P |
possibly damaging |
Het |
Vmn2r53 |
A |
G |
7: 12,601,142 |
V197A |
probably benign |
Het |
Wasf1 |
A |
T |
10: 40,920,369 |
I32F |
probably damaging |
Het |
Wasf2 |
G |
T |
4: 133,194,730 |
A387S |
unknown |
Het |
Wdr92 |
G |
A |
11: 17,222,309 |
V133M |
probably damaging |
Het |
Zbtb14 |
G |
A |
17: 69,387,679 |
C124Y |
probably damaging |
Het |
Zfp462 |
G |
T |
4: 55,007,671 |
A37S |
probably damaging |
Het |
Zfp532 |
A |
G |
18: 65,686,990 |
E882G |
possibly damaging |
Het |
|