Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
C |
T |
4: 53,061,481 (GRCm39) |
|
probably benign |
Het |
Abcc5 |
A |
T |
16: 20,190,906 (GRCm39) |
S815T |
probably benign |
Het |
Adamts17 |
T |
A |
7: 66,490,215 (GRCm39) |
L99Q |
possibly damaging |
Het |
Adamtsl1 |
A |
T |
4: 86,336,783 (GRCm39) |
Q1564L |
probably damaging |
Het |
Als2cl |
A |
G |
9: 110,718,377 (GRCm39) |
|
probably benign |
Het |
Antxrl |
C |
A |
14: 33,789,338 (GRCm39) |
H309Q |
probably benign |
Het |
Ap1g2 |
T |
C |
14: 55,342,363 (GRCm39) |
M165V |
probably benign |
Het |
Cacna2d3 |
A |
G |
14: 29,069,077 (GRCm39) |
|
probably null |
Het |
Cdh16 |
T |
C |
8: 105,344,473 (GRCm39) |
D22G |
possibly damaging |
Het |
Cdh17 |
A |
G |
4: 11,785,201 (GRCm39) |
D331G |
probably damaging |
Het |
Csmd1 |
C |
G |
8: 16,129,936 (GRCm39) |
V1729L |
probably benign |
Het |
Cul5 |
T |
G |
9: 53,529,286 (GRCm39) |
M800L |
probably benign |
Het |
Cwf19l1 |
T |
C |
19: 44,119,937 (GRCm39) |
Y68C |
probably benign |
Het |
Dst |
C |
T |
1: 34,228,355 (GRCm39) |
Q1658* |
probably null |
Het |
Dst |
C |
T |
1: 34,251,400 (GRCm39) |
S4165F |
probably damaging |
Het |
Fan1 |
T |
C |
7: 64,022,119 (GRCm39) |
Y378C |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,061,410 (GRCm39) |
V4331D |
probably benign |
Het |
Fbxl8 |
T |
C |
8: 105,993,781 (GRCm39) |
S46P |
probably benign |
Het |
Golgb1 |
C |
A |
16: 36,719,095 (GRCm39) |
Q334K |
probably benign |
Het |
Hoxc10 |
T |
C |
15: 102,875,879 (GRCm39) |
V196A |
probably benign |
Het |
Hsf4 |
T |
C |
8: 105,997,469 (GRCm39) |
F101L |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,290,561 (GRCm39) |
I3340T |
probably damaging |
Het |
Igfbpl1 |
C |
T |
4: 45,826,426 (GRCm39) |
R123H |
probably benign |
Het |
Mov10l1 |
A |
T |
15: 88,889,898 (GRCm39) |
|
probably null |
Het |
Mrc2 |
T |
C |
11: 105,183,729 (GRCm39) |
|
probably null |
Het |
Muc5b |
G |
A |
7: 141,416,375 (GRCm39) |
C3107Y |
possibly damaging |
Het |
Naip2 |
A |
T |
13: 100,315,940 (GRCm39) |
L280Q |
probably damaging |
Het |
Naip2 |
G |
C |
13: 100,315,941 (GRCm39) |
L280V |
probably damaging |
Het |
Nek1 |
T |
A |
8: 61,525,349 (GRCm39) |
F596I |
probably damaging |
Het |
Nfasc |
T |
C |
1: 132,559,471 (GRCm39) |
T214A |
probably damaging |
Het |
Or4a72 |
T |
C |
2: 89,405,378 (GRCm39) |
R231G |
probably damaging |
Het |
Or5aq1b |
T |
A |
2: 86,902,310 (GRCm39) |
H56L |
possibly damaging |
Het |
Pcdhga10 |
C |
T |
18: 37,882,074 (GRCm39) |
P612S |
probably damaging |
Het |
Picalm |
A |
G |
7: 89,840,912 (GRCm39) |
N456S |
probably damaging |
Het |
Pigo |
A |
G |
4: 43,025,084 (GRCm39) |
F5S |
probably benign |
Het |
Pikfyve |
T |
C |
1: 65,270,004 (GRCm39) |
F563S |
probably damaging |
Het |
Plod2 |
A |
G |
9: 92,424,598 (GRCm39) |
E29G |
probably benign |
Het |
Pm20d2 |
A |
G |
4: 33,174,414 (GRCm39) |
V403A |
probably damaging |
Het |
Proz |
A |
G |
8: 13,123,533 (GRCm39) |
E268G |
probably benign |
Het |
Rb1cc1 |
T |
A |
1: 6,320,337 (GRCm39) |
V1252D |
probably benign |
Het |
Rimbp3 |
A |
T |
16: 17,028,163 (GRCm39) |
H529L |
probably benign |
Het |
Rmdn3 |
A |
T |
2: 118,986,903 (GRCm39) |
H41Q |
possibly damaging |
Het |
Rnf17 |
T |
C |
14: 56,749,753 (GRCm39) |
V1433A |
probably damaging |
Het |
Ror1 |
A |
G |
4: 100,299,357 (GRCm39) |
Y910C |
possibly damaging |
Het |
Scn2a |
C |
T |
2: 65,512,375 (GRCm39) |
L171F |
probably benign |
Het |
Sh3pxd2b |
A |
G |
11: 32,361,505 (GRCm39) |
E239G |
probably damaging |
Het |
Smim33 |
G |
A |
18: 35,861,767 (GRCm39) |
V84I |
probably benign |
Het |
Snx27 |
G |
T |
3: 94,427,542 (GRCm39) |
T311K |
probably benign |
Het |
Sspo |
T |
A |
6: 48,469,424 (GRCm39) |
L4459Q |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,095,396 (GRCm39) |
L5241P |
probably damaging |
Het |
Tas2r110 |
T |
A |
6: 132,845,638 (GRCm39) |
I223N |
probably damaging |
Het |
Tead2 |
T |
A |
7: 44,881,752 (GRCm39) |
|
probably null |
Het |
Thap12 |
G |
T |
7: 98,365,870 (GRCm39) |
K679N |
probably damaging |
Het |
Vmn2r65 |
T |
A |
7: 84,595,859 (GRCm39) |
H275L |
probably benign |
Het |
Wfs1 |
C |
A |
5: 37,125,968 (GRCm39) |
V308L |
probably benign |
Het |
Zfp229 |
C |
A |
17: 21,964,843 (GRCm39) |
H358N |
probably damaging |
Het |
Zfp687 |
T |
C |
3: 94,915,225 (GRCm39) |
D1092G |
probably damaging |
Het |
|
Other mutations in Or7d10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01152:Or7d10
|
APN |
9 |
19,832,245 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01318:Or7d10
|
APN |
9 |
19,832,054 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01547:Or7d10
|
APN |
9 |
19,832,197 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01635:Or7d10
|
APN |
9 |
19,831,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02112:Or7d10
|
APN |
9 |
19,831,821 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02858:Or7d10
|
APN |
9 |
19,831,747 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02904:Or7d10
|
APN |
9 |
19,832,393 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02956:Or7d10
|
APN |
9 |
19,832,348 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03066:Or7d10
|
APN |
9 |
19,831,667 (GRCm39) |
missense |
probably benign |
0.12 |
R0662:Or7d10
|
UTSW |
9 |
19,831,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R1222:Or7d10
|
UTSW |
9 |
19,832,344 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1572:Or7d10
|
UTSW |
9 |
19,832,208 (GRCm39) |
missense |
probably benign |
0.35 |
R1761:Or7d10
|
UTSW |
9 |
19,832,445 (GRCm39) |
makesense |
probably null |
|
R2409:Or7d10
|
UTSW |
9 |
19,832,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2409:Or7d10
|
UTSW |
9 |
19,832,072 (GRCm39) |
missense |
probably benign |
0.31 |
R3621:Or7d10
|
UTSW |
9 |
19,832,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R3849:Or7d10
|
UTSW |
9 |
19,832,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R4277:Or7d10
|
UTSW |
9 |
19,831,685 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4768:Or7d10
|
UTSW |
9 |
19,831,841 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4979:Or7d10
|
UTSW |
9 |
19,831,655 (GRCm39) |
missense |
probably benign |
0.03 |
R5276:Or7d10
|
UTSW |
9 |
19,831,917 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5503:Or7d10
|
UTSW |
9 |
19,831,675 (GRCm39) |
missense |
probably benign |
0.36 |
R5760:Or7d10
|
UTSW |
9 |
19,832,050 (GRCm39) |
missense |
probably benign |
0.00 |
R5778:Or7d10
|
UTSW |
9 |
19,832,337 (GRCm39) |
missense |
probably benign |
0.20 |
R5930:Or7d10
|
UTSW |
9 |
19,832,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R6012:Or7d10
|
UTSW |
9 |
19,832,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R7269:Or7d10
|
UTSW |
9 |
19,831,631 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7977:Or7d10
|
UTSW |
9 |
19,831,610 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7987:Or7d10
|
UTSW |
9 |
19,831,610 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8174:Or7d10
|
UTSW |
9 |
19,832,020 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or7d10
|
UTSW |
9 |
19,832,008 (GRCm39) |
missense |
probably damaging |
1.00 |
|