Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
T |
C |
4: 103,088,604 (GRCm39) |
I302V |
probably benign |
Het |
Ackr2 |
A |
C |
9: 121,737,657 (GRCm39) |
T11P |
possibly damaging |
Het |
Ahnak |
A |
G |
19: 8,981,149 (GRCm39) |
N811S |
probably benign |
Het |
Atm |
T |
C |
9: 53,431,381 (GRCm39) |
I326V |
probably benign |
Het |
Ccn4 |
T |
A |
15: 66,784,764 (GRCm39) |
C146S |
possibly damaging |
Het |
Cdh23 |
A |
T |
10: 60,214,574 (GRCm39) |
F1480L |
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,322,578 (GRCm39) |
E78G |
possibly damaging |
Het |
Ces1f |
A |
T |
8: 93,983,494 (GRCm39) |
N504K |
probably benign |
Het |
Chrna4 |
G |
A |
2: 180,679,264 (GRCm39) |
S61L |
probably damaging |
Het |
Clcn3 |
G |
T |
8: 61,366,061 (GRCm39) |
T864K |
unknown |
Het |
Cym |
A |
C |
3: 107,126,941 (GRCm39) |
D71E |
possibly damaging |
Het |
Ddx19b |
T |
C |
8: 111,747,673 (GRCm39) |
D87G |
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,292,621 (GRCm39) |
V3002A |
possibly damaging |
Het |
Dnmt3a |
G |
A |
12: 3,946,997 (GRCm39) |
G408S |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,625,939 (GRCm39) |
D66E |
probably benign |
Het |
Dsg3 |
A |
G |
18: 20,672,789 (GRCm39) |
D820G |
probably damaging |
Het |
Dst |
G |
A |
1: 34,153,014 (GRCm39) |
V92I |
possibly damaging |
Het |
Dusp16 |
T |
A |
6: 134,695,185 (GRCm39) |
T549S |
probably benign |
Het |
Ephx1 |
T |
A |
1: 180,827,381 (GRCm39) |
K91* |
probably null |
Het |
Flii |
A |
G |
11: 60,617,991 (GRCm39) |
F9L |
probably benign |
Het |
Fmn2 |
T |
C |
1: 174,436,308 (GRCm39) |
S760P |
unknown |
Het |
Fmnl3 |
A |
T |
15: 99,223,210 (GRCm39) |
V378E |
probably damaging |
Het |
Gbp4 |
A |
G |
5: 105,284,740 (GRCm39) |
S50P |
probably damaging |
Het |
Glra3 |
G |
T |
8: 56,393,718 (GRCm39) |
|
probably benign |
Het |
Gm10188 |
T |
C |
1: 132,157,033 (GRCm39) |
D111G |
unknown |
Het |
Gnptab |
A |
T |
10: 88,247,876 (GRCm39) |
E101V |
probably damaging |
Het |
Hacl1 |
C |
A |
14: 31,332,197 (GRCm39) |
M525I |
probably benign |
Het |
Hid1 |
T |
A |
11: 115,239,738 (GRCm39) |
T731S |
probably damaging |
Het |
Ifi203 |
T |
C |
1: 173,751,522 (GRCm39) |
Y847C |
probably damaging |
Het |
Igfbpl1 |
C |
A |
4: 45,815,472 (GRCm39) |
L221F |
probably null |
Het |
Ighv1-12 |
A |
G |
12: 114,579,757 (GRCm39) |
Y22H |
probably benign |
Het |
Inpp5f |
A |
C |
7: 128,278,515 (GRCm39) |
D435A |
possibly damaging |
Het |
L3mbtl4 |
T |
A |
17: 68,866,767 (GRCm39) |
H335Q |
probably benign |
Het |
Mapre2 |
A |
G |
18: 24,016,707 (GRCm39) |
D287G |
probably benign |
Het |
Mfsd14b |
G |
A |
13: 65,214,522 (GRCm39) |
R477W |
probably benign |
Het |
Mfsd14b |
C |
A |
13: 65,221,414 (GRCm39) |
V293L |
probably benign |
Het |
Msh4 |
A |
T |
3: 153,607,148 (GRCm39) |
S131T |
possibly damaging |
Het |
Nat8f2 |
A |
T |
6: 85,844,848 (GRCm39) |
D171E |
probably benign |
Het |
Ndufb5 |
G |
T |
3: 32,795,881 (GRCm39) |
L24F |
probably benign |
Het |
Nkain2 |
T |
C |
10: 32,278,291 (GRCm39) |
I45V |
probably damaging |
Het |
Nlrp9b |
T |
G |
7: 19,753,302 (GRCm39) |
M69R |
probably benign |
Het |
Or4k37 |
A |
T |
2: 111,159,633 (GRCm39) |
R290* |
probably null |
Het |
Or5d39 |
A |
C |
2: 87,979,935 (GRCm39) |
C143G |
probably damaging |
Het |
Oxct2b |
T |
A |
4: 123,010,413 (GRCm39) |
V111E |
possibly damaging |
Het |
Parva |
T |
A |
7: 112,187,753 (GRCm39) |
V350D |
probably damaging |
Het |
Pcdhb7 |
A |
G |
18: 37,475,434 (GRCm39) |
D190G |
probably damaging |
Het |
Pik3c2b |
T |
C |
1: 133,012,725 (GRCm39) |
|
probably null |
Het |
Plcz1 |
T |
A |
6: 139,985,484 (GRCm39) |
Q19L |
possibly damaging |
Het |
Prag1 |
A |
G |
8: 36,571,069 (GRCm39) |
N551D |
probably benign |
Het |
Rb1cc1 |
G |
A |
1: 6,310,189 (GRCm39) |
V196I |
probably damaging |
Het |
Rnf113a2 |
T |
C |
12: 84,464,270 (GRCm39) |
V54A |
probably benign |
Het |
Sec14l1 |
G |
A |
11: 117,044,102 (GRCm39) |
E537K |
probably damaging |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Shtn1 |
T |
A |
19: 59,026,735 (GRCm39) |
I119F |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,266,358 (GRCm39) |
|
probably null |
Het |
Tasp1 |
T |
C |
2: 139,819,567 (GRCm39) |
D212G |
probably benign |
Het |
Tmpo |
A |
G |
10: 90,994,608 (GRCm39) |
|
probably null |
Het |
Usp17lb |
T |
C |
7: 104,489,718 (GRCm39) |
K403R |
probably benign |
Het |
Vcpip1 |
A |
G |
1: 9,816,019 (GRCm39) |
V788A |
probably benign |
Het |
Wdr25 |
C |
A |
12: 108,864,613 (GRCm39) |
H253N |
probably benign |
Het |
Wwc2 |
G |
A |
8: 48,328,360 (GRCm39) |
S367L |
probably damaging |
Het |
Zfr |
A |
G |
15: 12,162,292 (GRCm39) |
E814G |
probably damaging |
Het |
|
Other mutations in Or5d46 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01736:Or5d46
|
APN |
2 |
88,170,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02166:Or5d46
|
APN |
2 |
88,170,022 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02340:Or5d46
|
APN |
2 |
88,169,906 (GRCm39) |
unclassified |
probably benign |
|
IGL02598:Or5d46
|
APN |
2 |
88,170,595 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03069:Or5d46
|
APN |
2 |
88,170,643 (GRCm39) |
splice site |
probably null |
|
IGL03212:Or5d46
|
APN |
2 |
88,170,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Or5d46
|
UTSW |
2 |
88,170,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1960:Or5d46
|
UTSW |
2 |
88,170,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2907:Or5d46
|
UTSW |
2 |
88,170,827 (GRCm39) |
missense |
probably benign |
0.11 |
R2908:Or5d46
|
UTSW |
2 |
88,170,827 (GRCm39) |
missense |
probably benign |
0.11 |
R4049:Or5d46
|
UTSW |
2 |
88,174,144 (GRCm39) |
splice site |
probably null |
|
R4257:Or5d46
|
UTSW |
2 |
88,170,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Or5d46
|
UTSW |
2 |
88,170,179 (GRCm39) |
missense |
probably damaging |
0.96 |
R4897:Or5d46
|
UTSW |
2 |
88,174,686 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5106:Or5d46
|
UTSW |
2 |
88,170,454 (GRCm39) |
missense |
probably benign |
0.07 |
R5192:Or5d46
|
UTSW |
2 |
88,170,092 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5196:Or5d46
|
UTSW |
2 |
88,170,092 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5331:Or5d46
|
UTSW |
2 |
88,170,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Or5d46
|
UTSW |
2 |
88,170,757 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6283:Or5d46
|
UTSW |
2 |
88,170,002 (GRCm39) |
missense |
probably benign |
0.33 |
R6702:Or5d46
|
UTSW |
2 |
88,170,586 (GRCm39) |
missense |
probably benign |
0.02 |
R8155:Or5d46
|
UTSW |
2 |
88,170,296 (GRCm39) |
missense |
probably damaging |
0.98 |
R8904:Or5d46
|
UTSW |
2 |
88,169,949 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9094:Or5d46
|
UTSW |
2 |
88,170,248 (GRCm39) |
missense |
probably benign |
0.00 |
R9443:Or5d46
|
UTSW |
2 |
88,170,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R9719:Or5d46
|
UTSW |
2 |
88,169,928 (GRCm39) |
missense |
|
|
|