Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
G |
T |
5: 77,044,325 (GRCm39) |
D188E |
probably benign |
Het |
Ahcyl2 |
T |
C |
6: 29,878,619 (GRCm39) |
L273P |
probably damaging |
Het |
Amotl2 |
C |
T |
9: 102,600,968 (GRCm39) |
T345I |
probably benign |
Het |
Angpt1 |
T |
C |
15: 42,359,752 (GRCm39) |
T227A |
probably benign |
Het |
Ankle1 |
C |
T |
8: 71,860,665 (GRCm39) |
T374M |
probably damaging |
Het |
Arhgap18 |
T |
C |
10: 26,763,853 (GRCm39) |
V481A |
probably damaging |
Het |
Astn2 |
A |
T |
4: 66,184,587 (GRCm39) |
L170* |
probably null |
Het |
Bms1 |
T |
C |
6: 118,385,105 (GRCm39) |
T368A |
probably benign |
Het |
Boll |
A |
G |
1: 55,385,562 (GRCm39) |
I121T |
probably damaging |
Het |
Brca1 |
A |
C |
11: 101,416,296 (GRCm39) |
C613G |
probably benign |
Het |
Cdk14 |
T |
A |
5: 5,299,159 (GRCm39) |
I65F |
possibly damaging |
Het |
Chn1 |
T |
C |
2: 73,448,363 (GRCm39) |
D335G |
probably damaging |
Het |
Clpsl2 |
G |
A |
17: 28,769,702 (GRCm39) |
G55R |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,613,508 (GRCm39) |
|
probably null |
Het |
Cplane2 |
A |
C |
4: 140,947,348 (GRCm39) |
Q243P |
probably damaging |
Het |
Crtac1 |
T |
C |
19: 42,297,492 (GRCm39) |
|
probably benign |
Het |
Dhx40 |
A |
T |
11: 86,675,766 (GRCm39) |
C507* |
probably null |
Het |
Dok2 |
A |
G |
14: 71,015,482 (GRCm39) |
D403G |
probably damaging |
Het |
Eif1ad14 |
T |
C |
12: 87,886,335 (GRCm39) |
D98G |
probably benign |
Het |
Eif2b5 |
A |
G |
16: 20,325,154 (GRCm39) |
T556A |
possibly damaging |
Het |
Eml6 |
A |
T |
11: 29,708,981 (GRCm39) |
V1480E |
probably damaging |
Het |
Evl |
C |
T |
12: 108,647,783 (GRCm39) |
R295* |
probably null |
Het |
Glra1 |
A |
G |
11: 55,427,225 (GRCm39) |
S120P |
probably damaging |
Het |
Habp4 |
T |
C |
13: 64,322,656 (GRCm39) |
S242P |
probably benign |
Het |
Igkv12-46 |
A |
G |
6: 69,741,570 (GRCm39) |
I95T |
probably damaging |
Het |
Itch |
G |
T |
2: 155,052,422 (GRCm39) |
G674V |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,327,957 (GRCm39) |
L92P |
probably damaging |
Het |
Kcnk2 |
A |
G |
1: 188,990,933 (GRCm39) |
|
probably null |
Het |
Krt75 |
T |
C |
15: 101,481,199 (GRCm39) |
T192A |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,159,199 (GRCm39) |
K1694N |
|
Het |
Lrrc14 |
A |
G |
15: 76,598,731 (GRCm39) |
K456E |
possibly damaging |
Het |
Map1lc3a |
G |
T |
2: 155,119,129 (GRCm39) |
|
probably benign |
Het |
Naip5 |
T |
A |
13: 100,358,741 (GRCm39) |
M832L |
probably benign |
Het |
Nectin1 |
A |
G |
9: 43,703,798 (GRCm39) |
T263A |
probably benign |
Het |
Nnt |
A |
T |
13: 119,511,286 (GRCm39) |
M330K |
probably damaging |
Het |
Nrap |
T |
C |
19: 56,308,683 (GRCm39) |
N1711D |
possibly damaging |
Het |
Olfm1 |
A |
G |
2: 28,119,135 (GRCm39) |
N285D |
possibly damaging |
Het |
Or4b1d |
T |
A |
2: 89,969,159 (GRCm39) |
E108V |
probably damaging |
Het |
Or51ab3 |
T |
A |
7: 103,201,584 (GRCm39) |
S197R |
possibly damaging |
Het |
Pag1 |
A |
G |
3: 9,764,482 (GRCm39) |
Y224H |
probably damaging |
Het |
Pde8a |
T |
C |
7: 80,958,587 (GRCm39) |
C322R |
possibly damaging |
Het |
Pde8a |
A |
T |
7: 80,967,118 (GRCm39) |
T420S |
probably benign |
Het |
Per2 |
A |
C |
1: 91,363,425 (GRCm39) |
L365R |
possibly damaging |
Het |
Pml |
A |
G |
9: 58,154,256 (GRCm39) |
|
probably null |
Het |
Ppp1r1a |
T |
A |
15: 103,446,305 (GRCm39) |
M1L |
possibly damaging |
Het |
Ppp3r2 |
G |
T |
4: 49,681,913 (GRCm39) |
C12* |
probably null |
Het |
Rbm20 |
C |
A |
19: 53,806,402 (GRCm39) |
A494D |
probably benign |
Het |
Scyl1 |
C |
T |
19: 5,810,620 (GRCm39) |
R531Q |
possibly damaging |
Het |
Skp2 |
C |
A |
15: 9,139,687 (GRCm39) |
V38F |
probably damaging |
Het |
Slc27a3 |
A |
G |
3: 90,296,974 (GRCm39) |
C42R |
probably damaging |
Het |
Tekt5 |
A |
G |
16: 10,213,277 (GRCm39) |
F3L |
probably benign |
Het |
Tmem200c |
A |
G |
17: 69,147,513 (GRCm39) |
K32R |
probably benign |
Het |
Tmprss11f |
T |
A |
5: 86,676,132 (GRCm39) |
R350W |
probably damaging |
Het |
Tph2 |
A |
T |
10: 115,015,499 (GRCm39) |
I121N |
possibly damaging |
Het |
Trim37 |
A |
G |
11: 87,037,794 (GRCm39) |
D176G |
possibly damaging |
Het |
Trpc4 |
A |
T |
3: 54,102,335 (GRCm39) |
I78F |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,609,829 (GRCm39) |
K17526E |
probably damaging |
Het |
Tuba8 |
A |
C |
6: 121,199,832 (GRCm39) |
Y172S |
probably damaging |
Het |
Tubg1 |
G |
T |
11: 101,014,854 (GRCm39) |
A199S |
probably benign |
Het |
Urb2 |
A |
T |
8: 124,754,771 (GRCm39) |
R159S |
possibly damaging |
Het |
Usp25 |
T |
A |
16: 76,906,063 (GRCm39) |
C840S |
probably damaging |
Het |
Vmn1r36 |
T |
A |
6: 66,692,964 (GRCm39) |
K304* |
probably null |
Het |
Vmn1r37 |
C |
A |
6: 66,708,656 (GRCm39) |
T94N |
probably damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,614,479 (GRCm39) |
N445S |
probably damaging |
Het |
Wnk4 |
G |
A |
11: 101,164,918 (GRCm39) |
G749D |
probably benign |
Het |
Wscd2 |
G |
A |
5: 113,689,176 (GRCm39) |
V61I |
probably benign |
Het |
Zfp85 |
T |
A |
13: 67,897,098 (GRCm39) |
R325* |
probably null |
Het |
|
Other mutations in Or8b8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01362:Or8b8
|
APN |
9 |
37,809,359 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01586:Or8b8
|
APN |
9 |
37,809,272 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02185:Or8b8
|
APN |
9 |
37,809,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02895:Or8b8
|
APN |
9 |
37,809,278 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02956:Or8b8
|
APN |
9 |
37,809,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R0391:Or8b8
|
UTSW |
9 |
37,809,138 (GRCm39) |
missense |
probably benign |
0.31 |
R0513:Or8b8
|
UTSW |
9 |
37,809,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Or8b8
|
UTSW |
9 |
37,809,622 (GRCm39) |
missense |
probably benign |
|
R4610:Or8b8
|
UTSW |
9 |
37,809,622 (GRCm39) |
missense |
probably benign |
|
R4611:Or8b8
|
UTSW |
9 |
37,809,622 (GRCm39) |
missense |
probably benign |
|
R4982:Or8b8
|
UTSW |
9 |
37,808,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Or8b8
|
UTSW |
9 |
37,808,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Or8b8
|
UTSW |
9 |
37,809,078 (GRCm39) |
missense |
probably damaging |
0.98 |
R5688:Or8b8
|
UTSW |
9 |
37,809,359 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5906:Or8b8
|
UTSW |
9 |
37,809,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6286:Or8b8
|
UTSW |
9 |
37,809,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R7138:Or8b8
|
UTSW |
9 |
37,809,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R7145:Or8b8
|
UTSW |
9 |
37,808,859 (GRCm39) |
missense |
probably benign |
0.01 |
R7993:Or8b8
|
UTSW |
9 |
37,808,633 (GRCm39) |
intron |
probably benign |
|
R8185:Or8b8
|
UTSW |
9 |
37,809,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Or8b8
|
UTSW |
9 |
37,809,415 (GRCm39) |
missense |
probably benign |
0.04 |
R9352:Or8b8
|
UTSW |
9 |
37,808,712 (GRCm39) |
missense |
probably benign |
0.00 |
X0012:Or8b8
|
UTSW |
9 |
37,809,624 (GRCm39) |
nonsense |
probably null |
|
|