Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
G |
1: 71,334,215 (GRCm39) |
Y1096H |
probably damaging |
Het |
Aspa |
A |
T |
11: 73,196,420 (GRCm39) |
F261I |
probably damaging |
Het |
Atm |
C |
A |
9: 53,427,767 (GRCm39) |
G448* |
probably null |
Het |
Atmin |
T |
A |
8: 117,684,696 (GRCm39) |
D785E |
probably damaging |
Het |
Car1 |
G |
C |
3: 14,841,364 (GRCm39) |
R90G |
probably damaging |
Het |
Cdh11 |
T |
C |
8: 103,374,178 (GRCm39) |
D520G |
probably benign |
Het |
Cers5 |
T |
A |
15: 99,649,119 (GRCm39) |
K50* |
probably null |
Het |
Chad |
A |
T |
11: 94,459,118 (GRCm39) |
D340V |
probably benign |
Het |
Cspg5 |
T |
C |
9: 110,075,711 (GRCm39) |
I68T |
probably benign |
Het |
Fcgbpl1 |
C |
T |
7: 27,856,339 (GRCm39) |
T2042M |
probably damaging |
Het |
Fcrla |
T |
A |
1: 170,752,991 (GRCm39) |
|
probably benign |
Het |
Fer1l4 |
T |
A |
2: 155,865,177 (GRCm39) |
D1608V |
probably benign |
Het |
Gm7664 |
T |
A |
13: 62,676,464 (GRCm39) |
|
probably benign |
Het |
Hk3 |
T |
C |
13: 55,162,869 (GRCm39) |
E2G |
probably damaging |
Het |
Hmcn2 |
G |
A |
2: 31,296,428 (GRCm39) |
E2677K |
possibly damaging |
Het |
Hydin |
T |
C |
8: 111,291,741 (GRCm39) |
L3411P |
possibly damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Lysmd2 |
C |
T |
9: 75,533,254 (GRCm39) |
H70Y |
possibly damaging |
Het |
Msi2 |
A |
G |
11: 88,370,818 (GRCm39) |
|
probably benign |
Het |
Msi2 |
G |
A |
11: 88,608,921 (GRCm39) |
|
probably benign |
Het |
Napsa |
T |
A |
7: 44,230,817 (GRCm39) |
|
probably benign |
Het |
Nlrp4a |
T |
A |
7: 26,153,578 (GRCm39) |
L710M |
probably damaging |
Het |
Or10g1 |
T |
A |
14: 52,647,414 (GRCm39) |
K305M |
probably benign |
Het |
Or12d13 |
T |
C |
17: 37,647,159 (GRCm39) |
|
probably null |
Het |
Or5m13 |
T |
A |
2: 85,748,934 (GRCm39) |
F222I |
probably benign |
Het |
Or6ae1 |
T |
C |
7: 139,742,564 (GRCm39) |
T100A |
probably benign |
Het |
Or9a2 |
C |
T |
6: 41,748,782 (GRCm39) |
M150I |
probably benign |
Het |
Plbd2 |
T |
A |
5: 120,637,147 (GRCm39) |
Y105F |
probably benign |
Het |
Plppr5 |
A |
T |
3: 117,456,120 (GRCm39) |
I214F |
possibly damaging |
Het |
Pramel34 |
A |
T |
5: 93,784,456 (GRCm39) |
M139K |
possibly damaging |
Het |
Ptcd3 |
A |
G |
6: 71,858,505 (GRCm39) |
V655A |
possibly damaging |
Het |
Ptpn14 |
T |
C |
1: 189,530,767 (GRCm39) |
L78P |
probably damaging |
Het |
Ralgapa1 |
A |
C |
12: 55,766,408 (GRCm39) |
D1295E |
probably damaging |
Het |
Rnf213 |
G |
A |
11: 119,299,846 (GRCm39) |
D192N |
probably damaging |
Het |
Ropn1 |
A |
G |
16: 34,487,167 (GRCm39) |
I34M |
probably damaging |
Het |
Rpe65 |
G |
T |
3: 159,310,038 (GRCm39) |
G104C |
probably damaging |
Het |
Scgb2b27 |
T |
C |
7: 33,712,582 (GRCm39) |
|
probably benign |
Het |
Sh3bgr |
T |
C |
16: 96,007,117 (GRCm39) |
I29T |
possibly damaging |
Het |
Smg1 |
T |
C |
7: 117,794,304 (GRCm39) |
|
probably benign |
Het |
Stim2 |
T |
A |
5: 54,232,712 (GRCm39) |
C68* |
probably null |
Het |
Syne2 |
G |
A |
12: 76,035,917 (GRCm39) |
V3736I |
possibly damaging |
Het |
Tbx19 |
T |
C |
1: 164,981,249 (GRCm39) |
N82D |
probably damaging |
Het |
Tdp1 |
T |
A |
12: 99,876,544 (GRCm39) |
V353D |
probably damaging |
Het |
Tg |
T |
A |
15: 66,568,369 (GRCm39) |
I1352K |
possibly damaging |
Het |
Thsd4 |
T |
C |
9: 59,887,066 (GRCm39) |
T919A |
probably damaging |
Het |
Tmprss11f |
A |
T |
5: 86,676,062 (GRCm39) |
M373K |
probably damaging |
Het |
Tmprss15 |
T |
A |
16: 78,868,335 (GRCm39) |
|
probably null |
Het |
Tpd52 |
A |
T |
3: 9,068,466 (GRCm39) |
Y16* |
probably null |
Het |
Ube2o |
G |
A |
11: 116,435,268 (GRCm39) |
R507C |
probably damaging |
Het |
Unc93b1 |
T |
C |
19: 3,993,703 (GRCm39) |
F382L |
probably benign |
Het |
Vav2 |
A |
T |
2: 27,160,122 (GRCm39) |
|
probably benign |
Het |
Vmn1r207 |
T |
C |
13: 22,910,686 (GRCm39) |
|
noncoding transcript |
Het |
Zan |
T |
A |
5: 137,435,013 (GRCm39) |
I2127F |
unknown |
Het |
Zfp748 |
C |
A |
13: 67,688,737 (GRCm39) |
C841F |
probably damaging |
Het |
Zic4 |
C |
A |
9: 91,266,253 (GRCm39) |
P299Q |
probably damaging |
Het |
|
Other mutations in Fzd5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01959:Fzd5
|
APN |
1 |
64,775,105 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02015:Fzd5
|
APN |
1 |
64,775,501 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02673:Fzd5
|
APN |
1 |
64,774,265 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0060:Fzd5
|
UTSW |
1 |
64,774,835 (GRCm39) |
missense |
probably benign |
0.01 |
R1860:Fzd5
|
UTSW |
1 |
64,774,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Fzd5
|
UTSW |
1 |
64,774,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R2373:Fzd5
|
UTSW |
1 |
64,774,066 (GRCm39) |
missense |
probably damaging |
0.96 |
R3114:Fzd5
|
UTSW |
1 |
64,774,739 (GRCm39) |
missense |
probably benign |
0.45 |
R3725:Fzd5
|
UTSW |
1 |
64,775,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R4972:Fzd5
|
UTSW |
1 |
64,775,171 (GRCm39) |
missense |
probably benign |
0.06 |
R5154:Fzd5
|
UTSW |
1 |
64,775,131 (GRCm39) |
missense |
probably benign |
0.05 |
R6122:Fzd5
|
UTSW |
1 |
64,774,815 (GRCm39) |
nonsense |
probably null |
|
R6748:Fzd5
|
UTSW |
1 |
64,774,723 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7322:Fzd5
|
UTSW |
1 |
64,774,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R7526:Fzd5
|
UTSW |
1 |
64,775,251 (GRCm39) |
missense |
probably benign |
0.01 |
R7543:Fzd5
|
UTSW |
1 |
64,774,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R8163:Fzd5
|
UTSW |
1 |
64,774,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Fzd5
|
UTSW |
1 |
64,775,110 (GRCm39) |
missense |
possibly damaging |
0.63 |
|