Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd12 |
A |
T |
17: 66,291,175 (GRCm39) |
N1419K |
probably benign |
Het |
Arhgef18 |
A |
G |
8: 3,479,553 (GRCm39) |
E79G |
probably damaging |
Het |
Art4 |
T |
A |
6: 136,831,493 (GRCm39) |
Q216L |
probably damaging |
Het |
Bbs4 |
T |
C |
9: 59,231,348 (GRCm39) |
D407G |
probably benign |
Het |
Cherp |
A |
G |
8: 73,222,090 (GRCm39) |
I277T |
probably damaging |
Het |
Cnot2 |
A |
G |
10: 116,342,976 (GRCm39) |
M119T |
probably benign |
Het |
Disp2 |
T |
A |
2: 118,616,759 (GRCm39) |
C73S |
probably damaging |
Het |
Dock4 |
T |
C |
12: 40,884,390 (GRCm39) |
S1686P |
probably damaging |
Het |
Duox2 |
T |
A |
2: 122,122,781 (GRCm39) |
D551V |
possibly damaging |
Het |
Gmip |
T |
A |
8: 70,269,661 (GRCm39) |
Y585* |
probably null |
Het |
Gnal |
A |
G |
18: 67,267,360 (GRCm39) |
|
probably null |
Het |
Idh1 |
T |
G |
1: 65,205,281 (GRCm39) |
Q228P |
possibly damaging |
Het |
Igsf10 |
A |
T |
3: 59,226,938 (GRCm39) |
I2245N |
probably damaging |
Het |
Mrgpra4 |
A |
T |
7: 47,631,052 (GRCm39) |
M183K |
possibly damaging |
Het |
Npr2 |
T |
A |
4: 43,641,612 (GRCm39) |
V472D |
possibly damaging |
Het |
Pcdh7 |
A |
T |
5: 57,878,806 (GRCm39) |
N787I |
probably damaging |
Het |
Phf8-ps |
A |
G |
17: 33,286,361 (GRCm39) |
V147A |
probably damaging |
Het |
Ppp1r10 |
A |
T |
17: 36,235,751 (GRCm39) |
N111I |
probably damaging |
Het |
Ppp3ca |
A |
G |
3: 136,640,942 (GRCm39) |
N508D |
probably benign |
Het |
Rgs17 |
A |
G |
10: 5,862,624 (GRCm38) |
Q25P |
possibly damaging |
Het |
Slco6d1 |
T |
A |
1: 98,348,925 (GRCm39) |
|
probably benign |
Het |
Tab3 |
T |
A |
X: 84,665,210 (GRCm39) |
N591K |
probably damaging |
Het |
Tfcp2 |
T |
C |
15: 100,411,059 (GRCm39) |
|
probably benign |
Het |
Them5 |
A |
T |
3: 94,250,716 (GRCm39) |
D93V |
probably damaging |
Het |
Thoc5 |
T |
G |
11: 4,868,147 (GRCm39) |
V275G |
probably damaging |
Het |
Trmt1l |
T |
C |
1: 151,318,463 (GRCm39) |
|
probably null |
Het |
Zdbf2 |
G |
T |
1: 63,345,673 (GRCm39) |
V1351F |
possibly damaging |
Het |
Zfp14 |
G |
T |
7: 29,738,312 (GRCm39) |
Y224* |
probably null |
Het |
Zfp606 |
T |
G |
7: 12,228,159 (GRCm39) |
M702R |
probably damaging |
Het |
|
Other mutations in Dsc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Dsc1
|
APN |
18 |
20,234,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00571:Dsc1
|
APN |
18 |
20,243,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00963:Dsc1
|
APN |
18 |
20,245,043 (GRCm39) |
missense |
probably null |
0.01 |
IGL00972:Dsc1
|
APN |
18 |
20,221,420 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01112:Dsc1
|
APN |
18 |
20,227,679 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01458:Dsc1
|
APN |
18 |
20,232,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01607:Dsc1
|
APN |
18 |
20,222,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01794:Dsc1
|
APN |
18 |
20,243,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01959:Dsc1
|
APN |
18 |
20,230,282 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Dsc1
|
APN |
18 |
20,241,860 (GRCm39) |
unclassified |
probably benign |
|
IGL02365:Dsc1
|
APN |
18 |
20,241,873 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02714:Dsc1
|
APN |
18 |
20,220,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02959:Dsc1
|
APN |
18 |
20,241,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03019:Dsc1
|
APN |
18 |
20,221,421 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03106:Dsc1
|
APN |
18 |
20,219,701 (GRCm39) |
splice site |
probably null |
|
R0414:Dsc1
|
UTSW |
18 |
20,221,411 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0456:Dsc1
|
UTSW |
18 |
20,232,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Dsc1
|
UTSW |
18 |
20,247,573 (GRCm39) |
missense |
probably damaging |
0.96 |
R0630:Dsc1
|
UTSW |
18 |
20,218,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Dsc1
|
UTSW |
18 |
20,229,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R0928:Dsc1
|
UTSW |
18 |
20,243,306 (GRCm39) |
splice site |
probably null |
|
R0976:Dsc1
|
UTSW |
18 |
20,228,098 (GRCm39) |
splice site |
probably null |
|
R1221:Dsc1
|
UTSW |
18 |
20,247,599 (GRCm39) |
nonsense |
probably null |
|
R1398:Dsc1
|
UTSW |
18 |
20,221,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1902:Dsc1
|
UTSW |
18 |
20,229,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Dsc1
|
UTSW |
18 |
20,229,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Dsc1
|
UTSW |
18 |
20,221,353 (GRCm39) |
splice site |
probably null |
|
R2119:Dsc1
|
UTSW |
18 |
20,243,209 (GRCm39) |
missense |
probably benign |
0.07 |
R3935:Dsc1
|
UTSW |
18 |
20,230,298 (GRCm39) |
missense |
probably benign |
0.00 |
R4747:Dsc1
|
UTSW |
18 |
20,227,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5034:Dsc1
|
UTSW |
18 |
20,228,084 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5243:Dsc1
|
UTSW |
18 |
20,232,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5289:Dsc1
|
UTSW |
18 |
20,234,910 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5300:Dsc1
|
UTSW |
18 |
20,227,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Dsc1
|
UTSW |
18 |
20,220,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R5376:Dsc1
|
UTSW |
18 |
20,221,503 (GRCm39) |
missense |
probably benign |
0.21 |
R5808:Dsc1
|
UTSW |
18 |
20,219,886 (GRCm39) |
nonsense |
probably null |
|
R5860:Dsc1
|
UTSW |
18 |
20,228,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6059:Dsc1
|
UTSW |
18 |
20,243,299 (GRCm39) |
missense |
probably damaging |
0.98 |
R6116:Dsc1
|
UTSW |
18 |
20,230,356 (GRCm39) |
missense |
probably benign |
0.10 |
R6351:Dsc1
|
UTSW |
18 |
20,219,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R6422:Dsc1
|
UTSW |
18 |
20,228,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R6811:Dsc1
|
UTSW |
18 |
20,222,711 (GRCm39) |
missense |
probably benign |
|
R6880:Dsc1
|
UTSW |
18 |
20,221,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R6941:Dsc1
|
UTSW |
18 |
20,230,246 (GRCm39) |
missense |
probably benign |
0.00 |
R6997:Dsc1
|
UTSW |
18 |
20,219,701 (GRCm39) |
splice site |
probably null |
|
R7255:Dsc1
|
UTSW |
18 |
20,230,330 (GRCm39) |
missense |
probably benign |
0.12 |
R7456:Dsc1
|
UTSW |
18 |
20,219,879 (GRCm39) |
missense |
probably benign |
0.00 |
R7492:Dsc1
|
UTSW |
18 |
20,240,737 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7503:Dsc1
|
UTSW |
18 |
20,218,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Dsc1
|
UTSW |
18 |
20,222,628 (GRCm39) |
missense |
probably benign |
|
R8167:Dsc1
|
UTSW |
18 |
20,230,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R8444:Dsc1
|
UTSW |
18 |
20,222,636 (GRCm39) |
missense |
probably benign |
0.00 |
R8701:Dsc1
|
UTSW |
18 |
20,240,739 (GRCm39) |
nonsense |
probably null |
|
R8928:Dsc1
|
UTSW |
18 |
20,243,225 (GRCm39) |
missense |
probably benign |
0.01 |
R9133:Dsc1
|
UTSW |
18 |
20,234,904 (GRCm39) |
missense |
probably benign |
0.00 |
R9144:Dsc1
|
UTSW |
18 |
20,218,639 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9189:Dsc1
|
UTSW |
18 |
20,232,214 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9330:Dsc1
|
UTSW |
18 |
20,243,214 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9372:Dsc1
|
UTSW |
18 |
20,221,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Dsc1
|
UTSW |
18 |
20,240,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R9685:Dsc1
|
UTSW |
18 |
20,232,087 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9702:Dsc1
|
UTSW |
18 |
20,227,685 (GRCm39) |
missense |
probably benign |
0.06 |
Z1176:Dsc1
|
UTSW |
18 |
20,247,595 (GRCm39) |
missense |
probably benign |
0.15 |
|