Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
A |
G |
5: 8,903,607 (GRCm39) |
D1086G |
possibly damaging |
Het |
Ahcyl2 |
T |
C |
6: 29,906,768 (GRCm39) |
|
probably benign |
Het |
Ankrd42 |
T |
A |
7: 92,241,066 (GRCm39) |
Q431L |
probably benign |
Het |
Arhgap12 |
A |
T |
18: 6,031,766 (GRCm39) |
F592I |
probably damaging |
Het |
Arhgef28 |
A |
G |
13: 98,088,071 (GRCm39) |
|
probably null |
Het |
Boc |
A |
G |
16: 44,313,184 (GRCm39) |
F560S |
probably damaging |
Het |
Ccdc81 |
A |
T |
7: 89,545,916 (GRCm39) |
V96E |
probably benign |
Het |
Cep162 |
C |
T |
9: 87,107,839 (GRCm39) |
S517N |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 116,085,178 (GRCm39) |
N372S |
probably benign |
Het |
Dnah7a |
G |
A |
1: 53,458,766 (GRCm39) |
R3791C |
probably damaging |
Het |
Fdxr |
T |
C |
11: 115,166,918 (GRCm39) |
Q57R |
probably benign |
Het |
Fsip2l |
T |
A |
X: 47,961,825 (GRCm39) |
Q296L |
possibly damaging |
Het |
G3bp2 |
A |
G |
5: 92,216,367 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,678,660 (GRCm39) |
T487I |
probably benign |
Het |
Kpna7 |
A |
T |
5: 144,933,847 (GRCm39) |
I282N |
probably damaging |
Het |
Lif |
A |
T |
11: 4,219,201 (GRCm39) |
Y160F |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,361,134 (GRCm39) |
D556E |
possibly damaging |
Het |
Myom2 |
G |
T |
8: 15,161,844 (GRCm39) |
E954* |
probably null |
Het |
Nr6a1 |
A |
T |
2: 38,632,948 (GRCm39) |
I171N |
probably damaging |
Het |
Nup210 |
C |
A |
6: 90,992,832 (GRCm39) |
R1059L |
probably benign |
Het |
Or11g27 |
A |
G |
14: 50,770,877 (GRCm39) |
T3A |
probably benign |
Het |
Or2ag16 |
A |
G |
7: 106,351,980 (GRCm39) |
I205T |
probably benign |
Het |
Or5ak4 |
A |
T |
2: 85,161,864 (GRCm39) |
I126N |
probably damaging |
Het |
Or5aq6 |
A |
T |
2: 86,922,913 (GRCm39) |
V276E |
probably damaging |
Het |
Ostm1 |
T |
C |
10: 42,574,213 (GRCm39) |
V302A |
probably damaging |
Het |
Oxct1 |
A |
G |
15: 4,130,671 (GRCm39) |
M388V |
possibly damaging |
Het |
Ppp6r2 |
G |
A |
15: 89,152,758 (GRCm39) |
V300I |
possibly damaging |
Het |
Prmt1 |
T |
C |
7: 44,626,995 (GRCm39) |
Y205C |
probably damaging |
Het |
Slc45a4 |
A |
C |
15: 73,456,272 (GRCm39) |
V636G |
possibly damaging |
Het |
Spata18 |
T |
A |
5: 73,828,591 (GRCm39) |
L270Q |
probably damaging |
Het |
Stard9 |
G |
A |
2: 120,536,283 (GRCm39) |
D4151N |
probably damaging |
Het |
Thsd7b |
G |
A |
1: 129,556,646 (GRCm39) |
C334Y |
probably damaging |
Het |
Tmtc3 |
C |
T |
10: 100,294,896 (GRCm39) |
V406M |
probably benign |
Het |
Trpc5 |
T |
A |
X: 143,165,724 (GRCm39) |
M900L |
probably benign |
Het |
Ttc9c |
T |
C |
19: 8,793,344 (GRCm39) |
K99E |
probably benign |
Het |
Vmn1r73 |
A |
G |
7: 11,491,007 (GRCm39) |
E275G |
probably damaging |
Het |
|
Other mutations in Or2w25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Or2w25
|
APN |
11 |
59,504,147 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01835:Or2w25
|
APN |
11 |
59,504,165 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02006:Or2w25
|
APN |
11 |
59,503,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Or2w25
|
UTSW |
11 |
59,504,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R0831:Or2w25
|
UTSW |
11 |
59,504,480 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1924:Or2w25
|
UTSW |
11 |
59,503,949 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2184:Or2w25
|
UTSW |
11 |
59,503,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Or2w25
|
UTSW |
11 |
59,504,712 (GRCm39) |
missense |
probably benign |
|
R6986:Or2w25
|
UTSW |
11 |
59,504,924 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7405:Or2w25
|
UTSW |
11 |
59,504,899 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7755:Or2w25
|
UTSW |
11 |
59,504,467 (GRCm39) |
missense |
probably damaging |
0.97 |
R7851:Or2w25
|
UTSW |
11 |
59,504,789 (GRCm39) |
missense |
probably benign |
0.33 |
R9437:Or2w25
|
UTSW |
11 |
59,504,195 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9545:Or2w25
|
UTSW |
11 |
59,504,275 (GRCm39) |
missense |
probably benign |
0.27 |
R9562:Or2w25
|
UTSW |
11 |
59,504,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Or2w25
|
UTSW |
11 |
59,504,339 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Or2w25
|
UTSW |
11 |
59,504,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|