Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd16b |
G |
A |
2: 181,136,319 (GRCm39) |
R407H |
possibly damaging |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
Cadm1 |
A |
G |
9: 47,710,775 (GRCm39) |
E226G |
possibly damaging |
Het |
Caskin2 |
T |
C |
11: 115,695,623 (GRCm39) |
D246G |
probably damaging |
Het |
Cd80 |
T |
A |
16: 38,294,255 (GRCm39) |
V46E |
probably damaging |
Het |
Ctr9 |
C |
T |
7: 110,652,653 (GRCm39) |
R984C |
unknown |
Het |
Dach2 |
T |
C |
X: 112,729,664 (GRCm39) |
I417T |
possibly damaging |
Het |
Dcaf8l |
A |
T |
X: 88,448,327 (GRCm39) |
Y601N |
probably benign |
Het |
Drd3 |
T |
C |
16: 43,643,155 (GRCm39) |
F464L |
probably damaging |
Het |
Dyrk1a |
G |
A |
16: 94,469,660 (GRCm39) |
|
probably benign |
Het |
Fam227b |
T |
C |
2: 125,966,006 (GRCm39) |
T140A |
probably benign |
Het |
Fam91a1 |
A |
G |
15: 58,293,738 (GRCm39) |
I101V |
probably benign |
Het |
Fem1b |
T |
C |
9: 62,703,836 (GRCm39) |
I475V |
probably benign |
Het |
Glra3 |
A |
G |
8: 56,578,244 (GRCm39) |
R434G |
possibly damaging |
Het |
Hsd17b12 |
C |
T |
2: 93,864,303 (GRCm39) |
R268Q |
probably benign |
Het |
Iglc3 |
T |
C |
16: 18,884,345 (GRCm39) |
|
probably benign |
Het |
Khdrbs2 |
C |
A |
1: 32,558,858 (GRCm39) |
R408L |
probably damaging |
Het |
Loxhd1 |
A |
G |
18: 77,518,774 (GRCm39) |
D1860G |
probably damaging |
Het |
Mcpt8 |
A |
T |
14: 56,321,398 (GRCm39) |
I22K |
probably damaging |
Het |
Myo1h |
A |
G |
5: 114,466,860 (GRCm39) |
I303V |
probably benign |
Het |
Nipsnap2 |
G |
A |
5: 129,825,098 (GRCm39) |
|
probably null |
Het |
Nop2 |
G |
A |
6: 125,109,164 (GRCm39) |
|
probably benign |
Het |
Polr2a |
A |
T |
11: 69,626,536 (GRCm39) |
S1566T |
possibly damaging |
Het |
Pthlh |
A |
T |
6: 147,164,789 (GRCm39) |
V27E |
probably damaging |
Het |
Ralgps1 |
T |
C |
2: 33,048,968 (GRCm39) |
T314A |
possibly damaging |
Het |
Robo4 |
CGG |
CG |
9: 37,322,786 (GRCm39) |
|
probably null |
Het |
Skil |
A |
G |
3: 31,151,487 (GRCm39) |
N3S |
probably benign |
Het |
Tas2r140 |
T |
A |
6: 133,032,204 (GRCm39) |
I185L |
probably benign |
Het |
Tnpo1 |
GCACCTCTGCTTCCTC |
GCACCTCTGCTTCCTCACCTCTGCTTCCTC |
13: 99,003,637 (GRCm39) |
|
probably null |
Het |
Togaram1 |
G |
T |
12: 65,013,118 (GRCm39) |
R123L |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Trim12a |
G |
T |
7: 103,950,063 (GRCm39) |
T292K |
probably benign |
Het |
Trim9 |
C |
T |
12: 70,295,167 (GRCm39) |
G648R |
probably damaging |
Het |
Trmt13 |
T |
C |
3: 116,383,893 (GRCm39) |
I104V |
probably benign |
Het |
Vav3 |
G |
A |
3: 109,535,484 (GRCm39) |
|
probably null |
Het |
Vmn1r87 |
A |
G |
7: 12,865,493 (GRCm39) |
Y265H |
probably damaging |
Het |
Zfp574 |
G |
T |
7: 24,781,026 (GRCm39) |
A683S |
possibly damaging |
Het |
|
Other mutations in Tas2r129 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02227:Tas2r129
|
APN |
6 |
132,928,357 (GRCm39) |
nonsense |
probably null |
|
R0389:Tas2r129
|
UTSW |
6 |
132,928,159 (GRCm39) |
missense |
probably benign |
0.26 |
R0443:Tas2r129
|
UTSW |
6 |
132,928,159 (GRCm39) |
missense |
probably benign |
0.26 |
R0487:Tas2r129
|
UTSW |
6 |
132,928,907 (GRCm39) |
missense |
probably benign |
0.31 |
R0487:Tas2r129
|
UTSW |
6 |
132,928,906 (GRCm39) |
missense |
probably benign |
0.26 |
R0576:Tas2r129
|
UTSW |
6 |
132,928,497 (GRCm39) |
missense |
probably benign |
0.38 |
R1253:Tas2r129
|
UTSW |
6 |
132,928,999 (GRCm39) |
missense |
probably benign |
0.11 |
R4493:Tas2r129
|
UTSW |
6 |
132,928,317 (GRCm39) |
missense |
probably benign |
0.31 |
R4494:Tas2r129
|
UTSW |
6 |
132,928,317 (GRCm39) |
missense |
probably benign |
0.31 |
R4591:Tas2r129
|
UTSW |
6 |
132,928,574 (GRCm39) |
missense |
probably benign |
0.10 |
R6156:Tas2r129
|
UTSW |
6 |
132,928,455 (GRCm39) |
missense |
probably benign |
0.31 |
R6495:Tas2r129
|
UTSW |
6 |
132,928,128 (GRCm39) |
missense |
probably benign |
0.00 |
R7600:Tas2r129
|
UTSW |
6 |
132,928,137 (GRCm39) |
nonsense |
probably null |
|
R7608:Tas2r129
|
UTSW |
6 |
132,928,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R8498:Tas2r129
|
UTSW |
6 |
132,928,815 (GRCm39) |
missense |
probably benign |
0.01 |
R8870:Tas2r129
|
UTSW |
6 |
132,928,522 (GRCm39) |
missense |
probably damaging |
0.98 |
R9276:Tas2r129
|
UTSW |
6 |
132,928,576 (GRCm39) |
missense |
probably benign |
0.12 |
|