Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam5 |
A |
T |
8: 25,303,477 (GRCm39) |
V150E |
probably benign |
Het |
Alg11 |
A |
G |
8: 22,555,857 (GRCm39) |
K373E |
probably benign |
Het |
Arl14ep |
C |
T |
2: 106,799,398 (GRCm39) |
|
probably benign |
Het |
Ascc2 |
G |
A |
11: 4,608,284 (GRCm39) |
G227R |
probably benign |
Het |
Ash1l |
C |
T |
3: 88,976,300 (GRCm39) |
P2627S |
probably damaging |
Het |
Btla |
T |
G |
16: 45,059,402 (GRCm39) |
|
probably null |
Het |
Btnl10 |
C |
T |
11: 58,813,138 (GRCm39) |
P256S |
probably benign |
Het |
Cep162 |
C |
T |
9: 87,086,145 (GRCm39) |
A1060T |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,852,386 (GRCm39) |
K907* |
probably null |
Het |
Chpf |
A |
T |
1: 75,452,072 (GRCm39) |
F461I |
probably damaging |
Het |
Chrdl2 |
A |
G |
7: 99,670,114 (GRCm39) |
Y79C |
probably damaging |
Het |
Copb2 |
G |
A |
9: 98,450,161 (GRCm39) |
C40Y |
probably benign |
Het |
Cyfip1 |
T |
C |
7: 55,574,929 (GRCm39) |
L1060P |
probably damaging |
Het |
Drg1 |
G |
A |
11: 3,209,273 (GRCm39) |
|
probably benign |
Het |
Erich3 |
A |
G |
3: 154,468,134 (GRCm39) |
D862G |
possibly damaging |
Het |
Flii |
G |
T |
11: 60,607,137 (GRCm39) |
Y946* |
probably null |
Het |
Glt8d2 |
T |
C |
10: 82,507,915 (GRCm39) |
M1V |
probably null |
Het |
Gm21136 |
T |
A |
7: 38,567,165 (GRCm39) |
|
noncoding transcript |
Het |
Gramd1c |
T |
C |
16: 43,812,454 (GRCm39) |
T393A |
possibly damaging |
Het |
Gucy2d |
T |
A |
7: 98,101,090 (GRCm39) |
I471N |
probably benign |
Het |
Hps3 |
G |
A |
3: 20,063,034 (GRCm39) |
T711M |
probably benign |
Het |
Hs3st4 |
A |
T |
7: 123,582,831 (GRCm39) |
D143V |
probably benign |
Het |
Kif17 |
T |
A |
4: 138,018,744 (GRCm39) |
M461K |
possibly damaging |
Het |
Klhdc7a |
T |
A |
4: 139,694,885 (GRCm39) |
S21C |
probably damaging |
Het |
Klk15 |
G |
A |
7: 43,587,800 (GRCm39) |
R76H |
probably benign |
Het |
Lnpk |
G |
A |
2: 74,399,372 (GRCm39) |
T57I |
possibly damaging |
Het |
Ltbp2 |
A |
G |
12: 84,840,837 (GRCm39) |
V999A |
possibly damaging |
Het |
Ltbr |
T |
C |
6: 125,289,771 (GRCm39) |
H141R |
probably damaging |
Het |
Lvrn |
T |
C |
18: 47,026,816 (GRCm39) |
F805L |
probably damaging |
Het |
Ms4a13 |
A |
T |
19: 11,161,280 (GRCm39) |
C86* |
probably null |
Het |
Ncbp1 |
A |
G |
4: 46,163,026 (GRCm39) |
N480S |
probably benign |
Het |
Nelfcd |
T |
G |
2: 174,268,856 (GRCm39) |
*592G |
probably null |
Het |
Neurog2 |
T |
C |
3: 127,427,664 (GRCm39) |
V96A |
probably benign |
Het |
Nod1 |
A |
T |
6: 54,907,162 (GRCm39) |
W902R |
probably benign |
Het |
Or4k15c |
T |
A |
14: 50,321,484 (GRCm39) |
Y218F |
probably damaging |
Het |
Or55b3 |
T |
C |
7: 102,126,957 (GRCm39) |
Y40C |
possibly damaging |
Het |
Or6d13 |
T |
C |
6: 116,517,861 (GRCm39) |
L149P |
probably damaging |
Het |
Pcdha11 |
A |
T |
18: 37,140,336 (GRCm39) |
H655L |
probably damaging |
Het |
Plpp7 |
A |
G |
2: 31,985,996 (GRCm39) |
E58G |
probably benign |
Het |
Psph |
A |
T |
5: 129,867,685 (GRCm39) |
|
probably benign |
Het |
Rab11fip1 |
A |
C |
8: 27,644,748 (GRCm39) |
S346A |
probably damaging |
Het |
Rreb1 |
C |
A |
13: 38,131,384 (GRCm39) |
P1513T |
probably benign |
Het |
Rreb1 |
C |
T |
13: 38,131,385 (GRCm39) |
P1513L |
probably benign |
Het |
Rsf1 |
C |
T |
7: 97,334,766 (GRCm39) |
R1300C |
probably damaging |
Het |
Scap |
A |
G |
9: 110,203,115 (GRCm39) |
N263S |
probably benign |
Het |
Sec24d |
A |
T |
3: 123,072,961 (GRCm39) |
|
probably benign |
Het |
Slain2 |
T |
C |
5: 73,105,888 (GRCm39) |
|
probably benign |
Het |
Slc6a18 |
G |
T |
13: 73,816,278 (GRCm39) |
T367N |
probably benign |
Het |
Slk |
T |
A |
19: 47,597,481 (GRCm39) |
D96E |
probably benign |
Het |
Spag5 |
G |
A |
11: 78,204,360 (GRCm39) |
V514I |
probably benign |
Het |
St8sia2 |
T |
C |
7: 73,616,654 (GRCm39) |
D107G |
probably damaging |
Het |
Tgfbr3 |
T |
A |
5: 107,288,381 (GRCm39) |
I427F |
probably benign |
Het |
Tlr2 |
T |
G |
3: 83,743,810 (GRCm39) |
T758P |
possibly damaging |
Het |
Tmem270 |
A |
G |
5: 134,931,738 (GRCm39) |
V68A |
probably benign |
Het |
Vmn2r106 |
T |
A |
17: 20,505,583 (GRCm39) |
H37L |
possibly damaging |
Het |
Vmn2r27 |
T |
G |
6: 124,177,647 (GRCm39) |
R452S |
probably damaging |
Het |
Wdr5 |
A |
G |
2: 27,423,362 (GRCm39) |
Y252C |
probably damaging |
Het |
Zswim9 |
C |
T |
7: 12,995,371 (GRCm39) |
V262M |
probably damaging |
Het |
|
Other mutations in Or12d13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00333:Or12d13
|
APN |
17 |
37,647,474 (GRCm39) |
nonsense |
probably null |
|
IGL01953:Or12d13
|
APN |
17 |
37,647,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02556:Or12d13
|
APN |
17 |
37,647,887 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02574:Or12d13
|
APN |
17 |
37,647,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02737:Or12d13
|
APN |
17 |
37,647,664 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02995:Or12d13
|
APN |
17 |
37,647,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Or12d13
|
UTSW |
17 |
37,647,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Or12d13
|
UTSW |
17 |
37,647,847 (GRCm39) |
missense |
probably benign |
0.43 |
R1466:Or12d13
|
UTSW |
17 |
37,647,847 (GRCm39) |
missense |
probably benign |
0.43 |
R3024:Or12d13
|
UTSW |
17 |
37,647,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R3858:Or12d13
|
UTSW |
17 |
37,648,117 (GRCm39) |
nonsense |
probably null |
|
R4979:Or12d13
|
UTSW |
17 |
37,647,759 (GRCm39) |
missense |
probably benign |
0.06 |
R5062:Or12d13
|
UTSW |
17 |
37,647,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5215:Or12d13
|
UTSW |
17 |
37,647,704 (GRCm39) |
missense |
probably benign |
0.00 |
R5441:Or12d13
|
UTSW |
17 |
37,647,159 (GRCm39) |
splice site |
probably null |
|
R5453:Or12d13
|
UTSW |
17 |
37,647,953 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5525:Or12d13
|
UTSW |
17 |
37,647,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R5660:Or12d13
|
UTSW |
17 |
37,647,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Or12d13
|
UTSW |
17 |
37,647,599 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6958:Or12d13
|
UTSW |
17 |
37,647,308 (GRCm39) |
missense |
probably benign |
|
R7060:Or12d13
|
UTSW |
17 |
37,647,352 (GRCm39) |
missense |
probably benign |
0.02 |
R7567:Or12d13
|
UTSW |
17 |
37,648,062 (GRCm39) |
missense |
probably benign |
0.00 |
R7784:Or12d13
|
UTSW |
17 |
37,647,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R7784:Or12d13
|
UTSW |
17 |
37,647,469 (GRCm39) |
missense |
probably benign |
0.13 |
R7978:Or12d13
|
UTSW |
17 |
37,647,392 (GRCm39) |
missense |
probably benign |
0.00 |
R8284:Or12d13
|
UTSW |
17 |
37,647,587 (GRCm39) |
missense |
probably benign |
0.01 |
R8419:Or12d13
|
UTSW |
17 |
37,647,466 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8957:Or12d13
|
UTSW |
17 |
37,647,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Or12d13
|
UTSW |
17 |
37,648,057 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1088:Or12d13
|
UTSW |
17 |
37,647,596 (GRCm39) |
missense |
probably damaging |
0.99 |
|