Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,621,130 (GRCm39) |
Y278C |
probably damaging |
Het |
Abcd2 |
A |
G |
15: 91,062,444 (GRCm39) |
L498P |
possibly damaging |
Het |
Acot11 |
A |
G |
4: 106,615,578 (GRCm39) |
F271S |
probably damaging |
Het |
Acr |
T |
A |
15: 89,454,217 (GRCm39) |
Y185N |
probably damaging |
Het |
Adcy10 |
C |
T |
1: 165,365,949 (GRCm39) |
R489C |
probably damaging |
Het |
Arsb |
A |
G |
13: 93,930,670 (GRCm39) |
T213A |
probably benign |
Het |
Atg2a |
T |
A |
19: 6,291,858 (GRCm39) |
C11* |
probably null |
Het |
B3galt6 |
A |
T |
4: 156,076,152 (GRCm39) |
Y308N |
probably damaging |
Het |
Cd226 |
A |
G |
18: 89,225,451 (GRCm39) |
N116S |
probably benign |
Het |
Crat |
T |
A |
2: 30,297,146 (GRCm39) |
D269V |
probably damaging |
Het |
Crim1 |
T |
A |
17: 78,623,083 (GRCm39) |
I427N |
possibly damaging |
Het |
Dock3 |
T |
C |
9: 106,790,298 (GRCm39) |
|
probably benign |
Het |
Dsg1c |
T |
A |
18: 20,407,776 (GRCm39) |
V374E |
probably damaging |
Het |
Dtl |
A |
G |
1: 191,273,352 (GRCm39) |
S519P |
probably benign |
Het |
Fastkd1 |
C |
T |
2: 69,532,945 (GRCm39) |
R474H |
probably benign |
Het |
Fbxo10 |
T |
C |
4: 45,058,361 (GRCm39) |
T459A |
possibly damaging |
Het |
Frmd4b |
A |
G |
6: 97,272,770 (GRCm39) |
L828P |
probably damaging |
Het |
Gc |
T |
C |
5: 89,593,255 (GRCm39) |
S55G |
probably benign |
Het |
Gm6455 |
T |
G |
5: 10,917,257 (GRCm39) |
|
noncoding transcript |
Het |
Gnai2 |
T |
C |
9: 107,493,393 (GRCm39) |
T280A |
probably benign |
Het |
Hmgn2 |
A |
G |
4: 133,693,260 (GRCm39) |
|
probably null |
Het |
Jmjd1c |
G |
T |
10: 67,062,161 (GRCm39) |
A1505S |
probably benign |
Het |
Lrriq1 |
T |
C |
10: 102,982,142 (GRCm39) |
K1393E |
probably benign |
Het |
Mcam |
A |
G |
9: 44,051,547 (GRCm39) |
N469D |
probably benign |
Het |
Mrpl47 |
A |
G |
3: 32,790,789 (GRCm39) |
|
probably null |
Het |
Mslnl |
C |
T |
17: 25,966,972 (GRCm39) |
A659V |
possibly damaging |
Het |
Nlrp1a |
A |
G |
11: 71,013,456 (GRCm39) |
V598A |
probably benign |
Het |
Npff |
A |
T |
15: 102,433,000 (GRCm39) |
L15Q |
probably null |
Het |
Obsl1 |
G |
T |
1: 75,481,890 (GRCm39) |
Q327K |
probably damaging |
Het |
Or13a18 |
T |
C |
7: 140,190,844 (GRCm39) |
V255A |
probably damaging |
Het |
Or4c58 |
T |
A |
2: 89,675,315 (GRCm39) |
M1L |
probably benign |
Het |
Or52s1b |
T |
C |
7: 102,822,658 (GRCm39) |
Y62C |
probably damaging |
Het |
Or7e165 |
A |
T |
9: 19,694,711 (GRCm39) |
Y94F |
probably benign |
Het |
Or8b50 |
G |
A |
9: 38,518,417 (GRCm39) |
G219S |
possibly damaging |
Het |
Pdzd2 |
T |
A |
15: 12,375,851 (GRCm39) |
H1428L |
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,627,203 (GRCm39) |
E414G |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,106,617 (GRCm39) |
D3251G |
probably benign |
Het |
Secisbp2l |
G |
T |
2: 125,582,789 (GRCm39) |
S889* |
probably null |
Het |
Setx |
T |
A |
2: 29,023,942 (GRCm39) |
C133S |
probably damaging |
Het |
Slc22a29 |
A |
C |
19: 8,184,649 (GRCm39) |
S214A |
probably benign |
Het |
Slc30a5 |
A |
C |
13: 100,950,232 (GRCm39) |
L285R |
probably damaging |
Het |
Tfap2b |
T |
A |
1: 19,304,485 (GRCm39) |
F414I |
probably damaging |
Het |
Trpc4ap |
A |
T |
2: 155,512,989 (GRCm39) |
Y129N |
possibly damaging |
Het |
Vmn2r94 |
T |
C |
17: 18,473,523 (GRCm39) |
E501G |
probably benign |
Het |
Xpot |
T |
C |
10: 121,439,070 (GRCm39) |
H709R |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 109,682,004 (GRCm39) |
|
probably benign |
Het |
Zscan22 |
T |
G |
7: 12,640,426 (GRCm39) |
H223Q |
probably benign |
Het |
|
Other mutations in Taar7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Taar7a
|
APN |
10 |
23,868,294 (GRCm39) |
unclassified |
probably benign |
|
PIT4434001:Taar7a
|
UTSW |
10 |
23,869,319 (GRCm39) |
missense |
probably benign |
|
R0422:Taar7a
|
UTSW |
10 |
23,869,172 (GRCm39) |
missense |
probably benign |
0.02 |
R1029:Taar7a
|
UTSW |
10 |
23,868,439 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1742:Taar7a
|
UTSW |
10 |
23,869,117 (GRCm39) |
missense |
probably damaging |
0.98 |
R2104:Taar7a
|
UTSW |
10 |
23,868,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R2421:Taar7a
|
UTSW |
10 |
23,868,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Taar7a
|
UTSW |
10 |
23,868,457 (GRCm39) |
missense |
probably benign |
0.25 |
R4021:Taar7a
|
UTSW |
10 |
23,869,284 (GRCm39) |
missense |
probably benign |
0.00 |
R5180:Taar7a
|
UTSW |
10 |
23,869,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Taar7a
|
UTSW |
10 |
23,868,356 (GRCm39) |
missense |
probably benign |
0.00 |
R5507:Taar7a
|
UTSW |
10 |
23,868,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R5587:Taar7a
|
UTSW |
10 |
23,868,726 (GRCm39) |
missense |
probably benign |
0.00 |
R5766:Taar7a
|
UTSW |
10 |
23,869,260 (GRCm39) |
missense |
probably benign |
0.01 |
R5861:Taar7a
|
UTSW |
10 |
23,868,337 (GRCm39) |
missense |
probably benign |
|
R7201:Taar7a
|
UTSW |
10 |
23,868,358 (GRCm39) |
missense |
probably benign |
0.04 |
R7506:Taar7a
|
UTSW |
10 |
23,868,892 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8810:Taar7a
|
UTSW |
10 |
23,869,279 (GRCm39) |
missense |
probably benign |
0.20 |
R9015:Taar7a
|
UTSW |
10 |
23,868,733 (GRCm39) |
missense |
probably damaging |
0.97 |
R9172:Taar7a
|
UTSW |
10 |
23,868,677 (GRCm39) |
missense |
probably benign |
0.16 |
R9686:Taar7a
|
UTSW |
10 |
23,869,309 (GRCm39) |
missense |
probably benign |
0.01 |
R9717:Taar7a
|
UTSW |
10 |
23,868,799 (GRCm39) |
missense |
probably benign |
0.01 |
R9720:Taar7a
|
UTSW |
10 |
23,868,733 (GRCm39) |
missense |
probably benign |
0.10 |
X0064:Taar7a
|
UTSW |
10 |
23,868,515 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Taar7a
|
UTSW |
10 |
23,868,790 (GRCm39) |
missense |
probably benign |
0.01 |
|