Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
T |
A |
12: 118,849,911 (GRCm39) |
M951L |
probably benign |
Het |
Als2 |
T |
C |
1: 59,225,163 (GRCm39) |
|
probably benign |
Het |
Arhgap26 |
T |
C |
18: 39,244,856 (GRCm39) |
V167A |
probably damaging |
Het |
Bbs1 |
A |
G |
19: 4,952,867 (GRCm39) |
|
probably benign |
Het |
Capn11 |
A |
T |
17: 45,949,806 (GRCm39) |
|
probably benign |
Het |
Cenpl |
G |
T |
1: 160,910,857 (GRCm39) |
S268I |
possibly damaging |
Het |
Coq8b |
T |
C |
7: 26,939,282 (GRCm39) |
V144A |
possibly damaging |
Het |
Exo1 |
T |
A |
1: 175,728,963 (GRCm39) |
C10S |
possibly damaging |
Het |
Fam193b |
A |
T |
13: 55,691,266 (GRCm39) |
S203T |
probably damaging |
Het |
Ggact |
T |
C |
14: 123,129,167 (GRCm39) |
N16S |
probably damaging |
Het |
Gm3940 |
A |
T |
1: 52,129,882 (GRCm39) |
|
probably benign |
Het |
Gm5458 |
G |
T |
14: 19,649,760 (GRCm39) |
L155I |
probably damaging |
Het |
Golm1 |
T |
C |
13: 59,797,470 (GRCm39) |
K125R |
probably damaging |
Het |
Gpatch4 |
A |
G |
3: 87,962,312 (GRCm39) |
E175G |
probably damaging |
Het |
Gria1 |
A |
G |
11: 57,127,801 (GRCm39) |
N337D |
probably damaging |
Het |
Gripap1 |
G |
A |
X: 7,678,705 (GRCm39) |
G464D |
probably benign |
Het |
Grk1 |
A |
G |
8: 13,455,404 (GRCm39) |
D96G |
possibly damaging |
Het |
Hsf1 |
T |
C |
15: 76,382,403 (GRCm39) |
V258A |
probably benign |
Het |
Ighv7-4 |
A |
G |
12: 114,186,653 (GRCm39) |
S40P |
probably damaging |
Het |
Igkv4-50 |
G |
A |
6: 69,677,921 (GRCm39) |
S61L |
probably benign |
Het |
Igkv4-62 |
C |
T |
6: 69,377,035 (GRCm39) |
G38E |
probably damaging |
Het |
Ints1 |
T |
C |
5: 139,757,437 (GRCm39) |
D358G |
probably damaging |
Het |
Madd |
A |
G |
2: 90,984,888 (GRCm39) |
|
probably benign |
Het |
Map3k6 |
A |
G |
4: 132,974,439 (GRCm39) |
S580G |
probably damaging |
Het |
Myef2 |
A |
G |
2: 124,940,402 (GRCm39) |
M383T |
probably damaging |
Het |
Myo3b |
T |
C |
2: 70,119,730 (GRCm39) |
L930P |
probably damaging |
Het |
Ndufaf3 |
C |
T |
9: 108,444,068 (GRCm39) |
R20Q |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,640,248 (GRCm39) |
S328P |
probably damaging |
Het |
Or4k15b |
T |
A |
14: 50,272,507 (GRCm39) |
M118L |
probably benign |
Het |
Pdpr |
T |
C |
8: 111,839,342 (GRCm39) |
I155T |
possibly damaging |
Het |
Phf11b |
A |
T |
14: 59,560,631 (GRCm39) |
I216K |
probably benign |
Het |
Phkg1 |
T |
C |
5: 129,893,813 (GRCm39) |
|
probably null |
Het |
Pik3r6 |
A |
G |
11: 68,422,276 (GRCm39) |
Y225C |
probably benign |
Het |
Plekhh2 |
A |
T |
17: 84,914,356 (GRCm39) |
D1253V |
possibly damaging |
Het |
Plppr3 |
T |
C |
10: 79,702,757 (GRCm39) |
T155A |
probably damaging |
Het |
Ppp6r2 |
T |
C |
15: 89,166,192 (GRCm39) |
F732S |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,799,627 (GRCm39) |
|
probably benign |
Het |
Slc16a8 |
T |
G |
15: 79,135,432 (GRCm39) |
S459R |
probably damaging |
Het |
Slc25a12 |
A |
T |
2: 71,123,696 (GRCm39) |
|
probably benign |
Het |
Slc38a2 |
T |
C |
15: 96,591,066 (GRCm39) |
|
probably benign |
Het |
Slit1 |
C |
A |
19: 41,594,824 (GRCm39) |
W1182L |
possibly damaging |
Het |
Snx2 |
C |
T |
18: 53,327,495 (GRCm39) |
|
probably benign |
Het |
Sos1 |
A |
T |
17: 80,752,929 (GRCm39) |
V335D |
probably damaging |
Het |
St18 |
A |
G |
1: 6,872,856 (GRCm39) |
D197G |
probably damaging |
Het |
Ston2 |
G |
T |
12: 91,615,522 (GRCm39) |
N295K |
possibly damaging |
Het |
Stpg3 |
A |
G |
2: 25,103,191 (GRCm39) |
|
probably benign |
Het |
Tmem63a |
A |
G |
1: 180,799,654 (GRCm39) |
I675V |
probably damaging |
Het |
Vmn2r16 |
T |
A |
5: 109,488,294 (GRCm39) |
L389Q |
probably damaging |
Het |
Vps13d |
C |
A |
4: 144,699,320 (GRCm39) |
|
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,681,934 (GRCm39) |
D3012E |
probably damaging |
Het |
|
Other mutations in Or1r1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01084:Or1r1
|
APN |
11 |
73,875,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Or1r1
|
UTSW |
11 |
73,874,538 (GRCm39) |
missense |
probably benign |
|
R0242:Or1r1
|
UTSW |
11 |
73,874,538 (GRCm39) |
missense |
probably benign |
|
R0647:Or1r1
|
UTSW |
11 |
73,874,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R0906:Or1r1
|
UTSW |
11 |
73,874,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R1581:Or1r1
|
UTSW |
11 |
73,875,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Or1r1
|
UTSW |
11 |
73,874,673 (GRCm39) |
missense |
probably benign |
0.34 |
R1832:Or1r1
|
UTSW |
11 |
73,875,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R1879:Or1r1
|
UTSW |
11 |
73,875,368 (GRCm39) |
missense |
probably benign |
0.00 |
R2138:Or1r1
|
UTSW |
11 |
73,875,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R2988:Or1r1
|
UTSW |
11 |
73,874,627 (GRCm39) |
missense |
probably benign |
0.13 |
R4557:Or1r1
|
UTSW |
11 |
73,875,425 (GRCm39) |
missense |
probably benign |
0.25 |
R4606:Or1r1
|
UTSW |
11 |
73,874,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Or1r1
|
UTSW |
11 |
73,875,221 (GRCm39) |
missense |
probably benign |
0.01 |
R4783:Or1r1
|
UTSW |
11 |
73,874,834 (GRCm39) |
missense |
probably damaging |
0.97 |
R5047:Or1r1
|
UTSW |
11 |
73,875,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Or1r1
|
UTSW |
11 |
73,875,362 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6379:Or1r1
|
UTSW |
11 |
73,875,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Or1r1
|
UTSW |
11 |
73,875,121 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7254:Or1r1
|
UTSW |
11 |
73,874,603 (GRCm39) |
missense |
probably benign |
0.40 |
R7324:Or1r1
|
UTSW |
11 |
73,874,669 (GRCm39) |
missense |
probably benign |
0.06 |
R7444:Or1r1
|
UTSW |
11 |
73,874,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Or1r1
|
UTSW |
11 |
73,875,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R8540:Or1r1
|
UTSW |
11 |
73,875,153 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Or1r1
|
UTSW |
11 |
73,875,120 (GRCm39) |
missense |
probably benign |
0.01 |
|