Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130023H24Rik |
A |
G |
7: 128,236,725 (GRCm38) |
L232P |
possibly damaging |
Het |
Acaa1a |
T |
C |
9: 119,349,038 (GRCm38) |
V312A |
probably damaging |
Het |
Bmp2 |
A |
G |
2: 133,561,684 (GRCm38) |
D385G |
probably damaging |
Het |
C1qtnf9 |
T |
C |
14: 60,779,792 (GRCm38) |
V257A |
probably damaging |
Het |
Cd3d |
G |
A |
9: 44,985,693 (GRCm38) |
V122I |
probably damaging |
Het |
Cdc37 |
T |
C |
9: 21,142,223 (GRCm38) |
E199G |
probably damaging |
Het |
Crb2 |
T |
A |
2: 37,787,684 (GRCm38) |
D326E |
probably benign |
Het |
Cyp2c29 |
A |
C |
19: 39,330,337 (GRCm38) |
K420N |
possibly damaging |
Het |
Cyp2g1 |
A |
C |
7: 26,820,759 (GRCm38) |
D472A |
probably damaging |
Het |
Dab2 |
A |
C |
15: 6,422,251 (GRCm38) |
H116P |
probably damaging |
Het |
Dnah7b |
G |
C |
1: 46,236,809 (GRCm38) |
E2619Q |
probably benign |
Het |
Dsg4 |
A |
T |
18: 20,451,852 (GRCm38) |
M208L |
probably benign |
Het |
Eif4enif1 |
T |
G |
11: 3,234,040 (GRCm38) |
V521G |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,372,486 (GRCm38) |
N340Y |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,182,934 (GRCm38) |
M55T |
probably damaging |
Het |
Grhpr |
A |
G |
4: 44,985,362 (GRCm38) |
S101G |
probably damaging |
Het |
Kif15 |
T |
A |
9: 123,011,614 (GRCm38) |
D33E |
possibly damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,850,378 (GRCm38) |
|
probably benign |
Het |
Lama4 |
A |
G |
10: 39,060,162 (GRCm38) |
Q611R |
possibly damaging |
Het |
Lrrc47 |
T |
A |
4: 154,020,452 (GRCm38) |
*123R |
probably null |
Het |
Map4k3 |
A |
C |
17: 80,680,915 (GRCm38) |
V36G |
probably damaging |
Het |
Mme |
T |
A |
3: 63,368,923 (GRCm38) |
I707N |
probably damaging |
Het |
Muc2 |
A |
G |
7: 141,751,457 (GRCm38) |
E166G |
unknown |
Het |
Mucl1 |
T |
A |
15: 103,753,578 (GRCm38) |
T108S |
possibly damaging |
Het |
Myo1h |
A |
T |
5: 114,359,744 (GRCm38) |
D53V |
possibly damaging |
Het |
Naa15 |
T |
A |
3: 51,472,784 (GRCm38) |
L811Q |
possibly damaging |
Het |
Nalcn |
T |
C |
14: 123,287,855 (GRCm38) |
T1487A |
probably benign |
Het |
Nme8 |
A |
T |
13: 19,694,328 (GRCm38) |
L87H |
probably damaging |
Het |
Nr2e1 |
A |
G |
10: 42,568,378 (GRCm38) |
V245A |
probably damaging |
Het |
Nt5c2 |
A |
T |
19: 46,893,535 (GRCm38) |
F291Y |
possibly damaging |
Het |
Olfr1508 |
T |
C |
14: 52,463,475 (GRCm38) |
D178G |
possibly damaging |
Het |
Olfr556 |
A |
T |
7: 102,670,730 (GRCm38) |
Q270L |
probably benign |
Het |
Olfr668 |
A |
T |
7: 104,925,510 (GRCm38) |
C85S |
probably benign |
Het |
Ooep |
T |
C |
9: 78,378,401 (GRCm38) |
N43S |
possibly damaging |
Het |
Ovch2 |
A |
T |
7: 107,796,565 (GRCm38) |
I82N |
probably damaging |
Het |
Palb2 |
A |
T |
7: 122,114,399 (GRCm38) |
M524K |
possibly damaging |
Het |
Patj |
T |
C |
4: 98,441,080 (GRCm38) |
S524P |
probably benign |
Het |
Patl1 |
T |
A |
19: 11,929,954 (GRCm38) |
Y401N |
possibly damaging |
Het |
Pcdhb20 |
A |
T |
18: 37,504,717 (GRCm38) |
T99S |
probably benign |
Het |
Plcb4 |
G |
A |
2: 135,932,262 (GRCm38) |
A155T |
probably benign |
Het |
Rpap3 |
A |
G |
15: 97,679,112 (GRCm38) |
V585A |
possibly damaging |
Het |
Sorbs1 |
G |
C |
19: 40,376,800 (GRCm38) |
R180G |
probably benign |
Het |
Spen |
T |
A |
4: 141,494,382 (GRCm38) |
T302S |
unknown |
Het |
Tenm4 |
G |
A |
7: 96,553,496 (GRCm38) |
R106H |
probably benign |
Het |
Ube2o |
T |
C |
11: 116,541,860 (GRCm38) |
E760G |
probably benign |
Het |
Uimc1 |
T |
A |
13: 55,075,454 (GRCm38) |
|
probably null |
Het |
Usp16 |
C |
T |
16: 87,480,929 (GRCm38) |
A689V |
probably damaging |
Het |
Vmn2r60 |
G |
A |
7: 42,142,242 (GRCm38) |
A530T |
probably benign |
Het |
Vps8 |
T |
A |
16: 21,575,022 (GRCm38) |
M1185K |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 78,912,205 (GRCm38) |
S136P |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,834,462 (GRCm38) |
N175S |
probably benign |
Het |
Zfp160 |
A |
T |
17: 21,026,532 (GRCm38) |
H448L |
probably damaging |
Het |
Zfp90 |
T |
A |
8: 106,425,009 (GRCm38) |
C451* |
probably null |
Het |
Zfp945 |
A |
G |
17: 22,852,290 (GRCm38) |
C212R |
probably damaging |
Het |
|
Other mutations in Olfr1337 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02203:Olfr1337
|
APN |
4 |
118,782,429 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL02626:Olfr1337
|
APN |
4 |
118,782,334 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02699:Olfr1337
|
APN |
4 |
118,782,152 (GRCm38) |
nonsense |
probably null |
|
IGL02754:Olfr1337
|
APN |
4 |
118,781,920 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL03287:Olfr1337
|
APN |
4 |
118,782,354 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1341:Olfr1337
|
UTSW |
4 |
118,782,382 (GRCm38) |
missense |
probably benign |
0.01 |
R4894:Olfr1337
|
UTSW |
4 |
118,782,286 (GRCm38) |
missense |
probably damaging |
1.00 |
R6124:Olfr1337
|
UTSW |
4 |
118,782,195 (GRCm38) |
missense |
probably damaging |
1.00 |
R6515:Olfr1337
|
UTSW |
4 |
118,782,270 (GRCm38) |
missense |
probably benign |
0.13 |
R6529:Olfr1337
|
UTSW |
4 |
118,781,710 (GRCm38) |
missense |
probably benign |
0.15 |
R7398:Olfr1337
|
UTSW |
4 |
118,781,699 (GRCm38) |
missense |
possibly damaging |
0.80 |
R7684:Olfr1337
|
UTSW |
4 |
118,782,274 (GRCm38) |
missense |
probably benign |
0.40 |
R8377:Olfr1337
|
UTSW |
4 |
118,782,006 (GRCm38) |
missense |
probably benign |
0.22 |
R8717:Olfr1337
|
UTSW |
4 |
118,781,799 (GRCm38) |
missense |
probably damaging |
1.00 |
R9369:Olfr1337
|
UTSW |
4 |
118,781,880 (GRCm38) |
missense |
probably benign |
0.31 |
R9594:Olfr1337
|
UTSW |
4 |
118,781,755 (GRCm38) |
missense |
probably benign |
|
Z1189:Olfr1337
|
UTSW |
4 |
118,782,087 (GRCm38) |
missense |
possibly damaging |
0.85 |
|