Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt1s1 |
A |
G |
7: 44,503,363 (GRCm39) |
D180G |
probably damaging |
Het |
Aldh1a7 |
A |
T |
19: 20,673,762 (GRCm39) |
Y457* |
probably null |
Het |
Alpk3 |
C |
T |
7: 80,728,138 (GRCm39) |
P423S |
possibly damaging |
Het |
Aox1 |
A |
T |
1: 58,373,837 (GRCm39) |
|
probably null |
Het |
Crebbp |
T |
C |
16: 3,913,966 (GRCm39) |
T1316A |
probably benign |
Het |
Cul3 |
C |
A |
1: 80,261,407 (GRCm39) |
V273F |
probably damaging |
Het |
Dnah1 |
G |
T |
14: 31,028,985 (GRCm39) |
R582S |
probably benign |
Het |
Fbxl2 |
T |
C |
9: 113,832,261 (GRCm39) |
N51S |
probably damaging |
Het |
Gapvd1 |
T |
C |
2: 34,618,488 (GRCm39) |
D295G |
probably benign |
Het |
Gdf7 |
A |
G |
12: 8,348,845 (GRCm39) |
S151P |
unknown |
Het |
Gm10277 |
T |
C |
11: 77,676,827 (GRCm39) |
|
probably benign |
Het |
Hdac4 |
T |
C |
1: 91,898,690 (GRCm39) |
E688G |
possibly damaging |
Het |
Htr1d |
A |
G |
4: 136,170,548 (GRCm39) |
E259G |
probably benign |
Het |
Ifi204 |
T |
C |
1: 173,576,774 (GRCm39) |
H609R |
possibly damaging |
Het |
Ift80 |
T |
C |
3: 68,825,332 (GRCm39) |
D541G |
probably damaging |
Het |
Il18r1 |
A |
T |
1: 40,514,034 (GRCm39) |
H80L |
possibly damaging |
Het |
Lrp4 |
G |
A |
2: 91,304,294 (GRCm39) |
G158S |
probably damaging |
Het |
Mesd |
T |
A |
7: 83,546,993 (GRCm39) |
L152H |
probably damaging |
Het |
Mmut |
G |
A |
17: 41,266,030 (GRCm39) |
C531Y |
probably damaging |
Het |
Morf4l1 |
A |
T |
9: 89,976,501 (GRCm39) |
F276I |
possibly damaging |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,395,145 (GRCm39) |
T2480A |
probably benign |
Het |
Or2a52 |
A |
T |
6: 43,144,192 (GRCm39) |
I67F |
probably benign |
Het |
Or2y15 |
G |
A |
11: 49,350,766 (GRCm39) |
G87R |
possibly damaging |
Het |
Or4f47 |
T |
C |
2: 111,972,359 (GRCm39) |
I23T |
probably benign |
Het |
Or5k16 |
A |
G |
16: 58,736,702 (GRCm39) |
F101L |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,893,883 (GRCm39) |
|
probably benign |
Het |
Ovgp1 |
A |
G |
3: 105,893,912 (GRCm39) |
|
probably benign |
Het |
Pcbp4 |
A |
T |
9: 106,338,570 (GRCm39) |
Q59L |
possibly damaging |
Het |
Prg4 |
G |
C |
1: 150,330,510 (GRCm39) |
|
probably benign |
Het |
Rad50 |
T |
A |
11: 53,569,697 (GRCm39) |
I905L |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,266,756 (GRCm39) |
S781P |
probably benign |
Het |
Rps3 |
C |
T |
7: 99,129,103 (GRCm39) |
R173H |
probably benign |
Het |
Rtn3 |
T |
A |
19: 7,412,450 (GRCm39) |
T86S |
probably damaging |
Het |
Sdha |
A |
T |
13: 74,482,510 (GRCm39) |
S268T |
probably benign |
Het |
Sgo2b |
A |
T |
8: 64,381,767 (GRCm39) |
V355E |
possibly damaging |
Het |
Sh3glb2 |
T |
C |
2: 30,245,300 (GRCm39) |
T60A |
probably damaging |
Het |
Slc26a3 |
A |
C |
12: 31,514,719 (GRCm39) |
Y513S |
probably damaging |
Het |
Slc35b2 |
T |
C |
17: 45,877,368 (GRCm39) |
V165A |
probably benign |
Het |
Slco3a1 |
A |
G |
7: 73,934,361 (GRCm39) |
W604R |
probably damaging |
Het |
Tet2 |
A |
G |
3: 133,175,238 (GRCm39) |
S1370P |
possibly damaging |
Het |
Tmtc4 |
A |
T |
14: 123,158,731 (GRCm39) |
|
probably null |
Het |
Tsga13 |
A |
G |
6: 30,889,198 (GRCm39) |
V18A |
probably benign |
Het |
Ugt2a3 |
T |
C |
5: 87,477,449 (GRCm39) |
T317A |
probably benign |
Het |
Zcchc4 |
A |
T |
5: 52,941,442 (GRCm39) |
D79V |
probably damaging |
Het |
|
Other mutations in Or4g17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03024:Or4g17
|
APN |
2 |
111,209,935 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0526:Or4g17
|
UTSW |
2 |
111,209,837 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0731:Or4g17
|
UTSW |
2 |
111,209,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R1762:Or4g17
|
UTSW |
2 |
111,209,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R1765:Or4g17
|
UTSW |
2 |
111,209,491 (GRCm39) |
missense |
probably benign |
0.39 |
R3106:Or4g17
|
UTSW |
2 |
111,209,840 (GRCm39) |
missense |
probably benign |
0.23 |
R3803:Or4g17
|
UTSW |
2 |
111,209,638 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4005:Or4g17
|
UTSW |
2 |
111,210,088 (GRCm39) |
missense |
probably benign |
0.05 |
R4227:Or4g17
|
UTSW |
2 |
111,209,410 (GRCm39) |
missense |
probably benign |
|
R4637:Or4g17
|
UTSW |
2 |
111,209,927 (GRCm39) |
missense |
probably benign |
0.03 |
R4707:Or4g17
|
UTSW |
2 |
111,209,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R4762:Or4g17
|
UTSW |
2 |
111,210,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R5150:Or4g17
|
UTSW |
2 |
111,209,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Or4g17
|
UTSW |
2 |
111,210,179 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5312:Or4g17
|
UTSW |
2 |
111,210,179 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6554:Or4g17
|
UTSW |
2 |
111,209,504 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6913:Or4g17
|
UTSW |
2 |
111,209,347 (GRCm39) |
start codon destroyed |
probably null |
0.03 |
R6980:Or4g17
|
UTSW |
2 |
111,209,620 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6995:Or4g17
|
UTSW |
2 |
111,209,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R7168:Or4g17
|
UTSW |
2 |
111,210,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Or4g17
|
UTSW |
2 |
111,209,738 (GRCm39) |
missense |
not run |
|
R7464:Or4g17
|
UTSW |
2 |
111,209,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R8125:Or4g17
|
UTSW |
2 |
111,210,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R8963:Or4g17
|
UTSW |
2 |
111,209,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Or4g17
|
UTSW |
2 |
111,210,239 (GRCm39) |
missense |
probably damaging |
0.97 |
|