Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
C |
T |
1: 71,305,124 (GRCm39) |
V2044I |
possibly damaging |
Het |
Adgrv1 |
A |
G |
13: 81,614,279 (GRCm39) |
|
probably null |
Het |
Arhgef38 |
T |
C |
3: 132,839,465 (GRCm39) |
Q526R |
probably benign |
Het |
Atp2c2 |
A |
G |
8: 120,479,726 (GRCm39) |
N752D |
probably benign |
Het |
Atp6v0a1 |
T |
C |
11: 100,920,030 (GRCm39) |
I221T |
probably damaging |
Het |
Atp8b5 |
T |
C |
4: 43,355,673 (GRCm39) |
V551A |
possibly damaging |
Het |
B3galnt1 |
A |
G |
3: 69,483,040 (GRCm39) |
S74P |
possibly damaging |
Het |
Bcl2l13 |
A |
G |
6: 120,842,675 (GRCm39) |
I123V |
probably benign |
Het |
Brms1l |
A |
T |
12: 55,915,007 (GRCm39) |
K305N |
probably damaging |
Het |
Ccdc82 |
C |
T |
9: 13,252,385 (GRCm39) |
R226C |
probably damaging |
Het |
Chst9 |
T |
G |
18: 15,586,122 (GRCm39) |
K147T |
probably benign |
Het |
Clec16a |
A |
G |
16: 10,413,762 (GRCm39) |
R390G |
probably damaging |
Het |
Clec5a |
G |
T |
6: 40,562,153 (GRCm39) |
H4N |
probably benign |
Het |
Csmd1 |
T |
A |
8: 15,975,299 (GRCm39) |
Q2970L |
probably damaging |
Het |
Cyp2a4 |
T |
C |
7: 26,007,076 (GRCm39) |
I61T |
possibly damaging |
Het |
Cyp3a16 |
T |
A |
5: 145,378,884 (GRCm39) |
K379I |
possibly damaging |
Het |
Cyp3a16 |
T |
C |
5: 145,378,885 (GRCm39) |
K379E |
probably damaging |
Het |
Dok2 |
A |
G |
14: 71,014,397 (GRCm39) |
D195G |
probably benign |
Het |
Emilin1 |
A |
G |
5: 31,074,764 (GRCm39) |
E335G |
probably damaging |
Het |
Haus1 |
T |
C |
18: 77,854,620 (GRCm39) |
D50G |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,857,617 (GRCm39) |
V1099A |
probably benign |
Het |
Kif15 |
T |
C |
9: 122,789,021 (GRCm39) |
V71A |
probably benign |
Het |
Klk10 |
C |
T |
7: 43,432,286 (GRCm39) |
A73V |
probably damaging |
Het |
Lins1 |
C |
A |
7: 66,364,239 (GRCm39) |
D711E |
probably benign |
Het |
Mbtps1 |
C |
T |
8: 120,265,639 (GRCm39) |
V303I |
possibly damaging |
Het |
Mest |
G |
A |
6: 30,745,822 (GRCm39) |
|
probably benign |
Het |
Nup214 |
C |
T |
2: 31,924,478 (GRCm39) |
S1669F |
probably damaging |
Het |
Or14c43 |
A |
G |
7: 86,114,658 (GRCm39) |
E13G |
probably benign |
Het |
Or6c210 |
G |
T |
10: 129,496,184 (GRCm39) |
V170F |
probably benign |
Het |
Rfwd3 |
C |
T |
8: 112,014,874 (GRCm39) |
R326Q |
probably damaging |
Het |
Rtf2 |
A |
G |
2: 172,287,285 (GRCm39) |
D68G |
probably damaging |
Het |
Sbspon |
C |
A |
1: 15,962,692 (GRCm39) |
C62F |
probably damaging |
Het |
Spata31f3 |
T |
C |
4: 42,874,020 (GRCm39) |
|
probably null |
Het |
Spg7 |
T |
A |
8: 123,816,977 (GRCm39) |
|
probably benign |
Het |
Trabd2b |
T |
C |
4: 114,437,531 (GRCm39) |
V236A |
possibly damaging |
Het |
Vmn2r10 |
A |
T |
5: 109,154,117 (GRCm39) |
N62K |
possibly damaging |
Het |
Vmn2r45 |
T |
G |
7: 8,474,746 (GRCm39) |
S761R |
possibly damaging |
Het |
Zfp580 |
C |
T |
7: 5,056,284 (GRCm39) |
R215C |
probably damaging |
Het |
Zfpm2 |
A |
G |
15: 40,966,605 (GRCm39) |
D898G |
possibly damaging |
Het |
|
Other mutations in Gm7361 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02447:Gm7361
|
APN |
5 |
26,462,853 (GRCm39) |
missense |
probably benign |
|
IGL02550:Gm7361
|
APN |
5 |
26,466,120 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0011:Gm7361
|
UTSW |
5 |
26,463,876 (GRCm39) |
splice site |
probably benign |
|
R0959:Gm7361
|
UTSW |
5 |
26,467,051 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1246:Gm7361
|
UTSW |
5 |
26,466,225 (GRCm39) |
nonsense |
probably null |
|
R1654:Gm7361
|
UTSW |
5 |
26,466,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R2065:Gm7361
|
UTSW |
5 |
26,467,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Gm7361
|
UTSW |
5 |
26,467,008 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5386:Gm7361
|
UTSW |
5 |
26,463,903 (GRCm39) |
missense |
probably benign |
|
R6282:Gm7361
|
UTSW |
5 |
26,465,411 (GRCm39) |
missense |
probably benign |
0.13 |
R6391:Gm7361
|
UTSW |
5 |
26,463,960 (GRCm39) |
missense |
probably benign |
0.37 |
R6769:Gm7361
|
UTSW |
5 |
26,462,767 (GRCm39) |
nonsense |
probably null |
|
R7205:Gm7361
|
UTSW |
5 |
26,466,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R7497:Gm7361
|
UTSW |
5 |
26,466,188 (GRCm39) |
missense |
probably benign |
|
R7498:Gm7361
|
UTSW |
5 |
26,466,188 (GRCm39) |
missense |
probably benign |
|
R7499:Gm7361
|
UTSW |
5 |
26,466,188 (GRCm39) |
missense |
probably benign |
|
R8086:Gm7361
|
UTSW |
5 |
26,465,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R8325:Gm7361
|
UTSW |
5 |
26,467,154 (GRCm39) |
missense |
probably damaging |
0.98 |
R8349:Gm7361
|
UTSW |
5 |
26,465,387 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8449:Gm7361
|
UTSW |
5 |
26,465,387 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Gm7361
|
UTSW |
5 |
26,466,186 (GRCm39) |
missense |
probably benign |
0.01 |
|