Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921513D11Rik |
G |
T |
17: 79,935,638 (GRCm39) |
|
probably benign |
Het |
Apeh |
C |
T |
9: 107,971,486 (GRCm39) |
A29T |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,826,524 (GRCm39) |
Y1013* |
probably null |
Het |
Arhgef4 |
A |
G |
1: 34,762,355 (GRCm39) |
E537G |
unknown |
Het |
Asf1b |
T |
C |
8: 84,682,540 (GRCm39) |
F28S |
probably damaging |
Het |
Cd46 |
T |
A |
1: 194,767,693 (GRCm39) |
I123L |
possibly damaging |
Het |
Cdca7 |
A |
T |
2: 72,309,370 (GRCm39) |
T48S |
probably damaging |
Het |
Cfap53 |
T |
A |
18: 74,492,838 (GRCm39) |
|
probably benign |
Het |
Clca3a2 |
T |
A |
3: 144,511,599 (GRCm39) |
T599S |
probably benign |
Het |
Csf1 |
T |
A |
3: 107,656,252 (GRCm39) |
T148S |
probably benign |
Het |
Dmbt1 |
T |
C |
7: 130,699,400 (GRCm39) |
|
probably null |
Het |
Dmpk |
A |
G |
7: 18,818,050 (GRCm39) |
D44G |
probably damaging |
Het |
Dnajb12 |
T |
A |
10: 59,728,782 (GRCm39) |
N223K |
probably damaging |
Het |
Dync1h1 |
T |
A |
12: 110,595,264 (GRCm39) |
M1392K |
probably benign |
Het |
Edrf1 |
C |
T |
7: 133,261,908 (GRCm39) |
A867V |
probably damaging |
Het |
Efemp2 |
T |
A |
19: 5,527,706 (GRCm39) |
C94S |
possibly damaging |
Het |
Epha8 |
C |
T |
4: 136,666,037 (GRCm39) |
S373N |
probably benign |
Het |
Foxk1 |
A |
G |
5: 142,434,588 (GRCm39) |
D284G |
possibly damaging |
Het |
Fzd10 |
C |
A |
5: 128,678,366 (GRCm39) |
R29S |
possibly damaging |
Het |
Gm13991 |
T |
C |
2: 116,358,665 (GRCm39) |
|
noncoding transcript |
Het |
Gm6818 |
A |
T |
7: 38,101,471 (GRCm39) |
|
noncoding transcript |
Het |
Hydin |
T |
A |
8: 111,336,333 (GRCm39) |
C5037S |
probably benign |
Het |
Ikzf1 |
T |
A |
11: 11,719,448 (GRCm39) |
M492K |
probably damaging |
Het |
Krt20 |
G |
T |
11: 99,320,879 (GRCm39) |
S394R |
possibly damaging |
Het |
Lrrc71 |
T |
A |
3: 87,653,094 (GRCm39) |
R107S |
probably benign |
Het |
Mia2 |
A |
G |
12: 59,219,323 (GRCm39) |
T436A |
possibly damaging |
Het |
Muc19 |
T |
A |
15: 91,784,614 (GRCm39) |
|
noncoding transcript |
Het |
Neu4 |
T |
C |
1: 93,952,177 (GRCm39) |
V182A |
probably damaging |
Het |
Notch2 |
T |
G |
3: 98,031,626 (GRCm39) |
F1167V |
possibly damaging |
Het |
Nrap |
A |
G |
19: 56,360,277 (GRCm39) |
M189T |
possibly damaging |
Het |
Nt5m |
A |
T |
11: 59,765,487 (GRCm39) |
I172F |
probably damaging |
Het |
Or5b118 |
G |
T |
19: 13,449,037 (GRCm39) |
K234N |
probably damaging |
Het |
Or8k41 |
A |
T |
2: 86,313,362 (GRCm39) |
C241* |
probably null |
Het |
Plekha5 |
C |
T |
6: 140,372,254 (GRCm39) |
T68M |
probably damaging |
Het |
Ppef2 |
A |
G |
5: 92,392,461 (GRCm39) |
|
probably null |
Het |
Ppp1r37 |
T |
C |
7: 19,295,900 (GRCm39) |
|
probably benign |
Het |
Rfx4 |
T |
C |
10: 84,704,218 (GRCm39) |
Y238H |
probably damaging |
Het |
Sanbr |
A |
G |
11: 23,543,424 (GRCm39) |
|
probably null |
Het |
Sec13 |
G |
A |
6: 113,707,837 (GRCm39) |
A161V |
probably benign |
Het |
Serhl |
G |
A |
15: 82,986,895 (GRCm39) |
|
probably benign |
Het |
Slco4a1 |
T |
C |
2: 180,114,572 (GRCm39) |
V588A |
probably benign |
Het |
Slitrk3 |
T |
C |
3: 72,956,592 (GRCm39) |
T727A |
probably benign |
Het |
Sp100 |
T |
A |
1: 85,601,404 (GRCm39) |
D241E |
probably damaging |
Het |
Spata2 |
G |
T |
2: 167,325,494 (GRCm39) |
H442N |
probably damaging |
Het |
Speg |
T |
C |
1: 75,404,731 (GRCm39) |
V2588A |
probably damaging |
Het |
Tnfsf12 |
A |
G |
11: 69,578,155 (GRCm39) |
S141P |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,219,762 (GRCm39) |
I2166M |
probably damaging |
Het |
Trim10 |
T |
A |
17: 37,187,948 (GRCm39) |
V388E |
probably damaging |
Het |
Ttc23l |
G |
T |
15: 10,551,636 (GRCm39) |
T30K |
possibly damaging |
Het |
Vmn2r10 |
A |
G |
5: 109,143,466 (GRCm39) |
V828A |
probably benign |
Het |
Vmn2r75 |
T |
A |
7: 85,813,436 (GRCm39) |
L455F |
possibly damaging |
Het |
Vwa8 |
T |
A |
14: 79,221,666 (GRCm39) |
S541T |
probably benign |
Het |
|
Other mutations in Or5w15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02304:Or5w15
|
APN |
2 |
87,568,330 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02490:Or5w15
|
APN |
2 |
87,568,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02730:Or5w15
|
APN |
2 |
87,567,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03106:Or5w15
|
APN |
2 |
87,568,462 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03113:Or5w15
|
APN |
2 |
87,568,506 (GRCm39) |
missense |
probably benign |
0.01 |
R0450:Or5w15
|
UTSW |
2 |
87,567,825 (GRCm39) |
missense |
probably damaging |
0.98 |
R0469:Or5w15
|
UTSW |
2 |
87,567,825 (GRCm39) |
missense |
probably damaging |
0.98 |
R0510:Or5w15
|
UTSW |
2 |
87,567,825 (GRCm39) |
missense |
probably damaging |
0.98 |
R3696:Or5w15
|
UTSW |
2 |
87,568,360 (GRCm39) |
missense |
probably benign |
|
R3698:Or5w15
|
UTSW |
2 |
87,568,360 (GRCm39) |
missense |
probably benign |
|
R5149:Or5w15
|
UTSW |
2 |
87,567,749 (GRCm39) |
missense |
probably benign |
|
R6245:Or5w15
|
UTSW |
2 |
87,568,240 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6701:Or5w15
|
UTSW |
2 |
87,567,753 (GRCm39) |
missense |
probably benign |
|
R7170:Or5w15
|
UTSW |
2 |
87,568,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R7185:Or5w15
|
UTSW |
2 |
87,568,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Or5w15
|
UTSW |
2 |
87,568,852 (GRCm39) |
splice site |
probably null |
|
R8065:Or5w15
|
UTSW |
2 |
87,568,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R8067:Or5w15
|
UTSW |
2 |
87,568,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R8671:Or5w15
|
UTSW |
2 |
87,567,990 (GRCm39) |
missense |
probably damaging |
0.96 |
R8953:Or5w15
|
UTSW |
2 |
87,568,371 (GRCm39) |
missense |
probably benign |
0.01 |
R9254:Or5w15
|
UTSW |
2 |
87,568,372 (GRCm39) |
missense |
probably benign |
|
R9356:Or5w15
|
UTSW |
2 |
87,568,089 (GRCm39) |
missense |
probably benign |
0.01 |
R9481:Or5w15
|
UTSW |
2 |
87,568,576 (GRCm39) |
missense |
probably benign |
0.44 |
R9544:Or5w15
|
UTSW |
2 |
87,568,644 (GRCm39) |
missense |
probably benign |
|
R9588:Or5w15
|
UTSW |
2 |
87,568,644 (GRCm39) |
missense |
probably benign |
|
R9646:Or5w15
|
UTSW |
2 |
87,568,512 (GRCm39) |
missense |
probably damaging |
0.97 |
|