Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adap2 |
A |
G |
11: 80,068,032 (GRCm39) |
E348G |
probably damaging |
Het |
Ahnak |
G |
A |
19: 8,981,380 (GRCm39) |
G888D |
probably damaging |
Het |
Cfap97d1 |
T |
C |
11: 101,881,652 (GRCm39) |
V116A |
probably benign |
Het |
Csde1 |
T |
C |
3: 102,962,135 (GRCm39) |
C649R |
probably benign |
Het |
Cym |
A |
C |
3: 107,121,601 (GRCm39) |
D230E |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 31,009,835 (GRCm39) |
I1911N |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,403,360 (GRCm39) |
H37R |
probably benign |
Het |
Ggt6 |
T |
C |
11: 72,327,632 (GRCm39) |
V146A |
possibly damaging |
Het |
Glud1 |
T |
A |
14: 34,057,395 (GRCm39) |
L54* |
probably null |
Het |
Grk6 |
A |
G |
13: 55,606,750 (GRCm39) |
|
probably benign |
Het |
Gsta4 |
G |
A |
9: 78,116,447 (GRCm39) |
V219I |
probably benign |
Het |
Gucy1a2 |
G |
A |
9: 3,865,385 (GRCm39) |
V620M |
probably damaging |
Het |
Hspe1 |
T |
C |
1: 55,128,201 (GRCm39) |
|
probably benign |
Het |
Icmt |
T |
C |
4: 152,383,173 (GRCm39) |
V76A |
possibly damaging |
Het |
Ifrd1 |
A |
G |
12: 40,266,316 (GRCm39) |
|
probably benign |
Het |
Lgals12 |
T |
C |
19: 7,584,019 (GRCm39) |
|
probably benign |
Het |
Lypla1 |
T |
C |
1: 4,902,610 (GRCm39) |
|
probably benign |
Het |
Map1b |
A |
T |
13: 99,644,706 (GRCm39) |
W66R |
probably damaging |
Het |
Matn3 |
T |
A |
12: 9,017,678 (GRCm39) |
C443* |
probably null |
Het |
Mup8 |
T |
A |
4: 60,219,695 (GRCm39) |
R191W |
probably damaging |
Het |
Mycbp2 |
T |
C |
14: 103,551,811 (GRCm39) |
K140R |
probably benign |
Het |
Ndfip1 |
C |
T |
18: 38,580,789 (GRCm39) |
S66L |
probably damaging |
Het |
Neu1 |
A |
G |
17: 35,153,445 (GRCm39) |
I323V |
probably benign |
Het |
Nup205 |
A |
T |
6: 35,167,003 (GRCm39) |
T341S |
probably benign |
Het |
Or4f7 |
G |
A |
2: 111,644,336 (GRCm39) |
T245I |
probably benign |
Het |
Or5b112 |
T |
A |
19: 13,319,484 (GRCm39) |
C121S |
probably benign |
Het |
Or5b3 |
T |
A |
19: 13,388,351 (GRCm39) |
N139K |
probably benign |
Het |
Ovch2 |
T |
A |
7: 107,395,755 (GRCm39) |
I88F |
possibly damaging |
Het |
Pkd1 |
T |
A |
17: 24,784,200 (GRCm39) |
S249T |
probably benign |
Het |
Plekhg3 |
A |
T |
12: 76,625,127 (GRCm39) |
Q1324L |
probably benign |
Het |
Ppara |
T |
A |
15: 85,685,344 (GRCm39) |
V431E |
probably benign |
Het |
Prkaa1 |
T |
G |
15: 5,206,369 (GRCm39) |
H408Q |
probably damaging |
Het |
Sap25 |
T |
A |
5: 137,640,257 (GRCm39) |
N108K |
probably benign |
Het |
Setd5 |
A |
C |
6: 113,087,341 (GRCm39) |
I81L |
possibly damaging |
Het |
Sinhcaf |
A |
T |
6: 148,830,005 (GRCm39) |
|
probably null |
Het |
Sri |
T |
A |
5: 8,112,411 (GRCm39) |
M78K |
probably damaging |
Het |
Tyro3 |
A |
G |
2: 119,639,349 (GRCm39) |
N352S |
probably benign |
Het |
Ubr5 |
T |
A |
15: 38,038,145 (GRCm39) |
E332V |
possibly damaging |
Het |
Vmn2r19 |
G |
T |
6: 123,286,621 (GRCm39) |
V85F |
possibly damaging |
Het |
Vmn2r53 |
A |
T |
7: 12,315,656 (GRCm39) |
V721D |
probably damaging |
Het |
Vwa5a |
A |
G |
9: 38,646,080 (GRCm39) |
M483V |
probably benign |
Het |
Zfp786 |
T |
A |
6: 47,798,301 (GRCm39) |
Q212H |
probably benign |
Het |
|
Other mutations in Cdc45 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01528:Cdc45
|
APN |
16 |
18,630,311 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01677:Cdc45
|
APN |
16 |
18,605,750 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02079:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02080:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02105:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02106:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02237:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02238:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02239:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02371:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02441:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02465:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02466:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02468:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02469:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02470:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02471:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02472:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02473:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02489:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02490:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02491:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02492:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02511:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02558:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02559:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02560:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02561:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02562:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02566:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02567:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02576:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02583:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02589:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02626:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02627:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02628:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02629:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02687:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02688:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02689:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02720:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02724:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02731:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02738:Cdc45
|
APN |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02991:Cdc45
|
UTSW |
16 |
18,617,479 (GRCm39) |
missense |
probably benign |
0.06 |
R0051:Cdc45
|
UTSW |
16 |
18,613,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Cdc45
|
UTSW |
16 |
18,613,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0458:Cdc45
|
UTSW |
16 |
18,600,722 (GRCm39) |
splice site |
probably benign |
|
R1398:Cdc45
|
UTSW |
16 |
18,600,721 (GRCm39) |
splice site |
probably benign |
|
R1413:Cdc45
|
UTSW |
16 |
18,627,491 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1792:Cdc45
|
UTSW |
16 |
18,626,090 (GRCm39) |
missense |
probably benign |
0.01 |
R2919:Cdc45
|
UTSW |
16 |
18,627,543 (GRCm39) |
missense |
probably benign |
0.00 |
R3956:Cdc45
|
UTSW |
16 |
18,624,180 (GRCm39) |
missense |
probably benign |
0.00 |
R4079:Cdc45
|
UTSW |
16 |
18,630,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Cdc45
|
UTSW |
16 |
18,603,613 (GRCm39) |
missense |
probably damaging |
0.98 |
R5028:Cdc45
|
UTSW |
16 |
18,613,930 (GRCm39) |
missense |
probably benign |
0.43 |
R5214:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5215:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5353:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5355:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5424:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Cdc45
|
UTSW |
16 |
18,614,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Cdc45
|
UTSW |
16 |
18,626,029 (GRCm39) |
critical splice donor site |
probably null |
|
R6174:Cdc45
|
UTSW |
16 |
18,613,454 (GRCm39) |
splice site |
probably null |
|
R6796:Cdc45
|
UTSW |
16 |
18,603,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R7910:Cdc45
|
UTSW |
16 |
18,629,203 (GRCm39) |
missense |
probably damaging |
0.98 |
R8519:Cdc45
|
UTSW |
16 |
18,627,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Cdc45
|
UTSW |
16 |
18,630,300 (GRCm39) |
missense |
probably benign |
|
R9221:Cdc45
|
UTSW |
16 |
18,605,521 (GRCm39) |
missense |
probably benign |
0.08 |
|