Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
T |
C |
11: 48,839,003 (GRCm39) |
H528R |
probably damaging |
Het |
A530053G22Rik |
A |
T |
6: 60,379,047 (GRCm39) |
|
noncoding transcript |
Het |
Aagab |
A |
G |
9: 63,542,676 (GRCm39) |
|
probably benign |
Het |
Aknad1 |
A |
T |
3: 108,688,519 (GRCm39) |
I616F |
possibly damaging |
Het |
Ap2a1 |
A |
C |
7: 44,553,479 (GRCm39) |
D629E |
probably benign |
Het |
Apc2 |
C |
A |
10: 80,149,220 (GRCm39) |
Q1425K |
probably damaging |
Het |
Asf1b |
A |
C |
8: 84,694,542 (GRCm39) |
H102P |
probably benign |
Het |
Celf6 |
C |
T |
9: 59,489,565 (GRCm39) |
A90V |
probably damaging |
Het |
Chrna2 |
A |
T |
14: 66,379,688 (GRCm39) |
Q9L |
probably benign |
Het |
Csnk1g3 |
A |
G |
18: 54,086,356 (GRCm39) |
I420M |
possibly damaging |
Het |
Eml3 |
T |
C |
19: 8,916,543 (GRCm39) |
|
probably benign |
Het |
Epn3 |
T |
C |
11: 94,382,456 (GRCm39) |
N508S |
possibly damaging |
Het |
Fam120a |
T |
C |
13: 49,063,812 (GRCm39) |
Y608C |
probably damaging |
Het |
Fbn1 |
A |
C |
2: 125,162,888 (GRCm39) |
C2133G |
possibly damaging |
Het |
Fhl5 |
A |
G |
4: 25,211,309 (GRCm39) |
F128L |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,680,421 (GRCm39) |
N428S |
probably damaging |
Het |
Fxr2 |
T |
C |
11: 69,540,665 (GRCm39) |
|
probably null |
Het |
Gabrp |
T |
C |
11: 33,504,388 (GRCm39) |
Y309C |
probably damaging |
Het |
Golga2 |
A |
G |
2: 32,182,168 (GRCm39) |
I50V |
probably benign |
Het |
Ifi203 |
C |
T |
1: 173,764,158 (GRCm39) |
G105R |
possibly damaging |
Het |
Itgav |
A |
T |
2: 83,596,190 (GRCm39) |
Q201L |
possibly damaging |
Het |
Jade2 |
T |
C |
11: 51,716,198 (GRCm39) |
T336A |
probably damaging |
Het |
Kdm4b |
A |
G |
17: 56,708,649 (GRCm39) |
D996G |
probably damaging |
Het |
Me2 |
A |
G |
18: 73,903,797 (GRCm39) |
I557T |
probably benign |
Het |
Memo1 |
A |
C |
17: 74,551,996 (GRCm39) |
L100R |
probably damaging |
Het |
Mrps2 |
A |
G |
2: 28,359,818 (GRCm39) |
N225S |
probably damaging |
Het |
Ndufa2 |
A |
G |
18: 36,877,278 (GRCm39) |
|
probably null |
Het |
Or2g7 |
G |
T |
17: 38,378,275 (GRCm39) |
C71F |
probably damaging |
Het |
Pak5 |
G |
T |
2: 135,940,310 (GRCm39) |
Y501* |
probably null |
Het |
Pot1b |
A |
T |
17: 56,002,206 (GRCm39) |
F123I |
possibly damaging |
Het |
Rev3l |
T |
C |
10: 39,700,786 (GRCm39) |
V1761A |
probably benign |
Het |
Samd3 |
T |
A |
10: 26,106,064 (GRCm39) |
V14E |
probably damaging |
Het |
Slc4a8 |
G |
A |
15: 100,697,598 (GRCm39) |
A605T |
probably benign |
Het |
Smgc |
A |
T |
15: 91,744,642 (GRCm39) |
D333V |
probably damaging |
Het |
Spata4 |
A |
G |
8: 55,055,440 (GRCm39) |
I147V |
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,537,652 (GRCm39) |
S206L |
probably benign |
Het |
Vmn2r73 |
G |
A |
7: 85,507,495 (GRCm39) |
H606Y |
probably benign |
Het |
Vsig8 |
A |
G |
1: 172,387,916 (GRCm39) |
N2S |
probably damaging |
Het |
Wdr17 |
A |
C |
8: 55,114,515 (GRCm39) |
I667R |
probably damaging |
Het |
Yif1b |
A |
G |
7: 28,937,873 (GRCm39) |
|
probably null |
Het |
Zbtb5 |
A |
T |
4: 44,994,003 (GRCm39) |
H460Q |
possibly damaging |
Het |
Zdhhc21 |
G |
A |
4: 82,724,564 (GRCm39) |
|
probably benign |
Het |
Zfp944 |
A |
T |
17: 22,559,018 (GRCm39) |
H76Q |
probably damaging |
Het |
Zkscan1 |
A |
G |
5: 138,092,264 (GRCm39) |
Q146R |
probably benign |
Het |
|
Other mutations in Or7g19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03018:Or7g19
|
APN |
9 |
18,856,177 (GRCm39) |
missense |
probably damaging |
0.98 |
R0537:Or7g19
|
UTSW |
9 |
18,856,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R1923:Or7g19
|
UTSW |
9 |
18,856,781 (GRCm39) |
missense |
probably benign |
0.21 |
R2226:Or7g19
|
UTSW |
9 |
18,856,177 (GRCm39) |
missense |
probably damaging |
0.98 |
R2234:Or7g19
|
UTSW |
9 |
18,856,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2402:Or7g19
|
UTSW |
9 |
18,856,496 (GRCm39) |
missense |
probably damaging |
0.98 |
R4060:Or7g19
|
UTSW |
9 |
18,856,346 (GRCm39) |
missense |
probably benign |
0.09 |
R4537:Or7g19
|
UTSW |
9 |
18,856,526 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4715:Or7g19
|
UTSW |
9 |
18,856,742 (GRCm39) |
missense |
probably benign |
0.01 |
R5557:Or7g19
|
UTSW |
9 |
18,856,466 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6001:Or7g19
|
UTSW |
9 |
18,856,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R6172:Or7g19
|
UTSW |
9 |
18,856,042 (GRCm39) |
missense |
probably benign |
0.00 |
R6415:Or7g19
|
UTSW |
9 |
18,856,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R6594:Or7g19
|
UTSW |
9 |
18,856,127 (GRCm39) |
missense |
probably damaging |
0.98 |
R6874:Or7g19
|
UTSW |
9 |
18,856,777 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7801:Or7g19
|
UTSW |
9 |
18,856,555 (GRCm39) |
missense |
probably damaging |
0.97 |
R7818:Or7g19
|
UTSW |
9 |
18,856,305 (GRCm39) |
nonsense |
probably null |
|
R7880:Or7g19
|
UTSW |
9 |
18,856,024 (GRCm39) |
missense |
probably benign |
0.06 |
R7890:Or7g19
|
UTSW |
9 |
18,856,799 (GRCm39) |
missense |
probably benign |
0.10 |
R8352:Or7g19
|
UTSW |
9 |
18,856,459 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8452:Or7g19
|
UTSW |
9 |
18,856,459 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8776:Or7g19
|
UTSW |
9 |
18,856,286 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8776-TAIL:Or7g19
|
UTSW |
9 |
18,856,286 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8931:Or7g19
|
UTSW |
9 |
18,855,920 (GRCm39) |
splice site |
probably benign |
|
R9438:Or7g19
|
UTSW |
9 |
18,856,326 (GRCm39) |
nonsense |
probably null |
|
Z1088:Or7g19
|
UTSW |
9 |
18,856,717 (GRCm39) |
missense |
possibly damaging |
0.69 |
|