Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110082J24Rik |
G |
T |
5: 30,310,287 (GRCm39) |
A24E |
unknown |
Het |
Acap1 |
A |
G |
11: 69,781,003 (GRCm39) |
L117P |
probably damaging |
Het |
Actl6b |
G |
A |
5: 137,565,585 (GRCm39) |
G394S |
probably damaging |
Het |
Actr3b |
G |
T |
5: 26,030,202 (GRCm39) |
V177F |
possibly damaging |
Het |
Adamts6 |
A |
G |
13: 104,450,839 (GRCm39) |
T341A |
probably benign |
Het |
Agbl4 |
G |
T |
4: 111,520,156 (GRCm39) |
V474F |
probably benign |
Het |
Atosa |
A |
T |
9: 74,917,335 (GRCm39) |
T652S |
probably benign |
Het |
Bach1 |
T |
C |
16: 87,516,517 (GRCm39) |
S353P |
probably benign |
Het |
C1qtnf9 |
G |
A |
14: 61,017,141 (GRCm39) |
D224N |
probably damaging |
Het |
Camkmt |
A |
T |
17: 85,421,260 (GRCm39) |
N121Y |
probably damaging |
Het |
Card6 |
A |
T |
15: 5,129,078 (GRCm39) |
Y773N |
possibly damaging |
Het |
Cbfa2t2 |
C |
A |
2: 154,342,403 (GRCm39) |
P40T |
possibly damaging |
Het |
Colec10 |
A |
C |
15: 54,298,420 (GRCm39) |
E60D |
probably benign |
Het |
Cspg4 |
T |
C |
9: 56,800,280 (GRCm39) |
V1647A |
probably benign |
Het |
Cyp2d34 |
A |
G |
15: 82,502,471 (GRCm39) |
F222L |
probably benign |
Het |
Dennd1b |
A |
T |
1: 138,969,774 (GRCm39) |
I97F |
possibly damaging |
Het |
Deptor |
A |
C |
15: 55,083,596 (GRCm39) |
D388A |
possibly damaging |
Het |
Dhx40 |
T |
C |
11: 86,690,419 (GRCm39) |
K201E |
possibly damaging |
Het |
Dnah6 |
G |
A |
6: 73,145,850 (GRCm39) |
R854C |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,877,517 (GRCm39) |
I409V |
possibly damaging |
Het |
Eif1ad16 |
T |
G |
12: 87,985,278 (GRCm39) |
K88N |
probably damaging |
Het |
Esp31 |
G |
T |
17: 38,955,592 (GRCm39) |
L78F |
possibly damaging |
Het |
Fam98c |
A |
T |
7: 28,852,889 (GRCm39) |
V48E |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,853,264 (GRCm39) |
E1517V |
possibly damaging |
Het |
Fgfr1 |
A |
T |
8: 26,052,253 (GRCm39) |
D193V |
possibly damaging |
Het |
Furin |
C |
T |
7: 80,041,775 (GRCm39) |
|
probably benign |
Het |
Gm17078 |
A |
T |
14: 51,848,693 (GRCm39) |
F15I |
probably damaging |
Het |
Grid2 |
G |
T |
6: 63,480,321 (GRCm39) |
R45L |
probably damaging |
Het |
Hecw2 |
A |
G |
1: 53,904,223 (GRCm39) |
V1175A |
probably benign |
Het |
Hspa1b |
T |
C |
17: 35,176,072 (GRCm39) |
I638V |
possibly damaging |
Het |
Ighv6-7 |
A |
G |
12: 114,419,304 (GRCm39) |
V100A |
probably benign |
Het |
Itch |
G |
T |
2: 155,052,478 (GRCm39) |
E693* |
probably null |
Het |
Ivl |
G |
A |
3: 92,478,823 (GRCm39) |
S414L |
unknown |
Het |
Kif5b |
T |
A |
18: 6,225,787 (GRCm39) |
N160I |
probably benign |
Het |
Klhl5 |
A |
G |
5: 65,306,881 (GRCm39) |
|
probably benign |
Het |
Lpin1 |
C |
T |
12: 16,623,660 (GRCm39) |
|
probably benign |
Het |
Malsu1 |
C |
A |
6: 49,052,171 (GRCm39) |
H130Q |
probably benign |
Het |
Naip2 |
A |
C |
13: 100,297,676 (GRCm39) |
L787V |
probably damaging |
Het |
Nynrin |
C |
T |
14: 56,110,106 (GRCm39) |
R1738W |
probably damaging |
Het |
Or11g27 |
A |
G |
14: 50,770,910 (GRCm39) |
T14A |
probably benign |
Het |
Or4e1 |
A |
T |
14: 52,701,358 (GRCm39) |
I36N |
possibly damaging |
Het |
Or51d1 |
C |
T |
7: 102,347,777 (GRCm39) |
Q111* |
probably null |
Het |
Pclo |
A |
G |
5: 14,571,706 (GRCm39) |
T364A |
unknown |
Het |
Phlda2 |
A |
C |
7: 143,056,206 (GRCm39) |
S8A |
probably benign |
Het |
Pou3f1 |
G |
A |
4: 124,551,549 (GRCm39) |
G17E |
unknown |
Het |
Ppfibp2 |
A |
G |
7: 107,346,785 (GRCm39) |
D899G |
probably damaging |
Het |
Pskh1 |
T |
C |
8: 106,639,833 (GRCm39) |
V171A |
probably damaging |
Het |
Rictor |
A |
G |
15: 6,816,513 (GRCm39) |
T1262A |
probably damaging |
Het |
Rnf41 |
T |
C |
10: 128,274,077 (GRCm39) |
V243A |
probably benign |
Het |
Slc9c1 |
T |
A |
16: 45,427,182 (GRCm39) |
N1162K |
probably benign |
Het |
Spef2 |
A |
T |
15: 9,602,005 (GRCm39) |
L1419* |
probably null |
Het |
Tenm4 |
C |
T |
7: 96,555,148 (GRCm39) |
P2618S |
probably benign |
Het |
Tnc |
A |
G |
4: 63,880,313 (GRCm39) |
C1954R |
probably damaging |
Het |
Ttll11 |
T |
A |
2: 35,674,161 (GRCm39) |
I622F |
probably damaging |
Het |
Utp25 |
T |
C |
1: 192,796,110 (GRCm39) |
E673G |
probably benign |
Het |
Vmn2r104 |
A |
G |
17: 20,262,110 (GRCm39) |
I340T |
probably damaging |
Het |
Vmn2r110 |
G |
T |
17: 20,803,404 (GRCm39) |
D390E |
probably benign |
Het |
|
Other mutations in Or7e176 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01904:Or7e176
|
APN |
9 |
20,171,586 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02048:Or7e176
|
APN |
9 |
20,171,784 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02232:Or7e176
|
APN |
9 |
20,171,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02314:Or7e176
|
APN |
9 |
20,171,774 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03290:Or7e176
|
APN |
9 |
20,171,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0410:Or7e176
|
UTSW |
9 |
20,171,797 (GRCm39) |
missense |
probably benign |
0.03 |
R1482:Or7e176
|
UTSW |
9 |
20,172,020 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1521:Or7e176
|
UTSW |
9 |
20,171,728 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4930:Or7e176
|
UTSW |
9 |
20,171,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R5457:Or7e176
|
UTSW |
9 |
20,171,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R5870:Or7e176
|
UTSW |
9 |
20,171,874 (GRCm39) |
missense |
probably benign |
|
R6141:Or7e176
|
UTSW |
9 |
20,171,754 (GRCm39) |
missense |
probably benign |
0.00 |
R7283:Or7e176
|
UTSW |
9 |
20,171,555 (GRCm39) |
missense |
probably damaging |
0.98 |
R8882:Or7e176
|
UTSW |
9 |
20,171,256 (GRCm39) |
missense |
probably benign |
0.06 |
R9556:Or7e176
|
UTSW |
9 |
20,171,651 (GRCm39) |
missense |
probably benign |
0.00 |
R9618:Or7e176
|
UTSW |
9 |
20,171,639 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9752:Or7e176
|
UTSW |
9 |
20,171,204 (GRCm39) |
missense |
probably benign |
0.10 |
X0025:Or7e176
|
UTSW |
9 |
20,171,782 (GRCm39) |
missense |
probably benign |
0.01 |
|