Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Ano1 |
A |
T |
7: 144,172,600 (GRCm39) |
S528T |
probably benign |
Het |
Araf |
G |
T |
X: 20,726,339 (GRCm39) |
R601L |
probably damaging |
Homo |
Bcl2l10 |
T |
C |
9: 75,258,354 (GRCm39) |
I172T |
possibly damaging |
Het |
Bpifb3 |
A |
T |
2: 153,771,243 (GRCm39) |
N385I |
possibly damaging |
Het |
Bsnd |
A |
G |
4: 106,343,832 (GRCm39) |
V158A |
probably damaging |
Het |
Cacna1s |
A |
G |
1: 136,016,783 (GRCm39) |
N481S |
probably benign |
Het |
Cdk5rap1 |
A |
G |
2: 154,210,161 (GRCm39) |
V138A |
probably damaging |
Het |
Cep290 |
A |
G |
10: 100,366,069 (GRCm39) |
E1099G |
probably damaging |
Het |
Cers1 |
T |
A |
8: 70,783,727 (GRCm39) |
L225Q |
probably damaging |
Het |
Cfb |
T |
C |
17: 35,081,069 (GRCm39) |
Q7R |
probably benign |
Het |
Clk4 |
A |
G |
11: 51,162,748 (GRCm39) |
S98G |
possibly damaging |
Het |
Clock |
A |
G |
5: 76,385,000 (GRCm39) |
S406P |
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,484,833 (GRCm39) |
I3178V |
probably benign |
Het |
Dock10 |
A |
G |
1: 80,516,540 (GRCm39) |
S1397P |
probably damaging |
Het |
Fer1l4 |
A |
G |
2: 155,871,188 (GRCm39) |
L1421P |
probably damaging |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Greb1 |
G |
T |
12: 16,785,152 (GRCm39) |
T91K |
probably damaging |
Het |
Grid2ip |
G |
A |
5: 143,366,184 (GRCm39) |
S379N |
probably damaging |
Het |
Gucy1b2 |
A |
T |
14: 62,653,388 (GRCm39) |
C336S |
probably damaging |
Het |
Hdac1 |
A |
G |
4: 129,412,902 (GRCm39) |
C261R |
probably damaging |
Het |
Htt |
T |
C |
5: 35,009,431 (GRCm39) |
S1471P |
possibly damaging |
Het |
Ice1 |
A |
G |
13: 70,742,958 (GRCm39) |
V2134A |
probably damaging |
Het |
Ikzf1 |
C |
T |
11: 11,718,961 (GRCm39) |
Q310* |
probably null |
Het |
Il3ra |
G |
A |
14: 14,350,180 (GRCm38) |
V112I |
probably benign |
Het |
Kif21b |
A |
G |
1: 136,077,156 (GRCm39) |
I393V |
possibly damaging |
Het |
Krt74 |
T |
C |
15: 101,671,872 (GRCm39) |
|
noncoding transcript |
Het |
Krtap29-1 |
T |
C |
11: 99,869,809 (GRCm39) |
N24S |
probably null |
Het |
Mmut |
T |
C |
17: 41,267,136 (GRCm39) |
V570A |
probably benign |
Het |
Myh7 |
T |
C |
14: 55,216,943 (GRCm39) |
D1138G |
probably damaging |
Het |
Nktr |
T |
C |
9: 121,560,631 (GRCm39) |
I125T |
probably damaging |
Het |
Nlrp2 |
A |
T |
7: 5,320,554 (GRCm39) |
L861Q |
probably damaging |
Het |
Notch3 |
C |
A |
17: 32,366,264 (GRCm39) |
R990L |
probably benign |
Het |
Nrap |
T |
C |
19: 56,350,153 (GRCm39) |
D655G |
probably benign |
Het |
Or5b99 |
G |
A |
19: 12,977,234 (GRCm39) |
V295I |
probably damaging |
Het |
Osbpl11 |
T |
A |
16: 33,047,426 (GRCm39) |
I463N |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,683,592 (GRCm39) |
R749W |
probably damaging |
Het |
Plaat5 |
C |
T |
19: 7,614,831 (GRCm39) |
T231I |
probably damaging |
Het |
Plxnb1 |
T |
C |
9: 108,941,209 (GRCm39) |
|
probably null |
Het |
Polr1a |
T |
A |
6: 71,931,874 (GRCm39) |
|
probably null |
Het |
Ppm1g |
T |
C |
5: 31,363,750 (GRCm39) |
I153V |
probably damaging |
Het |
Ppp1r12a |
T |
C |
10: 108,096,751 (GRCm39) |
S191P |
probably benign |
Het |
Prodh |
T |
C |
16: 17,898,922 (GRCm39) |
K178E |
possibly damaging |
Het |
Rilpl2 |
A |
G |
5: 124,607,911 (GRCm39) |
V103A |
possibly damaging |
Het |
Sap18b |
C |
T |
8: 96,552,169 (GRCm39) |
H60Y |
probably benign |
Het |
Sclt1 |
A |
G |
3: 41,583,951 (GRCm39) |
|
probably null |
Het |
Serpinb1a |
G |
T |
13: 33,026,849 (GRCm39) |
H364Q |
probably damaging |
Het |
Sez6l |
G |
A |
5: 112,623,231 (GRCm39) |
Q107* |
probably null |
Het |
Sipa1l2 |
C |
T |
8: 126,196,611 (GRCm39) |
V708I |
probably damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Uaca |
T |
A |
9: 60,757,573 (GRCm39) |
|
probably null |
Het |
Uqcrc1 |
C |
A |
9: 108,771,224 (GRCm39) |
H95N |
probably damaging |
Het |
Usp9y |
C |
T |
Y: 1,316,735 (GRCm39) |
R1938H |
probably damaging |
Homo |
Wnk4 |
C |
T |
11: 101,156,257 (GRCm39) |
R42W |
probably damaging |
Het |
Zfp326 |
T |
A |
5: 106,053,846 (GRCm39) |
L242Q |
probably damaging |
Het |
|
Other mutations in Or10ak8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01064:Or10ak8
|
APN |
4 |
118,774,091 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02065:Or10ak8
|
APN |
4 |
118,773,968 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02085:Or10ak8
|
APN |
4 |
118,773,947 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02092:Or10ak8
|
APN |
4 |
118,774,187 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02557:Or10ak8
|
APN |
4 |
118,774,389 (GRCm39) |
missense |
probably benign |
0.00 |
R0129:Or10ak8
|
UTSW |
4 |
118,774,667 (GRCm39) |
splice site |
probably null |
|
R0411:Or10ak8
|
UTSW |
4 |
118,773,823 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5001:Or10ak8
|
UTSW |
4 |
118,774,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R5313:Or10ak8
|
UTSW |
4 |
118,773,995 (GRCm39) |
missense |
probably benign |
0.00 |
R5733:Or10ak8
|
UTSW |
4 |
118,774,035 (GRCm39) |
missense |
probably benign |
0.00 |
R6153:Or10ak8
|
UTSW |
4 |
118,773,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7671:Or10ak8
|
UTSW |
4 |
118,774,183 (GRCm39) |
missense |
probably benign |
0.02 |
R8358:Or10ak8
|
UTSW |
4 |
118,773,723 (GRCm39) |
makesense |
probably null |
|
R8696:Or10ak8
|
UTSW |
4 |
118,774,635 (GRCm39) |
missense |
probably benign |
0.23 |
R8881:Or10ak8
|
UTSW |
4 |
118,774,571 (GRCm39) |
missense |
probably benign |
0.01 |
R9599:Or10ak8
|
UTSW |
4 |
118,773,851 (GRCm39) |
missense |
probably benign |
0.00 |
R9655:Or10ak8
|
UTSW |
4 |
118,773,804 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or10ak8
|
UTSW |
4 |
118,773,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or10ak8
|
UTSW |
4 |
118,774,332 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Or10ak8
|
UTSW |
4 |
118,774,224 (GRCm39) |
missense |
probably benign |
0.21 |
|