Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130023H24Rik |
A |
C |
7: 127,836,362 (GRCm39) |
V77G |
probably benign |
Het |
Abcb1b |
A |
G |
5: 8,877,428 (GRCm39) |
R663G |
probably benign |
Het |
Acly |
A |
G |
11: 100,395,808 (GRCm39) |
V404A |
probably damaging |
Het |
Actg2 |
T |
A |
6: 83,497,725 (GRCm39) |
I103F |
probably damaging |
Het |
Anapc5 |
A |
G |
5: 122,956,919 (GRCm39) |
V120A |
probably damaging |
Het |
Ankk1 |
T |
G |
9: 49,327,371 (GRCm39) |
T603P |
probably damaging |
Het |
Ankmy2 |
T |
C |
12: 36,215,898 (GRCm39) |
S33P |
possibly damaging |
Het |
Arhgef19 |
A |
T |
4: 140,983,710 (GRCm39) |
T748S |
possibly damaging |
Het |
Atad5 |
T |
A |
11: 80,011,616 (GRCm39) |
|
probably benign |
Het |
Atxn10 |
T |
C |
15: 85,249,483 (GRCm39) |
L105P |
probably damaging |
Het |
Cacna1s |
T |
C |
1: 135,998,455 (GRCm39) |
V161A |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,735,426 (GRCm39) |
E741G |
possibly damaging |
Het |
Cpne9 |
G |
A |
6: 113,271,654 (GRCm39) |
G338E |
probably damaging |
Het |
Cyp3a13 |
G |
A |
5: 137,897,124 (GRCm39) |
P397S |
probably damaging |
Het |
Dbn1 |
C |
T |
13: 55,622,729 (GRCm39) |
E585K |
probably damaging |
Het |
Draxin |
A |
G |
4: 148,200,429 (GRCm39) |
L7P |
probably benign |
Het |
Exosc7 |
T |
A |
9: 122,960,025 (GRCm39) |
|
probably benign |
Het |
Far2 |
A |
G |
6: 148,058,968 (GRCm39) |
E218G |
probably damaging |
Het |
Ggps1 |
A |
C |
13: 14,228,462 (GRCm39) |
N240K |
possibly damaging |
Het |
Kcnip1 |
T |
C |
11: 33,601,529 (GRCm39) |
|
probably benign |
Het |
Kcnv2 |
A |
T |
19: 27,301,424 (GRCm39) |
Y425F |
probably benign |
Het |
Kdelr2 |
T |
A |
5: 143,398,272 (GRCm39) |
F40I |
probably damaging |
Het |
Kdm1b |
C |
T |
13: 47,207,195 (GRCm39) |
P173L |
probably benign |
Het |
Kif20b |
G |
A |
19: 34,925,132 (GRCm39) |
|
probably benign |
Het |
Klhl9 |
A |
T |
4: 88,638,691 (GRCm39) |
Y517N |
possibly damaging |
Het |
Lgals3bp |
A |
G |
11: 118,284,347 (GRCm39) |
S411P |
probably damaging |
Het |
Lmo3 |
G |
A |
6: 138,354,309 (GRCm39) |
T85M |
probably damaging |
Het |
Lvrn |
C |
A |
18: 46,997,820 (GRCm39) |
T256N |
probably damaging |
Het |
Malt1 |
T |
C |
18: 65,595,986 (GRCm39) |
|
probably null |
Het |
Mgst1 |
A |
G |
6: 138,133,155 (GRCm39) |
I157V |
possibly damaging |
Het |
Mob3a |
A |
T |
10: 80,525,819 (GRCm39) |
V164E |
possibly damaging |
Het |
Mprip |
T |
A |
11: 59,587,864 (GRCm39) |
|
probably benign |
Het |
Mst1 |
A |
G |
9: 107,959,712 (GRCm39) |
N276S |
probably benign |
Het |
Or5an1b |
A |
T |
19: 12,299,680 (GRCm39) |
C170* |
probably null |
Het |
P3h2 |
T |
A |
16: 25,789,681 (GRCm39) |
I529F |
possibly damaging |
Het |
Pikfyve |
T |
A |
1: 65,285,490 (GRCm39) |
S865T |
probably benign |
Het |
Rcbtb2 |
G |
A |
14: 73,415,909 (GRCm39) |
R474Q |
probably benign |
Het |
Rpl27 |
G |
A |
11: 101,334,321 (GRCm39) |
|
probably benign |
Het |
Rtp1 |
G |
A |
16: 23,250,210 (GRCm39) |
E192K |
probably damaging |
Het |
Sgk2 |
T |
C |
2: 162,837,592 (GRCm39) |
|
probably benign |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc49a4 |
T |
C |
16: 35,570,884 (GRCm39) |
D140G |
probably benign |
Het |
Spdl1 |
T |
C |
11: 34,714,347 (GRCm39) |
N114S |
possibly damaging |
Het |
Syne2 |
C |
T |
12: 76,110,936 (GRCm39) |
R5756W |
probably damaging |
Het |
Tor1aip1 |
T |
C |
1: 155,882,927 (GRCm39) |
E307G |
probably damaging |
Het |
Tpd52 |
T |
C |
3: 9,018,749 (GRCm39) |
T44A |
probably benign |
Het |
Trim67 |
A |
T |
8: 125,549,966 (GRCm39) |
Y532F |
probably damaging |
Het |
Ttll9 |
C |
A |
2: 152,842,018 (GRCm39) |
|
probably null |
Het |
Ush2a |
T |
C |
1: 188,680,571 (GRCm39) |
|
probably benign |
Het |
Vcam1 |
T |
C |
3: 115,909,709 (GRCm39) |
I539M |
probably benign |
Het |
Vmn1r19 |
T |
A |
6: 57,381,600 (GRCm39) |
M51K |
possibly damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,949,941 (GRCm39) |
M787K |
probably damaging |
Het |
Xdh |
T |
A |
17: 74,213,096 (GRCm39) |
|
probably benign |
Het |
Zfp109 |
A |
T |
7: 23,933,895 (GRCm39) |
V8E |
probably damaging |
Het |
Zfp595 |
G |
A |
13: 67,464,577 (GRCm39) |
A562V |
possibly damaging |
Het |
|
Other mutations in Zfp759 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01509:Zfp759
|
APN |
13 |
67,287,658 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03131:Zfp759
|
APN |
13 |
67,286,728 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03218:Zfp759
|
APN |
13 |
67,287,480 (GRCm39) |
missense |
probably benign |
0.00 |
R0243:Zfp759
|
UTSW |
13 |
67,286,877 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0520:Zfp759
|
UTSW |
13 |
67,285,419 (GRCm39) |
missense |
probably benign |
0.29 |
R0961:Zfp759
|
UTSW |
13 |
67,287,927 (GRCm39) |
missense |
probably benign |
0.32 |
R1435:Zfp759
|
UTSW |
13 |
67,286,830 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1649:Zfp759
|
UTSW |
13 |
67,287,668 (GRCm39) |
missense |
probably benign |
0.00 |
R1880:Zfp759
|
UTSW |
13 |
67,287,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Zfp759
|
UTSW |
13 |
67,287,578 (GRCm39) |
unclassified |
probably benign |
|
R2170:Zfp759
|
UTSW |
13 |
67,284,812 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3154:Zfp759
|
UTSW |
13 |
67,286,719 (GRCm39) |
missense |
probably benign |
0.20 |
R3551:Zfp759
|
UTSW |
13 |
67,287,031 (GRCm39) |
missense |
probably benign |
0.24 |
R4392:Zfp759
|
UTSW |
13 |
67,287,707 (GRCm39) |
nonsense |
probably null |
|
R4495:Zfp759
|
UTSW |
13 |
67,286,989 (GRCm39) |
splice site |
probably null |
|
R4736:Zfp759
|
UTSW |
13 |
67,287,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R4882:Zfp759
|
UTSW |
13 |
67,287,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5717:Zfp759
|
UTSW |
13 |
67,286,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R5921:Zfp759
|
UTSW |
13 |
67,288,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Zfp759
|
UTSW |
13 |
67,288,524 (GRCm39) |
missense |
probably benign |
0.00 |
R6381:Zfp759
|
UTSW |
13 |
67,286,969 (GRCm39) |
nonsense |
probably null |
|
R6427:Zfp759
|
UTSW |
13 |
67,287,162 (GRCm39) |
splice site |
probably null |
|
R6567:Zfp759
|
UTSW |
13 |
67,287,150 (GRCm39) |
missense |
probably benign |
0.34 |
R7140:Zfp759
|
UTSW |
13 |
67,288,177 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7731:Zfp759
|
UTSW |
13 |
67,287,690 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8504:Zfp759
|
UTSW |
13 |
67,286,947 (GRCm39) |
missense |
probably benign |
0.00 |
R8770:Zfp759
|
UTSW |
13 |
67,288,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:Zfp759
|
UTSW |
13 |
67,288,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R9695:Zfp759
|
UTSW |
13 |
67,287,198 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Zfp759
|
UTSW |
13 |
67,284,872 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Zfp759
|
UTSW |
13 |
67,288,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|