Other mutations in this stock |
Total: 62 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 |
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 |
Or7h8 |
G |
T |
9: 20,124,182 (GRCm39) |
C179F |
probably damaging |
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 Or10w1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01324:Or10w1
|
APN |
19 |
13,632,297 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01335:Or10w1
|
APN |
19 |
13,632,540 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01561:Or10w1
|
APN |
19 |
13,632,269 (GRCm39) |
missense |
probably benign |
|
IGL01644:Or10w1
|
APN |
19 |
13,632,768 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02257:Or10w1
|
APN |
19 |
13,632,629 (GRCm39) |
missense |
probably benign |
|
IGL02282:Or10w1
|
APN |
19 |
13,632,622 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Or10w1
|
APN |
19 |
13,632,597 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02362:Or10w1
|
APN |
19 |
13,632,597 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02639:Or10w1
|
APN |
19 |
13,631,960 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0078:Or10w1
|
UTSW |
19 |
13,632,179 (GRCm39) |
missense |
probably benign |
0.00 |
R0278:Or10w1
|
UTSW |
19 |
13,632,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Or10w1
|
UTSW |
19 |
13,632,261 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0927:Or10w1
|
UTSW |
19 |
13,631,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R1087:Or10w1
|
UTSW |
19 |
13,632,376 (GRCm39) |
nonsense |
probably null |
|
R1762:Or10w1
|
UTSW |
19 |
13,631,868 (GRCm39) |
missense |
probably benign |
|
R2901:Or10w1
|
UTSW |
19 |
13,632,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2907:Or10w1
|
UTSW |
19 |
13,632,611 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3625:Or10w1
|
UTSW |
19 |
13,632,346 (GRCm39) |
nonsense |
probably null |
|
R3838:Or10w1
|
UTSW |
19 |
13,632,321 (GRCm39) |
missense |
probably benign |
0.00 |
R4745:Or10w1
|
UTSW |
19 |
13,632,750 (GRCm39) |
missense |
probably benign |
|
R4804:Or10w1
|
UTSW |
19 |
13,631,882 (GRCm39) |
missense |
probably benign |
|
R5026:Or10w1
|
UTSW |
19 |
13,632,296 (GRCm39) |
missense |
probably benign |
0.03 |
R5314:Or10w1
|
UTSW |
19 |
13,632,630 (GRCm39) |
missense |
probably benign |
0.08 |
R6052:Or10w1
|
UTSW |
19 |
13,631,871 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6235:Or10w1
|
UTSW |
19 |
13,632,145 (GRCm39) |
nonsense |
probably null |
|
R7405:Or10w1
|
UTSW |
19 |
13,632,246 (GRCm39) |
missense |
probably benign |
0.14 |
R7557:Or10w1
|
UTSW |
19 |
13,632,390 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8038:Or10w1
|
UTSW |
19 |
13,632,719 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8338:Or10w1
|
UTSW |
19 |
13,632,216 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8366:Or10w1
|
UTSW |
19 |
13,631,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R8496:Or10w1
|
UTSW |
19 |
13,632,388 (GRCm39) |
missense |
probably damaging |
0.96 |
R8783:Or10w1
|
UTSW |
19 |
13,632,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R8838:Or10w1
|
UTSW |
19 |
13,632,371 (GRCm39) |
missense |
probably damaging |
0.98 |
R8859:Or10w1
|
UTSW |
19 |
13,632,246 (GRCm39) |
missense |
probably damaging |
0.99 |
R9064:Or10w1
|
UTSW |
19 |
13,632,719 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9161:Or10w1
|
UTSW |
19 |
13,632,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R9466:Or10w1
|
UTSW |
19 |
13,631,796 (GRCm39) |
start codon destroyed |
probably null |
|
R9596:Or10w1
|
UTSW |
19 |
13,632,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Or10w1
|
UTSW |
19 |
13,632,414 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or10w1
|
UTSW |
19 |
13,631,827 (GRCm39) |
missense |
probably benign |
0.00 |
|