Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
C |
6: 142,594,012 (GRCm38) |
N1545S |
probably benign |
Het |
Arid1b |
C |
A |
17: 5,040,663 (GRCm38) |
S546R |
probably damaging |
Het |
Arid3b |
A |
T |
9: 57,790,430 (GRCm38) |
|
probably benign |
Het |
Atf6b |
T |
A |
17: 34,652,674 (GRCm38) |
M428K |
probably benign |
Het |
Atpaf1 |
A |
T |
4: 115,788,359 (GRCm38) |
M142L |
probably benign |
Het |
Auts2 |
A |
G |
5: 131,474,971 (GRCm38) |
S225P |
probably damaging |
Het |
Bclaf1 |
A |
G |
10: 20,323,778 (GRCm38) |
Q20R |
probably damaging |
Het |
Bivm |
A |
T |
1: 44,138,633 (GRCm38) |
R364S |
probably damaging |
Het |
Brwd1 |
G |
A |
16: 96,017,604 (GRCm38) |
P1343S |
probably damaging |
Het |
Cckar |
A |
G |
5: 53,706,497 (GRCm38) |
S41P |
probably benign |
Het |
Cfap221 |
A |
G |
1: 119,930,920 (GRCm38) |
S728P |
probably benign |
Het |
Chrna9 |
A |
G |
5: 65,977,138 (GRCm38) |
K444R |
probably benign |
Het |
Cox10 |
A |
T |
11: 63,964,255 (GRCm38) |
V400E |
probably benign |
Het |
Dact2 |
C |
T |
17: 14,196,571 (GRCm38) |
E456K |
probably benign |
Het |
Ddr2 |
A |
G |
1: 169,990,609 (GRCm38) |
V443A |
probably benign |
Het |
Dlg3 |
A |
T |
X: 100,796,682 (GRCm38) |
|
probably benign |
Het |
En1 |
C |
A |
1: 120,603,757 (GRCm38) |
A242E |
unknown |
Het |
Fhdc1 |
C |
A |
3: 84,444,826 (GRCm38) |
V1031F |
probably benign |
Het |
Gm6124 |
A |
T |
7: 39,222,771 (GRCm38) |
|
noncoding transcript |
Het |
Gucy1a1 |
A |
T |
3: 82,094,759 (GRCm38) |
F671Y |
possibly damaging |
Het |
Hddc2 |
A |
T |
10: 31,314,587 (GRCm38) |
M48L |
possibly damaging |
Het |
Hepacam2 |
T |
A |
6: 3,487,237 (GRCm38) |
Y40F |
probably benign |
Het |
Ift80 |
A |
G |
3: 68,963,690 (GRCm38) |
I191T |
probably damaging |
Het |
Il19 |
T |
A |
1: 130,935,013 (GRCm38) |
T58S |
possibly damaging |
Het |
Itga2 |
G |
A |
13: 114,866,173 (GRCm38) |
R594C |
probably damaging |
Het |
Itga5 |
C |
T |
15: 103,352,257 (GRCm38) |
|
probably null |
Het |
Kcna1 |
T |
C |
6: 126,641,875 (GRCm38) |
D494G |
probably damaging |
Het |
Kcnv1 |
G |
A |
15: 45,114,444 (GRCm38) |
T66M |
probably damaging |
Het |
Kmt2b |
A |
T |
7: 30,581,836 (GRCm38) |
|
probably null |
Het |
Kmt5b |
T |
C |
19: 3,802,193 (GRCm38) |
Y125H |
possibly damaging |
Het |
Lbr |
C |
T |
1: 181,820,702 (GRCm38) |
C398Y |
probably damaging |
Het |
Lmf1 |
T |
C |
17: 25,654,481 (GRCm38) |
L320P |
probably damaging |
Het |
Man1c1 |
T |
A |
4: 134,563,785 (GRCm38) |
D600V |
probably damaging |
Het |
Mapkapk3 |
T |
C |
9: 107,258,932 (GRCm38) |
|
probably benign |
Het |
Mccc1 |
A |
G |
3: 35,990,068 (GRCm38) |
V203A |
probably damaging |
Het |
Mettl5 |
T |
C |
2: 69,880,832 (GRCm38) |
N114S |
probably benign |
Het |
Mindy2 |
T |
A |
9: 70,631,094 (GRCm38) |
R320W |
probably damaging |
Het |
Nrip1 |
A |
G |
16: 76,291,988 (GRCm38) |
S894P |
probably benign |
Het |
Nup210l |
A |
T |
3: 90,207,326 (GRCm38) |
H1736L |
probably benign |
Het |
Olfr1396 |
T |
A |
11: 49,113,427 (GRCm38) |
I100L |
probably benign |
Het |
Olfr1508 |
T |
C |
14: 52,463,985 (GRCm38) |
N8S |
probably damaging |
Het |
Olfr169 |
A |
T |
16: 19,566,244 (GRCm38) |
M213K |
possibly damaging |
Het |
Olfr310 |
A |
T |
7: 86,269,760 (GRCm38) |
F10I |
probably damaging |
Het |
Olfr373 |
A |
G |
8: 72,099,768 (GRCm38) |
T3A |
probably benign |
Het |
Olfr926 |
A |
G |
9: 38,877,313 (GRCm38) |
I46V |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,322,681 (GRCm38) |
S705T |
possibly damaging |
Het |
Phf14 |
C |
T |
6: 11,987,097 (GRCm38) |
P559S |
probably damaging |
Het |
Plpp4 |
A |
G |
7: 129,307,632 (GRCm38) |
E22G |
probably damaging |
Het |
Ppp4c |
A |
G |
7: 126,792,059 (GRCm38) |
|
probably null |
Het |
Rps15a-ps1 |
A |
G |
10: 106,192,635 (GRCm38) |
|
noncoding transcript |
Het |
Rps27a |
A |
G |
11: 29,545,933 (GRCm38) |
Y140H |
probably benign |
Het |
Sash1 |
A |
G |
10: 8,730,242 (GRCm38) |
S795P |
possibly damaging |
Het |
Slc22a21 |
T |
C |
11: 53,969,503 (GRCm38) |
D34G |
probably damaging |
Het |
Srsf6 |
T |
C |
2: 162,934,716 (GRCm38) |
|
probably benign |
Het |
Stk32c |
T |
C |
7: 139,120,788 (GRCm38) |
|
probably null |
Het |
Tmem237 |
A |
G |
1: 59,119,836 (GRCm38) |
|
probably benign |
Het |
Ttc19 |
A |
G |
11: 62,285,927 (GRCm38) |
|
probably null |
Het |
Ttf2 |
T |
C |
3: 100,962,761 (GRCm38) |
D332G |
probably benign |
Het |
Ttn |
A |
T |
2: 76,811,243 (GRCm38) |
L5176Q |
possibly damaging |
Het |
Vcan |
A |
G |
13: 89,725,486 (GRCm38) |
V83A |
probably damaging |
Het |
Vmn1r192 |
T |
A |
13: 22,187,295 (GRCm38) |
I252F |
probably damaging |
Het |
Vmn2r101 |
A |
T |
17: 19,612,041 (GRCm38) |
R766S |
probably damaging |
Het |
Xndc1 |
T |
A |
7: 102,081,487 (GRCm38) |
L288M |
possibly damaging |
Het |
Zfa-ps |
A |
T |
10: 52,543,711 (GRCm38) |
|
noncoding transcript |
Het |
|
Other mutations in Olfr711 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02600:Olfr711
|
APN |
7 |
106,971,549 (GRCm38) |
missense |
possibly damaging |
0.51 |
R0087:Olfr711
|
UTSW |
7 |
106,972,116 (GRCm38) |
missense |
probably benign |
0.01 |
R0580:Olfr711
|
UTSW |
7 |
106,972,240 (GRCm38) |
missense |
probably damaging |
1.00 |
R1375:Olfr711
|
UTSW |
7 |
106,972,098 (GRCm38) |
missense |
probably damaging |
1.00 |
R1538:Olfr711
|
UTSW |
7 |
106,971,983 (GRCm38) |
nonsense |
probably null |
|
R1875:Olfr711
|
UTSW |
7 |
106,972,182 (GRCm38) |
missense |
possibly damaging |
0.86 |
R2156:Olfr711
|
UTSW |
7 |
106,971,568 (GRCm38) |
missense |
probably damaging |
1.00 |
R4332:Olfr711
|
UTSW |
7 |
106,972,147 (GRCm38) |
missense |
probably benign |
0.00 |
R4400:Olfr711
|
UTSW |
7 |
106,972,002 (GRCm38) |
missense |
probably damaging |
1.00 |
R4688:Olfr711
|
UTSW |
7 |
106,971,861 (GRCm38) |
missense |
probably benign |
0.02 |
R4868:Olfr711
|
UTSW |
7 |
106,971,767 (GRCm38) |
missense |
probably benign |
|
R4970:Olfr711
|
UTSW |
7 |
106,971,571 (GRCm38) |
missense |
probably benign |
0.35 |
R5006:Olfr711
|
UTSW |
7 |
106,971,601 (GRCm38) |
missense |
probably damaging |
1.00 |
R5082:Olfr711
|
UTSW |
7 |
106,971,664 (GRCm38) |
missense |
probably benign |
0.00 |
R5121:Olfr711
|
UTSW |
7 |
106,972,231 (GRCm38) |
missense |
probably benign |
|
R6465:Olfr711
|
UTSW |
7 |
106,972,212 (GRCm38) |
missense |
possibly damaging |
0.63 |
R6541:Olfr711
|
UTSW |
7 |
106,972,203 (GRCm38) |
missense |
probably benign |
0.20 |
R7419:Olfr711
|
UTSW |
7 |
106,972,146 (GRCm38) |
missense |
probably benign |
0.01 |
R8048:Olfr711
|
UTSW |
7 |
106,972,464 (GRCm38) |
start gained |
probably benign |
|
R9310:Olfr711
|
UTSW |
7 |
106,971,471 (GRCm38) |
missense |
probably damaging |
1.00 |
R9470:Olfr711
|
UTSW |
7 |
106,972,254 (GRCm38) |
missense |
probably benign |
0.26 |
R9603:Olfr711
|
UTSW |
7 |
106,971,896 (GRCm38) |
nonsense |
probably null |
|
Z1177:Olfr711
|
UTSW |
7 |
106,971,915 (GRCm38) |
missense |
probably benign |
0.00 |
|