Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I06Rik |
G |
C |
14: 64,223,633 (GRCm39) |
L48V |
probably benign |
Het |
Acbd3 |
T |
C |
1: 180,566,095 (GRCm39) |
Y263H |
probably damaging |
Het |
Acot4 |
C |
A |
12: 84,088,809 (GRCm39) |
P219Q |
possibly damaging |
Het |
Adcy6 |
A |
G |
15: 98,498,919 (GRCm39) |
F294S |
probably damaging |
Het |
Ahcyl |
T |
C |
16: 45,974,786 (GRCm39) |
E197G |
probably damaging |
Het |
Aplf |
T |
C |
6: 87,606,987 (GRCm39) |
R476G |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,382,788 (GRCm39) |
T1292A |
probably benign |
Het |
Atp2c1 |
T |
A |
9: 105,295,778 (GRCm39) |
I649F |
probably damaging |
Het |
Bbs10 |
C |
T |
10: 111,136,104 (GRCm39) |
Q406* |
probably null |
Het |
Bcas3 |
T |
A |
11: 85,400,372 (GRCm39) |
M447K |
possibly damaging |
Het |
Bmal1 |
A |
T |
7: 112,884,258 (GRCm39) |
I92F |
probably damaging |
Het |
Cars1 |
T |
C |
7: 143,139,446 (GRCm39) |
D214G |
probably benign |
Het |
Ccdc88a |
A |
T |
11: 29,443,934 (GRCm39) |
I1410F |
probably benign |
Het |
Cd55b |
A |
T |
1: 130,316,415 (GRCm39) |
L378H |
probably damaging |
Het |
Cdh1 |
G |
A |
8: 107,330,979 (GRCm39) |
E37K |
probably benign |
Het |
Cep72 |
T |
C |
13: 74,206,465 (GRCm39) |
Y119C |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,634,879 (GRCm39) |
T176A |
possibly damaging |
Het |
D630045J12Rik |
T |
A |
6: 38,119,846 (GRCm39) |
|
probably null |
Het |
Ddi1 |
A |
T |
9: 6,265,524 (GRCm39) |
C282S |
probably damaging |
Het |
Ddit4 |
T |
C |
10: 59,787,277 (GRCm39) |
T20A |
probably benign |
Het |
Dpp10 |
T |
A |
1: 123,614,024 (GRCm39) |
T102S |
probably benign |
Het |
Ep400 |
T |
A |
5: 110,903,478 (GRCm39) |
K374* |
probably null |
Het |
Epha3 |
A |
G |
16: 63,403,917 (GRCm39) |
L728P |
probably damaging |
Het |
Fbxw21 |
C |
A |
9: 108,975,614 (GRCm39) |
|
probably null |
Het |
Frmpd1 |
A |
G |
4: 45,244,638 (GRCm39) |
E109G |
probably damaging |
Het |
Ggt1 |
C |
T |
10: 75,417,245 (GRCm39) |
P332L |
probably damaging |
Het |
Gm4779 |
G |
C |
X: 100,837,390 (GRCm39) |
T171S |
possibly damaging |
Het |
Gm5431 |
A |
T |
11: 48,785,556 (GRCm39) |
I273K |
probably benign |
Het |
Gon4l |
A |
G |
3: 88,799,937 (GRCm39) |
N861D |
probably damaging |
Het |
Grm5 |
T |
C |
7: 87,724,340 (GRCm39) |
|
probably null |
Het |
Helt |
T |
C |
8: 46,745,745 (GRCm39) |
N84S |
possibly damaging |
Het |
Hnrnpa0 |
G |
T |
13: 58,275,228 (GRCm39) |
Y300* |
probably null |
Het |
Ints1 |
T |
C |
5: 139,750,968 (GRCm39) |
T810A |
|
Het |
Irf2bp1 |
C |
T |
7: 18,740,079 (GRCm39) |
A573V |
possibly damaging |
Het |
Itgbl1 |
C |
A |
14: 124,065,246 (GRCm39) |
D133E |
probably benign |
Het |
Kctd15 |
A |
G |
7: 34,344,267 (GRCm39) |
F128S |
possibly damaging |
Het |
Klra17 |
T |
A |
6: 129,808,421 (GRCm39) |
N271Y |
probably damaging |
Het |
Kmt2c |
T |
A |
5: 25,610,514 (GRCm39) |
E197D |
possibly damaging |
Het |
Larp1 |
C |
A |
11: 57,949,515 (GRCm39) |
T1048K |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,365,863 (GRCm39) |
V2966A |
probably benign |
Het |
Magi3 |
A |
G |
3: 103,922,625 (GRCm39) |
L1364P |
probably benign |
Het |
Malrd1 |
T |
C |
2: 15,619,017 (GRCm39) |
S294P |
|
Het |
Med13l |
C |
T |
5: 118,886,794 (GRCm39) |
T1565I |
possibly damaging |
Het |
Mov10l1 |
A |
G |
15: 88,896,313 (GRCm39) |
D719G |
probably benign |
Het |
Mtcl3 |
T |
A |
10: 29,024,270 (GRCm39) |
H395Q |
possibly damaging |
Het |
Muc4 |
CAC |
CACTAC |
16: 32,575,367 (GRCm39) |
|
probably benign |
Het |
Myh14 |
T |
C |
7: 44,264,800 (GRCm39) |
E1654G |
probably damaging |
Het |
Myo1c |
C |
T |
11: 75,546,942 (GRCm39) |
|
probably benign |
Het |
Myo9a |
A |
G |
9: 59,817,961 (GRCm39) |
T2343A |
probably benign |
Het |
Or1j12 |
A |
G |
2: 36,342,897 (GRCm39) |
Q100R |
probably damaging |
Het |
Or2ag18 |
A |
T |
7: 106,405,234 (GRCm39) |
V145E |
possibly damaging |
Het |
Or2d2b |
A |
T |
7: 106,706,062 (GRCm39) |
M2K |
probably benign |
Het |
Or4m1 |
T |
C |
14: 50,557,615 (GRCm39) |
K226E |
probably benign |
Het |
Or52m2 |
T |
A |
7: 102,263,432 (GRCm39) |
I255F |
possibly damaging |
Het |
Or52n5 |
T |
A |
7: 104,587,879 (GRCm39) |
Y49N |
probably damaging |
Het |
Or6c2 |
T |
A |
10: 129,362,957 (GRCm39) |
I287N |
possibly damaging |
Het |
Or9g3 |
A |
T |
2: 85,589,820 (GRCm39) |
L300Q |
probably damaging |
Het |
Osmr |
A |
T |
15: 6,844,897 (GRCm39) |
D957E |
probably benign |
Het |
Pappa |
T |
A |
4: 65,234,419 (GRCm39) |
V1408E |
probably damaging |
Het |
Pcnx3 |
C |
T |
19: 5,715,412 (GRCm39) |
G1946E |
probably damaging |
Het |
Pdcd6ip |
A |
T |
9: 113,501,865 (GRCm39) |
D464E |
probably benign |
Het |
Pde1c |
T |
C |
6: 56,114,404 (GRCm39) |
Y503C |
probably benign |
Het |
Potefam3d |
A |
T |
8: 69,972,400 (GRCm39) |
D116E |
possibly damaging |
Het |
Prob1 |
T |
A |
18: 35,787,210 (GRCm39) |
E348V |
possibly damaging |
Het |
Rnls |
A |
G |
19: 33,180,048 (GRCm39) |
L134S |
probably damaging |
Het |
Scrn3 |
T |
C |
2: 73,166,202 (GRCm39) |
Y412H |
probably damaging |
Het |
Serpina3g |
T |
C |
12: 104,205,362 (GRCm39) |
S34P |
probably benign |
Het |
Sertad3 |
G |
A |
7: 27,175,784 (GRCm39) |
A73T |
probably benign |
Het |
Sez6l |
C |
T |
5: 112,609,122 (GRCm39) |
A576T |
probably benign |
Het |
Sh3tc2 |
G |
A |
18: 62,146,137 (GRCm39) |
R1172H |
probably damaging |
Het |
Sirt3 |
A |
G |
7: 140,456,319 (GRCm39) |
V110A |
|
Het |
Smpd3 |
A |
T |
8: 106,984,047 (GRCm39) |
D557E |
probably benign |
Het |
Sptssb |
A |
T |
3: 69,728,305 (GRCm39) |
M44K |
probably damaging |
Het |
Tars2 |
A |
G |
3: 95,662,132 (GRCm39) |
W7R |
probably damaging |
Het |
Tbc1d9b |
A |
G |
11: 50,055,013 (GRCm39) |
D964G |
probably benign |
Het |
Tiam2 |
A |
T |
17: 3,568,594 (GRCm39) |
D1580V |
possibly damaging |
Het |
Tmeff2 |
T |
A |
1: 50,977,478 (GRCm39) |
V130D |
probably damaging |
Het |
Top2a |
T |
A |
11: 98,891,595 (GRCm39) |
E1176V |
probably null |
Het |
Trappc9 |
C |
A |
15: 72,813,758 (GRCm39) |
E680* |
probably null |
Het |
Trip10 |
A |
G |
17: 57,564,314 (GRCm39) |
N355S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,596,337 (GRCm39) |
E20192G |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,804,243 (GRCm39) |
M306V |
probably benign |
Het |
Wdr90 |
A |
T |
17: 26,064,141 (GRCm39) |
H1860Q |
probably damaging |
Het |
Wrnip1 |
A |
G |
13: 32,989,339 (GRCm39) |
I276V |
possibly damaging |
Het |
Zfp608 |
T |
C |
18: 55,030,821 (GRCm39) |
K1040E |
possibly damaging |
Het |
Zfp808 |
T |
A |
13: 62,320,552 (GRCm39) |
C594S |
probably benign |
Het |
|
Other mutations in Or8k53 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01548:Or8k53
|
APN |
2 |
86,178,077 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02524:Or8k53
|
APN |
2 |
86,177,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Or8k53
|
UTSW |
2 |
86,178,072 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0134:Or8k53
|
UTSW |
2 |
86,178,072 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0225:Or8k53
|
UTSW |
2 |
86,178,072 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1981:Or8k53
|
UTSW |
2 |
86,177,486 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4181:Or8k53
|
UTSW |
2 |
86,177,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Or8k53
|
UTSW |
2 |
86,177,647 (GRCm39) |
missense |
probably benign |
0.00 |
R5013:Or8k53
|
UTSW |
2 |
86,177,647 (GRCm39) |
missense |
probably benign |
0.00 |
R5077:Or8k53
|
UTSW |
2 |
86,177,683 (GRCm39) |
missense |
probably benign |
0.00 |
R6312:Or8k53
|
UTSW |
2 |
86,177,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:Or8k53
|
UTSW |
2 |
86,177,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R6591:Or8k53
|
UTSW |
2 |
86,177,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R6626:Or8k53
|
UTSW |
2 |
86,177,364 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6680:Or8k53
|
UTSW |
2 |
86,177,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6691:Or8k53
|
UTSW |
2 |
86,177,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Or8k53
|
UTSW |
2 |
86,177,150 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7622:Or8k53
|
UTSW |
2 |
86,178,006 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8114:Or8k53
|
UTSW |
2 |
86,177,530 (GRCm39) |
missense |
probably benign |
0.00 |
R8138:Or8k53
|
UTSW |
2 |
86,177,930 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8242:Or8k53
|
UTSW |
2 |
86,177,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R8360:Or8k53
|
UTSW |
2 |
86,177,668 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8433:Or8k53
|
UTSW |
2 |
86,177,144 (GRCm39) |
missense |
unknown |
|
R8927:Or8k53
|
UTSW |
2 |
86,178,090 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8928:Or8k53
|
UTSW |
2 |
86,178,090 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9150:Or8k53
|
UTSW |
2 |
86,177,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Or8k53
|
UTSW |
2 |
86,177,768 (GRCm39) |
missense |
probably benign |
0.14 |
R9487:Or8k53
|
UTSW |
2 |
86,177,846 (GRCm39) |
missense |
probably benign |
0.10 |
R9712:Or8k53
|
UTSW |
2 |
86,177,583 (GRCm39) |
missense |
probably benign |
0.22 |
Z1176:Or8k53
|
UTSW |
2 |
86,177,227 (GRCm39) |
missense |
possibly damaging |
0.95 |
|