Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
T |
13: 61,001,387 (GRCm39) |
Y113* |
probably null |
Het |
Abcc2 |
C |
T |
19: 43,789,074 (GRCm39) |
T243M |
probably benign |
Het |
Actr6 |
A |
T |
10: 89,561,717 (GRCm39) |
L143Q |
probably damaging |
Het |
Adamts18 |
A |
G |
8: 114,425,642 (GRCm39) |
Y1207H |
probably benign |
Het |
Adamts2 |
A |
G |
11: 50,628,193 (GRCm39) |
I298V |
possibly damaging |
Het |
Adamts6 |
T |
A |
13: 104,433,998 (GRCm39) |
S142R |
probably damaging |
Het |
Adat2 |
A |
T |
10: 13,432,650 (GRCm39) |
N51Y |
probably damaging |
Het |
Alg6 |
G |
A |
4: 99,638,965 (GRCm39) |
|
probably null |
Het |
Aox3 |
G |
A |
1: 58,227,683 (GRCm39) |
|
probably null |
Het |
Atp2b2 |
T |
A |
6: 113,736,122 (GRCm39) |
I986F |
probably damaging |
Het |
Axin1 |
G |
T |
17: 26,413,045 (GRCm39) |
Q779H |
probably benign |
Het |
Axin1 |
A |
T |
17: 26,413,044 (GRCm39) |
Q779L |
probably benign |
Het |
Bltp3a |
T |
C |
17: 28,103,000 (GRCm39) |
S345P |
probably damaging |
Het |
Btaf1 |
T |
C |
19: 36,963,979 (GRCm39) |
V850A |
probably benign |
Het |
Camsap2 |
A |
G |
1: 136,232,124 (GRCm39) |
V157A |
probably damaging |
Het |
Ccdc191 |
T |
C |
16: 43,763,868 (GRCm39) |
V443A |
probably benign |
Het |
Cd1d1 |
T |
A |
3: 86,905,958 (GRCm39) |
M106L |
probably benign |
Het |
Cenpe |
A |
G |
3: 134,940,637 (GRCm39) |
D632G |
probably damaging |
Het |
Cnih2 |
T |
A |
19: 5,143,957 (GRCm39) |
|
probably null |
Het |
Crnkl1 |
G |
T |
2: 145,765,796 (GRCm39) |
Q425K |
possibly damaging |
Het |
Crnn |
T |
A |
3: 93,055,990 (GRCm39) |
S259T |
probably benign |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Ctc1 |
G |
T |
11: 68,918,152 (GRCm39) |
G425C |
probably damaging |
Het |
Dctn4 |
T |
A |
18: 60,689,464 (GRCm39) |
I445N |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,737,851 (GRCm39) |
D27E |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,545,711 (GRCm39) |
|
probably null |
Het |
Dst |
A |
T |
1: 34,235,050 (GRCm39) |
K3710* |
probably null |
Het |
Ecel1 |
T |
A |
1: 87,078,861 (GRCm39) |
Y526F |
probably benign |
Het |
Elp6 |
C |
T |
9: 110,143,141 (GRCm39) |
P118L |
probably damaging |
Het |
Enpp2 |
T |
A |
15: 54,733,701 (GRCm39) |
R420* |
probably null |
Het |
Ep400 |
A |
G |
5: 110,846,678 (GRCm39) |
F1480L |
unknown |
Het |
Ep400 |
T |
C |
5: 110,868,622 (GRCm39) |
E934G |
unknown |
Het |
Epb41 |
A |
C |
4: 131,664,747 (GRCm39) |
|
probably benign |
Het |
Epha5 |
A |
T |
5: 84,232,683 (GRCm39) |
V777E |
probably damaging |
Het |
Erp44 |
A |
T |
4: 48,208,797 (GRCm39) |
M221K |
probably benign |
Het |
Esp36 |
T |
C |
17: 38,728,177 (GRCm39) |
T35A |
possibly damaging |
Het |
Flvcr1 |
T |
C |
1: 190,757,692 (GRCm39) |
Q158R |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,818,535 (GRCm39) |
D4756V |
probably damaging |
Het |
Fzd10 |
T |
A |
5: 128,679,178 (GRCm39) |
Y299* |
probably null |
Het |
Gabrg1 |
C |
A |
5: 70,931,754 (GRCm39) |
V330L |
possibly damaging |
Het |
Gata4 |
A |
T |
14: 63,441,138 (GRCm39) |
N87K |
probably damaging |
Het |
Gdpd3 |
A |
T |
7: 126,366,454 (GRCm39) |
N97I |
probably damaging |
Het |
Gm28042 |
G |
A |
2: 119,865,124 (GRCm39) |
A250T |
probably damaging |
Het |
Golim4 |
T |
C |
3: 75,785,950 (GRCm39) |
|
probably null |
Het |
Gpr183 |
G |
T |
14: 122,192,275 (GRCm39) |
T82N |
possibly damaging |
Het |
Hsd17b4 |
T |
C |
18: 50,293,202 (GRCm39) |
L247S |
probably damaging |
Het |
Hsdl1 |
T |
A |
8: 120,292,606 (GRCm39) |
Y203F |
possibly damaging |
Het |
Igkv17-121 |
A |
G |
6: 68,014,068 (GRCm39) |
K40R |
probably benign |
Het |
Igsf3 |
T |
A |
3: 101,346,677 (GRCm39) |
|
probably null |
Het |
Ints1 |
C |
A |
5: 139,738,566 (GRCm39) |
G110C |
probably damaging |
Het |
Klhdc8b |
A |
T |
9: 108,328,386 (GRCm39) |
V22E |
probably damaging |
Het |
Kmt2d |
G |
A |
15: 98,745,075 (GRCm39) |
|
probably benign |
Het |
Kpna2 |
C |
T |
11: 106,882,295 (GRCm39) |
G204S |
probably damaging |
Het |
Ktn1 |
G |
A |
14: 47,907,756 (GRCm39) |
|
probably null |
Het |
Ldah |
G |
A |
12: 8,277,237 (GRCm39) |
A58T |
probably benign |
Het |
Lmx1a |
G |
T |
1: 167,619,123 (GRCm39) |
A161S |
possibly damaging |
Het |
Lrig1 |
T |
C |
6: 94,602,043 (GRCm39) |
Y270C |
probably damaging |
Het |
Lrrc24 |
T |
C |
15: 76,600,200 (GRCm39) |
Q313R |
probably benign |
Het |
Ltbp1 |
T |
C |
17: 75,628,090 (GRCm39) |
|
probably null |
Het |
Luzp1 |
A |
G |
4: 136,270,708 (GRCm39) |
D977G |
possibly damaging |
Het |
Mbd4 |
T |
C |
6: 115,827,685 (GRCm39) |
T43A |
possibly damaging |
Het |
Meak7 |
A |
C |
8: 120,494,882 (GRCm39) |
L292R |
probably damaging |
Het |
Meltf |
T |
C |
16: 31,713,532 (GRCm39) |
S592P |
probably benign |
Het |
Mrgpra4 |
A |
G |
7: 47,631,466 (GRCm39) |
L45P |
probably damaging |
Het |
Mrpl39 |
A |
G |
16: 84,531,293 (GRCm39) |
|
probably null |
Het |
Myocd |
T |
C |
11: 65,112,876 (GRCm39) |
T79A |
probably benign |
Het |
Myt1l |
A |
G |
12: 29,882,302 (GRCm39) |
E499G |
unknown |
Het |
Ncan |
C |
T |
8: 70,567,675 (GRCm39) |
E146K |
probably damaging |
Het |
Ncoa3 |
T |
A |
2: 165,889,820 (GRCm39) |
D68E |
probably damaging |
Het |
Nt5m |
T |
A |
11: 59,765,381 (GRCm39) |
Y136* |
probably null |
Het |
Or10h5 |
C |
T |
17: 33,434,728 (GRCm39) |
A200T |
probably benign |
Het |
Or4c12 |
A |
T |
2: 89,774,147 (GRCm39) |
I104N |
possibly damaging |
Het |
Or51m1 |
A |
T |
7: 103,578,944 (GRCm39) |
I305F |
probably benign |
Het |
Or5p66 |
A |
C |
7: 107,885,818 (GRCm39) |
C172G |
probably damaging |
Het |
Or7g21 |
G |
A |
9: 19,032,797 (GRCm39) |
C179Y |
probably damaging |
Het |
Pak6 |
A |
T |
2: 118,525,029 (GRCm39) |
I552F |
probably damaging |
Het |
Pcyox1 |
T |
A |
6: 86,365,708 (GRCm39) |
K502M |
probably damaging |
Het |
Phyhipl |
A |
T |
10: 70,404,904 (GRCm39) |
D56E |
probably damaging |
Het |
Ppp2r2a |
A |
T |
14: 67,254,086 (GRCm39) |
S361T |
possibly damaging |
Het |
Prim1 |
A |
T |
10: 127,851,131 (GRCm39) |
D5V |
probably damaging |
Het |
Prl7a1 |
A |
T |
13: 27,817,564 (GRCm39) |
H233Q |
possibly damaging |
Het |
Prpf40a |
A |
G |
2: 53,034,861 (GRCm39) |
F776L |
probably damaging |
Het |
Psmb1 |
T |
C |
17: 15,718,524 (GRCm39) |
M1V |
probably null |
Het |
Reln |
T |
A |
5: 22,176,868 (GRCm39) |
N1933Y |
probably benign |
Het |
Retsat |
T |
A |
6: 72,578,609 (GRCm39) |
M107K |
probably damaging |
Het |
Rhbdl1 |
C |
T |
17: 26,054,002 (GRCm39) |
W289* |
probably null |
Het |
Rlf |
G |
A |
4: 121,004,652 (GRCm39) |
H1443Y |
probably damaging |
Het |
Rpgrip1l |
T |
C |
8: 92,007,444 (GRCm39) |
E382G |
probably damaging |
Het |
Rprd2 |
T |
A |
3: 95,673,661 (GRCm39) |
T497S |
probably damaging |
Het |
Rps6kc1 |
T |
C |
1: 190,530,924 (GRCm39) |
T936A |
probably damaging |
Het |
Scgb1b10 |
A |
G |
7: 31,800,609 (GRCm39) |
Q66R |
possibly damaging |
Het |
Scrib |
C |
T |
15: 75,923,602 (GRCm39) |
|
probably null |
Het |
Setbp1 |
T |
A |
18: 79,129,927 (GRCm39) |
T102S |
probably damaging |
Het |
Shox2 |
T |
C |
3: 66,881,008 (GRCm39) |
|
probably benign |
Het |
Skp1 |
C |
A |
11: 52,134,458 (GRCm39) |
T63N |
probably benign |
Het |
Slc10a6 |
C |
T |
5: 103,754,470 (GRCm39) |
V354M |
probably benign |
Het |
Slc35f3 |
T |
C |
8: 127,116,020 (GRCm39) |
|
probably null |
Het |
Slc8b1 |
T |
A |
5: 120,663,740 (GRCm39) |
L320* |
probably null |
Het |
Snap29 |
T |
A |
16: 17,237,132 (GRCm39) |
L81Q |
probably damaging |
Het |
Sorl1 |
A |
G |
9: 41,894,299 (GRCm39) |
I1837T |
probably benign |
Het |
Spmip4 |
T |
A |
6: 50,566,164 (GRCm39) |
|
probably null |
Het |
Tacr3 |
A |
G |
3: 134,638,033 (GRCm39) |
T397A |
probably benign |
Het |
Tcte1 |
T |
C |
17: 45,845,854 (GRCm39) |
F153L |
probably damaging |
Het |
Them7 |
A |
G |
2: 105,209,153 (GRCm39) |
T158A |
probably benign |
Het |
Tmprss4 |
A |
G |
9: 45,084,706 (GRCm39) |
S433P |
possibly damaging |
Het |
Tpcn1 |
T |
C |
5: 120,698,387 (GRCm39) |
H45R |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,832,468 (GRCm39) |
S2813P |
possibly damaging |
Het |
Wdfy3 |
C |
T |
5: 102,090,985 (GRCm39) |
D532N |
probably benign |
Het |
Zbed6 |
T |
C |
1: 133,585,832 (GRCm39) |
T502A |
probably benign |
Het |
Zfp277 |
A |
G |
12: 40,378,687 (GRCm39) |
V390A |
possibly damaging |
Het |
|
Other mutations in Aoc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01488:Aoc3
|
APN |
11 |
101,228,304 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02026:Aoc3
|
APN |
11 |
101,228,421 (GRCm39) |
missense |
probably benign |
|
IGL02500:Aoc3
|
APN |
11 |
101,228,215 (GRCm39) |
nonsense |
probably null |
|
R0463:Aoc3
|
UTSW |
11 |
101,222,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R0524:Aoc3
|
UTSW |
11 |
101,228,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Aoc3
|
UTSW |
11 |
101,222,964 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0685:Aoc3
|
UTSW |
11 |
101,227,273 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0740:Aoc3
|
UTSW |
11 |
101,223,158 (GRCm39) |
missense |
probably benign |
0.01 |
R0946:Aoc3
|
UTSW |
11 |
101,223,131 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1723:Aoc3
|
UTSW |
11 |
101,227,261 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1869:Aoc3
|
UTSW |
11 |
101,222,293 (GRCm39) |
nonsense |
probably null |
|
R3735:Aoc3
|
UTSW |
11 |
101,223,045 (GRCm39) |
missense |
probably damaging |
0.99 |
R4497:Aoc3
|
UTSW |
11 |
101,222,871 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4613:Aoc3
|
UTSW |
11 |
101,228,485 (GRCm39) |
intron |
probably benign |
|
R4858:Aoc3
|
UTSW |
11 |
101,222,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R4954:Aoc3
|
UTSW |
11 |
101,222,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R5770:Aoc3
|
UTSW |
11 |
101,222,578 (GRCm39) |
nonsense |
probably null |
|
R6679:Aoc3
|
UTSW |
11 |
101,222,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Aoc3
|
UTSW |
11 |
101,228,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R7693:Aoc3
|
UTSW |
11 |
101,223,338 (GRCm39) |
missense |
probably benign |
0.00 |
R7888:Aoc3
|
UTSW |
11 |
101,223,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R8041:Aoc3
|
UTSW |
11 |
101,223,132 (GRCm39) |
missense |
probably benign |
0.00 |
R8444:Aoc3
|
UTSW |
11 |
101,232,573 (GRCm39) |
missense |
unknown |
|
R8491:Aoc3
|
UTSW |
11 |
101,223,042 (GRCm39) |
missense |
probably benign |
0.41 |
R8685:Aoc3
|
UTSW |
11 |
101,223,042 (GRCm39) |
missense |
probably benign |
0.00 |
R8732:Aoc3
|
UTSW |
11 |
101,222,643 (GRCm39) |
missense |
probably benign |
0.00 |
R9660:Aoc3
|
UTSW |
11 |
101,221,914 (GRCm39) |
missense |
possibly damaging |
0.49 |
|