Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd18 |
A |
C |
3: 40,871,325 (GRCm39) |
T50P |
probably damaging |
Het |
Adam5 |
T |
A |
8: 25,300,850 (GRCm39) |
L226F |
possibly damaging |
Het |
Adi1 |
T |
C |
12: 28,725,544 (GRCm39) |
|
probably benign |
Het |
Apc |
T |
C |
18: 34,447,343 (GRCm39) |
V1379A |
probably benign |
Het |
Atp13a4 |
G |
A |
16: 29,275,428 (GRCm39) |
T352M |
probably damaging |
Het |
Baat |
T |
A |
4: 49,490,070 (GRCm39) |
N338I |
probably benign |
Het |
Bdnf |
A |
G |
2: 109,554,327 (GRCm39) |
T234A |
probably benign |
Het |
Catsperd |
A |
C |
17: 56,967,235 (GRCm39) |
T539P |
possibly damaging |
Het |
Cd109 |
A |
T |
9: 78,617,434 (GRCm39) |
T1311S |
probably benign |
Het |
Ceacam18 |
T |
C |
7: 43,286,536 (GRCm39) |
|
probably null |
Het |
Cfap96 |
T |
C |
8: 46,415,373 (GRCm39) |
E211G |
probably benign |
Het |
Cfhr4 |
C |
T |
1: 139,668,233 (GRCm39) |
C300Y |
probably damaging |
Het |
Chsy3 |
T |
A |
18: 59,543,318 (GRCm39) |
S819T |
probably damaging |
Het |
Col4a4 |
G |
T |
1: 82,431,614 (GRCm39) |
R1557S |
unknown |
Het |
Ddx18 |
A |
G |
1: 121,495,518 (GRCm39) |
|
probably null |
Het |
Depdc5 |
C |
T |
5: 33,095,635 (GRCm39) |
P824L |
probably damaging |
Het |
Fam13c |
C |
G |
10: 70,276,893 (GRCm39) |
A17G |
probably benign |
Het |
Fermt1 |
T |
C |
2: 132,748,685 (GRCm39) |
Y646C |
probably damaging |
Het |
Fra10ac1 |
A |
G |
19: 38,188,110 (GRCm39) |
S229P |
probably benign |
Het |
Gbp8 |
A |
T |
5: 105,198,845 (GRCm39) |
H23Q |
probably benign |
Het |
Gdf2 |
T |
C |
14: 33,666,788 (GRCm39) |
V170A |
probably benign |
Het |
Gm15723 |
T |
C |
10: 114,652,722 (GRCm39) |
|
noncoding transcript |
Het |
Gm815 |
G |
A |
19: 26,863,806 (GRCm39) |
V16I |
unknown |
Het |
Ighv1-75 |
T |
A |
12: 115,797,797 (GRCm39) |
K42* |
probably null |
Het |
Isx |
A |
G |
8: 75,619,473 (GRCm39) |
T222A |
probably benign |
Het |
Itgax |
G |
A |
7: 127,747,450 (GRCm39) |
D1018N |
probably damaging |
Het |
Kcnc4 |
A |
G |
3: 107,355,401 (GRCm39) |
F349S |
probably damaging |
Het |
Lama3 |
A |
C |
18: 12,598,565 (GRCm39) |
S991R |
probably damaging |
Het |
Larp4b |
C |
T |
13: 9,208,220 (GRCm39) |
A398V |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,670,357 (GRCm39) |
N1466S |
probably benign |
Het |
Metrn |
A |
T |
17: 26,015,514 (GRCm39) |
L67Q |
probably damaging |
Het |
Morc1 |
G |
A |
16: 48,451,132 (GRCm39) |
R937Q |
probably benign |
Het |
Mta3 |
A |
G |
17: 84,112,003 (GRCm39) |
Y577C |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,753,063 (GRCm39) |
F308L |
possibly damaging |
Het |
Nat8 |
A |
T |
6: 85,807,873 (GRCm39) |
S87T |
probably benign |
Het |
Oplah |
A |
T |
15: 76,185,410 (GRCm39) |
|
probably null |
Het |
Or2ak6 |
A |
G |
11: 58,592,778 (GRCm39) |
N84D |
probably benign |
Het |
Or2ak6 |
A |
C |
11: 58,592,779 (GRCm39) |
N84T |
possibly damaging |
Het |
Pcdh15 |
A |
T |
10: 74,232,204 (GRCm39) |
I668L |
possibly damaging |
Het |
Pecr |
A |
G |
1: 72,316,444 (GRCm39) |
|
probably null |
Het |
Plxna4 |
T |
C |
6: 32,493,956 (GRCm39) |
E220G |
possibly damaging |
Het |
Pnma8b |
A |
G |
7: 16,679,199 (GRCm39) |
K61R |
unknown |
Het |
Prl8a6 |
C |
T |
13: 27,620,179 (GRCm39) |
W81* |
probably null |
Het |
Rab33b |
C |
T |
3: 51,392,033 (GRCm39) |
|
probably benign |
Het |
Rbm33 |
T |
A |
5: 28,557,772 (GRCm39) |
|
probably null |
Het |
Relch |
A |
G |
1: 105,649,101 (GRCm39) |
S747G |
probably benign |
Het |
Reln |
C |
T |
5: 22,308,395 (GRCm39) |
V325M |
possibly damaging |
Het |
Rheb |
A |
C |
5: 25,008,743 (GRCm39) |
D158E |
probably benign |
Het |
Rhebl1 |
T |
A |
15: 98,778,464 (GRCm39) |
|
probably benign |
Het |
Rmdn2 |
T |
A |
17: 79,975,446 (GRCm39) |
Y312N |
probably damaging |
Het |
Scamp1 |
T |
G |
13: 94,368,594 (GRCm39) |
N58T |
probably benign |
Het |
Semp2l1 |
A |
T |
1: 32,584,598 (GRCm39) |
C437* |
probably null |
Het |
Slc35a1 |
C |
T |
4: 34,683,322 (GRCm39) |
V53M |
probably benign |
Het |
Slc35f3 |
A |
T |
8: 127,115,872 (GRCm39) |
L266F |
probably damaging |
Het |
Slc45a2 |
C |
T |
15: 11,027,871 (GRCm39) |
T480I |
probably damaging |
Het |
Ticrr |
T |
A |
7: 79,344,471 (GRCm39) |
S1445R |
probably benign |
Het |
Ttc23l |
T |
C |
15: 10,515,236 (GRCm39) |
N381D |
probably damaging |
Het |
Usp17ld |
T |
A |
7: 102,899,781 (GRCm39) |
K384* |
probably null |
Het |
Vmn1r20 |
T |
A |
6: 57,409,050 (GRCm39) |
Y125* |
probably null |
Het |
Zfp738 |
G |
T |
13: 67,817,805 (GRCm39) |
Q729K |
probably benign |
Het |
Zfp770 |
T |
A |
2: 114,027,674 (GRCm39) |
M132L |
probably benign |
Het |
|
Other mutations in Or7e166 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01510:Or7e166
|
APN |
9 |
19,624,575 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01919:Or7e166
|
APN |
9 |
19,624,638 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02157:Or7e166
|
APN |
9 |
19,624,585 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02550:Or7e166
|
APN |
9 |
19,624,343 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03329:Or7e166
|
APN |
9 |
19,624,597 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02799:Or7e166
|
UTSW |
9 |
19,624,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R0356:Or7e166
|
UTSW |
9 |
19,624,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Or7e166
|
UTSW |
9 |
19,624,945 (GRCm39) |
missense |
probably benign |
0.39 |
R1161:Or7e166
|
UTSW |
9 |
19,624,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Or7e166
|
UTSW |
9 |
19,624,386 (GRCm39) |
missense |
probably benign |
0.01 |
R5191:Or7e166
|
UTSW |
9 |
19,624,630 (GRCm39) |
missense |
probably damaging |
0.98 |
R5216:Or7e166
|
UTSW |
9 |
19,624,585 (GRCm39) |
missense |
probably benign |
0.07 |
R5342:Or7e166
|
UTSW |
9 |
19,624,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R5506:Or7e166
|
UTSW |
9 |
19,624,570 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5526:Or7e166
|
UTSW |
9 |
19,624,994 (GRCm39) |
nonsense |
probably null |
|
R5594:Or7e166
|
UTSW |
9 |
19,624,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R5928:Or7e166
|
UTSW |
9 |
19,625,049 (GRCm39) |
missense |
probably benign |
0.02 |
R6569:Or7e166
|
UTSW |
9 |
19,624,638 (GRCm39) |
missense |
probably benign |
0.00 |
R6858:Or7e166
|
UTSW |
9 |
19,624,765 (GRCm39) |
missense |
probably damaging |
0.98 |
R7077:Or7e166
|
UTSW |
9 |
19,624,428 (GRCm39) |
missense |
probably benign |
|
R7378:Or7e166
|
UTSW |
9 |
19,624,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Or7e166
|
UTSW |
9 |
19,624,767 (GRCm39) |
missense |
probably benign |
|
R8038:Or7e166
|
UTSW |
9 |
19,624,976 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8160:Or7e166
|
UTSW |
9 |
19,624,085 (GRCm39) |
intron |
probably benign |
|
R8223:Or7e166
|
UTSW |
9 |
19,624,705 (GRCm39) |
missense |
probably benign |
|
R8400:Or7e166
|
UTSW |
9 |
19,624,389 (GRCm39) |
missense |
probably benign |
0.45 |
R8780:Or7e166
|
UTSW |
9 |
19,624,653 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8946:Or7e166
|
UTSW |
9 |
19,624,885 (GRCm39) |
missense |
probably damaging |
0.99 |
R9164:Or7e166
|
UTSW |
9 |
19,624,954 (GRCm39) |
missense |
probably benign |
0.25 |
R9475:Or7e166
|
UTSW |
9 |
19,624,939 (GRCm39) |
missense |
probably benign |
0.01 |
|