Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
A |
G |
5: 138,563,576 (GRCm38) |
F116S |
probably damaging |
Het |
4930467E23Rik |
T |
C |
8: 19,747,799 (GRCm38) |
|
probably null |
Het |
Abhd18 |
G |
A |
3: 40,930,227 (GRCm38) |
|
probably null |
Het |
Akr1c6 |
G |
T |
13: 4,438,497 (GRCm38) |
C34F |
probably benign |
Het |
Ankef1 |
T |
A |
2: 136,544,775 (GRCm38) |
I180N |
possibly damaging |
Het |
Ap1b1 |
G |
A |
11: 5,019,294 (GRCm38) |
V217I |
probably benign |
Het |
Arhgap27 |
T |
C |
11: 103,333,163 (GRCm38) |
Q608R |
probably benign |
Het |
Arhgap32 |
A |
G |
9: 32,259,331 (GRCm38) |
T1136A |
probably benign |
Het |
Ascc3 |
T |
A |
10: 50,728,154 (GRCm38) |
Y1323* |
probably null |
Het |
Bsx |
A |
C |
9: 40,874,221 (GRCm38) |
Q15P |
probably benign |
Het |
Cdh20 |
A |
G |
1: 104,954,039 (GRCm38) |
I410V |
probably null |
Het |
Cfhr4 |
T |
A |
1: 139,781,097 (GRCm38) |
E24D |
probably benign |
Het |
Col20a1 |
A |
G |
2: 181,007,159 (GRCm38) |
D945G |
probably damaging |
Het |
Cox20 |
A |
G |
1: 178,322,478 (GRCm38) |
|
probably null |
Het |
Cplane1 |
A |
G |
15: 8,175,025 (GRCm38) |
K96E |
probably damaging |
Het |
Cpne9 |
A |
G |
6: 113,293,738 (GRCm38) |
D305G |
possibly damaging |
Het |
Cyp2d12 |
A |
G |
15: 82,555,243 (GRCm38) |
T33A |
probably benign |
Het |
Dvl3 |
A |
G |
16: 20,523,743 (GRCm38) |
R149G |
possibly damaging |
Het |
Dysf |
A |
G |
6: 84,186,464 (GRCm38) |
I1624V |
possibly damaging |
Het |
Echs1 |
A |
T |
7: 140,111,710 (GRCm38) |
L167Q |
probably damaging |
Het |
Ect2 |
A |
T |
3: 27,138,719 (GRCm38) |
N358K |
probably benign |
Het |
Eml4 |
A |
G |
17: 83,441,366 (GRCm38) |
I230V |
probably benign |
Het |
Fut10 |
A |
G |
8: 31,236,258 (GRCm38) |
Y347C |
probably damaging |
Het |
Gfm2 |
C |
A |
13: 97,162,975 (GRCm38) |
N401K |
probably damaging |
Het |
Gm4795 |
C |
T |
10: 45,006,639 (GRCm38) |
|
noncoding transcript |
Het |
Gm5592 |
C |
A |
7: 41,286,788 (GRCm38) |
T238N |
probably benign |
Het |
Gm9892 |
T |
C |
8: 52,196,225 (GRCm38) |
|
noncoding transcript |
Het |
Greb1l |
G |
T |
18: 10,469,388 (GRCm38) |
M134I |
possibly damaging |
Het |
Grk3 |
A |
G |
5: 112,937,803 (GRCm38) |
Y314H |
probably damaging |
Het |
Hrh2 |
T |
C |
13: 54,214,650 (GRCm38) |
I215T |
probably damaging |
Het |
Ilkap |
A |
G |
1: 91,385,238 (GRCm38) |
|
probably null |
Het |
Inpp4a |
T |
C |
1: 37,368,303 (GRCm38) |
Y233H |
probably damaging |
Het |
Itgb4 |
G |
A |
11: 115,988,926 (GRCm38) |
V635I |
probably damaging |
Het |
Lmo7 |
C |
T |
14: 101,900,066 (GRCm38) |
|
probably benign |
Het |
Luc7l3 |
C |
T |
11: 94,292,993 (GRCm38) |
R440Q |
probably benign |
Het |
Mis18bp1 |
A |
C |
12: 65,158,741 (GRCm38) |
I219S |
probably benign |
Het |
Myo9b |
G |
A |
8: 71,354,124 (GRCm38) |
E1581K |
probably damaging |
Het |
Nfs1 |
T |
A |
2: 156,124,271 (GRCm38) |
Q458L |
probably damaging |
Het |
Numb |
A |
T |
12: 83,831,918 (GRCm38) |
|
probably null |
Het |
Nxf1 |
G |
A |
19: 8,764,150 (GRCm38) |
|
probably null |
Het |
Or52z1 |
A |
G |
7: 103,788,268 (GRCm38) |
V3A |
probably benign |
Het |
Pacc1 |
A |
G |
1: 191,348,408 (GRCm38) |
E275G |
possibly damaging |
Het |
Pde2a |
A |
T |
7: 101,503,343 (GRCm38) |
Y371F |
possibly damaging |
Het |
Phlpp2 |
G |
T |
8: 109,939,873 (GRCm38) |
L1011F |
probably benign |
Het |
Prss27 |
G |
T |
17: 24,045,597 (GRCm38) |
V245L |
probably benign |
Het |
Rbm7 |
T |
C |
9: 48,494,111 (GRCm38) |
N56S |
probably damaging |
Het |
Rftn1 |
T |
C |
17: 50,036,970 (GRCm38) |
I97V |
possibly damaging |
Het |
Ric3 |
T |
C |
7: 109,048,080 (GRCm38) |
T178A |
probably damaging |
Het |
Rock1 |
A |
G |
18: 10,104,323 (GRCm38) |
|
probably benign |
Het |
Sall2 |
T |
C |
14: 52,315,565 (GRCm38) |
T56A |
probably damaging |
Het |
Sgk1 |
T |
C |
10: 21,995,541 (GRCm38) |
S60P |
probably damaging |
Het |
Smarcad1 |
G |
A |
6: 65,073,239 (GRCm38) |
A281T |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,174,463 (GRCm38) |
H53R |
possibly damaging |
Het |
Thbs4 |
T |
C |
13: 92,763,584 (GRCm38) |
D468G |
probably damaging |
Het |
Tmem108 |
A |
T |
9: 103,499,782 (GRCm38) |
V156E |
probably benign |
Het |
Tnfaip3 |
T |
G |
10: 19,004,467 (GRCm38) |
R617S |
probably benign |
Het |
Traf3 |
A |
G |
12: 111,237,597 (GRCm38) |
M7V |
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,979,397 (GRCm38) |
I1237N |
probably damaging |
Het |
Vmn2r23 |
T |
C |
6: 123,741,836 (GRCm38) |
V716A |
probably benign |
Het |
|
Other mutations in Or2n1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01677:Or2n1
|
APN |
17 |
38,175,875 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01749:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01750:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01751:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01753:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01757:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01765:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01766:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01767:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01822:Or2n1
|
APN |
17 |
38,175,448 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02256:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02257:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02258:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02259:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02275:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02293:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02295:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02317:Or2n1
|
APN |
17 |
38,175,686 (GRCm38) |
missense |
probably benign |
0.04 |
R0230:Or2n1
|
UTSW |
17 |
38,175,950 (GRCm38) |
missense |
probably damaging |
1.00 |
R0363:Or2n1
|
UTSW |
17 |
38,175,447 (GRCm38) |
missense |
probably damaging |
1.00 |
R1074:Or2n1
|
UTSW |
17 |
38,175,440 (GRCm38) |
missense |
probably damaging |
1.00 |
R1506:Or2n1
|
UTSW |
17 |
38,175,200 (GRCm38) |
missense |
probably benign |
|
R2300:Or2n1
|
UTSW |
17 |
38,175,550 (GRCm38) |
nonsense |
probably null |
|
R3743:Or2n1
|
UTSW |
17 |
38,175,902 (GRCm38) |
missense |
probably damaging |
1.00 |
R3975:Or2n1
|
UTSW |
17 |
38,175,495 (GRCm38) |
missense |
probably benign |
0.03 |
R4230:Or2n1
|
UTSW |
17 |
38,175,881 (GRCm38) |
missense |
possibly damaging |
0.67 |
R5158:Or2n1
|
UTSW |
17 |
38,175,454 (GRCm38) |
nonsense |
probably null |
|
R5439:Or2n1
|
UTSW |
17 |
38,176,026 (GRCm38) |
splice site |
probably null |
|
R6144:Or2n1
|
UTSW |
17 |
38,175,225 (GRCm38) |
missense |
probably damaging |
1.00 |
R6309:Or2n1
|
UTSW |
17 |
38,175,519 (GRCm38) |
missense |
probably benign |
0.00 |
R6675:Or2n1
|
UTSW |
17 |
38,176,014 (GRCm38) |
missense |
probably benign |
|
R6800:Or2n1
|
UTSW |
17 |
38,175,122 (GRCm38) |
missense |
probably benign |
0.01 |
R6873:Or2n1
|
UTSW |
17 |
38,175,368 (GRCm38) |
missense |
probably benign |
|
R7193:Or2n1
|
UTSW |
17 |
38,175,096 (GRCm38) |
missense |
probably benign |
0.44 |
R7534:Or2n1
|
UTSW |
17 |
38,175,297 (GRCm38) |
missense |
probably benign |
0.22 |
R7869:Or2n1
|
UTSW |
17 |
38,175,939 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7912:Or2n1
|
UTSW |
17 |
38,175,267 (GRCm38) |
missense |
probably damaging |
0.99 |
R8048:Or2n1
|
UTSW |
17 |
38,175,528 (GRCm38) |
missense |
probably benign |
0.11 |
R8305:Or2n1
|
UTSW |
17 |
38,175,573 (GRCm38) |
missense |
probably damaging |
1.00 |
R9396:Or2n1
|
UTSW |
17 |
38,175,530 (GRCm38) |
missense |
probably damaging |
1.00 |
R9445:Or2n1
|
UTSW |
17 |
38,175,803 (GRCm38) |
missense |
probably damaging |
1.00 |
X0011:Or2n1
|
UTSW |
17 |
38,175,851 (GRCm38) |
missense |
probably damaging |
1.00 |
|