Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
A |
T |
6: 124,324,778 (GRCm39) |
L81H |
probably damaging |
Het |
Abca8b |
A |
G |
11: 109,868,667 (GRCm39) |
C166R |
probably damaging |
Het |
Adgrv1 |
T |
A |
13: 81,671,868 (GRCm39) |
E2242D |
probably damaging |
Het |
Agap1 |
T |
C |
1: 89,694,045 (GRCm39) |
S448P |
probably benign |
Het |
Aldh1a2 |
T |
C |
9: 71,160,334 (GRCm39) |
L120P |
probably damaging |
Het |
Alkbh2 |
T |
C |
5: 114,262,115 (GRCm39) |
N205S |
probably benign |
Het |
Anapc1 |
C |
A |
2: 128,511,608 (GRCm39) |
G493C |
possibly damaging |
Het |
Aox3 |
A |
T |
1: 58,192,220 (GRCm39) |
I497F |
possibly damaging |
Het |
Atp2b1 |
T |
C |
10: 98,850,354 (GRCm39) |
S826P |
possibly damaging |
Het |
Atp8b4 |
T |
A |
2: 126,164,928 (GRCm39) |
R1129S |
probably damaging |
Het |
Bche |
T |
A |
3: 73,609,159 (GRCm39) |
Q89L |
probably benign |
Het |
Bche |
G |
T |
3: 73,609,160 (GRCm39) |
Q89K |
probably benign |
Het |
Bcl9 |
T |
C |
3: 97,121,050 (GRCm39) |
K171E |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,538,998 (GRCm39) |
Y1488N |
probably damaging |
Het |
Dock8 |
A |
G |
19: 25,098,545 (GRCm39) |
N623S |
probably null |
Het |
Dok6 |
T |
C |
18: 89,578,234 (GRCm39) |
E61G |
probably damaging |
Het |
Duxf4 |
T |
A |
10: 58,071,785 (GRCm39) |
Q143L |
possibly damaging |
Het |
Esf1 |
A |
T |
2: 139,990,806 (GRCm39) |
D559E |
possibly damaging |
Het |
F11r |
A |
G |
1: 171,289,438 (GRCm39) |
I254V |
probably benign |
Het |
Fkrp |
A |
G |
7: 16,545,802 (GRCm39) |
V20A |
probably benign |
Het |
Fscb |
T |
C |
12: 64,521,457 (GRCm39) |
E3G |
unknown |
Het |
Hdlbp |
A |
G |
1: 93,358,840 (GRCm39) |
I237T |
probably damaging |
Het |
Hfm1 |
A |
T |
5: 107,046,442 (GRCm39) |
D481E |
probably damaging |
Het |
Hspa4l |
T |
C |
3: 40,714,833 (GRCm39) |
V156A |
probably damaging |
Het |
Igfn1 |
A |
G |
1: 135,889,782 (GRCm39) |
S2422P |
probably benign |
Het |
Il23r |
T |
A |
6: 67,467,652 (GRCm39) |
|
probably null |
Het |
Il24 |
G |
A |
1: 130,810,268 (GRCm39) |
T196I |
probably benign |
Het |
Isg15 |
T |
C |
4: 156,284,250 (GRCm39) |
I93V |
probably benign |
Het |
Kcna6 |
T |
C |
6: 126,715,473 (GRCm39) |
E472G |
probably benign |
Het |
Kif21b |
G |
A |
1: 136,075,284 (GRCm39) |
D166N |
probably damaging |
Het |
Lilrb4b |
A |
T |
10: 51,357,831 (GRCm39) |
Q80L |
possibly damaging |
Het |
Lrrc69 |
T |
C |
4: 14,708,669 (GRCm39) |
E225G |
possibly damaging |
Het |
Marchf6 |
A |
T |
15: 31,469,792 (GRCm39) |
L726Q |
probably damaging |
Het |
Megf6 |
G |
T |
4: 154,352,124 (GRCm39) |
G1210C |
probably damaging |
Het |
Msh2 |
C |
T |
17: 88,026,724 (GRCm39) |
T740I |
probably damaging |
Het |
Myh14 |
T |
C |
7: 44,288,446 (GRCm39) |
Y514C |
probably damaging |
Het |
Myorg |
C |
A |
4: 41,497,501 (GRCm39) |
A710S |
possibly damaging |
Het |
Nedd1 |
T |
C |
10: 92,550,022 (GRCm39) |
T88A |
possibly damaging |
Het |
Nfkb1 |
G |
A |
3: 135,321,110 (GRCm39) |
T215I |
possibly damaging |
Het |
Obox1 |
A |
T |
7: 15,289,135 (GRCm39) |
I17L |
probably benign |
Het |
Palb2 |
A |
C |
7: 121,726,303 (GRCm39) |
H522Q |
probably damaging |
Het |
Pde4c |
C |
T |
8: 71,177,191 (GRCm39) |
T6M |
probably damaging |
Het |
Plekhg1 |
A |
G |
10: 3,908,181 (GRCm39) |
K97E |
probably damaging |
Het |
Plod3 |
A |
G |
5: 137,019,707 (GRCm39) |
|
probably null |
Het |
Plppr3 |
A |
T |
10: 79,703,294 (GRCm39) |
Y63* |
probably null |
Het |
Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Het |
Qrich1 |
T |
C |
9: 108,411,246 (GRCm39) |
V257A |
probably damaging |
Het |
Rpl14 |
A |
G |
9: 120,401,253 (GRCm39) |
D32G |
possibly damaging |
Het |
Senp8 |
A |
G |
9: 59,644,721 (GRCm39) |
V132A |
possibly damaging |
Het |
Serac1 |
A |
G |
17: 6,095,964 (GRCm39) |
|
probably null |
Het |
Sh2d3c |
T |
A |
2: 32,639,256 (GRCm39) |
C295* |
probably null |
Het |
Stab1 |
A |
G |
14: 30,872,605 (GRCm39) |
F1142L |
probably benign |
Het |
Stam2 |
T |
C |
2: 52,599,638 (GRCm39) |
T257A |
possibly damaging |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tg |
A |
G |
15: 66,554,691 (GRCm39) |
E702G |
probably benign |
Het |
Tgif2lx2 |
A |
T |
X: 117,337,690 (GRCm39) |
K218* |
probably null |
Het |
Tpp1 |
C |
A |
7: 105,400,905 (GRCm39) |
V41L |
probably benign |
Het |
Tulp3 |
A |
T |
6: 128,303,769 (GRCm39) |
S277T |
probably benign |
Het |
Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
Zfp683 |
T |
C |
4: 133,784,766 (GRCm39) |
F338L |
probably damaging |
Het |
|
Other mutations in Or11g24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01719:Or11g24
|
APN |
14 |
50,662,018 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02430:Or11g24
|
APN |
14 |
50,662,608 (GRCm39) |
missense |
probably benign |
|
IGL02603:Or11g24
|
APN |
14 |
50,662,657 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02959:Or11g24
|
APN |
14 |
50,662,389 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03154:Or11g24
|
APN |
14 |
50,662,080 (GRCm39) |
missense |
probably benign |
0.00 |
R0455:Or11g24
|
UTSW |
14 |
50,662,359 (GRCm39) |
missense |
possibly damaging |
0.45 |
R3160:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3161:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3162:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R4821:Or11g24
|
UTSW |
14 |
50,662,206 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4880:Or11g24
|
UTSW |
14 |
50,662,758 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5047:Or11g24
|
UTSW |
14 |
50,662,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5385:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5386:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5640:Or11g24
|
UTSW |
14 |
50,662,111 (GRCm39) |
missense |
probably benign |
0.18 |
R5809:Or11g24
|
UTSW |
14 |
50,662,905 (GRCm39) |
makesense |
probably null |
|
R6035:Or11g24
|
UTSW |
14 |
50,661,984 (GRCm39) |
missense |
probably benign |
|
R6035:Or11g24
|
UTSW |
14 |
50,661,984 (GRCm39) |
missense |
probably benign |
|
R6229:Or11g24
|
UTSW |
14 |
50,662,662 (GRCm39) |
missense |
probably benign |
0.38 |
R6614:Or11g24
|
UTSW |
14 |
50,662,546 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Or11g24
|
UTSW |
14 |
50,662,722 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7443:Or11g24
|
UTSW |
14 |
50,662,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Or11g24
|
UTSW |
14 |
50,662,792 (GRCm39) |
missense |
probably benign |
|
R7700:Or11g24
|
UTSW |
14 |
50,662,792 (GRCm39) |
missense |
probably benign |
|
R7851:Or11g24
|
UTSW |
14 |
50,662,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R8397:Or11g24
|
UTSW |
14 |
50,662,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Or11g24
|
UTSW |
14 |
50,662,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Or11g24
|
UTSW |
14 |
50,662,255 (GRCm39) |
missense |
probably benign |
0.00 |
|