Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA474408 |
A |
T |
7: 109,660,177 (GRCm39) |
|
probably benign |
Het |
Abcc1 |
T |
A |
16: 14,207,732 (GRCm39) |
V23D |
probably damaging |
Het |
Adam8 |
G |
T |
7: 139,568,456 (GRCm39) |
N260K |
possibly damaging |
Het |
Ap3b1 |
A |
T |
13: 94,591,906 (GRCm39) |
I457L |
probably benign |
Het |
Apaf1 |
T |
C |
10: 90,867,421 (GRCm39) |
N808S |
possibly damaging |
Het |
Arhgef26 |
A |
G |
3: 62,327,082 (GRCm39) |
T532A |
possibly damaging |
Het |
Cfap65 |
G |
T |
1: 74,967,592 (GRCm39) |
T162N |
possibly damaging |
Het |
Creb3 |
T |
C |
4: 43,563,081 (GRCm39) |
V60A |
probably benign |
Het |
Cyp11b1 |
A |
G |
15: 74,707,703 (GRCm39) |
F469L |
probably benign |
Het |
Defb28 |
A |
T |
2: 152,362,047 (GRCm39) |
E69V |
possibly damaging |
Het |
Etnppl |
T |
C |
3: 130,415,967 (GRCm39) |
L118S |
probably damaging |
Het |
Fsip1 |
T |
C |
2: 118,072,144 (GRCm39) |
Y213C |
probably damaging |
Het |
Glb1l2 |
A |
G |
9: 26,676,421 (GRCm39) |
W480R |
probably damaging |
Het |
Herc1 |
A |
T |
9: 66,395,279 (GRCm39) |
M4205L |
probably benign |
Het |
Kif5a |
A |
T |
10: 127,071,478 (GRCm39) |
|
probably benign |
Het |
Lmbrd2 |
C |
T |
15: 9,186,695 (GRCm39) |
R557C |
probably damaging |
Het |
Map4k3 |
A |
G |
17: 80,963,284 (GRCm39) |
|
probably null |
Het |
Npc1 |
A |
G |
18: 12,331,596 (GRCm39) |
I858T |
probably benign |
Het |
Or7e173 |
T |
C |
9: 19,938,725 (GRCm39) |
T170A |
probably benign |
Het |
Pecam1 |
A |
G |
11: 106,588,177 (GRCm39) |
V92A |
probably damaging |
Het |
Rbm43 |
A |
T |
2: 51,816,757 (GRCm39) |
I70N |
probably benign |
Het |
Rps6kb1 |
T |
C |
11: 86,393,708 (GRCm39) |
Y474C |
probably benign |
Het |
Slco2a1 |
G |
A |
9: 102,954,205 (GRCm39) |
G459R |
possibly damaging |
Het |
Snca |
T |
A |
6: 60,804,595 (GRCm39) |
|
probably benign |
Het |
Spata31f1e |
T |
C |
4: 42,793,424 (GRCm39) |
D236G |
possibly damaging |
Het |
Stap2 |
T |
A |
17: 56,309,029 (GRCm39) |
I113F |
probably damaging |
Het |
Tas2r140 |
T |
C |
6: 40,468,764 (GRCm39) |
M198T |
probably benign |
Het |
Trim9 |
T |
C |
12: 70,393,428 (GRCm39) |
E172G |
probably damaging |
Het |
Ttll7 |
T |
C |
3: 146,602,445 (GRCm39) |
V81A |
possibly damaging |
Het |
Vmn2r103 |
A |
G |
17: 19,993,782 (GRCm39) |
Y53C |
probably damaging |
Het |
Vmn2r22 |
C |
A |
6: 123,614,295 (GRCm39) |
A432S |
probably benign |
Het |
Zfp943 |
T |
C |
17: 22,211,156 (GRCm39) |
S81P |
probably damaging |
Het |
|
Other mutations in Clec12b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01014:Clec12b
|
APN |
6 |
129,362,393 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01328:Clec12b
|
APN |
6 |
129,356,517 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Clec12b
|
APN |
6 |
129,359,334 (GRCm39) |
splice site |
probably benign |
|
R0662:Clec12b
|
UTSW |
6 |
129,353,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0786:Clec12b
|
UTSW |
6 |
129,357,651 (GRCm39) |
missense |
probably benign |
0.07 |
R1468:Clec12b
|
UTSW |
6 |
129,357,603 (GRCm39) |
missense |
probably damaging |
0.98 |
R1468:Clec12b
|
UTSW |
6 |
129,357,603 (GRCm39) |
missense |
probably damaging |
0.98 |
R1513:Clec12b
|
UTSW |
6 |
129,353,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R4757:Clec12b
|
UTSW |
6 |
129,357,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Clec12b
|
UTSW |
6 |
129,362,438 (GRCm39) |
missense |
probably damaging |
0.99 |
R5643:Clec12b
|
UTSW |
6 |
129,356,923 (GRCm39) |
missense |
probably benign |
|
R5644:Clec12b
|
UTSW |
6 |
129,356,923 (GRCm39) |
missense |
probably benign |
|
R7351:Clec12b
|
UTSW |
6 |
129,356,874 (GRCm39) |
critical splice donor site |
probably null |
|
R7600:Clec12b
|
UTSW |
6 |
129,353,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R8347:Clec12b
|
UTSW |
6 |
129,357,450 (GRCm39) |
critical splice donor site |
probably null |
|
R9076:Clec12b
|
UTSW |
6 |
129,356,580 (GRCm39) |
missense |
possibly damaging |
0.94 |
|