Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh1l2 |
G |
A |
10: 83,356,234 (GRCm39) |
T52I |
probably damaging |
Het |
Arhgef28 |
G |
A |
13: 98,114,952 (GRCm39) |
R633W |
probably damaging |
Het |
Atg9a |
T |
C |
1: 75,162,389 (GRCm39) |
N507S |
possibly damaging |
Het |
Bsn |
A |
G |
9: 107,991,193 (GRCm39) |
S1520P |
probably benign |
Het |
Cacul1 |
G |
T |
19: 60,568,837 (GRCm39) |
A107E |
probably damaging |
Het |
Cd74 |
A |
G |
18: 60,944,438 (GRCm39) |
D216G |
probably damaging |
Het |
Cdh16 |
A |
T |
8: 105,348,702 (GRCm39) |
W109R |
probably damaging |
Het |
Cdip1 |
C |
T |
16: 4,586,775 (GRCm39) |
V100I |
probably damaging |
Het |
Ceacam3 |
A |
G |
7: 16,897,071 (GRCm39) |
D679G |
probably damaging |
Het |
Comp |
A |
G |
8: 70,826,563 (GRCm39) |
D46G |
possibly damaging |
Het |
Dlx3 |
T |
C |
11: 95,011,430 (GRCm39) |
Y95H |
probably benign |
Het |
Dmrta2 |
T |
C |
4: 109,837,072 (GRCm39) |
S5P |
unknown |
Het |
E130308A19Rik |
A |
G |
4: 59,719,746 (GRCm39) |
Y426C |
probably damaging |
Het |
Entpd3 |
A |
G |
9: 120,383,225 (GRCm39) |
S87G |
probably benign |
Het |
Eps8l1 |
A |
G |
7: 4,473,888 (GRCm39) |
R232G |
probably damaging |
Het |
Gart |
A |
T |
16: 91,421,232 (GRCm39) |
V812D |
probably damaging |
Het |
Gm10153 |
C |
T |
7: 141,743,879 (GRCm39) |
C83Y |
unknown |
Het |
Gpd2 |
T |
C |
2: 57,245,487 (GRCm39) |
V394A |
probably damaging |
Het |
Hpcal1 |
A |
T |
12: 17,836,225 (GRCm39) |
E18D |
probably benign |
Het |
Mdga2 |
T |
C |
12: 66,844,530 (GRCm39) |
D156G |
probably benign |
Het |
Mks1 |
A |
G |
11: 87,753,595 (GRCm39) |
K510E |
probably benign |
Het |
Ms4a19 |
A |
G |
19: 11,118,902 (GRCm39) |
I69T |
probably benign |
Het |
Mtmr4 |
G |
A |
11: 87,503,051 (GRCm39) |
R1035Q |
probably damaging |
Het |
Myh6 |
T |
A |
14: 55,200,175 (GRCm39) |
K235* |
probably null |
Het |
Nedd1 |
A |
G |
10: 92,536,660 (GRCm39) |
F214S |
probably damaging |
Het |
Or1e32 |
A |
G |
11: 73,705,197 (GRCm39) |
V237A |
possibly damaging |
Het |
Or1o3 |
A |
G |
17: 37,573,733 (GRCm39) |
M274T |
probably benign |
Het |
Or52e15 |
A |
G |
7: 104,645,700 (GRCm39) |
I137T |
possibly damaging |
Het |
Pfkfb2 |
A |
C |
1: 130,625,626 (GRCm39) |
|
probably null |
Het |
Pfkfb4 |
T |
C |
9: 108,856,688 (GRCm39) |
L398P |
probably damaging |
Het |
Pfn3 |
T |
G |
13: 55,562,732 (GRCm39) |
D83A |
probably damaging |
Het |
Pi4ka |
C |
A |
16: 17,204,132 (GRCm39) |
W54L |
probably damaging |
Het |
Ppp3r1 |
A |
G |
11: 17,148,275 (GRCm39) |
D161G |
probably benign |
Het |
Prrc2a |
A |
G |
17: 35,372,230 (GRCm39) |
S1757P |
probably benign |
Het |
Samd7 |
A |
G |
3: 30,812,502 (GRCm39) |
E314G |
probably benign |
Het |
Slc17a4 |
A |
G |
13: 24,088,736 (GRCm39) |
I217T |
probably benign |
Het |
Slc22a1 |
A |
T |
17: 12,881,780 (GRCm39) |
|
probably null |
Het |
Slc7a7 |
C |
T |
14: 54,646,103 (GRCm39) |
R120H |
probably damaging |
Het |
Sos1 |
A |
T |
17: 80,721,104 (GRCm39) |
H905Q |
probably benign |
Het |
Thada |
G |
A |
17: 84,754,029 (GRCm39) |
T314I |
possibly damaging |
Het |
Tirap |
ACTGCTGCTGCTGCTGCTG |
ACTGCTGCTGCTGCTG |
9: 35,100,362 (GRCm39) |
|
probably benign |
Het |
Tlr11 |
A |
C |
14: 50,600,633 (GRCm39) |
H873P |
probably benign |
Het |
Tlr4 |
A |
T |
4: 66,757,611 (GRCm39) |
T135S |
possibly damaging |
Het |
Tmem116 |
T |
C |
5: 121,633,174 (GRCm39) |
S183P |
probably damaging |
Het |
Tubgcp3 |
A |
T |
8: 12,689,550 (GRCm39) |
I572K |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Ush2a |
C |
T |
1: 188,092,038 (GRCm39) |
T523I |
probably benign |
Het |
Usp40 |
G |
A |
1: 87,916,687 (GRCm39) |
Q364* |
probably null |
Het |
Vmn1r61 |
T |
C |
7: 5,614,242 (GRCm39) |
Q24R |
probably benign |
Het |
Wdfy4 |
C |
A |
14: 32,874,495 (GRCm39) |
|
probably null |
Het |
Zfp458 |
G |
A |
13: 67,405,573 (GRCm39) |
P286S |
probably damaging |
Het |
Zfp68 |
A |
T |
5: 138,605,091 (GRCm39) |
C373S |
probably benign |
Het |
Zfp768 |
T |
A |
7: 126,942,803 (GRCm39) |
I442F |
probably damaging |
Het |
Zfp990 |
A |
G |
4: 145,263,853 (GRCm39) |
R284G |
probably benign |
Het |
|
Other mutations in Or2l13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01559:Or2l13
|
APN |
16 |
19,306,209 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01639:Or2l13
|
APN |
16 |
19,305,914 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02105:Or2l13
|
APN |
16 |
19,306,011 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02352:Or2l13
|
APN |
16 |
19,305,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02359:Or2l13
|
APN |
16 |
19,305,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03053:Or2l13
|
APN |
16 |
19,305,969 (GRCm39) |
missense |
probably benign |
0.36 |
IGL03168:Or2l13
|
APN |
16 |
19,305,969 (GRCm39) |
missense |
probably benign |
0.36 |
R0576:Or2l13
|
UTSW |
16 |
19,305,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Or2l13
|
UTSW |
16 |
19,305,680 (GRCm39) |
missense |
probably benign |
0.00 |
R1335:Or2l13
|
UTSW |
16 |
19,305,803 (GRCm39) |
missense |
probably benign |
0.01 |
R1468:Or2l13
|
UTSW |
16 |
19,306,378 (GRCm39) |
missense |
probably benign |
0.15 |
R1468:Or2l13
|
UTSW |
16 |
19,306,378 (GRCm39) |
missense |
probably benign |
0.15 |
R2095:Or2l13
|
UTSW |
16 |
19,305,681 (GRCm39) |
missense |
probably benign |
|
R3123:Or2l13
|
UTSW |
16 |
19,305,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Or2l13
|
UTSW |
16 |
19,305,653 (GRCm39) |
missense |
probably benign |
|
R5093:Or2l13
|
UTSW |
16 |
19,306,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Or2l13
|
UTSW |
16 |
19,305,680 (GRCm39) |
missense |
probably benign |
|
R7149:Or2l13
|
UTSW |
16 |
19,306,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7305:Or2l13
|
UTSW |
16 |
19,306,449 (GRCm39) |
missense |
probably damaging |
0.98 |
R7484:Or2l13
|
UTSW |
16 |
19,305,753 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9394:Or2l13
|
UTSW |
16 |
19,306,421 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9640:Or2l13
|
UTSW |
16 |
19,305,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Or2l13
|
UTSW |
16 |
19,306,113 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0020:Or2l13
|
UTSW |
16 |
19,305,840 (GRCm39) |
missense |
probably benign |
0.22 |
Z1088:Or2l13
|
UTSW |
16 |
19,305,798 (GRCm39) |
missense |
possibly damaging |
0.52 |
|