Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,213,957 (GRCm39) |
M728K |
probably benign |
Het |
2700049A03Rik |
T |
A |
12: 71,213,955 (GRCm39) |
Y727* |
probably null |
Het |
Adam23 |
T |
C |
1: 63,582,278 (GRCm39) |
Y309H |
probably damaging |
Het |
Ash2l |
C |
T |
8: 26,329,868 (GRCm39) |
V97M |
probably damaging |
Het |
Cyp4f13 |
A |
G |
17: 33,149,588 (GRCm39) |
F83L |
probably benign |
Het |
Dnah6 |
A |
T |
6: 73,112,784 (GRCm39) |
S1607T |
probably damaging |
Het |
Dock2 |
T |
A |
11: 34,260,435 (GRCm39) |
M969L |
possibly damaging |
Het |
Dse |
T |
A |
10: 34,036,213 (GRCm39) |
|
probably benign |
Het |
Dusp22 |
C |
T |
13: 30,892,666 (GRCm39) |
|
probably null |
Het |
F5 |
G |
A |
1: 164,021,937 (GRCm39) |
V1471I |
probably benign |
Het |
Gm14403 |
A |
T |
2: 177,199,049 (GRCm39) |
E48D |
probably damaging |
Het |
Gm6309 |
G |
A |
5: 146,105,085 (GRCm39) |
A276V |
probably damaging |
Het |
Icam4 |
A |
T |
9: 20,941,086 (GRCm39) |
T113S |
probably damaging |
Het |
Ipo5 |
T |
C |
14: 121,163,650 (GRCm39) |
V236A |
probably benign |
Het |
Mrc2 |
T |
G |
11: 105,227,503 (GRCm39) |
F579V |
probably damaging |
Het |
Myl4 |
T |
A |
11: 104,468,279 (GRCm39) |
M1K |
probably null |
Het |
Oas3 |
A |
T |
5: 120,904,193 (GRCm39) |
C560* |
probably null |
Het |
Or2w25 |
T |
C |
11: 59,504,165 (GRCm39) |
V125A |
probably damaging |
Het |
Or52e18 |
T |
C |
7: 104,609,669 (GRCm39) |
N90S |
probably benign |
Het |
Prlr |
G |
A |
15: 10,329,129 (GRCm39) |
V535I |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,165,058 (GRCm39) |
T48A |
probably benign |
Het |
Rasa4 |
A |
G |
5: 136,131,461 (GRCm39) |
H485R |
possibly damaging |
Het |
Rnf13 |
A |
T |
3: 57,728,007 (GRCm39) |
H229L |
probably damaging |
Het |
Rpap3 |
T |
C |
15: 97,601,120 (GRCm39) |
D39G |
possibly damaging |
Het |
Sec23ip |
T |
A |
7: 128,357,035 (GRCm39) |
|
probably null |
Het |
Sirpa |
T |
A |
2: 129,457,484 (GRCm39) |
F186Y |
possibly damaging |
Het |
Slc26a11 |
T |
C |
11: 119,268,040 (GRCm39) |
Y473H |
probably benign |
Het |
Slc36a2 |
T |
C |
11: 55,053,559 (GRCm39) |
I360V |
probably benign |
Het |
Spg11 |
G |
A |
2: 121,918,705 (GRCm39) |
R975C |
probably benign |
Het |
Sppl2b |
T |
A |
10: 80,701,175 (GRCm39) |
I350N |
probably damaging |
Het |
Trav14n-3 |
A |
G |
14: 53,607,786 (GRCm39) |
T39A |
possibly damaging |
Het |
Vmn2r61 |
A |
G |
7: 41,950,015 (GRCm39) |
M812V |
probably benign |
Het |
Vmn2r87 |
A |
C |
10: 130,314,978 (GRCm39) |
F203V |
probably damaging |
Het |
Vwde |
A |
C |
6: 13,186,823 (GRCm39) |
V888G |
probably benign |
Het |
Zbtb17 |
T |
C |
4: 141,192,749 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Tas2r139 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00863:Tas2r139
|
APN |
6 |
42,118,055 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01593:Tas2r139
|
APN |
6 |
42,117,891 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02990:Tas2r139
|
APN |
6 |
42,118,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R0517:Tas2r139
|
UTSW |
6 |
42,118,425 (GRCm39) |
missense |
probably damaging |
0.98 |
R1106:Tas2r139
|
UTSW |
6 |
42,118,479 (GRCm39) |
missense |
probably benign |
0.36 |
R1352:Tas2r139
|
UTSW |
6 |
42,117,874 (GRCm39) |
missense |
probably benign |
0.28 |
R4352:Tas2r139
|
UTSW |
6 |
42,118,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Tas2r139
|
UTSW |
6 |
42,118,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Tas2r139
|
UTSW |
6 |
42,118,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Tas2r139
|
UTSW |
6 |
42,118,500 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5888:Tas2r139
|
UTSW |
6 |
42,118,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Tas2r139
|
UTSW |
6 |
42,118,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R8058:Tas2r139
|
UTSW |
6 |
42,118,753 (GRCm39) |
missense |
probably benign |
0.01 |
R8075:Tas2r139
|
UTSW |
6 |
42,118,154 (GRCm39) |
missense |
probably benign |
0.00 |
R8319:Tas2r139
|
UTSW |
6 |
42,118,720 (GRCm39) |
missense |
probably benign |
0.01 |
R9087:Tas2r139
|
UTSW |
6 |
42,118,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9185:Tas2r139
|
UTSW |
6 |
42,118,099 (GRCm39) |
missense |
probably benign |
0.25 |
R9803:Tas2r139
|
UTSW |
6 |
42,118,066 (GRCm39) |
missense |
probably damaging |
1.00 |
|