Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
C |
T |
5: 109,887,101 (GRCm39) |
V32M |
possibly damaging |
Het |
Abca1 |
T |
C |
4: 53,034,046 (GRCm39) |
D2228G |
probably damaging |
Het |
Actr5 |
A |
G |
2: 158,480,728 (GRCm39) |
K582R |
probably benign |
Het |
Armc8 |
T |
C |
9: 99,409,122 (GRCm39) |
|
probably benign |
Het |
Atp7b |
T |
C |
8: 22,518,454 (GRCm39) |
D128G |
possibly damaging |
Het |
Cemip |
C |
A |
7: 83,613,383 (GRCm39) |
G605V |
probably damaging |
Het |
Cep112 |
A |
G |
11: 108,409,509 (GRCm39) |
H133R |
probably benign |
Het |
Cops3 |
C |
T |
11: 59,723,864 (GRCm39) |
D98N |
probably benign |
Het |
Crlf3 |
T |
C |
11: 79,950,150 (GRCm39) |
D160G |
probably damaging |
Het |
Csn1s1 |
T |
C |
5: 87,825,501 (GRCm39) |
|
probably null |
Het |
Ddx60 |
C |
A |
8: 62,395,470 (GRCm39) |
|
probably null |
Het |
Depdc1a |
T |
A |
3: 159,221,147 (GRCm39) |
N159K |
probably benign |
Het |
Dsg3 |
A |
T |
18: 20,662,004 (GRCm39) |
|
probably benign |
Het |
Eif4g3 |
A |
C |
4: 137,824,677 (GRCm39) |
|
probably benign |
Het |
Ercc6l2 |
T |
A |
13: 64,001,437 (GRCm39) |
|
probably null |
Het |
Fus |
T |
A |
7: 127,584,794 (GRCm39) |
L100H |
probably damaging |
Het |
Gm29247 |
A |
G |
1: 44,146,269 (GRCm39) |
|
probably benign |
Het |
Gucy2e |
T |
C |
11: 69,115,857 (GRCm39) |
T842A |
probably damaging |
Het |
Inpp4a |
A |
T |
1: 37,418,115 (GRCm39) |
Q519L |
probably benign |
Het |
Kcnip1 |
C |
A |
11: 33,593,290 (GRCm39) |
|
probably benign |
Het |
Lyst |
T |
A |
13: 13,855,975 (GRCm39) |
L2432H |
probably damaging |
Het |
Mastl |
A |
G |
2: 23,022,857 (GRCm39) |
V622A |
probably benign |
Het |
Myh15 |
A |
G |
16: 48,997,317 (GRCm39) |
T1712A |
probably benign |
Het |
Nlrp1a |
T |
C |
11: 71,013,826 (GRCm39) |
T475A |
possibly damaging |
Het |
Nr4a3 |
G |
A |
4: 48,051,649 (GRCm39) |
M134I |
probably benign |
Het |
Or2a56 |
T |
G |
6: 42,932,663 (GRCm39) |
V77G |
probably damaging |
Het |
Or52m1 |
T |
A |
7: 102,290,290 (GRCm39) |
L279Q |
probably damaging |
Het |
Or5p60 |
T |
A |
7: 107,723,595 (GRCm39) |
I292F |
probably damaging |
Het |
Paqr6 |
T |
G |
3: 88,273,085 (GRCm39) |
I52S |
probably damaging |
Het |
Pcdhb4 |
T |
A |
18: 37,442,721 (GRCm39) |
L677Q |
probably benign |
Het |
Phax |
C |
T |
18: 56,717,372 (GRCm39) |
R250* |
probably null |
Het |
Pkn3 |
A |
G |
2: 29,973,158 (GRCm39) |
D356G |
probably benign |
Het |
Pnpla2 |
T |
C |
7: 141,035,285 (GRCm39) |
L29P |
probably damaging |
Het |
Rad18 |
G |
A |
6: 112,664,948 (GRCm39) |
T62I |
probably damaging |
Het |
Riok3 |
C |
T |
18: 12,276,017 (GRCm39) |
R238C |
probably benign |
Het |
Ror2 |
C |
T |
13: 53,264,764 (GRCm39) |
S764N |
probably damaging |
Het |
Sccpdh |
G |
T |
1: 179,504,025 (GRCm39) |
G125W |
probably damaging |
Het |
Skint11 |
T |
A |
4: 114,051,925 (GRCm39) |
L91H |
probably damaging |
Het |
Slc25a45 |
A |
G |
19: 5,928,725 (GRCm39) |
|
probably benign |
Het |
Slco2a1 |
C |
T |
9: 102,954,128 (GRCm39) |
Q370* |
probably null |
Het |
Szt2 |
A |
G |
4: 118,250,087 (GRCm39) |
S474P |
probably damaging |
Het |
Tchh |
C |
A |
3: 93,350,719 (GRCm39) |
T53K |
probably damaging |
Het |
Tiam1 |
T |
C |
16: 89,595,588 (GRCm39) |
T1298A |
possibly damaging |
Het |
Tmem161a |
C |
T |
8: 70,633,887 (GRCm39) |
Q183* |
probably null |
Het |
Trim26 |
C |
A |
17: 37,161,797 (GRCm39) |
A72E |
probably damaging |
Het |
Trmt11 |
A |
T |
10: 30,435,169 (GRCm39) |
I330K |
probably benign |
Het |
Tspan1 |
A |
G |
4: 116,021,052 (GRCm39) |
|
probably benign |
Het |
Ubr4 |
C |
A |
4: 139,194,561 (GRCm39) |
C4286* |
probably null |
Het |
Unc13a |
T |
C |
8: 72,105,158 (GRCm39) |
|
probably null |
Het |
Vmn1r20 |
T |
A |
6: 57,409,583 (GRCm39) |
F303Y |
probably damaging |
Het |
Washc2 |
T |
C |
6: 116,190,979 (GRCm39) |
|
probably benign |
Het |
Xab2 |
C |
T |
8: 3,661,699 (GRCm39) |
D585N |
probably benign |
Het |
Ythdc2 |
C |
T |
18: 44,993,001 (GRCm39) |
L791F |
probably damaging |
Het |
Zfp319 |
C |
A |
8: 96,055,589 (GRCm39) |
V205F |
probably damaging |
Het |
Zscan25 |
A |
T |
5: 145,227,512 (GRCm39) |
H392L |
probably damaging |
Het |
Zswim6 |
A |
T |
13: 107,884,786 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Fbxw19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01094:Fbxw19
|
APN |
9 |
109,322,614 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01878:Fbxw19
|
APN |
9 |
109,312,347 (GRCm39) |
splice site |
probably benign |
|
IGL02752:Fbxw19
|
APN |
9 |
109,323,709 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02795:Fbxw19
|
APN |
9 |
109,324,886 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL03401:Fbxw19
|
APN |
9 |
109,324,038 (GRCm39) |
critical splice donor site |
probably null |
|
R0402:Fbxw19
|
UTSW |
9 |
109,313,493 (GRCm39) |
missense |
probably benign |
0.00 |
R0423:Fbxw19
|
UTSW |
9 |
109,315,134 (GRCm39) |
missense |
probably benign |
0.22 |
R0466:Fbxw19
|
UTSW |
9 |
109,307,717 (GRCm39) |
missense |
probably benign |
0.32 |
R0513:Fbxw19
|
UTSW |
9 |
109,310,621 (GRCm39) |
splice site |
probably null |
|
R1538:Fbxw19
|
UTSW |
9 |
109,324,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Fbxw19
|
UTSW |
9 |
109,323,840 (GRCm39) |
nonsense |
probably null |
|
R1869:Fbxw19
|
UTSW |
9 |
109,311,100 (GRCm39) |
missense |
probably benign |
0.11 |
R1933:Fbxw19
|
UTSW |
9 |
109,310,718 (GRCm39) |
missense |
probably benign |
0.20 |
R1960:Fbxw19
|
UTSW |
9 |
109,315,004 (GRCm39) |
missense |
probably benign |
|
R2288:Fbxw19
|
UTSW |
9 |
109,322,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R2877:Fbxw19
|
UTSW |
9 |
109,315,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R2878:Fbxw19
|
UTSW |
9 |
109,315,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Fbxw19
|
UTSW |
9 |
109,323,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R5192:Fbxw19
|
UTSW |
9 |
109,313,496 (GRCm39) |
missense |
probably benign |
0.01 |
R5196:Fbxw19
|
UTSW |
9 |
109,313,496 (GRCm39) |
missense |
probably benign |
0.01 |
R5533:Fbxw19
|
UTSW |
9 |
109,315,133 (GRCm39) |
missense |
probably benign |
0.00 |
R6107:Fbxw19
|
UTSW |
9 |
109,324,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R6333:Fbxw19
|
UTSW |
9 |
109,323,751 (GRCm39) |
missense |
probably benign |
0.01 |
R6820:Fbxw19
|
UTSW |
9 |
109,311,079 (GRCm39) |
missense |
probably benign |
0.07 |
R7631:Fbxw19
|
UTSW |
9 |
109,311,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R7651:Fbxw19
|
UTSW |
9 |
109,323,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Fbxw19
|
UTSW |
9 |
109,313,482 (GRCm39) |
missense |
probably benign |
0.26 |
R8678:Fbxw19
|
UTSW |
9 |
109,312,376 (GRCm39) |
nonsense |
probably null |
|
R9121:Fbxw19
|
UTSW |
9 |
109,324,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9256:Fbxw19
|
UTSW |
9 |
109,310,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R9324:Fbxw19
|
UTSW |
9 |
109,313,440 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9393:Fbxw19
|
UTSW |
9 |
109,324,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Fbxw19
|
UTSW |
9 |
109,315,101 (GRCm39) |
missense |
probably benign |
|
Z1176:Fbxw19
|
UTSW |
9 |
109,310,650 (GRCm39) |
missense |
probably benign |
0.00 |
|