Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
C |
A |
12: 72,939,669 (GRCm39) |
E415* |
probably null |
Het |
Abcb10 |
C |
T |
8: 124,688,791 (GRCm39) |
G495D |
probably damaging |
Het |
Acad12 |
C |
T |
5: 121,742,385 (GRCm39) |
A408T |
probably benign |
Het |
Acox2 |
T |
A |
14: 8,230,247 (GRCm38) |
H632L |
probably benign |
Het |
Anxa5 |
A |
T |
3: 36,506,441 (GRCm39) |
|
probably null |
Het |
Ap1m2 |
A |
T |
9: 21,209,500 (GRCm39) |
I392N |
possibly damaging |
Het |
Casp2 |
T |
C |
6: 42,253,725 (GRCm39) |
|
probably benign |
Het |
Cel |
C |
T |
2: 28,449,636 (GRCm39) |
A243T |
probably damaging |
Het |
Depp1 |
A |
G |
6: 116,628,966 (GRCm39) |
N103S |
possibly damaging |
Het |
Dgka |
A |
T |
10: 128,569,202 (GRCm39) |
S177T |
possibly damaging |
Het |
Dnajc6 |
A |
G |
4: 101,496,544 (GRCm39) |
T836A |
possibly damaging |
Het |
Dock3 |
T |
C |
9: 106,790,392 (GRCm39) |
S1444G |
probably damaging |
Het |
Dtl |
T |
C |
1: 191,293,649 (GRCm39) |
D176G |
probably benign |
Het |
Eif4g1 |
T |
C |
16: 20,497,692 (GRCm39) |
I230T |
probably benign |
Het |
Fam227a |
T |
A |
15: 79,518,309 (GRCm39) |
I328F |
probably benign |
Het |
Fam98a |
A |
G |
17: 75,847,173 (GRCm39) |
L179S |
probably damaging |
Het |
Fmo1 |
C |
T |
1: 162,657,635 (GRCm39) |
R502Q |
probably damaging |
Het |
Fndc3a |
C |
T |
14: 72,811,811 (GRCm39) |
A340T |
probably damaging |
Het |
Gli3 |
C |
A |
13: 15,900,899 (GRCm39) |
Q1429K |
probably benign |
Het |
Gm3443 |
A |
T |
19: 21,534,959 (GRCm39) |
I75F |
possibly damaging |
Het |
Gtpbp6 |
C |
T |
5: 110,252,155 (GRCm39) |
|
probably null |
Het |
Gtsf1 |
A |
T |
15: 103,318,070 (GRCm39) |
Y156* |
probably null |
Het |
Hmcn1 |
T |
C |
1: 150,522,545 (GRCm39) |
T3452A |
probably benign |
Het |
Kcnj10 |
T |
A |
1: 172,196,822 (GRCm39) |
V112E |
probably damaging |
Het |
Lama3 |
C |
A |
18: 12,653,048 (GRCm39) |
T256K |
probably benign |
Het |
Lrrc8d |
G |
A |
5: 105,974,782 (GRCm39) |
V63M |
unknown |
Het |
Matn3 |
G |
T |
12: 9,011,132 (GRCm39) |
A348S |
possibly damaging |
Het |
Mmp16 |
A |
G |
4: 18,112,121 (GRCm39) |
|
probably null |
Het |
Nsd3 |
A |
G |
8: 26,190,594 (GRCm39) |
N175S |
probably damaging |
Het |
Or11h4 |
A |
T |
14: 50,974,521 (GRCm39) |
F33I |
probably benign |
Het |
Or1d2 |
C |
A |
11: 74,255,780 (GRCm39) |
P95Q |
probably benign |
Het |
Or4c35 |
C |
T |
2: 89,808,415 (GRCm39) |
Q98* |
probably null |
Het |
Or4k5 |
C |
A |
14: 50,385,922 (GRCm39) |
M136I |
possibly damaging |
Het |
Pcdhb12 |
T |
A |
18: 37,571,132 (GRCm39) |
N759K |
probably benign |
Het |
Pcsk2 |
T |
C |
2: 143,415,348 (GRCm39) |
|
probably benign |
Het |
Polq |
G |
A |
16: 36,906,890 (GRCm39) |
D2284N |
probably damaging |
Het |
Prdm12 |
C |
T |
2: 31,533,823 (GRCm39) |
R147C |
probably damaging |
Het |
Ptprz1 |
A |
G |
6: 23,000,382 (GRCm39) |
D824G |
probably benign |
Het |
Rere |
C |
T |
4: 150,701,495 (GRCm39) |
R1292C |
probably damaging |
Het |
Rptor |
T |
A |
11: 119,671,419 (GRCm39) |
L294* |
probably null |
Het |
Sbf2 |
A |
T |
7: 109,914,233 (GRCm39) |
C1650S |
probably damaging |
Het |
Sdk1 |
C |
T |
5: 142,147,621 (GRCm39) |
T1751I |
probably damaging |
Het |
Sh3bp1 |
T |
C |
15: 78,787,899 (GRCm39) |
|
probably null |
Het |
Shank2 |
T |
A |
7: 143,606,109 (GRCm39) |
D97E |
probably damaging |
Het |
Tab2 |
A |
C |
10: 7,795,812 (GRCm39) |
S149R |
possibly damaging |
Het |
Taok1 |
G |
T |
11: 77,440,190 (GRCm39) |
R606S |
probably benign |
Het |
Tas2r121 |
A |
G |
6: 132,677,645 (GRCm39) |
L109P |
probably damaging |
Het |
Tmem117 |
A |
G |
15: 94,829,689 (GRCm39) |
M175V |
probably benign |
Het |
Tmprss11b |
T |
C |
5: 86,812,832 (GRCm39) |
K155E |
probably benign |
Het |
Tmtc2 |
G |
T |
10: 105,249,229 (GRCm39) |
T168N |
probably benign |
Het |
Top2b |
G |
A |
14: 16,383,177 (GRCm38) |
R55H |
probably damaging |
Het |
Tsga10ip |
C |
T |
19: 5,440,942 (GRCm39) |
|
probably null |
Het |
Tuba8 |
A |
G |
6: 121,197,470 (GRCm39) |
N44S |
probably benign |
Het |
Ube2o |
A |
G |
11: 116,434,558 (GRCm39) |
V590A |
probably benign |
Het |
Ush2a |
T |
G |
1: 188,275,075 (GRCm39) |
|
probably null |
Het |
Vmn2r23 |
T |
A |
6: 123,690,229 (GRCm39) |
Y368* |
probably null |
Het |
|
Other mutations in Fgb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00839:Fgb
|
APN |
3 |
82,950,598 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02129:Fgb
|
APN |
3 |
82,950,725 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02148:Fgb
|
APN |
3 |
82,950,594 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02286:Fgb
|
APN |
3 |
82,950,633 (GRCm39) |
missense |
probably benign |
|
IGL02601:Fgb
|
APN |
3 |
82,952,367 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02721:Fgb
|
APN |
3 |
82,950,674 (GRCm39) |
missense |
possibly damaging |
0.89 |
G1patch:Fgb
|
UTSW |
3 |
82,951,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Fgb
|
UTSW |
3 |
82,950,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R1913:Fgb
|
UTSW |
3 |
82,952,287 (GRCm39) |
missense |
probably benign |
0.03 |
R1990:Fgb
|
UTSW |
3 |
82,951,560 (GRCm39) |
nonsense |
probably null |
|
R2063:Fgb
|
UTSW |
3 |
82,956,996 (GRCm39) |
missense |
probably benign |
0.09 |
R2065:Fgb
|
UTSW |
3 |
82,956,996 (GRCm39) |
missense |
probably benign |
0.09 |
R2066:Fgb
|
UTSW |
3 |
82,956,996 (GRCm39) |
missense |
probably benign |
0.09 |
R2067:Fgb
|
UTSW |
3 |
82,956,996 (GRCm39) |
missense |
probably benign |
0.09 |
R2251:Fgb
|
UTSW |
3 |
82,950,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R4682:Fgb
|
UTSW |
3 |
82,950,572 (GRCm39) |
missense |
probably benign |
0.00 |
R5045:Fgb
|
UTSW |
3 |
82,950,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R5573:Fgb
|
UTSW |
3 |
82,956,984 (GRCm39) |
splice site |
probably null |
|
R5766:Fgb
|
UTSW |
3 |
82,953,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R6103:Fgb
|
UTSW |
3 |
82,951,170 (GRCm39) |
missense |
probably benign |
0.22 |
R6315:Fgb
|
UTSW |
3 |
82,952,362 (GRCm39) |
missense |
probably benign |
0.00 |
R6469:Fgb
|
UTSW |
3 |
82,953,449 (GRCm39) |
nonsense |
probably null |
|
R6664:Fgb
|
UTSW |
3 |
82,954,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6725:Fgb
|
UTSW |
3 |
82,951,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R6727:Fgb
|
UTSW |
3 |
82,954,094 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6830:Fgb
|
UTSW |
3 |
82,952,332 (GRCm39) |
missense |
probably benign |
0.07 |
R7016:Fgb
|
UTSW |
3 |
82,953,371 (GRCm39) |
missense |
probably benign |
0.01 |
R7132:Fgb
|
UTSW |
3 |
82,954,053 (GRCm39) |
nonsense |
probably null |
|
R7371:Fgb
|
UTSW |
3 |
82,953,359 (GRCm39) |
missense |
probably damaging |
0.99 |
R7430:Fgb
|
UTSW |
3 |
82,954,014 (GRCm39) |
missense |
probably benign |
0.26 |
R7681:Fgb
|
UTSW |
3 |
82,957,139 (GRCm39) |
start gained |
probably benign |
|
R7811:Fgb
|
UTSW |
3 |
82,957,004 (GRCm39) |
missense |
probably benign |
|
R8171:Fgb
|
UTSW |
3 |
82,949,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R8787:Fgb
|
UTSW |
3 |
82,953,969 (GRCm39) |
missense |
probably benign |
0.00 |
R9526:Fgb
|
UTSW |
3 |
82,957,122 (GRCm39) |
start gained |
probably benign |
|
R9562:Fgb
|
UTSW |
3 |
82,952,409 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Fgb
|
UTSW |
3 |
82,952,363 (GRCm39) |
missense |
probably benign |
0.01 |
|