Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
G |
A |
7: 78,746,492 (GRCm39) |
V711I |
probably benign |
Het |
Adprh |
A |
T |
16: 38,267,871 (GRCm39) |
M138K |
probably damaging |
Het |
Ahctf1 |
A |
G |
1: 179,591,107 (GRCm39) |
|
probably benign |
Het |
Atg9a |
G |
A |
1: 75,162,870 (GRCm39) |
T410M |
probably damaging |
Het |
Atxn1 |
A |
T |
13: 45,721,426 (GRCm39) |
S156R |
possibly damaging |
Het |
Bptf |
T |
C |
11: 106,934,524 (GRCm39) |
T2850A |
probably benign |
Het |
Cc2d2a |
A |
T |
5: 43,852,581 (GRCm39) |
Y386F |
probably damaging |
Het |
Ccdc97 |
T |
C |
7: 25,414,427 (GRCm39) |
D109G |
probably damaging |
Het |
Chd5 |
C |
T |
4: 152,441,147 (GRCm39) |
R196* |
probably null |
Het |
Clec4a2 |
T |
C |
6: 123,100,630 (GRCm39) |
|
probably null |
Het |
Col13a1 |
A |
G |
10: 61,720,477 (GRCm39) |
I317T |
probably damaging |
Het |
D630003M21Rik |
G |
T |
2: 158,058,852 (GRCm39) |
S349R |
probably benign |
Het |
Eml5 |
C |
A |
12: 98,842,560 (GRCm39) |
L179F |
probably damaging |
Het |
Entrep1 |
T |
A |
19: 23,965,866 (GRCm39) |
N211I |
probably damaging |
Het |
Ets2 |
A |
T |
16: 95,516,019 (GRCm39) |
M200L |
probably benign |
Het |
Fat3 |
T |
C |
9: 16,158,263 (GRCm39) |
T1116A |
probably benign |
Het |
Fhit |
A |
G |
14: 10,751,616 (GRCm38) |
V24A |
probably benign |
Het |
Gm6685 |
T |
C |
11: 28,289,195 (GRCm39) |
N207S |
probably benign |
Het |
Hdc |
G |
A |
2: 126,436,125 (GRCm39) |
T582M |
probably benign |
Het |
Hmgxb4 |
G |
A |
8: 75,756,222 (GRCm39) |
C575Y |
probably damaging |
Het |
Kidins220 |
T |
A |
12: 25,090,527 (GRCm39) |
S1164T |
probably benign |
Het |
Ldb1 |
C |
A |
19: 46,024,709 (GRCm39) |
D5Y |
probably null |
Het |
Lpcat1 |
G |
A |
13: 73,659,044 (GRCm39) |
R320H |
probably benign |
Het |
Lrfn4 |
T |
C |
19: 4,664,333 (GRCm39) |
D67G |
probably damaging |
Het |
Myo15b |
C |
T |
11: 115,774,083 (GRCm39) |
Q550* |
probably null |
Het |
Myo18b |
C |
A |
5: 113,019,489 (GRCm39) |
E43* |
probably null |
Het |
Neurl1a |
T |
C |
19: 47,241,719 (GRCm39) |
C271R |
probably damaging |
Het |
Nfasc |
T |
C |
1: 132,532,827 (GRCm39) |
S690G |
probably damaging |
Het |
Ngly1 |
T |
C |
14: 16,310,377 (GRCm38) |
S501P |
probably benign |
Het |
Nlrp1a |
A |
T |
11: 70,999,901 (GRCm39) |
|
probably null |
Het |
Npw |
A |
G |
17: 24,876,396 (GRCm39) |
W172R |
probably benign |
Het |
Nudt8 |
T |
C |
19: 4,050,849 (GRCm39) |
|
probably null |
Het |
Nyap2 |
A |
T |
1: 81,219,352 (GRCm39) |
Y458F |
probably damaging |
Het |
Osbpl5 |
T |
A |
7: 143,258,731 (GRCm39) |
T280S |
probably benign |
Het |
Pex1 |
A |
T |
5: 3,662,923 (GRCm39) |
I505F |
probably benign |
Het |
Pfkm |
A |
G |
15: 98,029,864 (GRCm39) |
E756G |
probably benign |
Het |
Pkd2l2 |
A |
G |
18: 34,558,166 (GRCm39) |
I282V |
possibly damaging |
Het |
Pnpla8 |
T |
C |
12: 44,330,410 (GRCm39) |
S321P |
probably benign |
Het |
Prxl2a |
C |
T |
14: 40,719,723 (GRCm39) |
E164K |
probably benign |
Het |
Qdpr |
G |
T |
5: 45,596,688 (GRCm39) |
Q159K |
probably benign |
Het |
Rac2 |
T |
C |
15: 78,450,206 (GRCm39) |
M45V |
probably benign |
Het |
Rnaset2b |
G |
A |
17: 7,263,908 (GRCm39) |
|
probably null |
Het |
Rpl38 |
T |
A |
11: 114,563,114 (GRCm39) |
*71R |
probably null |
Het |
Sacs |
G |
T |
14: 61,440,404 (GRCm39) |
V817L |
probably benign |
Het |
Selenot |
T |
C |
3: 58,495,889 (GRCm39) |
F133S |
probably damaging |
Het |
Sgcg |
G |
A |
14: 61,477,856 (GRCm39) |
L78F |
probably damaging |
Het |
Slc19a1 |
A |
G |
10: 76,885,497 (GRCm39) |
R466G |
probably benign |
Het |
Tpr |
A |
G |
1: 150,309,451 (GRCm39) |
T1736A |
probably damaging |
Het |
Zfhx3 |
A |
G |
8: 109,674,511 (GRCm39) |
I1854V |
probably benign |
Het |
Zfp652 |
T |
C |
11: 95,643,719 (GRCm39) |
S306P |
probably damaging |
Het |
Zfp998 |
C |
T |
13: 66,579,797 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or10ag56 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01328:Or10ag56
|
APN |
2 |
87,139,925 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01458:Or10ag56
|
APN |
2 |
87,139,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02544:Or10ag56
|
APN |
2 |
87,139,471 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02748:Or10ag56
|
APN |
2 |
87,140,009 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03077:Or10ag56
|
APN |
2 |
87,140,056 (GRCm39) |
makesense |
probably null |
|
R0411:Or10ag56
|
UTSW |
2 |
87,139,402 (GRCm39) |
missense |
probably benign |
0.07 |
R0525:Or10ag56
|
UTSW |
2 |
87,139,693 (GRCm39) |
missense |
probably benign |
0.10 |
R1703:Or10ag56
|
UTSW |
2 |
87,139,754 (GRCm39) |
missense |
probably benign |
0.00 |
R1750:Or10ag56
|
UTSW |
2 |
87,139,196 (GRCm39) |
missense |
probably benign |
0.02 |
R2005:Or10ag56
|
UTSW |
2 |
87,139,792 (GRCm39) |
missense |
probably benign |
0.24 |
R2090:Or10ag56
|
UTSW |
2 |
87,139,762 (GRCm39) |
missense |
probably benign |
0.02 |
R3846:Or10ag56
|
UTSW |
2 |
87,139,526 (GRCm39) |
missense |
probably benign |
0.15 |
R4011:Or10ag56
|
UTSW |
2 |
87,139,555 (GRCm39) |
missense |
probably benign |
0.03 |
R4077:Or10ag56
|
UTSW |
2 |
87,139,208 (GRCm39) |
splice site |
probably null |
0.42 |
R5132:Or10ag56
|
UTSW |
2 |
87,139,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Or10ag56
|
UTSW |
2 |
87,139,126 (GRCm39) |
splice site |
probably null |
|
R7355:Or10ag56
|
UTSW |
2 |
87,139,754 (GRCm39) |
missense |
probably benign |
0.00 |
R7405:Or10ag56
|
UTSW |
2 |
87,139,339 (GRCm39) |
missense |
probably benign |
0.00 |
R7437:Or10ag56
|
UTSW |
2 |
87,139,687 (GRCm39) |
missense |
probably benign |
|
R7554:Or10ag56
|
UTSW |
2 |
87,139,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R7609:Or10ag56
|
UTSW |
2 |
87,139,853 (GRCm39) |
missense |
probably benign |
0.01 |
R8156:Or10ag56
|
UTSW |
2 |
87,139,318 (GRCm39) |
missense |
probably damaging |
0.97 |
R8558:Or10ag56
|
UTSW |
2 |
87,139,583 (GRCm39) |
missense |
probably benign |
0.11 |
R9136:Or10ag56
|
UTSW |
2 |
87,139,219 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9229:Or10ag56
|
UTSW |
2 |
87,139,165 (GRCm39) |
missense |
probably benign |
0.00 |
R9326:Or10ag56
|
UTSW |
2 |
87,139,730 (GRCm39) |
missense |
probably benign |
0.37 |
RF010:Or10ag56
|
UTSW |
2 |
87,139,184 (GRCm39) |
missense |
possibly damaging |
0.83 |
|