Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700088E04Rik |
T |
C |
15: 79,020,608 (GRCm39) |
Y62C |
probably benign |
Het |
A1bg |
T |
C |
15: 60,791,564 (GRCm39) |
T291A |
probably damaging |
Het |
Abcb11 |
A |
G |
2: 69,115,642 (GRCm39) |
I574T |
possibly damaging |
Het |
Abcb5 |
T |
A |
12: 118,929,000 (GRCm39) |
Y17F |
possibly damaging |
Het |
Arfgef3 |
A |
T |
10: 18,522,478 (GRCm39) |
L516* |
probably null |
Het |
Arhgap21 |
A |
G |
2: 20,885,321 (GRCm39) |
S619P |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,347,261 (GRCm39) |
V65A |
probably benign |
Het |
Calm3 |
T |
A |
7: 16,653,568 (GRCm39) |
Q9L |
probably benign |
Het |
Cd300c2 |
C |
T |
11: 114,891,503 (GRCm39) |
D124N |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,706,390 (GRCm39) |
T958A |
probably benign |
Het |
Cemip2 |
T |
C |
19: 21,809,487 (GRCm39) |
S956P |
possibly damaging |
Het |
Cfap69 |
T |
C |
5: 5,671,958 (GRCm39) |
T317A |
probably benign |
Het |
Cluh |
T |
A |
11: 74,556,210 (GRCm39) |
I887K |
probably damaging |
Het |
Dag1 |
A |
T |
9: 108,086,457 (GRCm39) |
V228E |
probably damaging |
Het |
Dhtkd1 |
T |
C |
2: 5,924,248 (GRCm39) |
|
probably null |
Het |
Dnah1 |
T |
A |
14: 30,993,018 (GRCm39) |
K2959* |
probably null |
Het |
Dnttip2 |
T |
A |
3: 122,069,457 (GRCm39) |
V224E |
probably damaging |
Het |
Drosha |
C |
T |
15: 12,907,479 (GRCm39) |
P1071L |
probably benign |
Het |
E030025P04Rik |
T |
A |
11: 109,030,993 (GRCm39) |
H84L |
unknown |
Het |
Elac2 |
A |
T |
11: 64,890,589 (GRCm39) |
S698C |
probably null |
Het |
Elf2 |
A |
T |
3: 51,201,586 (GRCm39) |
*88R |
probably null |
Het |
Fastkd1 |
T |
A |
2: 69,538,958 (GRCm39) |
I143L |
probably benign |
Het |
Fbxw10 |
C |
T |
11: 62,746,193 (GRCm39) |
R366C |
probably damaging |
Het |
Frg2f1 |
T |
C |
4: 119,388,329 (GRCm39) |
M57V |
probably benign |
Het |
Gbp4 |
T |
C |
5: 105,273,444 (GRCm39) |
S129G |
probably damaging |
Het |
Gnat2 |
A |
C |
3: 108,002,947 (GRCm39) |
|
probably benign |
Het |
Golgb1 |
C |
A |
16: 36,738,565 (GRCm39) |
F2301L |
probably damaging |
Het |
Il18bp |
T |
C |
7: 101,666,518 (GRCm39) |
T2A |
possibly damaging |
Het |
Kpna2 |
T |
C |
11: 106,883,520 (GRCm39) |
|
probably null |
Het |
Lrrfip2 |
A |
T |
9: 111,045,187 (GRCm39) |
|
probably benign |
Het |
Map4k1 |
T |
G |
7: 28,701,096 (GRCm39) |
|
probably null |
Het |
Mcm3ap |
T |
C |
10: 76,306,049 (GRCm39) |
V54A |
probably benign |
Het |
Nup133 |
A |
G |
8: 124,626,246 (GRCm39) |
I1112T |
probably benign |
Het |
Pcdhac1 |
T |
A |
18: 37,225,140 (GRCm39) |
V651D |
probably damaging |
Het |
Pde10a |
A |
G |
17: 9,186,356 (GRCm39) |
T571A |
possibly damaging |
Het |
Phc3 |
A |
G |
3: 30,990,910 (GRCm39) |
S403P |
probably damaging |
Het |
Prl7b1 |
T |
C |
13: 27,788,516 (GRCm39) |
E113G |
probably damaging |
Het |
Psmd2 |
T |
G |
16: 20,480,593 (GRCm39) |
M744R |
probably benign |
Het |
Qrich2 |
T |
C |
11: 116,346,156 (GRCm39) |
D1556G |
probably damaging |
Het |
Septin1 |
C |
T |
7: 126,816,876 (GRCm39) |
V46M |
probably benign |
Het |
Shank2 |
C |
A |
7: 143,606,197 (GRCm39) |
Q127K |
probably damaging |
Het |
Siah1a |
A |
G |
8: 87,451,653 (GRCm39) |
V277A |
possibly damaging |
Het |
Slc4a7 |
T |
A |
14: 14,733,846 (GRCm38) |
D85E |
probably damaging |
Het |
Slc5a12 |
A |
T |
2: 110,472,155 (GRCm39) |
I526F |
probably damaging |
Het |
Svil |
T |
C |
18: 5,063,231 (GRCm39) |
V834A |
possibly damaging |
Het |
Sycp1 |
T |
A |
3: 102,842,919 (GRCm39) |
S17C |
probably damaging |
Het |
Tssk6 |
G |
A |
8: 70,355,673 (GRCm39) |
R239Q |
probably benign |
Het |
Txnrd1 |
A |
G |
10: 82,709,042 (GRCm39) |
D80G |
probably benign |
Het |
Tyk2 |
A |
G |
9: 21,036,250 (GRCm39) |
F79S |
probably damaging |
Het |
Tyrp1 |
T |
C |
4: 80,769,014 (GRCm39) |
S503P |
probably benign |
Het |
Upf1 |
A |
T |
8: 70,794,211 (GRCm39) |
C232S |
probably benign |
Het |
Zeb2 |
G |
A |
2: 44,878,922 (GRCm39) |
T1080I |
probably damaging |
Het |
|
Other mutations in Or8b1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03127:Or8b1
|
APN |
9 |
38,399,882 (GRCm39) |
missense |
probably benign |
0.13 |
R0948:Or8b1
|
UTSW |
9 |
38,400,244 (GRCm39) |
missense |
probably benign |
0.00 |
R1236:Or8b1
|
UTSW |
9 |
38,399,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1246:Or8b1
|
UTSW |
9 |
38,400,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Or8b1
|
UTSW |
9 |
38,399,939 (GRCm39) |
missense |
probably benign |
0.10 |
R2016:Or8b1
|
UTSW |
9 |
38,399,309 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2264:Or8b1
|
UTSW |
9 |
38,399,351 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2268:Or8b1
|
UTSW |
9 |
38,399,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R3853:Or8b1
|
UTSW |
9 |
38,400,247 (GRCm39) |
missense |
probably benign |
0.18 |
R4066:Or8b1
|
UTSW |
9 |
38,399,778 (GRCm39) |
missense |
probably benign |
0.17 |
R4594:Or8b1
|
UTSW |
9 |
38,400,057 (GRCm39) |
missense |
probably damaging |
0.98 |
R5192:Or8b1
|
UTSW |
9 |
38,400,101 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5436:Or8b1
|
UTSW |
9 |
38,399,835 (GRCm39) |
missense |
probably benign |
0.31 |
R5598:Or8b1
|
UTSW |
9 |
38,399,821 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5694:Or8b1
|
UTSW |
9 |
38,399,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Or8b1
|
UTSW |
9 |
38,399,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R5959:Or8b1
|
UTSW |
9 |
38,400,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Or8b1
|
UTSW |
9 |
38,399,673 (GRCm39) |
missense |
probably benign |
|
R7482:Or8b1
|
UTSW |
9 |
38,399,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R7571:Or8b1
|
UTSW |
9 |
38,399,952 (GRCm39) |
missense |
probably benign |
0.08 |
R7917:Or8b1
|
UTSW |
9 |
38,399,905 (GRCm39) |
nonsense |
probably null |
|
R8837:Or8b1
|
UTSW |
9 |
38,399,597 (GRCm39) |
missense |
probably benign |
0.05 |
R9562:Or8b1
|
UTSW |
9 |
38,400,092 (GRCm39) |
missense |
possibly damaging |
0.45 |
R9628:Or8b1
|
UTSW |
9 |
38,399,871 (GRCm39) |
missense |
probably benign |
0.17 |
|