Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
A |
7: 119,995,829 (GRCm39) |
I1322N |
probably benign |
Het |
Adamts1 |
A |
T |
16: 85,592,713 (GRCm39) |
M565K |
probably benign |
Het |
Akr1b7 |
T |
A |
6: 34,392,333 (GRCm39) |
Y49N |
probably damaging |
Het |
Cacna2d2 |
T |
A |
9: 107,390,757 (GRCm39) |
V363E |
probably damaging |
Het |
Cdh10 |
C |
T |
15: 19,013,605 (GRCm39) |
T735I |
probably damaging |
Het |
Cds1 |
T |
A |
5: 101,962,302 (GRCm39) |
C306S |
possibly damaging |
Het |
Cfap251 |
T |
C |
5: 123,440,486 (GRCm39) |
Y1091H |
probably damaging |
Het |
Clasp2 |
T |
C |
9: 113,709,088 (GRCm39) |
C644R |
probably damaging |
Het |
Coil |
T |
C |
11: 88,872,580 (GRCm39) |
S314P |
probably benign |
Het |
D630045J12Rik |
T |
A |
6: 38,173,329 (GRCm39) |
M280L |
probably benign |
Het |
Dmxl2 |
C |
T |
9: 54,352,717 (GRCm39) |
V795M |
probably damaging |
Het |
Dock10 |
A |
G |
1: 80,511,510 (GRCm39) |
V1533A |
probably damaging |
Het |
Fbxo40 |
T |
C |
16: 36,789,536 (GRCm39) |
N525D |
possibly damaging |
Het |
Fezf2 |
T |
C |
14: 12,344,494 (GRCm38) |
E231G |
probably damaging |
Het |
Fmn1 |
T |
C |
2: 113,412,470 (GRCm39) |
V870A |
possibly damaging |
Het |
Ifi44 |
A |
G |
3: 151,438,019 (GRCm39) |
*423Q |
probably null |
Het |
Invs |
T |
C |
4: 48,390,029 (GRCm39) |
V173A |
probably damaging |
Het |
Krt88 |
A |
G |
15: 101,350,486 (GRCm39) |
|
probably benign |
Het |
Mctp2 |
A |
T |
7: 71,739,953 (GRCm39) |
Y812* |
probably null |
Het |
Neto2 |
T |
C |
8: 86,396,292 (GRCm39) |
I118V |
probably damaging |
Het |
Nutm2 |
T |
G |
13: 50,625,075 (GRCm39) |
M264R |
probably damaging |
Het |
Or2d2 |
A |
G |
7: 106,728,244 (GRCm39) |
S119P |
probably damaging |
Het |
Or8u8 |
T |
C |
2: 86,011,939 (GRCm39) |
|
probably null |
Het |
Pcnx1 |
G |
A |
12: 81,964,688 (GRCm39) |
R285Q |
probably damaging |
Het |
Pi16 |
G |
T |
17: 29,545,269 (GRCm39) |
K177N |
probably damaging |
Het |
Pigg |
C |
T |
5: 108,466,794 (GRCm39) |
S225F |
possibly damaging |
Het |
Prrc2b |
T |
A |
2: 32,103,429 (GRCm39) |
V969E |
probably damaging |
Het |
Rab4b |
A |
C |
7: 26,872,154 (GRCm39) |
Y189D |
probably benign |
Het |
Ran |
A |
G |
5: 129,099,246 (GRCm39) |
N143D |
possibly damaging |
Het |
Rfc4 |
A |
T |
16: 22,933,219 (GRCm39) |
F286L |
probably damaging |
Het |
Sel1l2 |
T |
C |
2: 140,089,859 (GRCm39) |
Y418C |
probably damaging |
Het |
Slc13a1 |
T |
C |
6: 24,103,482 (GRCm39) |
I354V |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 41,361,193 (GRCm39) |
T386S |
probably benign |
Het |
Tm2d2 |
G |
T |
8: 25,512,787 (GRCm39) |
V212F |
probably benign |
Het |
Tmem247 |
A |
T |
17: 87,225,721 (GRCm39) |
N54Y |
probably damaging |
Het |
Txnrd3 |
T |
A |
6: 89,633,117 (GRCm39) |
Y206N |
probably benign |
Het |
Uba5 |
T |
C |
9: 103,931,259 (GRCm39) |
|
probably benign |
Het |
Vmn2r54 |
A |
G |
7: 12,369,910 (GRCm39) |
L51P |
probably damaging |
Het |
Zfp735 |
A |
G |
11: 73,601,319 (GRCm39) |
K88E |
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 |
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 |
IGL02442: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 |
|