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 |
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 |
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 Gm15446 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01584:Gm15446
|
APN |
5 |
110,088,668 (GRCm39) |
makesense |
probably null |
|
R0606:Gm15446
|
UTSW |
5 |
110,091,347 (GRCm39) |
missense |
probably benign |
|
R1608:Gm15446
|
UTSW |
5 |
110,090,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Gm15446
|
UTSW |
5 |
110,090,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R1892:Gm15446
|
UTSW |
5 |
110,091,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R2000:Gm15446
|
UTSW |
5 |
110,090,677 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2059:Gm15446
|
UTSW |
5 |
110,090,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R3083:Gm15446
|
UTSW |
5 |
110,091,158 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3883:Gm15446
|
UTSW |
5 |
110,088,313 (GRCm39) |
missense |
probably damaging |
0.98 |
R4086:Gm15446
|
UTSW |
5 |
110,091,121 (GRCm39) |
missense |
probably benign |
0.02 |
R4095:Gm15446
|
UTSW |
5 |
110,088,590 (GRCm39) |
splice site |
probably null |
|
R4459:Gm15446
|
UTSW |
5 |
110,091,107 (GRCm39) |
missense |
probably benign |
0.03 |
R4721:Gm15446
|
UTSW |
5 |
110,090,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Gm15446
|
UTSW |
5 |
110,090,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5229:Gm15446
|
UTSW |
5 |
110,091,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Gm15446
|
UTSW |
5 |
110,088,364 (GRCm39) |
nonsense |
probably null |
|
R6116:Gm15446
|
UTSW |
5 |
110,090,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R6166:Gm15446
|
UTSW |
5 |
110,090,646 (GRCm39) |
nonsense |
probably null |
|
R6322:Gm15446
|
UTSW |
5 |
110,091,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Gm15446
|
UTSW |
5 |
110,091,165 (GRCm39) |
nonsense |
probably null |
|
R7939:Gm15446
|
UTSW |
5 |
110,090,360 (GRCm39) |
missense |
probably benign |
0.22 |
R8045:Gm15446
|
UTSW |
5 |
110,088,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Gm15446
|
UTSW |
5 |
110,088,306 (GRCm39) |
nonsense |
probably null |
|
R8528:Gm15446
|
UTSW |
5 |
110,090,896 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9074:Gm15446
|
UTSW |
5 |
110,091,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9198:Gm15446
|
UTSW |
5 |
110,090,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R9604:Gm15446
|
UTSW |
5 |
110,088,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R9706:Gm15446
|
UTSW |
5 |
110,091,161 (GRCm39) |
missense |
probably damaging |
0.96 |
|