Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019D03Rik |
T |
C |
1: 52,964,657 (GRCm39) |
S24G |
probably damaging |
Het |
1810064F22Rik |
A |
G |
9: 22,119,039 (GRCm39) |
|
noncoding transcript |
Het |
Aacs |
A |
T |
5: 125,592,078 (GRCm39) |
M589L |
probably benign |
Het |
Adamts8 |
A |
C |
9: 30,873,012 (GRCm39) |
H739P |
probably benign |
Het |
Atp8b2 |
T |
C |
3: 89,860,216 (GRCm39) |
|
probably benign |
Het |
BC030500 |
A |
G |
8: 59,366,043 (GRCm39) |
|
probably benign |
Het |
Btnl9 |
T |
A |
11: 49,066,830 (GRCm39) |
|
probably benign |
Het |
Cd74 |
G |
T |
18: 60,940,993 (GRCm39) |
A31S |
probably benign |
Het |
Ceacam3 |
G |
A |
7: 16,893,808 (GRCm39) |
A440T |
possibly damaging |
Het |
Ces1d |
G |
A |
8: 93,912,664 (GRCm39) |
T258I |
probably benign |
Het |
Col10a1 |
A |
G |
10: 34,266,735 (GRCm39) |
|
probably benign |
Het |
Coro1b |
C |
T |
19: 4,203,449 (GRCm39) |
A430V |
probably benign |
Het |
Cyp2c65 |
A |
T |
19: 39,081,928 (GRCm39) |
I485L |
probably benign |
Het |
Dio1 |
A |
T |
4: 107,163,977 (GRCm39) |
|
probably benign |
Het |
Dmxl1 |
G |
A |
18: 50,000,966 (GRCm39) |
|
probably null |
Het |
Dynlt5 |
A |
G |
4: 102,859,700 (GRCm39) |
E84G |
possibly damaging |
Het |
Elp6 |
A |
G |
9: 110,144,851 (GRCm39) |
Y136C |
probably damaging |
Het |
Gon4l |
A |
T |
3: 88,803,532 (GRCm39) |
Q1382L |
possibly damaging |
Het |
Guca1a |
T |
C |
17: 47,711,295 (GRCm39) |
E17G |
probably damaging |
Het |
Gucy2d |
G |
A |
7: 98,098,982 (GRCm39) |
G267E |
probably damaging |
Het |
Gvin3 |
T |
A |
7: 106,199,314 (GRCm39) |
|
noncoding transcript |
Het |
Hspg2 |
T |
A |
4: 137,256,105 (GRCm39) |
|
probably null |
Het |
Il1a |
G |
T |
2: 129,149,821 (GRCm39) |
D26E |
possibly damaging |
Het |
Il22b |
T |
A |
10: 118,130,789 (GRCm39) |
I36F |
probably damaging |
Het |
Kcna1 |
A |
T |
6: 126,620,075 (GRCm39) |
F82I |
probably damaging |
Het |
Klhl18 |
G |
C |
9: 110,265,195 (GRCm39) |
N335K |
possibly damaging |
Het |
Lamtor5 |
T |
G |
3: 107,189,323 (GRCm39) |
C120G |
probably benign |
Het |
Lars1 |
A |
G |
18: 42,384,363 (GRCm39) |
C72R |
possibly damaging |
Het |
Lrrfip1 |
T |
G |
1: 91,014,848 (GRCm39) |
|
probably null |
Het |
Mapkapk3 |
T |
C |
9: 107,133,491 (GRCm39) |
D349G |
probably damaging |
Het |
Mknk2 |
A |
T |
10: 80,503,059 (GRCm39) |
I421N |
probably benign |
Het |
Myh6 |
A |
G |
14: 55,191,381 (GRCm39) |
I820T |
probably benign |
Het |
Notch2 |
T |
G |
3: 98,033,450 (GRCm39) |
V1182G |
probably damaging |
Het |
Or1af1 |
T |
G |
2: 37,109,684 (GRCm39) |
F61C |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Ppfia4 |
A |
T |
1: 134,245,632 (GRCm39) |
S641T |
probably damaging |
Het |
Prok1 |
T |
A |
3: 107,146,949 (GRCm39) |
H6L |
probably benign |
Het |
Ptprm |
A |
T |
17: 67,000,468 (GRCm39) |
V1172E |
probably damaging |
Het |
Rasal3 |
C |
T |
17: 32,612,575 (GRCm39) |
R762Q |
probably benign |
Het |
Rgs20 |
G |
T |
1: 5,140,333 (GRCm39) |
A23E |
possibly damaging |
Het |
Rprd1a |
T |
C |
18: 24,640,288 (GRCm39) |
T163A |
probably benign |
Het |
Rrm1 |
A |
T |
7: 102,114,974 (GRCm39) |
N37I |
probably damaging |
Het |
Shc4 |
T |
A |
2: 125,481,350 (GRCm39) |
E520V |
probably damaging |
Het |
Slc14a2 |
G |
T |
18: 78,252,143 (GRCm39) |
P56Q |
probably damaging |
Het |
Slc22a3 |
C |
T |
17: 12,677,377 (GRCm39) |
G264S |
probably damaging |
Het |
Svil |
A |
G |
18: 5,059,294 (GRCm39) |
E770G |
probably damaging |
Het |
Svop |
A |
G |
5: 114,198,186 (GRCm39) |
V129A |
probably damaging |
Het |
Szt2 |
A |
T |
4: 118,232,663 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,951,105 (GRCm39) |
|
probably benign |
Het |
Tmem30a |
T |
A |
9: 79,687,930 (GRCm39) |
I80F |
probably damaging |
Het |
Vmn2r16 |
G |
T |
5: 109,511,708 (GRCm39) |
L638F |
probably damaging |
Het |
Xkr7 |
T |
A |
2: 152,896,244 (GRCm39) |
I366N |
probably damaging |
Het |
Zer1 |
A |
G |
2: 29,990,998 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or2z2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01305:Or2z2
|
APN |
11 |
58,346,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02001:Or2z2
|
APN |
11 |
58,346,335 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02170:Or2z2
|
APN |
11 |
58,345,906 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02638:Or2z2
|
APN |
11 |
58,345,873 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU22:Or2z2
|
UTSW |
11 |
58,346,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R0502:Or2z2
|
UTSW |
11 |
58,346,140 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0784:Or2z2
|
UTSW |
11 |
58,346,131 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1300:Or2z2
|
UTSW |
11 |
58,346,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1451:Or2z2
|
UTSW |
11 |
58,346,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1642:Or2z2
|
UTSW |
11 |
58,346,664 (GRCm39) |
missense |
probably benign |
|
R1754:Or2z2
|
UTSW |
11 |
58,346,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Or2z2
|
UTSW |
11 |
58,346,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R2920:Or2z2
|
UTSW |
11 |
58,346,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Or2z2
|
UTSW |
11 |
58,346,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Or2z2
|
UTSW |
11 |
58,346,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4791:Or2z2
|
UTSW |
11 |
58,346,370 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4964:Or2z2
|
UTSW |
11 |
58,346,733 (GRCm39) |
missense |
probably benign |
0.05 |
R5543:Or2z2
|
UTSW |
11 |
58,345,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6649:Or2z2
|
UTSW |
11 |
58,346,394 (GRCm39) |
missense |
probably damaging |
0.98 |
R6653:Or2z2
|
UTSW |
11 |
58,346,394 (GRCm39) |
missense |
probably damaging |
0.98 |
R7388:Or2z2
|
UTSW |
11 |
58,346,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7492:Or2z2
|
UTSW |
11 |
58,346,715 (GRCm39) |
missense |
probably benign |
0.28 |
R7566:Or2z2
|
UTSW |
11 |
58,346,489 (GRCm39) |
missense |
probably benign |
0.02 |
R7567:Or2z2
|
UTSW |
11 |
58,345,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R8557:Or2z2
|
UTSW |
11 |
58,346,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Or2z2
|
UTSW |
11 |
58,346,757 (GRCm39) |
nonsense |
probably null |
|
R8777-TAIL:Or2z2
|
UTSW |
11 |
58,346,757 (GRCm39) |
nonsense |
probably null |
|
R8810:Or2z2
|
UTSW |
11 |
58,345,936 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9139:Or2z2
|
UTSW |
11 |
58,345,999 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:Or2z2
|
UTSW |
11 |
58,346,363 (GRCm39) |
missense |
probably damaging |
1.00 |
|