Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
G |
11: 119,901,696 (GRCm39) |
V900A |
probably benign |
Het |
Adam28 |
C |
T |
14: 68,879,479 (GRCm39) |
A190T |
probably benign |
Het |
Ager |
T |
C |
17: 34,817,541 (GRCm39) |
V116A |
probably damaging |
Het |
Agt |
G |
T |
8: 125,291,065 (GRCm39) |
H81N |
probably benign |
Het |
Apc2 |
T |
C |
10: 80,146,872 (GRCm39) |
V642A |
probably damaging |
Het |
Atg4b |
C |
T |
1: 93,713,648 (GRCm39) |
T325M |
probably damaging |
Het |
Atp10b |
A |
G |
11: 43,150,711 (GRCm39) |
S1470G |
probably benign |
Het |
Cacul1 |
A |
G |
19: 60,533,942 (GRCm39) |
I220T |
probably benign |
Het |
Ccdc7a |
T |
C |
8: 129,671,136 (GRCm39) |
|
probably null |
Het |
Cnnm1 |
A |
C |
19: 43,429,827 (GRCm39) |
D315A |
probably damaging |
Het |
Fbxo24 |
A |
G |
5: 137,611,096 (GRCm39) |
F565L |
probably damaging |
Het |
Fpr-rs4 |
T |
A |
17: 18,242,211 (GRCm39) |
S73T |
probably damaging |
Het |
Gbp7 |
T |
C |
3: 142,248,889 (GRCm39) |
V384A |
probably benign |
Het |
Gcnt2 |
A |
T |
13: 41,041,732 (GRCm39) |
H297L |
possibly damaging |
Het |
Glo1 |
T |
C |
17: 30,831,518 (GRCm39) |
E3G |
probably benign |
Het |
Ifi213 |
T |
A |
1: 173,396,392 (GRCm39) |
M561L |
probably benign |
Het |
Ighv1-63 |
A |
G |
12: 115,459,478 (GRCm39) |
S40P |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,260,814 (GRCm39) |
L971P |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,336,917 (GRCm39) |
I1285N |
probably damaging |
Het |
Map1b |
A |
T |
13: 99,566,708 (GRCm39) |
Y2004* |
probably null |
Het |
Mindy1 |
C |
T |
3: 95,202,590 (GRCm39) |
L394F |
probably benign |
Het |
Mug1 |
A |
G |
6: 121,852,450 (GRCm39) |
D846G |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,463,268 (GRCm39) |
E500G |
probably damaging |
Het |
Myo18a |
C |
T |
11: 77,733,014 (GRCm39) |
T1348M |
probably damaging |
Het |
Myo7b |
A |
T |
18: 32,093,129 (GRCm39) |
I2027N |
probably damaging |
Het |
Neb |
T |
C |
2: 52,069,580 (GRCm39) |
|
probably null |
Het |
Obscn |
G |
A |
11: 58,929,592 (GRCm39) |
R5208C |
probably damaging |
Het |
Parg |
G |
A |
14: 31,996,874 (GRCm39) |
D827N |
probably damaging |
Het |
Pcdha6 |
A |
T |
18: 37,102,226 (GRCm39) |
H473L |
probably benign |
Het |
Pde4dip |
A |
G |
3: 97,625,645 (GRCm39) |
S1318P |
probably benign |
Het |
Ppan |
T |
C |
9: 20,801,220 (GRCm39) |
S166P |
possibly damaging |
Het |
Ppargc1b |
C |
A |
18: 61,448,939 (GRCm39) |
A128S |
probably damaging |
Het |
Rdh16f2 |
T |
A |
10: 127,712,915 (GRCm39) |
D304E |
possibly damaging |
Het |
Sh3pxd2a |
A |
T |
19: 47,260,448 (GRCm39) |
L435Q |
probably damaging |
Het |
Slc35d1 |
A |
T |
4: 103,065,333 (GRCm39) |
Y183N |
|
Het |
Sspo |
T |
C |
6: 48,443,989 (GRCm39) |
S2166P |
possibly damaging |
Het |
Tent5a |
A |
T |
9: 85,208,672 (GRCm39) |
N50K |
probably benign |
Het |
Twf2 |
T |
C |
9: 106,092,100 (GRCm39) |
F319S |
probably benign |
Het |
Ush2a |
C |
T |
1: 188,607,147 (GRCm39) |
T4014M |
probably benign |
Het |
Vmn1r3 |
T |
G |
4: 3,185,149 (GRCm39) |
T53P |
probably damaging |
Het |
Vmn2r76 |
T |
C |
7: 85,880,428 (GRCm39) |
E86G |
probably benign |
Het |
Wdtc1 |
A |
G |
4: 133,023,782 (GRCm39) |
Y530H |
probably damaging |
Het |
Xdh |
A |
G |
17: 74,214,711 (GRCm39) |
F745L |
probably damaging |
Het |
Xdh |
A |
C |
17: 74,233,541 (GRCm39) |
|
probably null |
Het |
Zfp358 |
T |
C |
8: 3,545,568 (GRCm39) |
L50P |
probably damaging |
Het |
|
Other mutations in Gsdmc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00730:Gsdmc4
|
APN |
15 |
63,769,653 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02301:Gsdmc4
|
APN |
15 |
63,767,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02586:Gsdmc4
|
APN |
15 |
63,765,641 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02747:Gsdmc4
|
APN |
15 |
63,765,720 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02829:Gsdmc4
|
APN |
15 |
63,764,497 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03233:Gsdmc4
|
APN |
15 |
63,774,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Gsdmc4
|
UTSW |
15 |
63,765,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R0981:Gsdmc4
|
UTSW |
15 |
63,763,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1946:Gsdmc4
|
UTSW |
15 |
63,774,629 (GRCm39) |
missense |
probably benign |
0.19 |
R2350:Gsdmc4
|
UTSW |
15 |
63,765,014 (GRCm39) |
missense |
probably benign |
|
R2967:Gsdmc4
|
UTSW |
15 |
63,773,909 (GRCm39) |
missense |
probably benign |
0.19 |
R3409:Gsdmc4
|
UTSW |
15 |
63,763,895 (GRCm39) |
missense |
probably benign |
0.09 |
R3410:Gsdmc4
|
UTSW |
15 |
63,763,895 (GRCm39) |
missense |
probably benign |
0.09 |
R4067:Gsdmc4
|
UTSW |
15 |
63,765,736 (GRCm39) |
splice site |
probably null |
|
R4840:Gsdmc4
|
UTSW |
15 |
63,765,596 (GRCm39) |
missense |
probably benign |
0.24 |
R5182:Gsdmc4
|
UTSW |
15 |
63,765,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5624:Gsdmc4
|
UTSW |
15 |
63,764,503 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5910:Gsdmc4
|
UTSW |
15 |
63,767,101 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6533:Gsdmc4
|
UTSW |
15 |
63,763,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R6698:Gsdmc4
|
UTSW |
15 |
63,765,613 (GRCm39) |
missense |
probably benign |
0.10 |
R7291:Gsdmc4
|
UTSW |
15 |
63,774,689 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7598:Gsdmc4
|
UTSW |
15 |
63,772,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7691:Gsdmc4
|
UTSW |
15 |
63,765,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R7851:Gsdmc4
|
UTSW |
15 |
63,774,595 (GRCm39) |
nonsense |
probably null |
|
R7881:Gsdmc4
|
UTSW |
15 |
63,769,568 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8300:Gsdmc4
|
UTSW |
15 |
63,766,790 (GRCm39) |
missense |
probably damaging |
0.97 |
R8512:Gsdmc4
|
UTSW |
15 |
63,763,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Gsdmc4
|
UTSW |
15 |
63,774,586 (GRCm39) |
missense |
probably benign |
0.10 |
R9680:Gsdmc4
|
UTSW |
15 |
63,774,706 (GRCm39) |
missense |
possibly damaging |
0.61 |
|