Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,771,971 (GRCm39) |
N387Y |
probably damaging |
Het |
Abhd17a |
T |
C |
10: 80,422,421 (GRCm39) |
E87G |
probably damaging |
Het |
Aco1 |
T |
A |
4: 40,188,330 (GRCm39) |
|
probably null |
Het |
Adcy6 |
T |
C |
15: 98,494,086 (GRCm39) |
N817S |
probably benign |
Het |
Ak8 |
T |
A |
2: 28,599,957 (GRCm39) |
L63* |
probably null |
Het |
Arhgef28 |
G |
A |
13: 98,211,755 (GRCm39) |
S76L |
probably damaging |
Het |
Asap1 |
A |
G |
15: 63,966,261 (GRCm39) |
L891S |
possibly damaging |
Het |
Cacng5 |
C |
A |
11: 107,768,379 (GRCm39) |
M209I |
probably benign |
Het |
Casr |
T |
C |
16: 36,335,950 (GRCm39) |
I120V |
probably benign |
Het |
Ccnq |
T |
C |
11: 78,641,950 (GRCm39) |
Y180C |
probably damaging |
Het |
Chd7 |
T |
C |
4: 8,833,866 (GRCm39) |
Y1207H |
probably damaging |
Het |
Chrnb2 |
A |
T |
3: 89,668,883 (GRCm39) |
F144Y |
probably damaging |
Het |
Cyp4a14 |
T |
A |
4: 115,348,391 (GRCm39) |
H362L |
probably damaging |
Het |
Dnaaf4 |
A |
G |
9: 72,869,257 (GRCm39) |
T156A |
probably benign |
Het |
Dym |
G |
A |
18: 75,419,718 (GRCm39) |
V630M |
probably damaging |
Het |
Dync2i1 |
A |
T |
12: 116,177,076 (GRCm39) |
V842E |
possibly damaging |
Het |
Dyrk1b |
C |
A |
7: 27,886,134 (GRCm39) |
P619Q |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,831,659 (GRCm39) |
D433G |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,561,086 (GRCm39) |
S1140R |
probably damaging |
Het |
Gabra5 |
T |
C |
7: 57,068,082 (GRCm39) |
R255G |
probably damaging |
Het |
Galnt17 |
T |
A |
5: 131,110,428 (GRCm39) |
I304F |
probably damaging |
Het |
Gpc5 |
A |
G |
14: 115,607,363 (GRCm39) |
S322G |
probably benign |
Het |
Herc1 |
TCCC |
TCC |
9: 66,408,470 (GRCm39) |
|
probably null |
Het |
Hmcn1 |
T |
A |
1: 150,610,269 (GRCm39) |
N1467Y |
probably damaging |
Het |
Ifna6 |
T |
C |
4: 88,745,987 (GRCm39) |
L112P |
probably damaging |
Het |
Ifrd1 |
C |
T |
12: 40,253,913 (GRCm39) |
|
probably null |
Het |
Il17f |
A |
G |
1: 20,849,713 (GRCm39) |
M17T |
probably benign |
Het |
Itga11 |
G |
A |
9: 62,675,866 (GRCm39) |
V892I |
probably benign |
Het |
Nckap5l |
A |
G |
15: 99,321,042 (GRCm39) |
L1246P |
probably damaging |
Het |
Nlrp4f |
A |
T |
13: 65,342,243 (GRCm39) |
H467Q |
probably damaging |
Het |
Ntng2 |
A |
G |
2: 29,118,055 (GRCm39) |
V131A |
possibly damaging |
Het |
Or51r1 |
G |
A |
7: 102,227,706 (GRCm39) |
M1I |
probably null |
Het |
Or8b40 |
T |
G |
9: 38,027,271 (GRCm39) |
Y60D |
probably damaging |
Het |
Or8g37 |
T |
A |
9: 39,731,193 (GRCm39) |
V86E |
probably benign |
Het |
Osbpl8 |
T |
C |
10: 111,110,874 (GRCm39) |
Y459H |
possibly damaging |
Het |
Pabpc1 |
A |
T |
15: 36,597,778 (GRCm39) |
V537D |
possibly damaging |
Het |
Pde4b |
A |
T |
4: 102,459,868 (GRCm39) |
M583L |
probably damaging |
Het |
Phlda1 |
T |
C |
10: 111,342,555 (GRCm39) |
V97A |
possibly damaging |
Het |
Pik3cb |
G |
T |
9: 98,976,574 (GRCm39) |
H174Q |
probably benign |
Het |
Plxdc2 |
A |
T |
2: 16,552,952 (GRCm39) |
I117F |
probably benign |
Het |
Psapl1 |
C |
A |
5: 36,362,303 (GRCm39) |
C298* |
probably null |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Homo |
Rtkn2 |
T |
A |
10: 67,877,283 (GRCm39) |
F448I |
probably benign |
Het |
Scn10a |
T |
C |
9: 119,500,617 (GRCm39) |
R221G |
probably damaging |
Het |
Serpina3c |
A |
G |
12: 104,117,759 (GRCm39) |
L193P |
probably damaging |
Het |
Sox12 |
T |
C |
2: 152,238,678 (GRCm39) |
Y314C |
probably damaging |
Het |
Spata31h1 |
A |
G |
10: 82,119,331 (GRCm39) |
S4560P |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,067,859 (GRCm39) |
E1772G |
probably damaging |
Het |
Supt6 |
A |
G |
11: 78,099,775 (GRCm39) |
V1570A |
probably benign |
Het |
Synrg |
T |
C |
11: 83,872,251 (GRCm39) |
F125S |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,494,919 (GRCm39) |
I1116F |
possibly damaging |
Het |
Tfap2a |
T |
A |
13: 40,882,230 (GRCm39) |
N25I |
probably damaging |
Het |
Tfap2d |
C |
A |
1: 19,173,507 (GRCm39) |
H10N |
possibly damaging |
Het |
Trpm8 |
T |
C |
1: 88,312,428 (GRCm39) |
I1103T |
possibly damaging |
Het |
Vmn1r158 |
C |
T |
7: 22,489,306 (GRCm39) |
C301Y |
probably damaging |
Het |
Vmn2r56 |
T |
C |
7: 12,428,719 (GRCm39) |
I516V |
probably benign |
Het |
Vmn2r71 |
G |
A |
7: 85,269,095 (GRCm39) |
|
probably null |
Het |
Vnn3 |
C |
T |
10: 23,745,523 (GRCm39) |
R491C |
probably benign |
Het |
Vps50 |
A |
G |
6: 3,600,274 (GRCm39) |
Y911C |
probably damaging |
Het |
Zfp772 |
C |
T |
7: 7,206,716 (GRCm39) |
R325Q |
possibly damaging |
Het |
Zranb3 |
T |
A |
1: 127,887,556 (GRCm39) |
H957L |
probably benign |
Het |
Zscan20 |
G |
T |
4: 128,479,668 (GRCm39) |
T941K |
probably damaging |
Het |
Zscan25 |
T |
A |
5: 145,227,373 (GRCm39) |
F346I |
probably damaging |
Het |
|
Other mutations in Or8g55 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01805:Or8g55
|
APN |
9 |
39,785,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02008:Or8g55
|
APN |
9 |
39,784,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02556:Or8g55
|
APN |
9 |
39,784,906 (GRCm39) |
missense |
possibly damaging |
0.73 |
BB008:Or8g55
|
UTSW |
9 |
39,785,146 (GRCm39) |
missense |
possibly damaging |
0.86 |
BB018:Or8g55
|
UTSW |
9 |
39,785,146 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02991:Or8g55
|
UTSW |
9 |
39,785,362 (GRCm39) |
missense |
probably benign |
0.36 |
R0494:Or8g55
|
UTSW |
9 |
39,784,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R0725:Or8g55
|
UTSW |
9 |
39,784,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R1179:Or8g55
|
UTSW |
9 |
39,785,371 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1500:Or8g55
|
UTSW |
9 |
39,784,707 (GRCm39) |
missense |
probably benign |
0.36 |
R1796:Or8g55
|
UTSW |
9 |
39,785,267 (GRCm39) |
missense |
probably benign |
0.12 |
R1970:Or8g55
|
UTSW |
9 |
39,785,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Or8g55
|
UTSW |
9 |
39,785,354 (GRCm39) |
missense |
probably benign |
0.35 |
R4065:Or8g55
|
UTSW |
9 |
39,784,718 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5254:Or8g55
|
UTSW |
9 |
39,784,741 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5799:Or8g55
|
UTSW |
9 |
39,785,392 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7525:Or8g55
|
UTSW |
9 |
39,785,435 (GRCm39) |
nonsense |
probably null |
|
R7570:Or8g55
|
UTSW |
9 |
39,784,751 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7803:Or8g55
|
UTSW |
9 |
39,785,378 (GRCm39) |
missense |
probably benign |
0.23 |
R7931:Or8g55
|
UTSW |
9 |
39,785,146 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8344:Or8g55
|
UTSW |
9 |
39,785,231 (GRCm39) |
missense |
probably benign |
0.42 |
R8859:Or8g55
|
UTSW |
9 |
39,784,894 (GRCm39) |
missense |
probably benign |
0.05 |
R9404:Or8g55
|
UTSW |
9 |
39,784,708 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1177:Or8g55
|
UTSW |
9 |
39,784,819 (GRCm39) |
missense |
probably benign |
0.33 |
|