Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy4 |
C |
A |
14: 56,019,403 (GRCm39) |
E82D |
probably damaging |
Het |
Ago1 |
G |
A |
4: 126,333,732 (GRCm39) |
R486* |
probably null |
Het |
Ago2 |
T |
A |
15: 72,996,091 (GRCm39) |
N346I |
possibly damaging |
Het |
Apol11a |
A |
T |
15: 77,401,395 (GRCm39) |
D294V |
probably benign |
Het |
Atp13a5 |
A |
G |
16: 29,116,215 (GRCm39) |
F634L |
possibly damaging |
Het |
Atp2a2 |
G |
A |
5: 122,595,576 (GRCm39) |
P953L |
probably damaging |
Het |
Brca2 |
A |
G |
5: 150,463,137 (GRCm39) |
D967G |
probably benign |
Het |
Bud13 |
A |
T |
9: 46,199,446 (GRCm39) |
H269L |
probably benign |
Het |
Cachd1 |
A |
T |
4: 100,838,079 (GRCm39) |
|
probably null |
Het |
Cog3 |
T |
C |
14: 75,979,182 (GRCm39) |
D188G |
probably benign |
Het |
Col15a1 |
T |
C |
4: 47,208,492 (GRCm39) |
S20P |
probably damaging |
Het |
Col4a3 |
A |
G |
1: 82,658,431 (GRCm39) |
D838G |
unknown |
Het |
Cwh43 |
A |
T |
5: 73,578,886 (GRCm39) |
T298S |
probably benign |
Het |
Dip2c |
A |
G |
13: 9,659,041 (GRCm39) |
R847G |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,407,470 (GRCm39) |
D438N |
probably damaging |
Het |
Drg2 |
T |
C |
11: 60,358,954 (GRCm39) |
V358A |
probably damaging |
Het |
Eif4enif1 |
T |
A |
11: 3,171,168 (GRCm39) |
W220R |
probably damaging |
Het |
Enpp2 |
A |
T |
15: 54,783,090 (GRCm39) |
I75K |
probably damaging |
Het |
Fam110c |
T |
C |
12: 31,125,238 (GRCm39) |
I400T |
probably damaging |
Het |
Fam193b |
C |
A |
13: 55,690,629 (GRCm39) |
R711L |
probably damaging |
Het |
Fgfr1 |
T |
C |
8: 26,053,462 (GRCm39) |
Y246H |
probably damaging |
Het |
Frs3 |
G |
A |
17: 48,013,997 (GRCm39) |
R230Q |
probably benign |
Het |
Galnt5 |
A |
G |
2: 57,889,425 (GRCm39) |
K342E |
probably benign |
Het |
Glrb |
A |
T |
3: 80,769,054 (GRCm39) |
L189Q |
probably damaging |
Het |
Gmeb2 |
T |
C |
2: 180,900,819 (GRCm39) |
T193A |
probably benign |
Het |
Gnl3 |
A |
G |
14: 30,736,120 (GRCm39) |
S307P |
probably damaging |
Het |
Golim4 |
A |
T |
3: 75,800,166 (GRCm39) |
F443I |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Klf10 |
A |
C |
15: 38,297,357 (GRCm39) |
Y228D |
probably benign |
Het |
Klrc3 |
A |
T |
6: 129,616,520 (GRCm39) |
W166R |
probably damaging |
Het |
Kng2 |
A |
T |
16: 22,807,065 (GRCm39) |
I378N |
probably benign |
Het |
Map3k10 |
T |
C |
7: 27,362,688 (GRCm39) |
K466R |
possibly damaging |
Het |
Mrrf |
C |
T |
2: 36,079,109 (GRCm39) |
T245M |
probably benign |
Het |
Msi1 |
A |
G |
5: 115,583,517 (GRCm39) |
Y239C |
probably damaging |
Het |
Nfasc |
A |
G |
1: 132,525,501 (GRCm39) |
|
probably null |
Het |
Or1x6 |
T |
A |
11: 50,939,300 (GRCm39) |
L122Q |
probably damaging |
Het |
P3r3urf |
A |
G |
4: 116,030,791 (GRCm39) |
D65G |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,908,900 (GRCm39) |
E368G |
unknown |
Het |
Polq |
G |
A |
16: 36,909,687 (GRCm39) |
G2078D |
probably damaging |
Het |
Ppfibp1 |
A |
C |
6: 146,893,942 (GRCm39) |
I134L |
probably damaging |
Het |
Rasip1 |
A |
T |
7: 45,284,247 (GRCm39) |
I608F |
probably damaging |
Het |
Ripk3 |
A |
T |
14: 56,025,492 (GRCm39) |
V24E |
probably damaging |
Het |
Rtkn |
T |
A |
6: 83,124,526 (GRCm39) |
I110N |
probably damaging |
Het |
Scn1a |
C |
T |
2: 66,104,176 (GRCm39) |
V1695I |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,606,042 (GRCm39) |
N75S |
possibly damaging |
Het |
Snu13 |
C |
A |
15: 81,928,182 (GRCm39) |
A14S |
probably benign |
Het |
Snx27 |
A |
C |
3: 94,438,541 (GRCm39) |
D231E |
probably damaging |
Het |
Spef2 |
A |
G |
15: 9,725,283 (GRCm39) |
I158T |
possibly damaging |
Het |
Sptb |
A |
G |
12: 76,696,643 (GRCm39) |
I19T |
possibly damaging |
Het |
Ssu72 |
T |
C |
4: 155,817,970 (GRCm39) |
L175P |
probably damaging |
Het |
Tcstv2a |
T |
A |
13: 120,725,475 (GRCm39) |
C46* |
probably null |
Het |
Tecr |
C |
T |
8: 84,299,204 (GRCm39) |
V248I |
probably benign |
Het |
Tnfrsf13b |
T |
G |
11: 61,032,302 (GRCm39) |
S59A |
probably benign |
Het |
Tom1l1 |
T |
C |
11: 90,561,951 (GRCm39) |
T150A |
possibly damaging |
Het |
Ubr3 |
A |
T |
2: 69,766,362 (GRCm39) |
Y410F |
probably damaging |
Het |
Vmn2r108 |
A |
G |
17: 20,692,577 (GRCm39) |
I93T |
probably damaging |
Het |
Vmn2r19 |
A |
G |
6: 123,306,937 (GRCm39) |
T482A |
probably benign |
Het |
Vstm4 |
T |
A |
14: 32,585,664 (GRCm39) |
M77K |
probably benign |
Het |
Zbtb17 |
C |
T |
4: 141,191,896 (GRCm39) |
T309I |
probably damaging |
Het |
Zfp957 |
T |
C |
14: 79,451,494 (GRCm39) |
T102A |
probably damaging |
Het |
|
Other mutations in Or7g25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02104:Or7g25
|
APN |
9 |
19,160,166 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02338:Or7g25
|
APN |
9 |
19,159,960 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03197:Or7g25
|
APN |
9 |
19,160,098 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03227:Or7g25
|
APN |
9 |
19,160,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03046:Or7g25
|
UTSW |
9 |
19,160,441 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03052:Or7g25
|
UTSW |
9 |
19,159,938 (GRCm39) |
nonsense |
probably null |
|
R0423:Or7g25
|
UTSW |
9 |
19,160,248 (GRCm39) |
nonsense |
probably null |
|
R1316:Or7g25
|
UTSW |
9 |
19,160,035 (GRCm39) |
missense |
probably benign |
0.06 |
R1759:Or7g25
|
UTSW |
9 |
19,160,384 (GRCm39) |
missense |
probably benign |
0.36 |
R1782:Or7g25
|
UTSW |
9 |
19,159,877 (GRCm39) |
missense |
probably benign |
0.04 |
R3196:Or7g25
|
UTSW |
9 |
19,160,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R3742:Or7g25
|
UTSW |
9 |
19,159,979 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4191:Or7g25
|
UTSW |
9 |
19,160,383 (GRCm39) |
missense |
probably benign |
0.05 |
R4320:Or7g25
|
UTSW |
9 |
19,160,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4523:Or7g25
|
UTSW |
9 |
19,160,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R4756:Or7g25
|
UTSW |
9 |
19,160,153 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4908:Or7g25
|
UTSW |
9 |
19,160,149 (GRCm39) |
missense |
probably benign |
0.00 |
R5319:Or7g25
|
UTSW |
9 |
19,160,329 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5554:Or7g25
|
UTSW |
9 |
19,160,039 (GRCm39) |
missense |
probably benign |
0.02 |
R6011:Or7g25
|
UTSW |
9 |
19,159,807 (GRCm39) |
missense |
probably damaging |
0.98 |
R7330:Or7g25
|
UTSW |
9 |
19,160,567 (GRCm39) |
missense |
probably benign |
0.01 |
R7862:Or7g25
|
UTSW |
9 |
19,160,736 (GRCm39) |
start gained |
probably benign |
|
R9544:Or7g25
|
UTSW |
9 |
19,160,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|