Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
G |
A |
6: 92,784,156 (GRCm39) |
T985M |
probably damaging |
Het |
Alpk1 |
A |
G |
3: 127,473,592 (GRCm39) |
S804P |
possibly damaging |
Het |
Ap3b1 |
A |
G |
13: 94,664,835 (GRCm39) |
I925V |
unknown |
Het |
Cep135 |
T |
A |
5: 76,788,796 (GRCm39) |
S1130T |
probably damaging |
Het |
Cers3 |
A |
T |
7: 66,431,573 (GRCm39) |
M183L |
probably benign |
Het |
Col5a1 |
A |
G |
2: 27,842,352 (GRCm39) |
E409G |
unknown |
Het |
Cyp4a32 |
G |
T |
4: 115,471,818 (GRCm39) |
V410F |
probably damaging |
Het |
Ddx1 |
G |
A |
12: 13,277,318 (GRCm39) |
Q528* |
probably null |
Het |
Dio2 |
G |
A |
12: 90,696,178 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
G |
T |
11: 65,931,172 (GRCm39) |
A2008E |
probably damaging |
Het |
Dnajc2 |
A |
G |
5: 21,965,408 (GRCm39) |
V457A |
probably benign |
Het |
Dytn |
T |
C |
1: 63,682,532 (GRCm39) |
T372A |
probably benign |
Het |
Fam135a |
T |
C |
1: 24,067,714 (GRCm39) |
I152V |
probably benign |
Het |
Fmnl2 |
C |
T |
2: 52,748,261 (GRCm39) |
A36V |
possibly damaging |
Het |
Galnt7 |
G |
A |
8: 58,005,531 (GRCm39) |
T234I |
probably damaging |
Het |
Gba1 |
A |
C |
3: 89,110,809 (GRCm39) |
I6L |
probably benign |
Het |
Gja10 |
A |
G |
4: 32,602,147 (GRCm39) |
V79A |
probably damaging |
Het |
Gpd2 |
T |
A |
2: 57,228,991 (GRCm39) |
V265E |
probably damaging |
Het |
Gpld1 |
T |
C |
13: 25,136,861 (GRCm39) |
Y60H |
probably damaging |
Het |
H2bc27 |
A |
G |
11: 58,839,869 (GRCm39) |
K35R |
probably benign |
Het |
Heatr9 |
A |
G |
11: 83,409,672 (GRCm39) |
|
probably benign |
Het |
Krt75 |
T |
A |
15: 101,476,508 (GRCm39) |
D419V |
probably benign |
Het |
Lrig3 |
A |
T |
10: 125,842,871 (GRCm39) |
I599F |
probably benign |
Het |
Lrp4 |
A |
G |
2: 91,341,925 (GRCm39) |
D1846G |
probably damaging |
Het |
Mamdc2 |
C |
T |
19: 23,281,215 (GRCm39) |
A653T |
probably damaging |
Het |
Myo7a |
A |
T |
7: 97,740,227 (GRCm39) |
|
probably null |
Het |
Notch2 |
A |
G |
3: 98,044,689 (GRCm39) |
D1537G |
probably benign |
Het |
Or10k2 |
G |
A |
8: 84,268,100 (GRCm39) |
C109Y |
probably damaging |
Het |
Or51a25 |
G |
T |
7: 102,372,858 (GRCm39) |
H280N |
probably benign |
Het |
Papss1 |
A |
C |
3: 131,288,280 (GRCm39) |
D84A |
probably damaging |
Het |
Pcdhb16 |
T |
A |
18: 37,611,527 (GRCm39) |
D162E |
probably damaging |
Het |
Rab11fip1 |
C |
T |
8: 27,642,840 (GRCm39) |
R653Q |
possibly damaging |
Het |
Rap1gap2 |
A |
T |
11: 74,303,281 (GRCm39) |
|
probably benign |
Het |
Rasal2 |
T |
C |
1: 156,984,777 (GRCm39) |
D990G |
probably damaging |
Het |
Rnf32 |
T |
C |
5: 29,410,701 (GRCm39) |
|
probably null |
Het |
Rp1 |
T |
C |
1: 4,419,936 (GRCm39) |
D392G |
probably benign |
Het |
Scn9a |
T |
C |
2: 66,398,373 (GRCm39) |
D79G |
probably damaging |
Het |
Selenon |
A |
T |
4: 134,268,219 (GRCm39) |
V438D |
probably damaging |
Het |
Slc47a1 |
G |
A |
11: 61,254,239 (GRCm39) |
H158Y |
probably benign |
Het |
Slc5a12 |
A |
T |
2: 110,471,160 (GRCm39) |
E463D |
probably benign |
Het |
Taf2 |
C |
T |
15: 54,879,959 (GRCm39) |
V1126M |
probably benign |
Het |
Tas2r143 |
G |
T |
6: 42,377,259 (GRCm39) |
V30L |
possibly damaging |
Het |
Tcea3 |
G |
A |
4: 135,995,424 (GRCm39) |
V256M |
probably damaging |
Het |
Thy1 |
A |
G |
9: 43,958,111 (GRCm39) |
T80A |
probably benign |
Het |
Tmem9 |
A |
G |
1: 135,947,469 (GRCm39) |
N47S |
probably damaging |
Het |
Tmprss11g |
T |
C |
5: 86,645,128 (GRCm39) |
Q101R |
probably benign |
Het |
Trim66 |
C |
T |
7: 109,059,704 (GRCm39) |
C792Y |
probably damaging |
Het |
Tstd2 |
A |
T |
4: 46,124,949 (GRCm39) |
M226K |
probably damaging |
Het |
Utrn |
G |
T |
10: 12,613,937 (GRCm39) |
T378K |
possibly damaging |
Het |
Vmn2r23 |
A |
G |
6: 123,681,355 (GRCm39) |
I88V |
probably benign |
Het |
|
Other mutations in Or52ae7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01735:Or52ae7
|
APN |
7 |
103,119,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02428:Or52ae7
|
APN |
7 |
103,119,590 (GRCm39) |
missense |
probably benign |
0.03 |
R0546:Or52ae7
|
UTSW |
7 |
103,119,907 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1518:Or52ae7
|
UTSW |
7 |
103,119,249 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R1696:Or52ae7
|
UTSW |
7 |
103,119,384 (GRCm39) |
missense |
probably benign |
0.18 |
R1735:Or52ae7
|
UTSW |
7 |
103,119,353 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2927:Or52ae7
|
UTSW |
7 |
103,120,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R3856:Or52ae7
|
UTSW |
7 |
103,119,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R4374:Or52ae7
|
UTSW |
7 |
103,119,278 (GRCm39) |
missense |
probably damaging |
0.97 |
R4375:Or52ae7
|
UTSW |
7 |
103,119,278 (GRCm39) |
missense |
probably damaging |
0.97 |
R4377:Or52ae7
|
UTSW |
7 |
103,119,278 (GRCm39) |
missense |
probably damaging |
0.97 |
R5059:Or52ae7
|
UTSW |
7 |
103,119,488 (GRCm39) |
nonsense |
probably null |
|
R5174:Or52ae7
|
UTSW |
7 |
103,119,610 (GRCm39) |
missense |
probably benign |
0.14 |
R5579:Or52ae7
|
UTSW |
7 |
103,120,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Or52ae7
|
UTSW |
7 |
103,119,596 (GRCm39) |
missense |
probably benign |
0.02 |
R7888:Or52ae7
|
UTSW |
7 |
103,120,006 (GRCm39) |
nonsense |
probably null |
|
R7980:Or52ae7
|
UTSW |
7 |
103,119,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R8150:Or52ae7
|
UTSW |
7 |
103,119,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Or52ae7
|
UTSW |
7 |
103,119,524 (GRCm39) |
missense |
probably benign |
0.07 |
R9369:Or52ae7
|
UTSW |
7 |
103,119,555 (GRCm39) |
missense |
probably benign |
0.14 |
R9683:Or52ae7
|
UTSW |
7 |
103,119,157 (GRCm39) |
start gained |
probably benign |
|
R9713:Or52ae7
|
UTSW |
7 |
103,119,914 (GRCm39) |
missense |
possibly damaging |
0.47 |
|