Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alyref |
T |
C |
11: 120,489,074 (GRCm39) |
R31G |
probably benign |
Het |
Arfgef2 |
GTGTGCAGAAACT |
GT |
2: 166,676,383 (GRCm39) |
92 |
probably null |
Het |
Arhgap31 |
G |
T |
16: 38,445,991 (GRCm39) |
A118E |
probably damaging |
Het |
Asb5 |
T |
A |
8: 55,003,541 (GRCm39) |
I21K |
probably damaging |
Het |
Asxl2 |
A |
G |
12: 3,546,760 (GRCm39) |
I515V |
probably benign |
Het |
Bend7 |
C |
T |
2: 4,757,665 (GRCm39) |
P236S |
probably benign |
Het |
C4bp |
T |
C |
1: 130,566,824 (GRCm39) |
T351A |
probably benign |
Het |
Cd1d2 |
T |
A |
3: 86,894,569 (GRCm39) |
|
probably null |
Het |
Chd1 |
T |
A |
17: 15,981,666 (GRCm39) |
D1368E |
probably benign |
Het |
Chrnb3 |
A |
G |
8: 27,883,682 (GRCm39) |
I140V |
probably benign |
Het |
Cip2a |
A |
G |
16: 48,817,825 (GRCm39) |
D65G |
probably damaging |
Het |
Col6a2 |
T |
C |
10: 76,432,625 (GRCm39) |
T843A |
possibly damaging |
Het |
Dnajc2 |
A |
G |
5: 21,986,317 (GRCm39) |
|
probably null |
Het |
Dop1a |
A |
G |
9: 86,376,510 (GRCm39) |
D248G |
probably damaging |
Het |
Dtna |
T |
A |
18: 23,723,388 (GRCm39) |
C197* |
probably null |
Het |
Flg2 |
T |
C |
3: 93,127,390 (GRCm39) |
S2101P |
unknown |
Het |
Foxg1 |
A |
G |
12: 49,431,429 (GRCm39) |
H54R |
unknown |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Gpr35 |
A |
G |
1: 92,910,437 (GRCm39) |
T50A |
probably damaging |
Het |
Gsta3 |
A |
T |
1: 21,330,322 (GRCm39) |
Y108F |
probably benign |
Het |
Hdac4 |
G |
T |
1: 91,886,138 (GRCm39) |
A811E |
probably damaging |
Het |
Hephl1 |
A |
T |
9: 14,972,210 (GRCm39) |
V910E |
possibly damaging |
Het |
Kcnb2 |
A |
T |
1: 15,780,280 (GRCm39) |
Y384F |
probably damaging |
Het |
Kmt2a |
T |
C |
9: 44,733,686 (GRCm39) |
I2210M |
unknown |
Het |
Lamb2 |
C |
T |
9: 108,357,845 (GRCm39) |
R123W |
probably damaging |
Het |
Lrriq1 |
A |
G |
10: 102,992,196 (GRCm39) |
|
probably null |
Het |
Lsm4 |
G |
A |
8: 71,131,018 (GRCm39) |
G112S |
probably damaging |
Het |
Myt1 |
T |
C |
2: 181,464,554 (GRCm39) |
|
probably null |
Het |
Ndor1 |
T |
C |
2: 25,138,746 (GRCm39) |
R396G |
probably benign |
Het |
Or10ag56 |
A |
C |
2: 87,139,318 (GRCm39) |
I82L |
probably damaging |
Het |
Pcnx1 |
C |
T |
12: 81,965,593 (GRCm39) |
R59* |
probably null |
Het |
Prdm2 |
A |
G |
4: 142,861,338 (GRCm39) |
S651P |
probably benign |
Het |
Prkaa2 |
T |
C |
4: 104,909,172 (GRCm39) |
M91V |
probably benign |
Het |
Pskh1 |
G |
A |
8: 106,640,226 (GRCm39) |
R302H |
probably benign |
Het |
Rab11fip4 |
A |
G |
11: 79,577,415 (GRCm39) |
T390A |
probably benign |
Het |
Snx10 |
T |
C |
6: 51,538,999 (GRCm39) |
|
probably benign |
Het |
Tcf20 |
A |
G |
15: 82,737,138 (GRCm39) |
C1438R |
probably benign |
Het |
Tfap2d |
A |
G |
1: 19,173,486 (GRCm39) |
T3A |
probably benign |
Het |
Toporsl |
A |
G |
4: 52,609,975 (GRCm39) |
|
probably benign |
Het |
Trim71 |
A |
G |
9: 114,342,192 (GRCm39) |
S697P |
probably benign |
Het |
Ufl1 |
T |
C |
4: 25,269,057 (GRCm39) |
D258G |
probably damaging |
Het |
Vmn1r28 |
T |
C |
6: 58,242,183 (GRCm39) |
Y9H |
probably damaging |
Het |
Zfp995 |
T |
A |
17: 22,099,115 (GRCm39) |
H373L |
probably damaging |
Het |
|
Other mutations in Taar5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01602:Taar5
|
APN |
10 |
23,846,962 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01605:Taar5
|
APN |
10 |
23,846,962 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02935:Taar5
|
APN |
10 |
23,847,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02962:Taar5
|
APN |
10 |
23,846,883 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0136:Taar5
|
UTSW |
10 |
23,847,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Taar5
|
UTSW |
10 |
23,847,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1537:Taar5
|
UTSW |
10 |
23,846,620 (GRCm39) |
missense |
probably benign |
0.25 |
R2033:Taar5
|
UTSW |
10 |
23,846,992 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2158:Taar5
|
UTSW |
10 |
23,846,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R4914:Taar5
|
UTSW |
10 |
23,847,468 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4999:Taar5
|
UTSW |
10 |
23,847,445 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5084:Taar5
|
UTSW |
10 |
23,846,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Taar5
|
UTSW |
10 |
23,847,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R6516:Taar5
|
UTSW |
10 |
23,847,564 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7974:Taar5
|
UTSW |
10 |
23,847,120 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8147:Taar5
|
UTSW |
10 |
23,846,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R9306:Taar5
|
UTSW |
10 |
23,846,781 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Taar5
|
UTSW |
10 |
23,847,339 (GRCm39) |
missense |
probably benign |
0.00 |
|