Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
G |
T |
11: 9,251,259 (GRCm39) |
|
probably null |
Het |
Ache |
T |
C |
5: 137,290,117 (GRCm39) |
I394T |
probably damaging |
Het |
Acsm1 |
G |
A |
7: 119,232,289 (GRCm39) |
G62D |
probably damaging |
Het |
Actrt3 |
T |
A |
3: 30,653,899 (GRCm39) |
I34F |
probably damaging |
Het |
Adgrf5 |
T |
C |
17: 43,761,974 (GRCm39) |
I1223T |
possibly damaging |
Het |
Adora2a |
T |
C |
10: 75,161,981 (GRCm39) |
F40S |
possibly damaging |
Het |
Ano8 |
T |
C |
8: 71,933,441 (GRCm39) |
|
probably benign |
Het |
Arid1b |
T |
A |
17: 5,293,107 (GRCm39) |
L675Q |
probably damaging |
Het |
Atg2b |
T |
C |
12: 105,589,741 (GRCm39) |
I1837V |
possibly damaging |
Het |
Atp10b |
A |
G |
11: 43,145,109 (GRCm39) |
Y1284C |
probably damaging |
Het |
B3gnt7 |
G |
T |
1: 86,233,237 (GRCm39) |
G44V |
probably damaging |
Het |
Chrna1 |
G |
T |
2: 73,403,653 (GRCm39) |
H99N |
probably benign |
Het |
Cnksr1 |
T |
C |
4: 133,961,204 (GRCm39) |
H220R |
probably damaging |
Het |
Cpsf2 |
T |
A |
12: 101,965,619 (GRCm39) |
|
probably null |
Het |
Daglb |
T |
C |
5: 143,489,096 (GRCm39) |
L651P |
probably benign |
Het |
Ddx60 |
A |
G |
8: 62,398,974 (GRCm39) |
D231G |
possibly damaging |
Het |
Ehd4 |
A |
C |
2: 119,932,904 (GRCm39) |
F174C |
probably damaging |
Het |
Emsy |
G |
T |
7: 98,260,060 (GRCm39) |
P9T |
probably damaging |
Het |
Fnbp1l |
T |
C |
3: 122,352,805 (GRCm39) |
E217G |
probably benign |
Het |
Gm11596 |
A |
T |
11: 99,683,524 (GRCm39) |
C199S |
unknown |
Het |
Gmps |
T |
G |
3: 63,908,964 (GRCm39) |
C489G |
probably benign |
Het |
Gpsm1 |
T |
C |
2: 26,215,425 (GRCm39) |
Y296H |
probably benign |
Het |
Heatr5b |
T |
C |
17: 79,138,870 (GRCm39) |
T91A |
possibly damaging |
Het |
Hs3st3b1 |
A |
T |
11: 63,780,324 (GRCm39) |
W268R |
probably damaging |
Het |
Il27ra |
T |
C |
8: 84,758,773 (GRCm39) |
|
probably null |
Het |
Itga5 |
T |
A |
15: 103,265,880 (GRCm39) |
I156F |
probably damaging |
Het |
Kcnmb3 |
T |
A |
3: 32,527,976 (GRCm39) |
D96V |
probably damaging |
Het |
Khdrbs1 |
T |
A |
4: 129,609,965 (GRCm39) |
N417Y |
probably damaging |
Het |
Loxhd1 |
A |
G |
18: 77,383,454 (GRCm39) |
N118D |
possibly damaging |
Het |
Mdm4 |
A |
G |
1: 132,919,845 (GRCm39) |
L341P |
probably damaging |
Het |
Mecom |
T |
C |
3: 30,047,797 (GRCm39) |
E225G |
possibly damaging |
Het |
Megf8 |
G |
A |
7: 25,046,796 (GRCm39) |
G1560S |
possibly damaging |
Het |
Mfsd13a |
A |
T |
19: 46,356,321 (GRCm39) |
D142V |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,415,181 (GRCm39) |
Y2709F |
possibly damaging |
Het |
Nelfa |
A |
T |
5: 34,056,223 (GRCm39) |
I480N |
probably damaging |
Het |
Or10ak8 |
G |
A |
4: 118,773,944 (GRCm39) |
S240F |
probably damaging |
Het |
Palld |
G |
T |
8: 62,003,186 (GRCm39) |
N304K |
probably damaging |
Het |
Pcsk5 |
A |
G |
19: 17,488,856 (GRCm39) |
L988P |
probably damaging |
Het |
Prmt1 |
A |
T |
7: 44,631,251 (GRCm39) |
F34I |
probably damaging |
Het |
Pzp |
A |
G |
6: 128,465,979 (GRCm39) |
S1234P |
probably benign |
Het |
Ralb |
A |
T |
1: 119,405,870 (GRCm39) |
|
probably null |
Het |
Robo2 |
T |
A |
16: 73,717,617 (GRCm39) |
D141V |
probably damaging |
Het |
Rsrc1 |
T |
C |
3: 67,262,895 (GRCm39) |
I283T |
probably benign |
Het |
Sec62 |
A |
T |
3: 30,864,631 (GRCm39) |
K165M |
unknown |
Het |
Sez6 |
A |
G |
11: 77,868,648 (GRCm39) |
D974G |
probably damaging |
Het |
Shc2 |
T |
A |
10: 79,465,752 (GRCm39) |
I187F |
possibly damaging |
Het |
Shroom3 |
G |
A |
5: 93,112,267 (GRCm39) |
R1876Q |
probably damaging |
Het |
Siglecg |
C |
A |
7: 43,061,441 (GRCm39) |
N481K |
possibly damaging |
Het |
Skil |
T |
A |
3: 31,152,002 (GRCm39) |
F175I |
probably damaging |
Het |
Slc1a1 |
T |
C |
19: 28,886,935 (GRCm39) |
V432A |
probably damaging |
Het |
Slit3 |
G |
T |
11: 35,591,310 (GRCm39) |
G1374V |
possibly damaging |
Het |
Snx14 |
T |
C |
9: 88,273,859 (GRCm39) |
Y644C |
probably damaging |
Het |
Snx33 |
T |
A |
9: 56,833,983 (GRCm39) |
I29F |
possibly damaging |
Het |
Sos1 |
T |
A |
17: 80,756,764 (GRCm39) |
I263L |
probably benign |
Het |
Susd2 |
C |
T |
10: 75,473,853 (GRCm39) |
A581T |
probably damaging |
Het |
Tbpl2 |
C |
A |
2: 23,966,028 (GRCm39) |
V320F |
probably damaging |
Het |
Tmem209 |
A |
G |
6: 30,505,794 (GRCm39) |
S171P |
probably benign |
Het |
Tprkb |
T |
A |
6: 85,893,172 (GRCm39) |
|
probably null |
Het |
Tspan11 |
G |
A |
6: 127,916,061 (GRCm39) |
S119N |
probably benign |
Het |
Ulk2 |
A |
T |
11: 61,672,572 (GRCm39) |
V922D |
probably damaging |
Het |
Zfp267 |
A |
G |
3: 36,219,303 (GRCm39) |
H442R |
possibly damaging |
Het |
Zfp976 |
A |
C |
7: 42,263,610 (GRCm39) |
Y76D |
probably damaging |
Het |
Zkscan2 |
G |
A |
7: 123,088,993 (GRCm39) |
T426I |
probably benign |
Het |
|
Other mutations in Or8b36 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00980:Or8b36
|
APN |
9 |
37,937,107 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02092:Or8b36
|
APN |
9 |
37,937,917 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02351:Or8b36
|
APN |
9 |
37,937,332 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02358:Or8b36
|
APN |
9 |
37,937,332 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02807:Or8b36
|
APN |
9 |
37,937,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R0972:Or8b36
|
UTSW |
9 |
37,937,856 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1016:Or8b36
|
UTSW |
9 |
37,937,987 (GRCm39) |
missense |
probably damaging |
0.98 |
R1818:Or8b36
|
UTSW |
9 |
37,937,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R4466:Or8b36
|
UTSW |
9 |
37,937,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R4871:Or8b36
|
UTSW |
9 |
37,937,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R5977:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R5979:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6026:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6027:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6029:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6035:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6035:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6053:Or8b36
|
UTSW |
9 |
37,937,837 (GRCm39) |
frame shift |
probably null |
|
R6092:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6106:Or8b36
|
UTSW |
9 |
37,937,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6132:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6133:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6134:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6251:Or8b36
|
UTSW |
9 |
37,937,842 (GRCm39) |
frame shift |
probably null |
|
R6251:Or8b36
|
UTSW |
9 |
37,937,841 (GRCm39) |
frame shift |
probably null |
|
R6251:Or8b36
|
UTSW |
9 |
37,937,833 (GRCm39) |
frame shift |
probably null |
|
R6251:Or8b36
|
UTSW |
9 |
37,937,844 (GRCm39) |
frame shift |
probably null |
|
R6300:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6301:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6305:Or8b36
|
UTSW |
9 |
37,937,838 (GRCm39) |
frame shift |
probably null |
|
R6305:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6307:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6312:Or8b36
|
UTSW |
9 |
37,937,842 (GRCm39) |
frame shift |
probably null |
|
R6312:Or8b36
|
UTSW |
9 |
37,937,837 (GRCm39) |
frame shift |
probably null |
|
R6312:Or8b36
|
UTSW |
9 |
37,937,836 (GRCm39) |
frame shift |
probably null |
|
R6312:Or8b36
|
UTSW |
9 |
37,937,845 (GRCm39) |
frame shift |
probably null |
|
R6312:Or8b36
|
UTSW |
9 |
37,937,843 (GRCm39) |
nonsense |
probably null |
|
R6813:Or8b36
|
UTSW |
9 |
37,937,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R7134:Or8b36
|
UTSW |
9 |
37,937,795 (GRCm39) |
missense |
probably benign |
0.00 |
R7775:Or8b36
|
UTSW |
9 |
37,937,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7778:Or8b36
|
UTSW |
9 |
37,937,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7984:Or8b36
|
UTSW |
9 |
37,937,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:Or8b36
|
UTSW |
9 |
37,938,014 (GRCm39) |
missense |
probably benign |
0.00 |
R9154:Or8b36
|
UTSW |
9 |
37,937,690 (GRCm39) |
nonsense |
probably null |
|
|