Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot11 |
A |
G |
4: 106,617,329 (GRCm39) |
F259S |
probably damaging |
Het |
Aldh16a1 |
T |
A |
7: 44,793,931 (GRCm39) |
|
probably benign |
Het |
Ankrd24 |
A |
T |
10: 81,478,547 (GRCm39) |
|
probably benign |
Het |
Arhgap5 |
T |
C |
12: 52,564,951 (GRCm39) |
S641P |
probably damaging |
Het |
Arpp21 |
A |
C |
9: 111,986,824 (GRCm39) |
S242R |
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,070,820 (GRCm39) |
T204A |
probably benign |
Het |
Bud31 |
A |
G |
5: 145,083,265 (GRCm39) |
Y77C |
probably damaging |
Het |
Ccdc65 |
G |
A |
15: 98,607,095 (GRCm39) |
V101I |
possibly damaging |
Het |
Ccr7 |
T |
A |
11: 99,036,809 (GRCm39) |
T38S |
probably damaging |
Het |
Ces2f |
C |
T |
8: 105,677,618 (GRCm39) |
H208Y |
possibly damaging |
Het |
Chst1 |
C |
A |
2: 92,443,964 (GRCm39) |
N145K |
possibly damaging |
Het |
Clock |
A |
G |
5: 76,374,976 (GRCm39) |
V731A |
possibly damaging |
Het |
Cog6 |
C |
T |
3: 52,921,283 (GRCm39) |
V108I |
possibly damaging |
Het |
Cplane1 |
T |
A |
15: 8,287,805 (GRCm39) |
N2881K |
unknown |
Het |
Crtc2 |
T |
A |
3: 90,170,804 (GRCm39) |
F626I |
probably damaging |
Het |
Dicer1 |
A |
T |
12: 104,673,144 (GRCm39) |
F792I |
probably damaging |
Het |
Dnajc13 |
T |
C |
9: 104,049,781 (GRCm39) |
K1780R |
probably benign |
Het |
Dph5 |
A |
C |
3: 115,708,782 (GRCm39) |
N155H |
probably benign |
Het |
Dscam |
T |
C |
16: 96,626,982 (GRCm39) |
|
probably null |
Het |
Etl4 |
C |
A |
2: 20,810,382 (GRCm39) |
|
probably benign |
Het |
Flt3l |
T |
C |
7: 44,785,450 (GRCm39) |
S9G |
probably benign |
Het |
Fmnl2 |
A |
G |
2: 52,944,498 (GRCm39) |
E159G |
possibly damaging |
Het |
Fryl |
A |
G |
5: 73,240,715 (GRCm39) |
I1295T |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gatad2b |
T |
A |
3: 90,263,489 (GRCm39) |
S529T |
probably benign |
Het |
Herc6 |
G |
A |
6: 57,639,347 (GRCm39) |
G905E |
possibly damaging |
Het |
Hhip |
T |
A |
8: 80,724,884 (GRCm39) |
N296I |
probably damaging |
Het |
Hmgcr |
A |
T |
13: 96,787,151 (GRCm39) |
|
probably benign |
Het |
Kalrn |
T |
G |
16: 33,830,951 (GRCm39) |
N723H |
possibly damaging |
Het |
Mroh5 |
T |
A |
15: 73,662,588 (GRCm39) |
Y242F |
possibly damaging |
Het |
Msh3 |
T |
A |
13: 92,483,848 (GRCm39) |
K258* |
probably null |
Het |
Myo1a |
T |
C |
10: 127,555,732 (GRCm39) |
|
probably benign |
Het |
Nlrp4f |
C |
T |
13: 65,342,317 (GRCm39) |
E443K |
probably benign |
Het |
Nupr2 |
A |
G |
5: 129,937,533 (GRCm39) |
Y34C |
probably damaging |
Het |
Ociad1 |
T |
C |
5: 73,452,255 (GRCm39) |
|
probably benign |
Het |
Or1af1 |
A |
T |
2: 37,110,208 (GRCm39) |
K236* |
probably null |
Het |
Or5af2 |
T |
A |
11: 58,708,577 (GRCm39) |
L248M |
probably damaging |
Het |
Or5b3 |
A |
T |
19: 13,388,784 (GRCm39) |
M284L |
probably benign |
Het |
Or5p5 |
A |
G |
7: 107,414,331 (GRCm39) |
D182G |
probably damaging |
Het |
Or6ae1 |
T |
C |
7: 139,742,002 (GRCm39) |
N287S |
probably damaging |
Het |
P2ry12 |
C |
A |
3: 59,124,908 (GRCm39) |
V256F |
probably damaging |
Het |
Pcdhb22 |
T |
A |
18: 37,651,904 (GRCm39) |
I124N |
probably damaging |
Het |
Pcnt |
A |
G |
10: 76,256,375 (GRCm39) |
F622L |
probably damaging |
Het |
Pfas |
A |
T |
11: 68,888,863 (GRCm39) |
N361K |
probably benign |
Het |
Plod2 |
T |
G |
9: 92,487,480 (GRCm39) |
L600V |
possibly damaging |
Het |
Pole |
T |
C |
5: 110,446,854 (GRCm39) |
Y631H |
probably damaging |
Het |
Proser1 |
T |
C |
3: 53,386,197 (GRCm39) |
L693P |
probably damaging |
Het |
Ptprd |
A |
G |
4: 75,875,476 (GRCm39) |
Y1195H |
probably damaging |
Het |
Rbm27 |
T |
A |
18: 42,459,091 (GRCm39) |
|
probably null |
Het |
Ric8a |
A |
G |
7: 140,437,886 (GRCm39) |
|
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rimkla |
C |
T |
4: 119,335,177 (GRCm39) |
V69M |
probably damaging |
Het |
Scfd1 |
A |
T |
12: 51,459,360 (GRCm39) |
K307M |
probably damaging |
Het |
Sh2b2 |
A |
G |
5: 136,261,117 (GRCm39) |
F33S |
probably damaging |
Het |
Smg7 |
T |
G |
1: 152,746,508 (GRCm39) |
|
probably null |
Het |
Srebf1 |
T |
C |
11: 60,094,942 (GRCm39) |
T486A |
probably benign |
Het |
Strn3 |
G |
A |
12: 51,657,187 (GRCm39) |
T642I |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,028,837 (GRCm39) |
|
probably null |
Het |
Syne3 |
A |
G |
12: 104,935,619 (GRCm39) |
L53P |
probably damaging |
Het |
Tcea1 |
T |
A |
1: 4,950,569 (GRCm39) |
|
probably benign |
Het |
Tmem30b |
T |
C |
12: 73,592,942 (GRCm39) |
N58D |
probably benign |
Het |
Tnpo1 |
A |
G |
13: 98,991,954 (GRCm39) |
Y641H |
probably damaging |
Het |
Trim25 |
A |
T |
11: 88,890,564 (GRCm39) |
T84S |
probably benign |
Het |
Trip4 |
A |
T |
9: 65,746,286 (GRCm39) |
F537I |
possibly damaging |
Het |
Uaca |
G |
A |
9: 60,755,900 (GRCm39) |
|
probably benign |
Het |
Ugt2b34 |
T |
A |
5: 87,040,758 (GRCm39) |
Y388F |
possibly damaging |
Het |
Vmn2r71 |
T |
C |
7: 85,268,640 (GRCm39) |
V281A |
probably benign |
Het |
Vps13d |
A |
T |
4: 144,882,502 (GRCm39) |
D1030E |
probably damaging |
Het |
Vps8 |
C |
A |
16: 21,261,107 (GRCm39) |
F82L |
probably damaging |
Het |
Zfp296 |
A |
G |
7: 19,313,661 (GRCm39) |
D172G |
probably benign |
Het |
Zfp977 |
C |
A |
7: 42,229,958 (GRCm39) |
C189F |
probably damaging |
Het |
|
Other mutations in Cdc14a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00801:Cdc14a
|
APN |
3 |
116,088,493 (GRCm39) |
nonsense |
probably null |
|
IGL01062:Cdc14a
|
APN |
3 |
116,068,361 (GRCm39) |
splice site |
probably benign |
|
IGL01584:Cdc14a
|
APN |
3 |
116,186,474 (GRCm39) |
nonsense |
probably null |
|
IGL03084:Cdc14a
|
APN |
3 |
116,142,101 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03237:Cdc14a
|
APN |
3 |
116,198,275 (GRCm39) |
intron |
probably benign |
|
IGL03296:Cdc14a
|
APN |
3 |
116,090,807 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4131001:Cdc14a
|
UTSW |
3 |
116,122,310 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0782:Cdc14a
|
UTSW |
3 |
116,115,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Cdc14a
|
UTSW |
3 |
116,122,171 (GRCm39) |
missense |
probably benign |
0.12 |
R1363:Cdc14a
|
UTSW |
3 |
116,087,509 (GRCm39) |
small deletion |
probably benign |
|
R1507:Cdc14a
|
UTSW |
3 |
116,087,646 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1545:Cdc14a
|
UTSW |
3 |
116,087,373 (GRCm39) |
critical splice donor site |
probably null |
|
R1795:Cdc14a
|
UTSW |
3 |
116,092,122 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1797:Cdc14a
|
UTSW |
3 |
116,115,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Cdc14a
|
UTSW |
3 |
116,216,296 (GRCm39) |
nonsense |
probably null |
|
R4229:Cdc14a
|
UTSW |
3 |
116,087,413 (GRCm39) |
missense |
probably damaging |
0.99 |
R4655:Cdc14a
|
UTSW |
3 |
116,122,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R4769:Cdc14a
|
UTSW |
3 |
116,088,399 (GRCm39) |
critical splice donor site |
probably null |
|
R4870:Cdc14a
|
UTSW |
3 |
116,217,109 (GRCm39) |
missense |
probably benign |
0.30 |
R4980:Cdc14a
|
UTSW |
3 |
116,186,506 (GRCm39) |
nonsense |
probably null |
|
R6228:Cdc14a
|
UTSW |
3 |
116,144,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R6248:Cdc14a
|
UTSW |
3 |
116,101,843 (GRCm39) |
missense |
probably benign |
0.01 |
R6402:Cdc14a
|
UTSW |
3 |
116,142,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R6749:Cdc14a
|
UTSW |
3 |
116,090,807 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6852:Cdc14a
|
UTSW |
3 |
116,122,325 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6996:Cdc14a
|
UTSW |
3 |
116,122,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Cdc14a
|
UTSW |
3 |
116,087,676 (GRCm39) |
missense |
probably benign |
|
R7783:Cdc14a
|
UTSW |
3 |
116,198,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Cdc14a
|
UTSW |
3 |
116,088,482 (GRCm39) |
missense |
probably benign |
0.00 |
R7991:Cdc14a
|
UTSW |
3 |
116,101,887 (GRCm39) |
missense |
probably benign |
0.01 |
R8049:Cdc14a
|
UTSW |
3 |
116,087,577 (GRCm39) |
missense |
probably benign |
0.33 |
R9163:Cdc14a
|
UTSW |
3 |
116,122,213 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9434:Cdc14a
|
UTSW |
3 |
116,217,092 (GRCm39) |
missense |
probably benign |
|
R9526:Cdc14a
|
UTSW |
3 |
116,087,509 (GRCm39) |
small deletion |
probably benign |
|
R9662:Cdc14a
|
UTSW |
3 |
116,088,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R9781:Cdc14a
|
UTSW |
3 |
116,122,274 (GRCm39) |
missense |
probably benign |
0.01 |
|