Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adad1 |
T |
C |
3: 37,146,140 (GRCm39) |
Y503H |
probably benign |
Het |
Adck1 |
T |
C |
12: 88,338,550 (GRCm39) |
|
probably null |
Het |
Afap1l1 |
T |
C |
18: 61,879,859 (GRCm39) |
D337G |
probably damaging |
Het |
Afg1l |
G |
A |
10: 42,189,587 (GRCm39) |
T448M |
probably damaging |
Het |
Aqp6 |
T |
C |
15: 99,499,409 (GRCm39) |
S41P |
|
Het |
Atad5 |
T |
G |
11: 80,023,388 (GRCm39) |
V1500G |
probably benign |
Het |
B3galt9 |
C |
T |
2: 34,728,623 (GRCm39) |
Q141* |
probably null |
Het |
Btbd18 |
T |
A |
2: 84,497,524 (GRCm39) |
D387E |
probably benign |
Het |
Catsperd |
A |
G |
17: 56,969,720 (GRCm39) |
N605D |
possibly damaging |
Het |
Ccdc24 |
C |
T |
4: 117,728,355 (GRCm39) |
V102I |
probably benign |
Het |
Cenpe |
T |
A |
3: 134,976,609 (GRCm39) |
D2405E |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,195,023 (GRCm39) |
D2249G |
|
Het |
Chrm1 |
A |
T |
19: 8,655,550 (GRCm39) |
Y85F |
possibly damaging |
Het |
Clstn3 |
C |
T |
6: 124,428,358 (GRCm39) |
G465S |
probably damaging |
Het |
Col7a1 |
G |
A |
9: 108,785,059 (GRCm39) |
G262D |
unknown |
Het |
Copg2 |
T |
C |
6: 30,750,578 (GRCm39) |
T736A |
probably benign |
Het |
Coro2b |
T |
C |
9: 62,333,080 (GRCm39) |
E435G |
probably benign |
Het |
Cp |
A |
T |
3: 20,033,083 (GRCm39) |
I637F |
possibly damaging |
Het |
Cpne7 |
T |
C |
8: 123,853,411 (GRCm39) |
F239L |
probably damaging |
Het |
Cstdc2 |
C |
T |
2: 148,689,878 (GRCm39) |
E92K |
probably damaging |
Het |
Cul2 |
T |
A |
18: 3,434,041 (GRCm39) |
Y679* |
probably null |
Het |
Dhx8 |
T |
C |
11: 101,655,740 (GRCm39) |
Y1158H |
probably damaging |
Het |
Eda |
G |
T |
X: 99,019,775 (GRCm39) |
R130L |
unknown |
Het |
Elp6 |
T |
A |
9: 110,150,004 (GRCm39) |
V265D |
probably damaging |
Het |
Eomes |
A |
G |
9: 118,313,640 (GRCm39) |
T562A |
|
Het |
Fam187b |
A |
T |
7: 30,677,067 (GRCm39) |
E192V |
probably damaging |
Het |
Foxi1 |
T |
C |
11: 34,155,671 (GRCm39) |
T320A |
probably benign |
Het |
Gga1 |
C |
T |
15: 78,765,247 (GRCm39) |
T18I |
possibly damaging |
Het |
Grik4 |
T |
A |
9: 42,571,037 (GRCm39) |
M223L |
probably benign |
Het |
Hdac7 |
T |
C |
15: 97,700,352 (GRCm39) |
N594S |
probably benign |
Het |
Ifnar1 |
C |
T |
16: 91,292,367 (GRCm39) |
P207L |
probably benign |
Het |
Itpr3 |
T |
G |
17: 27,324,523 (GRCm39) |
F1235C |
probably damaging |
Het |
Klhdc4 |
A |
G |
8: 122,523,765 (GRCm39) |
S484P |
possibly damaging |
Het |
Kmt2c |
A |
G |
5: 25,515,045 (GRCm39) |
S2933P |
probably damaging |
Het |
Lama5 |
T |
A |
2: 179,843,522 (GRCm39) |
H475L |
probably benign |
Het |
Ly6g6f |
A |
G |
17: 35,299,826 (GRCm39) |
L292P |
possibly damaging |
Het |
Macf1 |
T |
A |
4: 123,365,668 (GRCm39) |
Q3031L |
probably benign |
Het |
Mbd5 |
T |
G |
2: 49,146,712 (GRCm39) |
S307R |
probably damaging |
Het |
Mertk |
T |
C |
2: 128,604,029 (GRCm39) |
F388L |
probably benign |
Het |
Mmp11 |
A |
G |
10: 75,762,733 (GRCm39) |
F240S |
probably damaging |
Het |
Mroh1 |
T |
A |
15: 76,318,964 (GRCm39) |
F949I |
probably damaging |
Het |
Mroh2b |
T |
C |
15: 4,973,821 (GRCm39) |
L1113P |
probably damaging |
Het |
Ndufv1 |
C |
A |
19: 4,057,614 (GRCm39) |
A454S |
probably benign |
Het |
Or13e8 |
A |
G |
4: 43,696,591 (GRCm39) |
L194P |
probably damaging |
Het |
Or56b2j |
T |
C |
7: 104,352,821 (GRCm39) |
S16P |
probably benign |
Het |
Osbpl1a |
C |
A |
18: 13,031,244 (GRCm39) |
D329Y |
probably benign |
Het |
Pcdh1 |
C |
A |
18: 38,330,633 (GRCm39) |
R929L |
probably damaging |
Het |
Phactr2 |
C |
T |
10: 13,122,841 (GRCm39) |
R427K |
probably benign |
Het |
Pip5k1c |
T |
C |
10: 81,153,184 (GRCm39) |
Y670H |
probably damaging |
Het |
Plbd1 |
T |
A |
6: 136,611,555 (GRCm39) |
N241Y |
probably damaging |
Het |
Pmvk |
C |
A |
3: 89,374,956 (GRCm39) |
Q139K |
probably benign |
Het |
Pramel30 |
T |
A |
4: 144,059,678 (GRCm39) |
I463N |
possibly damaging |
Het |
Rab3gap2 |
T |
A |
1: 184,967,523 (GRCm39) |
C136S |
probably damaging |
Het |
Rcor3 |
A |
G |
1: 191,786,050 (GRCm39) |
V396A |
probably damaging |
Het |
Rgs20 |
C |
A |
1: 4,982,629 (GRCm39) |
E147* |
probably null |
Het |
Rnf167 |
G |
T |
11: 70,540,777 (GRCm39) |
L170F |
probably damaging |
Het |
Scn9a |
T |
C |
2: 66,395,553 (GRCm39) |
T164A |
probably damaging |
Het |
Skic3 |
A |
G |
13: 76,266,288 (GRCm39) |
Q210R |
probably benign |
Het |
Slc52a3 |
A |
T |
2: 151,846,299 (GRCm39) |
I87F |
probably benign |
Het |
Sntn |
A |
T |
14: 13,682,364 (GRCm38) |
M146L |
|
Het |
Svep1 |
C |
T |
4: 58,179,697 (GRCm39) |
R182H |
possibly damaging |
Het |
Taar7f |
A |
G |
10: 23,926,311 (GRCm39) |
I302V |
probably benign |
Het |
Tm4sf20 |
T |
C |
1: 82,746,090 (GRCm39) |
I17V |
probably benign |
Het |
Traf1 |
T |
C |
2: 34,836,748 (GRCm39) |
T270A |
probably benign |
Het |
Trpm5 |
C |
T |
7: 142,638,860 (GRCm39) |
E304K |
probably benign |
Het |
Ttll8 |
T |
C |
15: 88,809,863 (GRCm39) |
D311G |
possibly damaging |
Het |
Unc79 |
T |
A |
12: 103,037,035 (GRCm39) |
F608I |
probably damaging |
Het |
Vmn2r11 |
A |
T |
5: 109,195,159 (GRCm39) |
C722* |
probably null |
Het |
Wdr7 |
A |
G |
18: 63,853,407 (GRCm39) |
T36A |
probably damaging |
Het |
Ybx2 |
C |
T |
11: 69,831,188 (GRCm39) |
P261L |
|
Het |
Zfp101 |
C |
T |
17: 33,601,418 (GRCm39) |
V113I |
probably benign |
Het |
Zfp260 |
T |
C |
7: 29,804,249 (GRCm39) |
S50P |
probably benign |
Het |
Zfp319 |
A |
T |
8: 96,054,922 (GRCm39) |
F427Y |
probably benign |
Het |
Zfp369 |
T |
C |
13: 65,444,347 (GRCm39) |
S497P |
possibly 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 |
R9598:Or5d46
|
UTSW |
2 |
88,170,821 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9719:Or5d46
|
UTSW |
2 |
88,169,928 (GRCm39) |
missense |
|
|
|