Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts17 |
A |
G |
7: 66,725,064 (GRCm39) |
H795R |
probably damaging |
Het |
Adgrl2 |
A |
T |
3: 148,565,016 (GRCm39) |
I188K |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,431,507 (GRCm39) |
Y5974H |
probably damaging |
Het |
Angpt4 |
A |
G |
2: 151,778,623 (GRCm39) |
T336A |
probably damaging |
Het |
Arhgap30 |
C |
A |
1: 171,236,662 (GRCm39) |
T1012N |
probably damaging |
Het |
Asl |
A |
T |
5: 130,040,908 (GRCm39) |
Y178N |
probably damaging |
Het |
Brd1 |
C |
A |
15: 88,591,454 (GRCm39) |
L714F |
possibly damaging |
Het |
Ccdc47 |
A |
G |
11: 106,095,788 (GRCm39) |
S303P |
probably damaging |
Het |
Cdcp3 |
T |
A |
7: 130,848,420 (GRCm39) |
I858N |
probably damaging |
Het |
Cdk16 |
A |
G |
X: 20,561,998 (GRCm39) |
K264E |
probably damaging |
Het |
Cenpc1 |
A |
T |
5: 86,164,181 (GRCm39) |
F813L |
probably damaging |
Het |
Cfp |
A |
C |
X: 20,794,248 (GRCm39) |
F291C |
possibly damaging |
Het |
Chordc1 |
T |
G |
9: 18,223,762 (GRCm39) |
F276V |
probably damaging |
Het |
Clic4 |
C |
T |
4: 134,945,889 (GRCm39) |
R176H |
possibly damaging |
Het |
Fcer1a |
T |
G |
1: 173,053,040 (GRCm39) |
N52T |
possibly damaging |
Het |
Fndc7 |
A |
T |
3: 108,774,624 (GRCm39) |
C545S |
probably damaging |
Het |
Frem2 |
T |
C |
3: 53,559,674 (GRCm39) |
D1611G |
probably damaging |
Het |
Fryl |
G |
A |
5: 73,234,038 (GRCm39) |
P1496S |
probably benign |
Het |
Gga3 |
A |
T |
11: 115,483,312 (GRCm39) |
N82K |
probably damaging |
Het |
Gm43638 |
G |
A |
5: 87,608,484 (GRCm39) |
P452S |
possibly damaging |
Het |
Gpn1 |
T |
C |
5: 31,662,309 (GRCm39) |
S244P |
probably damaging |
Het |
Hspa12a |
T |
C |
19: 58,787,828 (GRCm39) |
S665G |
probably benign |
Het |
Htt |
A |
G |
5: 34,983,385 (GRCm39) |
I995V |
probably benign |
Het |
Iars1 |
A |
T |
13: 49,878,223 (GRCm39) |
I916L |
probably benign |
Het |
Ice1 |
C |
A |
13: 70,751,048 (GRCm39) |
L1679F |
probably damaging |
Het |
Inpp1 |
A |
T |
1: 52,838,486 (GRCm39) |
D54E |
probably damaging |
Het |
Irf2bpl |
T |
C |
12: 86,929,713 (GRCm39) |
E320G |
possibly damaging |
Het |
Itprid1 |
T |
G |
6: 55,945,569 (GRCm39) |
D763E |
probably damaging |
Het |
Kcnn2 |
T |
C |
18: 45,810,026 (GRCm39) |
V421A |
probably damaging |
Het |
Micu2 |
A |
G |
14: 58,154,768 (GRCm39) |
V419A |
probably benign |
Het |
Nek9 |
C |
T |
12: 85,350,383 (GRCm39) |
C897Y |
probably damaging |
Het |
Ofcc1 |
A |
C |
13: 40,226,140 (GRCm39) |
H797Q |
probably benign |
Het |
Or2y16 |
C |
A |
11: 49,335,070 (GRCm39) |
H131N |
probably damaging |
Het |
Or5m12 |
T |
C |
2: 85,735,285 (GRCm39) |
T38A |
probably benign |
Het |
Or6c69c |
T |
G |
10: 129,911,125 (GRCm39) |
L282R |
probably damaging |
Het |
Pakap |
C |
T |
4: 57,688,502 (GRCm39) |
T115M |
probably damaging |
Het |
Papss1 |
G |
A |
3: 131,288,950 (GRCm39) |
G151S |
probably benign |
Het |
Plxnb1 |
A |
G |
9: 108,943,780 (GRCm39) |
T1956A |
probably damaging |
Het |
Pomt1 |
A |
G |
2: 32,143,724 (GRCm39) |
|
probably benign |
Het |
Ppfibp2 |
T |
A |
7: 107,337,126 (GRCm39) |
Y570* |
probably null |
Het |
Ppp1r9a |
A |
G |
6: 5,046,015 (GRCm39) |
E493G |
probably damaging |
Het |
Ptk2b |
A |
G |
14: 66,406,870 (GRCm39) |
F621L |
probably benign |
Het |
Ptpn13 |
G |
T |
5: 103,702,816 (GRCm39) |
D1261Y |
possibly damaging |
Het |
Ptprd |
C |
T |
4: 75,977,966 (GRCm39) |
G181D |
probably damaging |
Het |
Rabgap1l |
T |
C |
1: 160,270,853 (GRCm39) |
T645A |
probably benign |
Het |
Slc2a7 |
T |
C |
4: 150,252,797 (GRCm39) |
I479T |
probably damaging |
Het |
Smc3 |
A |
G |
19: 53,602,273 (GRCm39) |
N40S |
probably damaging |
Het |
Spata31 |
A |
T |
13: 65,067,587 (GRCm39) |
D83V |
probably benign |
Het |
Sptb |
C |
T |
12: 76,630,330 (GRCm39) |
|
probably benign |
Het |
Ssc4d |
A |
T |
5: 135,990,028 (GRCm39) |
C493* |
probably null |
Het |
Styxl2 |
T |
C |
1: 165,927,017 (GRCm39) |
D865G |
probably benign |
Het |
Ubr2 |
C |
A |
17: 47,262,844 (GRCm39) |
V1256L |
probably benign |
Het |
Ubr3 |
T |
C |
2: 69,803,490 (GRCm39) |
|
probably benign |
Het |
Vmn2r105 |
C |
T |
17: 20,446,631 (GRCm39) |
W456* |
probably null |
Het |
Vmn2r24 |
T |
A |
6: 123,793,070 (GRCm39) |
I799N |
probably damaging |
Het |
Vps13b |
G |
A |
15: 35,917,316 (GRCm39) |
G3720D |
possibly damaging |
Het |
|
Other mutations in Or12d17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01813:Or12d17
|
APN |
17 |
37,777,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02039:Or12d17
|
APN |
17 |
37,777,340 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02391:Or12d17
|
APN |
17 |
37,777,477 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02730:Or12d17
|
APN |
17 |
37,777,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02751:Or12d17
|
APN |
17 |
37,777,306 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02891:Or12d17
|
APN |
17 |
37,777,835 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03023:Or12d17
|
APN |
17 |
37,777,885 (GRCm39) |
missense |
probably benign |
|
R0026:Or12d17
|
UTSW |
17 |
37,777,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R0579:Or12d17
|
UTSW |
17 |
37,777,238 (GRCm39) |
missense |
probably benign |
0.01 |
R1751:Or12d17
|
UTSW |
17 |
37,777,792 (GRCm39) |
missense |
probably benign |
0.00 |
R1848:Or12d17
|
UTSW |
17 |
37,777,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R2392:Or12d17
|
UTSW |
17 |
37,777,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R4249:Or12d17
|
UTSW |
17 |
37,777,715 (GRCm39) |
missense |
probably damaging |
0.98 |
R4464:Or12d17
|
UTSW |
17 |
37,777,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Or12d17
|
UTSW |
17 |
37,777,714 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4947:Or12d17
|
UTSW |
17 |
37,777,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R5107:Or12d17
|
UTSW |
17 |
37,777,144 (GRCm39) |
missense |
probably damaging |
0.97 |
R5526:Or12d17
|
UTSW |
17 |
37,778,003 (GRCm39) |
missense |
unknown |
|
R6147:Or12d17
|
UTSW |
17 |
37,777,430 (GRCm39) |
missense |
probably benign |
0.00 |
R6416:Or12d17
|
UTSW |
17 |
37,777,971 (GRCm39) |
nonsense |
probably null |
|
R7450:Or12d17
|
UTSW |
17 |
37,777,507 (GRCm39) |
missense |
probably benign |
0.00 |
R7487:Or12d17
|
UTSW |
17 |
37,777,457 (GRCm39) |
missense |
probably damaging |
0.96 |
R7822:Or12d17
|
UTSW |
17 |
37,777,994 (GRCm39) |
missense |
probably benign |
0.00 |
R8041:Or12d17
|
UTSW |
17 |
37,777,540 (GRCm39) |
missense |
probably benign |
|
R8051:Or12d17
|
UTSW |
17 |
37,777,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R9013:Or12d17
|
UTSW |
17 |
37,777,441 (GRCm39) |
missense |
probably benign |
0.13 |
X0063:Or12d17
|
UTSW |
17 |
37,777,415 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Or12d17
|
UTSW |
17 |
37,777,209 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or12d17
|
UTSW |
17 |
37,777,552 (GRCm39) |
missense |
possibly damaging |
0.93 |
|