Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apc |
G |
T |
18: 34,354,213 (GRCm39) |
|
probably benign |
Het |
Apol11b |
T |
A |
15: 77,519,793 (GRCm39) |
K96* |
probably null |
Het |
Arhgap35 |
C |
T |
7: 16,296,849 (GRCm39) |
G739S |
probably damaging |
Het |
Atp6v0a4 |
A |
C |
6: 38,069,752 (GRCm39) |
F47V |
probably damaging |
Het |
Bcl9 |
G |
A |
3: 97,117,881 (GRCm39) |
P271L |
probably benign |
Het |
Cd109 |
T |
C |
9: 78,587,446 (GRCm39) |
|
probably null |
Het |
Col12a1 |
T |
A |
9: 79,521,645 (GRCm39) |
I2771F |
probably benign |
Het |
Col6a1 |
A |
G |
10: 76,559,288 (GRCm39) |
V116A |
probably damaging |
Het |
Cpsf2 |
C |
G |
12: 101,963,138 (GRCm39) |
L401V |
probably benign |
Het |
Cwf19l2 |
G |
A |
9: 3,475,549 (GRCm39) |
E829K |
probably damaging |
Het |
D7Ertd443e |
G |
A |
7: 133,951,004 (GRCm39) |
T223I |
probably damaging |
Het |
Dtx4 |
G |
A |
19: 12,469,681 (GRCm39) |
R149C |
probably damaging |
Het |
Fam186b |
C |
T |
15: 99,171,734 (GRCm39) |
A838T |
possibly damaging |
Het |
Fzd4 |
G |
T |
7: 89,057,326 (GRCm39) |
E458* |
probably null |
Het |
Gm17669 |
C |
T |
18: 67,695,526 (GRCm39) |
P24S |
possibly damaging |
Het |
Grin2b |
C |
T |
6: 135,713,304 (GRCm39) |
G859D |
probably damaging |
Het |
Gucy2e |
T |
C |
11: 69,114,472 (GRCm39) |
Y1019C |
probably damaging |
Het |
Gzme |
T |
A |
14: 56,355,910 (GRCm39) |
N134I |
possibly damaging |
Het |
Havcr1 |
A |
T |
11: 46,643,197 (GRCm39) |
Y39F |
probably damaging |
Het |
Hint3 |
A |
T |
10: 30,494,347 (GRCm39) |
M1K |
probably null |
Het |
Hspa4l |
A |
G |
3: 40,736,008 (GRCm39) |
K543R |
probably damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Lipo2 |
A |
G |
19: 33,698,258 (GRCm39) |
I373T |
probably benign |
Het |
Myo5c |
T |
A |
9: 75,165,407 (GRCm39) |
I405N |
possibly damaging |
Het |
Or10a49 |
T |
C |
7: 108,467,833 (GRCm39) |
H176R |
probably damaging |
Het |
P2rx1 |
A |
G |
11: 72,899,329 (GRCm39) |
M108V |
probably benign |
Het |
Pcsk2 |
T |
A |
2: 143,388,463 (GRCm39) |
V18E |
probably benign |
Het |
Pigr |
A |
T |
1: 130,777,359 (GRCm39) |
|
probably null |
Het |
Pkp1 |
A |
T |
1: 135,810,230 (GRCm39) |
C447S |
probably benign |
Het |
Prom1 |
T |
A |
5: 44,215,988 (GRCm39) |
I96F |
probably benign |
Het |
Prpf4b |
T |
C |
13: 35,068,076 (GRCm39) |
|
probably benign |
Het |
Ropn1 |
C |
A |
16: 34,491,542 (GRCm39) |
D102E |
probably benign |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Sphk1 |
T |
G |
11: 116,425,714 (GRCm39) |
V17G |
possibly damaging |
Het |
Syngr1 |
A |
G |
15: 79,982,219 (GRCm39) |
N2S |
probably benign |
Het |
Syt9 |
T |
G |
7: 107,101,330 (GRCm39) |
S359A |
possibly damaging |
Het |
Terb1 |
T |
C |
8: 105,215,131 (GRCm39) |
I282V |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,585,168 (GRCm39) |
I22042F |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,739,600 (GRCm39) |
D3646E |
probably benign |
Het |
Ube2d1 |
A |
G |
10: 71,091,682 (GRCm39) |
W141R |
probably damaging |
Het |
Vmn2r41 |
T |
A |
7: 8,141,362 (GRCm39) |
I701F |
probably damaging |
Het |
Zfp770 |
T |
C |
2: 114,026,596 (GRCm39) |
D491G |
probably benign |
Het |
|
Other mutations in Ifna9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01788:Ifna9
|
APN |
4 |
88,510,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Ifna9
|
APN |
4 |
88,510,591 (GRCm39) |
nonsense |
probably null |
|
R0579:Ifna9
|
UTSW |
4 |
88,510,508 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1530:Ifna9
|
UTSW |
4 |
88,510,409 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1663:Ifna9
|
UTSW |
4 |
88,510,220 (GRCm39) |
missense |
probably benign |
0.00 |
R1872:Ifna9
|
UTSW |
4 |
88,510,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R3923:Ifna9
|
UTSW |
4 |
88,510,508 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4534:Ifna9
|
UTSW |
4 |
88,510,285 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4882:Ifna9
|
UTSW |
4 |
88,510,540 (GRCm39) |
missense |
probably benign |
0.01 |
R6008:Ifna9
|
UTSW |
4 |
88,510,600 (GRCm39) |
missense |
probably null |
1.00 |
R6464:Ifna9
|
UTSW |
4 |
88,510,487 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6584:Ifna9
|
UTSW |
4 |
88,510,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R6899:Ifna9
|
UTSW |
4 |
88,510,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|