Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17b |
C |
T |
19: 21,655,888 (GRCm39) |
Q57* |
probably null |
Het |
Acad8 |
C |
T |
9: 26,890,352 (GRCm39) |
A288T |
possibly damaging |
Het |
Adamtsl3 |
G |
A |
7: 82,197,187 (GRCm39) |
C711Y |
probably damaging |
Het |
Ahcyl2 |
C |
A |
6: 29,768,869 (GRCm39) |
D111E |
probably benign |
Het |
Asxl3 |
T |
C |
18: 22,649,174 (GRCm39) |
F388L |
probably benign |
Het |
Bcr |
T |
A |
10: 74,981,271 (GRCm39) |
S697T |
probably damaging |
Het |
Catspere2 |
G |
A |
1: 177,842,724 (GRCm39) |
V50M |
possibly damaging |
Het |
Dgka |
C |
A |
10: 128,563,997 (GRCm39) |
V451F |
probably damaging |
Het |
Dnajc2 |
A |
T |
5: 21,962,705 (GRCm39) |
C617S |
unknown |
Het |
Erich3 |
C |
A |
3: 154,469,991 (GRCm39) |
T1481K |
unknown |
Het |
Golm2 |
A |
T |
2: 121,697,632 (GRCm39) |
|
probably benign |
Het |
Hdac2 |
T |
A |
10: 36,874,059 (GRCm39) |
D396E |
probably benign |
Het |
Hmgcs2 |
A |
T |
3: 98,204,724 (GRCm39) |
D294V |
possibly damaging |
Het |
Hnf1a |
A |
G |
5: 115,091,391 (GRCm39) |
V434A |
possibly damaging |
Het |
Il4ra |
T |
C |
7: 125,169,138 (GRCm39) |
L130P |
probably damaging |
Het |
Inpp5j |
T |
C |
11: 3,449,767 (GRCm39) |
K672E |
probably damaging |
Het |
Kif16b |
G |
A |
2: 142,553,777 (GRCm39) |
A1007V |
probably benign |
Het |
Kif26b |
T |
C |
1: 178,743,938 (GRCm39) |
S1345P |
probably benign |
Het |
Lrrc28 |
A |
T |
7: 67,290,909 (GRCm39) |
D37E |
probably benign |
Het |
Mlx |
G |
T |
11: 100,978,140 (GRCm39) |
|
probably benign |
Het |
Muc16 |
T |
C |
9: 18,436,554 (GRCm39) |
H7878R |
probably benign |
Het |
Mybpc1 |
C |
A |
10: 88,409,359 (GRCm39) |
E32* |
probably null |
Het |
Nebl |
C |
T |
2: 17,465,298 (GRCm39) |
V18M |
probably benign |
Het |
Nhsl3 |
C |
T |
4: 129,117,995 (GRCm39) |
R268Q |
possibly damaging |
Het |
Nlrp3 |
T |
C |
11: 59,440,229 (GRCm39) |
V602A |
probably benign |
Het |
Npepps |
G |
A |
11: 97,120,665 (GRCm39) |
P532S |
probably benign |
Het |
Or7g12 |
T |
A |
9: 18,900,139 (GRCm39) |
M285K |
probably benign |
Het |
Or8k53 |
T |
C |
2: 86,177,668 (GRCm39) |
I147M |
possibly damaging |
Het |
Pfdn1 |
G |
A |
18: 36,584,214 (GRCm39) |
T40M |
probably benign |
Het |
Pkd2 |
G |
T |
5: 104,607,653 (GRCm39) |
E51* |
probably null |
Het |
Prss40 |
T |
A |
1: 34,599,876 (GRCm39) |
H37L |
probably benign |
Het |
Rab11fip1 |
A |
T |
8: 27,642,374 (GRCm39) |
C808* |
probably null |
Het |
Rab3gap2 |
A |
T |
1: 184,999,270 (GRCm39) |
|
probably benign |
Het |
Sall3 |
C |
T |
18: 81,017,232 (GRCm39) |
R232H |
probably benign |
Het |
Sbk3 |
A |
G |
7: 4,970,707 (GRCm39) |
F221L |
probably damaging |
Het |
Sema7a |
T |
G |
9: 57,862,974 (GRCm39) |
|
probably benign |
Het |
Serpina3b |
C |
A |
12: 104,104,962 (GRCm39) |
N379K |
probably benign |
Het |
Ssbp4 |
A |
G |
8: 71,052,039 (GRCm39) |
L208P |
probably benign |
Het |
Stxbp5 |
C |
T |
10: 9,688,003 (GRCm39) |
|
probably null |
Het |
Tecrl |
A |
G |
5: 83,448,764 (GRCm39) |
Y160H |
probably damaging |
Het |
Tnc |
T |
C |
4: 63,885,511 (GRCm39) |
I1773V |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,198,468 (GRCm39) |
T1511A |
probably benign |
Het |
Utp15 |
T |
C |
13: 98,391,499 (GRCm39) |
N246S |
probably damaging |
Het |
Vmn1r49 |
C |
T |
6: 90,049,991 (GRCm39) |
A4T |
probably benign |
Het |
Vmn2r57 |
A |
T |
7: 41,049,640 (GRCm39) |
I703N |
probably damaging |
Het |
Wdr93 |
A |
G |
7: 79,398,974 (GRCm39) |
D36G |
probably damaging |
Het |
Zfp334 |
A |
G |
2: 165,225,278 (GRCm39) |
I8T |
probably benign |
Het |
|
Other mutations in Or8g19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Or8g19
|
APN |
9 |
39,056,053 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00905:Or8g19
|
APN |
9 |
39,056,326 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02346:Or8g19
|
APN |
9 |
39,055,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Or8g19
|
UTSW |
9 |
39,056,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R0118:Or8g19
|
UTSW |
9 |
39,055,399 (GRCm39) |
start codon destroyed |
probably null |
0.97 |
R0590:Or8g19
|
UTSW |
9 |
39,056,017 (GRCm39) |
missense |
probably benign |
0.01 |
R2915:Or8g19
|
UTSW |
9 |
39,055,762 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4299:Or8g19
|
UTSW |
9 |
39,056,295 (GRCm39) |
missense |
probably benign |
0.11 |
R4367:Or8g19
|
UTSW |
9 |
39,055,725 (GRCm39) |
missense |
probably damaging |
0.98 |
R4663:Or8g19
|
UTSW |
9 |
39,056,145 (GRCm39) |
missense |
probably damaging |
0.97 |
R5276:Or8g19
|
UTSW |
9 |
39,055,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R5503:Or8g19
|
UTSW |
9 |
39,055,780 (GRCm39) |
missense |
probably benign |
0.02 |
R5742:Or8g19
|
UTSW |
9 |
39,055,974 (GRCm39) |
missense |
probably benign |
0.07 |
R5986:Or8g19
|
UTSW |
9 |
39,056,278 (GRCm39) |
missense |
probably null |
1.00 |
R6801:Or8g19
|
UTSW |
9 |
39,055,506 (GRCm39) |
missense |
probably benign |
0.01 |
R7247:Or8g19
|
UTSW |
9 |
39,056,153 (GRCm39) |
nonsense |
probably null |
|
R7520:Or8g19
|
UTSW |
9 |
39,055,414 (GRCm39) |
missense |
probably benign |
|
R7787:Or8g19
|
UTSW |
9 |
39,055,548 (GRCm39) |
missense |
probably benign |
0.22 |
R8721:Or8g19
|
UTSW |
9 |
39,055,386 (GRCm39) |
start gained |
probably benign |
|
R8880:Or8g19
|
UTSW |
9 |
39,055,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8883:Or8g19
|
UTSW |
9 |
39,056,083 (GRCm39) |
missense |
probably benign |
0.00 |
R9143:Or8g19
|
UTSW |
9 |
39,055,722 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9445:Or8g19
|
UTSW |
9 |
39,055,766 (GRCm39) |
nonsense |
probably null |
|
|