Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
T |
6: 121,645,253 (GRCm38) |
V372F |
probably benign |
Het |
Adcy10 |
G |
A |
1: 165,519,895 (GRCm38) |
C393Y |
probably damaging |
Het |
Adgrg7 |
A |
C |
16: 56,730,306 (GRCm38) |
I681S |
possibly damaging |
Het |
Akap8l |
T |
C |
17: 32,321,511 (GRCm38) |
|
probably benign |
Het |
Akr1a1 |
A |
T |
4: 116,639,895 (GRCm38) |
V156E |
probably damaging |
Het |
Alk |
T |
G |
17: 71,895,739 (GRCm38) |
D1167A |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 122,893,714 (GRCm38) |
|
probably null |
Het |
Aspm |
A |
G |
1: 139,470,395 (GRCm38) |
|
probably null |
Het |
Aspm |
T |
A |
1: 139,457,483 (GRCm38) |
N288K |
probably damaging |
Het |
Asxl2 |
G |
A |
12: 3,474,618 (GRCm38) |
|
probably null |
Het |
Atp6v0a1 |
A |
G |
11: 101,055,587 (GRCm38) |
H802R |
probably damaging |
Het |
B4galnt1 |
A |
G |
10: 127,171,822 (GRCm38) |
T531A |
possibly damaging |
Het |
Ccdc114 |
C |
T |
7: 45,942,082 (GRCm38) |
R257* |
probably null |
Het |
Cecr2 |
A |
G |
6: 120,756,569 (GRCm38) |
N506D |
possibly damaging |
Het |
Crebrf |
T |
C |
17: 26,759,865 (GRCm38) |
V509A |
probably damaging |
Het |
Cyp4f40 |
A |
T |
17: 32,675,616 (GRCm38) |
I413F |
probably null |
Het |
Defb12 |
C |
A |
8: 19,114,326 (GRCm38) |
|
probably null |
Het |
Dnah2 |
T |
C |
11: 69,421,848 (GRCm38) |
E4297G |
probably damaging |
Het |
Dpysl5 |
A |
T |
5: 30,791,513 (GRCm38) |
N371Y |
probably damaging |
Het |
Eef1d |
G |
T |
15: 75,903,189 (GRCm38) |
T207N |
probably benign |
Het |
Esrrb |
C |
T |
12: 86,519,009 (GRCm38) |
Q416* |
probably null |
Het |
Exd2 |
T |
C |
12: 80,489,448 (GRCm38) |
L284P |
probably damaging |
Het |
Fat3 |
T |
A |
9: 16,376,443 (GRCm38) |
I595F |
probably benign |
Het |
Gm9920 |
A |
G |
15: 55,108,975 (GRCm38) |
|
probably benign |
Het |
Hephl1 |
T |
C |
9: 15,069,788 (GRCm38) |
K783E |
probably damaging |
Het |
Irs2 |
A |
G |
8: 11,005,277 (GRCm38) |
S1052P |
probably benign |
Het |
Kctd18 |
T |
C |
1: 57,963,093 (GRCm38) |
I192V |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,453,746 (GRCm38) |
D722G |
probably damaging |
Het |
Lepr |
T |
C |
4: 101,815,019 (GRCm38) |
V1080A |
possibly damaging |
Het |
Lpin1 |
C |
T |
12: 16,563,655 (GRCm38) |
G504S |
probably damaging |
Het |
Lrit2 |
A |
C |
14: 37,069,183 (GRCm38) |
Q273P |
possibly damaging |
Het |
Mgea5 |
A |
T |
19: 45,758,022 (GRCm38) |
Y779* |
probably null |
Het |
Mlkl |
T |
A |
8: 111,327,937 (GRCm38) |
E189D |
probably benign |
Het |
Mttp |
C |
T |
3: 138,105,029 (GRCm38) |
R608H |
probably benign |
Het |
Nav2 |
T |
C |
7: 49,589,160 (GRCm38) |
V2011A |
probably benign |
Het |
Nos2 |
A |
T |
11: 78,957,491 (GRCm38) |
I1075F |
probably benign |
Het |
Npat |
A |
G |
9: 53,550,036 (GRCm38) |
|
probably null |
Het |
Nucks1 |
T |
C |
1: 131,919,033 (GRCm38) |
F16L |
probably damaging |
Het |
Nus1 |
T |
C |
10: 52,429,213 (GRCm38) |
S150P |
possibly damaging |
Het |
Olfr1230 |
G |
T |
2: 89,297,162 (GRCm38) |
T36K |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,681,353 (GRCm38) |
T3290A |
unknown |
Het |
Pign |
A |
T |
1: 105,657,812 (GRCm38) |
F4Y |
probably benign |
Het |
Rfx4 |
A |
G |
10: 84,860,542 (GRCm38) |
N233D |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,160,195 (GRCm38) |
M1325L |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,147,663 (GRCm38) |
C537R |
probably damaging |
Het |
Scaf11 |
T |
A |
15: 96,417,120 (GRCm38) |
H1227L |
possibly damaging |
Het |
Sec31b |
G |
T |
19: 44,518,637 (GRCm38) |
P840T |
probably damaging |
Het |
Slc16a9 |
T |
A |
10: 70,283,128 (GRCm38) |
L426I |
probably damaging |
Het |
Slc17a2 |
T |
C |
13: 23,812,592 (GRCm38) |
S27P |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,344,393 (GRCm38) |
Q436* |
probably null |
Het |
Tacc1 |
A |
G |
8: 25,182,283 (GRCm38) |
S310P |
possibly damaging |
Het |
Tmem245 |
G |
A |
4: 56,947,084 (GRCm38) |
R110C |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,757,431 (GRCm38) |
Y953C |
probably damaging |
Het |
Trpm7 |
C |
A |
2: 126,842,855 (GRCm38) |
|
probably null |
Het |
Ush2a |
G |
A |
1: 188,912,123 (GRCm38) |
V4561I |
probably benign |
Het |
Vmn1r192 |
C |
T |
13: 22,187,631 (GRCm38) |
V140I |
probably benign |
Het |
Vmn2r66 |
A |
T |
7: 85,006,818 (GRCm38) |
I330N |
probably damaging |
Het |
Vmn2r99 |
T |
C |
17: 19,379,269 (GRCm38) |
V405A |
probably damaging |
Het |
Wdhd1 |
A |
C |
14: 47,272,221 (GRCm38) |
V172G |
probably benign |
Het |
Zfhx3 |
C |
T |
8: 108,951,185 (GRCm38) |
R2956C |
possibly damaging |
Het |
Zfp446 |
T |
C |
7: 12,982,251 (GRCm38) |
L283P |
possibly damaging |
Het |
Zfp82 |
T |
C |
7: 30,057,166 (GRCm38) |
K164E |
probably damaging |
Het |
|
Other mutations in Olfr881 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01882:Olfr881
|
APN |
9 |
37,992,560 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02282:Olfr881
|
APN |
9 |
37,993,022 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02714:Olfr881
|
APN |
9 |
37,993,086 (GRCm38) |
missense |
possibly damaging |
0.83 |
R0308:Olfr881
|
UTSW |
9 |
37,992,845 (GRCm38) |
missense |
probably benign |
0.01 |
R0486:Olfr881
|
UTSW |
9 |
37,992,702 (GRCm38) |
missense |
possibly damaging |
0.72 |
R0504:Olfr881
|
UTSW |
9 |
37,993,142 (GRCm38) |
missense |
probably benign |
0.05 |
R1939:Olfr881
|
UTSW |
9 |
37,993,089 (GRCm38) |
missense |
probably benign |
0.12 |
R4669:Olfr881
|
UTSW |
9 |
37,993,085 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5468:Olfr881
|
UTSW |
9 |
37,993,011 (GRCm38) |
missense |
probably damaging |
1.00 |
R5601:Olfr881
|
UTSW |
9 |
37,992,714 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6799:Olfr881
|
UTSW |
9 |
37,993,182 (GRCm38) |
missense |
possibly damaging |
0.79 |
R7212:Olfr881
|
UTSW |
9 |
37,992,957 (GRCm38) |
missense |
possibly damaging |
0.47 |
R7648:Olfr881
|
UTSW |
9 |
37,992,560 (GRCm38) |
missense |
probably damaging |
1.00 |
R8286:Olfr881
|
UTSW |
9 |
37,993,105 (GRCm38) |
nonsense |
probably null |
|
X0064:Olfr881
|
UTSW |
9 |
37,993,340 (GRCm38) |
missense |
probably benign |
0.07 |
|