Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,328,215 (GRCm39) |
S3429R |
probably damaging |
Het |
Abca3 |
A |
G |
17: 24,600,894 (GRCm39) |
D436G |
probably benign |
Het |
Acacb |
C |
A |
5: 114,371,320 (GRCm39) |
Y1816* |
probably null |
Het |
Acer3 |
T |
C |
7: 97,910,804 (GRCm39) |
Y86C |
probably damaging |
Het |
Adgre1 |
A |
G |
17: 57,754,872 (GRCm39) |
I657V |
probably benign |
Het |
Akap1 |
A |
G |
11: 88,736,020 (GRCm39) |
V214A |
probably benign |
Het |
Ankrd42 |
T |
C |
7: 92,280,865 (GRCm39) |
R22G |
possibly damaging |
Het |
Apc2 |
C |
T |
10: 80,148,647 (GRCm39) |
P1234S |
possibly damaging |
Het |
Atp13a4 |
A |
G |
16: 29,273,652 (GRCm39) |
I441T |
probably damaging |
Het |
Cenpu |
G |
A |
8: 47,031,344 (GRCm39) |
A242T |
probably damaging |
Het |
Col6a6 |
A |
T |
9: 105,644,487 (GRCm39) |
V1267E |
possibly damaging |
Het |
Crhr2 |
T |
C |
6: 55,094,516 (GRCm39) |
T58A |
probably benign |
Het |
Ddx6 |
T |
G |
9: 44,542,722 (GRCm39) |
C385G |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,543,305 (GRCm39) |
N2288K |
probably benign |
Het |
Egfl8 |
A |
T |
17: 34,833,342 (GRCm39) |
|
probably null |
Het |
Elmo2 |
A |
T |
2: 165,139,287 (GRCm39) |
I420N |
probably damaging |
Het |
Elovl4 |
A |
G |
9: 83,665,248 (GRCm39) |
F113L |
probably benign |
Het |
Fancd2 |
T |
A |
6: 113,525,409 (GRCm39) |
|
probably null |
Het |
Fbxl13 |
A |
G |
5: 21,728,908 (GRCm39) |
V456A |
probably benign |
Het |
Fgfr2 |
A |
T |
7: 129,863,592 (GRCm39) |
|
probably null |
Het |
Fkbpl |
A |
T |
17: 34,864,384 (GRCm39) |
R51* |
probably null |
Het |
Fn3krp |
G |
A |
11: 121,312,406 (GRCm39) |
V40M |
probably damaging |
Het |
Fnip1 |
A |
G |
11: 54,380,169 (GRCm39) |
|
probably null |
Het |
Gm15446 |
A |
T |
5: 110,091,281 (GRCm39) |
Q511L |
probably benign |
Het |
Gm7334 |
A |
G |
17: 51,006,289 (GRCm39) |
K192E |
probably damaging |
Het |
H2-Q10 |
A |
T |
17: 35,784,204 (GRCm39) |
T282S |
possibly damaging |
Het |
Hspa9 |
A |
G |
18: 35,073,963 (GRCm39) |
V482A |
possibly damaging |
Het |
Ica1l |
A |
T |
1: 60,053,155 (GRCm39) |
S128T |
probably benign |
Het |
Il7r |
A |
T |
15: 9,516,423 (GRCm39) |
I126K |
probably damaging |
Het |
Kcnj8 |
T |
C |
6: 142,516,074 (GRCm39) |
E11G |
probably benign |
Het |
Klkb1 |
A |
C |
8: 45,725,446 (GRCm39) |
F498V |
probably benign |
Het |
Lama1 |
A |
G |
17: 68,117,178 (GRCm39) |
E2491G |
probably null |
Het |
Lhfpl2 |
T |
C |
13: 94,310,943 (GRCm39) |
V71A |
probably benign |
Het |
Lin9 |
T |
C |
1: 180,493,488 (GRCm39) |
I198T |
probably damaging |
Het |
Lrrc7 |
T |
A |
3: 157,885,432 (GRCm39) |
M431L |
possibly damaging |
Het |
Nmt2 |
A |
G |
2: 3,326,424 (GRCm39) |
T519A |
probably benign |
Het |
Or10w1 |
C |
A |
19: 13,632,128 (GRCm39) |
L112I |
probably damaging |
Het |
Or10w1 |
T |
A |
19: 13,632,129 (GRCm39) |
L112H |
probably damaging |
Het |
Or1d2 |
T |
C |
11: 74,256,028 (GRCm39) |
F178L |
probably damaging |
Het |
Or4a74 |
G |
T |
2: 89,440,108 (GRCm39) |
L113M |
probably damaging |
Het |
Or4a74 |
A |
T |
2: 89,440,107 (GRCm39) |
L113Q |
probably damaging |
Het |
Or5al7 |
A |
T |
2: 85,992,923 (GRCm39) |
Y123* |
probably null |
Het |
Parp4 |
A |
G |
14: 56,844,980 (GRCm39) |
R624G |
probably damaging |
Het |
Pex16 |
C |
T |
2: 92,211,401 (GRCm39) |
P325S |
probably damaging |
Het |
Pik3ca |
T |
C |
3: 32,493,902 (GRCm39) |
M288T |
possibly damaging |
Het |
Pla2g5 |
C |
T |
4: 138,527,967 (GRCm39) |
D100N |
probably benign |
Het |
Prss43 |
T |
A |
9: 110,656,430 (GRCm39) |
M39K |
probably benign |
Het |
Psd4 |
T |
C |
2: 24,284,450 (GRCm39) |
S105P |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,000,816 (GRCm39) |
S969T |
probably benign |
Het |
Rad23b |
T |
A |
4: 55,383,575 (GRCm39) |
|
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rpl10l |
A |
G |
12: 66,331,130 (GRCm39) |
M1T |
probably null |
Het |
Sec16a |
A |
G |
2: 26,318,328 (GRCm39) |
S1588P |
probably damaging |
Het |
Sh3rf1 |
A |
T |
8: 61,827,052 (GRCm39) |
H602L |
probably damaging |
Het |
Sparcl1 |
A |
T |
5: 104,236,263 (GRCm39) |
S497T |
probably benign |
Het |
Spata13 |
A |
G |
14: 60,929,537 (GRCm39) |
Y365C |
probably benign |
Het |
Trim5 |
T |
C |
7: 103,928,882 (GRCm39) |
N20D |
probably benign |
Het |
Vmn1r201 |
G |
T |
13: 22,659,194 (GRCm39) |
W136L |
probably damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,821,987 (GRCm39) |
I222V |
probably benign |
Het |
Vmn2r56 |
A |
T |
7: 12,449,644 (GRCm39) |
V198D |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,414,569 (GRCm39) |
D477G |
possibly damaging |
Het |
Zfp202 |
C |
A |
9: 40,119,778 (GRCm39) |
H194N |
probably benign |
Het |
Zfp212 |
C |
T |
6: 47,903,453 (GRCm39) |
R13W |
probably damaging |
Het |
|
Other mutations in Or7h8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01977:Or7h8
|
APN |
9 |
20,123,755 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02291:Or7h8
|
APN |
9 |
20,124,098 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02312:Or7h8
|
APN |
9 |
20,124,377 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02345:Or7h8
|
APN |
9 |
20,124,314 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0520:Or7h8
|
UTSW |
9 |
20,123,791 (GRCm39) |
missense |
probably benign |
0.01 |
R1606:Or7h8
|
UTSW |
9 |
20,124,242 (GRCm39) |
missense |
probably benign |
0.05 |
R3751:Or7h8
|
UTSW |
9 |
20,124,556 (GRCm39) |
missense |
probably damaging |
0.98 |
R4701:Or7h8
|
UTSW |
9 |
20,123,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Or7h8
|
UTSW |
9 |
20,124,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Or7h8
|
UTSW |
9 |
20,123,878 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5406:Or7h8
|
UTSW |
9 |
20,124,454 (GRCm39) |
missense |
probably benign |
0.08 |
R6541:Or7h8
|
UTSW |
9 |
20,123,695 (GRCm39) |
missense |
probably benign |
0.01 |
R6730:Or7h8
|
UTSW |
9 |
20,123,798 (GRCm39) |
missense |
probably benign |
0.04 |
R7195:Or7h8
|
UTSW |
9 |
20,123,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R7197:Or7h8
|
UTSW |
9 |
20,123,851 (GRCm39) |
missense |
probably benign |
0.00 |
R7384:Or7h8
|
UTSW |
9 |
20,124,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R7715:Or7h8
|
UTSW |
9 |
20,123,732 (GRCm39) |
missense |
probably benign |
0.06 |
R7715:Or7h8
|
UTSW |
9 |
20,123,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R8108:Or7h8
|
UTSW |
9 |
20,123,747 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8409:Or7h8
|
UTSW |
9 |
20,123,542 (GRCm39) |
start gained |
probably benign |
|
R8861:Or7h8
|
UTSW |
9 |
20,124,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Or7h8
|
UTSW |
9 |
20,124,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Or7h8
|
UTSW |
9 |
20,124,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R9154:Or7h8
|
UTSW |
9 |
20,124,173 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9665:Or7h8
|
UTSW |
9 |
20,124,402 (GRCm39) |
nonsense |
probably null |
|
R9743:Or7h8
|
UTSW |
9 |
20,123,840 (GRCm39) |
missense |
probably damaging |
0.99 |
RF013:Or7h8
|
UTSW |
9 |
20,124,190 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Or7h8
|
UTSW |
9 |
20,124,140 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Or7h8
|
UTSW |
9 |
20,124,482 (GRCm39) |
missense |
probably damaging |
1.00 |
|