Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadm |
C |
A |
3: 153,647,607 (GRCm39) |
V11F |
probably damaging |
Het |
Alk |
A |
T |
17: 72,209,620 (GRCm39) |
Y941* |
probably null |
Het |
Blm |
A |
T |
7: 80,153,125 (GRCm39) |
|
probably null |
Het |
Blvrb |
T |
C |
7: 27,158,765 (GRCm39) |
V55A |
possibly damaging |
Het |
Cdh23 |
T |
A |
10: 60,153,721 (GRCm39) |
T2288S |
probably damaging |
Het |
Csnk1g1 |
T |
A |
9: 65,915,067 (GRCm39) |
M242K |
probably damaging |
Het |
Cyp2c29 |
G |
A |
19: 39,279,291 (GRCm39) |
G96D |
possibly damaging |
Het |
Cyp2d26 |
T |
A |
15: 82,676,827 (GRCm39) |
H173L |
probably benign |
Het |
Cyp2g1 |
T |
A |
7: 26,510,871 (GRCm39) |
S131T |
probably benign |
Het |
Dusp29 |
G |
A |
14: 21,752,990 (GRCm39) |
T52I |
probably damaging |
Het |
Dzip3 |
T |
A |
16: 48,758,900 (GRCm39) |
|
probably benign |
Het |
Espl1 |
T |
C |
15: 102,208,274 (GRCm39) |
S427P |
probably damaging |
Het |
Fasn |
A |
T |
11: 120,699,006 (GRCm39) |
D2424E |
probably benign |
Het |
Flrt2 |
G |
A |
12: 95,746,257 (GRCm39) |
M198I |
probably benign |
Het |
Gen1 |
A |
T |
12: 11,292,576 (GRCm39) |
S404R |
probably benign |
Het |
Gm11596 |
A |
T |
11: 99,683,806 (GRCm39) |
C105S |
unknown |
Het |
Hdlbp |
A |
T |
1: 93,345,233 (GRCm39) |
V714D |
probably damaging |
Het |
Igkv4-80 |
A |
G |
6: 68,993,816 (GRCm39) |
V25A |
probably benign |
Het |
Igkv8-27 |
C |
T |
6: 70,148,925 (GRCm39) |
W76* |
probably null |
Het |
Ikzf1 |
T |
C |
11: 11,698,545 (GRCm39) |
L132P |
probably damaging |
Het |
Kcna6 |
C |
A |
6: 126,715,443 (GRCm39) |
C482F |
possibly damaging |
Het |
Lhx9 |
A |
T |
1: 138,769,580 (GRCm39) |
L47Q |
probably damaging |
Het |
Lrp4 |
T |
A |
2: 91,304,347 (GRCm39) |
D175E |
probably damaging |
Het |
Lrrtm3 |
T |
C |
10: 63,923,815 (GRCm39) |
K451E |
probably damaging |
Het |
Mcm9 |
C |
T |
10: 53,417,653 (GRCm39) |
V17M |
probably damaging |
Het |
Mios |
T |
A |
6: 8,222,492 (GRCm39) |
S475R |
probably benign |
Het |
Mmp24 |
C |
T |
2: 155,657,708 (GRCm39) |
R533C |
probably damaging |
Het |
Moxd1 |
C |
T |
10: 24,158,650 (GRCm39) |
P435S |
probably damaging |
Het |
Mta2 |
T |
A |
19: 8,927,670 (GRCm39) |
I497N |
probably benign |
Het |
Mtus2 |
T |
C |
5: 148,014,473 (GRCm39) |
V422A |
probably benign |
Het |
Ndufaf1 |
A |
T |
2: 119,486,907 (GRCm39) |
F260Y |
probably damaging |
Het |
Nfasc |
C |
T |
1: 132,548,662 (GRCm39) |
|
probably null |
Het |
Nid1 |
A |
T |
13: 13,683,305 (GRCm39) |
T1128S |
probably benign |
Het |
Odad2 |
C |
T |
18: 7,129,461 (GRCm39) |
E906K |
probably damaging |
Het |
Pcdh12 |
G |
A |
18: 38,414,746 (GRCm39) |
P793L |
probably benign |
Het |
Pclo |
A |
T |
5: 14,726,980 (GRCm39) |
|
probably benign |
Het |
Prpf31 |
T |
A |
7: 3,637,185 (GRCm39) |
N161K |
possibly damaging |
Het |
Prpf6 |
T |
G |
2: 181,290,878 (GRCm39) |
N656K |
probably benign |
Het |
Ptprn |
T |
A |
1: 75,234,813 (GRCm39) |
H258L |
probably benign |
Het |
Rab19 |
A |
G |
6: 39,366,732 (GRCm39) |
T216A |
probably benign |
Het |
Ryr3 |
A |
C |
2: 112,664,335 (GRCm39) |
L1652W |
probably damaging |
Het |
Six2 |
A |
C |
17: 85,992,806 (GRCm39) |
S232R |
possibly damaging |
Het |
Spag17 |
T |
C |
3: 99,934,707 (GRCm39) |
V663A |
probably benign |
Het |
Spag5 |
A |
G |
11: 78,195,449 (GRCm39) |
N252S |
probably benign |
Het |
Spata31e4 |
A |
T |
13: 50,857,113 (GRCm39) |
H917L |
probably damaging |
Het |
Sptb |
C |
T |
12: 76,655,810 (GRCm39) |
|
probably null |
Het |
Synj1 |
A |
G |
16: 90,758,253 (GRCm39) |
|
probably benign |
Het |
Tekt2 |
T |
C |
4: 126,218,645 (GRCm39) |
H36R |
possibly damaging |
Het |
Tjp1 |
A |
T |
7: 64,962,403 (GRCm39) |
M1258K |
probably damaging |
Het |
Txnrd3 |
T |
C |
6: 89,651,777 (GRCm39) |
*502Q |
probably null |
Het |
|
Other mutations in Or51f1d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02172:Or51f1d
|
APN |
7 |
102,700,582 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02200:Or51f1d
|
APN |
7 |
102,701,000 (GRCm39) |
missense |
probably benign |
|
IGL02412:Or51f1d
|
APN |
7 |
102,701,359 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02859:Or51f1d
|
APN |
7 |
102,701,345 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03078:Or51f1d
|
APN |
7 |
102,701,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Or51f1d
|
UTSW |
7 |
102,700,909 (GRCm39) |
missense |
probably benign |
0.22 |
R1474:Or51f1d
|
UTSW |
7 |
102,701,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R1531:Or51f1d
|
UTSW |
7 |
102,700,795 (GRCm39) |
missense |
probably benign |
0.00 |
R1535:Or51f1d
|
UTSW |
7 |
102,700,576 (GRCm39) |
missense |
probably benign |
0.14 |
R1777:Or51f1d
|
UTSW |
7 |
102,700,583 (GRCm39) |
missense |
probably benign |
0.41 |
R1883:Or51f1d
|
UTSW |
7 |
102,701,189 (GRCm39) |
missense |
probably benign |
0.00 |
R1884:Or51f1d
|
UTSW |
7 |
102,701,189 (GRCm39) |
missense |
probably benign |
0.00 |
R2265:Or51f1d
|
UTSW |
7 |
102,701,344 (GRCm39) |
missense |
probably benign |
0.00 |
R2267:Or51f1d
|
UTSW |
7 |
102,701,344 (GRCm39) |
missense |
probably benign |
0.00 |
R2269:Or51f1d
|
UTSW |
7 |
102,701,344 (GRCm39) |
missense |
probably benign |
0.00 |
R2299:Or51f1d
|
UTSW |
7 |
102,700,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R3802:Or51f1d
|
UTSW |
7 |
102,701,372 (GRCm39) |
missense |
probably benign |
0.05 |
R4239:Or51f1d
|
UTSW |
7 |
102,701,003 (GRCm39) |
missense |
probably benign |
0.17 |
R4426:Or51f1d
|
UTSW |
7 |
102,701,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Or51f1d
|
UTSW |
7 |
102,700,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Or51f1d
|
UTSW |
7 |
102,700,526 (GRCm39) |
missense |
probably benign |
0.00 |
R6270:Or51f1d
|
UTSW |
7 |
102,700,538 (GRCm39) |
missense |
probably benign |
0.27 |
R6837:Or51f1d
|
UTSW |
7 |
102,700,929 (GRCm39) |
nonsense |
probably null |
|
R7257:Or51f1d
|
UTSW |
7 |
102,700,837 (GRCm39) |
missense |
probably benign |
0.39 |
R8506:Or51f1d
|
UTSW |
7 |
102,700,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Or51f1d
|
UTSW |
7 |
102,701,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R9638:Or51f1d
|
UTSW |
7 |
102,701,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|