Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
T |
A |
3: 59,843,701 (GRCm39) |
Y132N |
probably damaging |
Het |
Adam21 |
T |
C |
12: 81,605,594 (GRCm39) |
T723A |
probably damaging |
Het |
Alox5 |
C |
T |
6: 116,397,219 (GRCm39) |
V322I |
probably benign |
Het |
Alpk1 |
C |
T |
3: 127,523,022 (GRCm39) |
V7M |
probably damaging |
Het |
Ankhd1 |
A |
T |
18: 36,776,096 (GRCm39) |
K1482* |
probably null |
Het |
Cacna1e |
A |
C |
1: 154,319,727 (GRCm39) |
D1324E |
probably damaging |
Het |
Ccdc150 |
A |
G |
1: 54,392,213 (GRCm39) |
D657G |
probably damaging |
Het |
Celsr1 |
A |
G |
15: 85,863,028 (GRCm39) |
S1335P |
probably damaging |
Het |
Cfhr4 |
T |
A |
1: 139,660,048 (GRCm39) |
K621N |
probably damaging |
Het |
Cspg5 |
A |
G |
9: 110,085,245 (GRCm39) |
D391G |
probably damaging |
Het |
Defa30 |
A |
T |
8: 21,624,821 (GRCm39) |
D48V |
possibly damaging |
Het |
E2f7 |
T |
C |
10: 110,595,712 (GRCm39) |
Y136H |
probably damaging |
Het |
Fam3d |
A |
G |
14: 8,349,314 (GRCm38) |
L212P |
probably damaging |
Het |
Fgg |
A |
T |
3: 82,920,250 (GRCm39) |
D343V |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,922,700 (GRCm38) |
M1712K |
probably benign |
Het |
Fnbp4 |
T |
C |
2: 90,588,683 (GRCm39) |
S485P |
probably damaging |
Het |
Ftsj3 |
G |
A |
11: 106,144,502 (GRCm39) |
A134V |
probably benign |
Het |
Gast |
C |
A |
11: 100,227,373 (GRCm39) |
S22Y |
probably damaging |
Het |
Gm20834 |
T |
A |
Y: 10,322,962 (GRCm39) |
H158L |
possibly damaging |
Het |
Ids |
C |
A |
X: 69,389,950 (GRCm39) |
G506C |
probably damaging |
Het |
Ifna15 |
G |
T |
4: 88,476,079 (GRCm39) |
T135N |
probably benign |
Het |
Igsf9b |
G |
A |
9: 27,220,774 (GRCm39) |
V47I |
possibly damaging |
Het |
Impg2 |
C |
T |
16: 56,080,527 (GRCm39) |
T777I |
probably damaging |
Het |
Kif11 |
C |
A |
19: 37,399,883 (GRCm39) |
T790K |
probably benign |
Het |
Kif24 |
A |
G |
4: 41,413,827 (GRCm39) |
|
probably null |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lrp10 |
C |
T |
14: 54,705,823 (GRCm39) |
R338C |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,751,844 (GRCm39) |
N242S |
probably benign |
Het |
Nectin1 |
A |
G |
9: 43,703,802 (GRCm39) |
D264G |
probably benign |
Het |
Nipsnap3a |
T |
C |
4: 52,995,979 (GRCm39) |
|
probably null |
Het |
Or10al3 |
G |
T |
17: 38,011,790 (GRCm39) |
E76D |
probably damaging |
Het |
Or5w14 |
G |
A |
2: 87,542,229 (GRCm39) |
S7F |
possibly damaging |
Het |
P3h4 |
A |
G |
11: 100,304,452 (GRCm39) |
F263S |
probably damaging |
Het |
Pcdhga4 |
C |
T |
18: 37,820,664 (GRCm39) |
H738Y |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,388,490 (GRCm39) |
I304K |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,444,225 (GRCm39) |
Y1460N |
probably damaging |
Het |
Rbl2 |
A |
G |
8: 91,833,735 (GRCm39) |
D812G |
probably damaging |
Het |
Rbm19 |
A |
G |
5: 120,278,427 (GRCm39) |
T737A |
possibly damaging |
Het |
Rbsn |
G |
A |
6: 92,184,029 (GRCm39) |
L95F |
possibly damaging |
Het |
Sall4 |
T |
C |
2: 168,597,400 (GRCm39) |
E480G |
probably benign |
Het |
Scfd1 |
T |
A |
12: 51,486,068 (GRCm39) |
N541K |
probably benign |
Het |
Scube3 |
G |
A |
17: 28,383,283 (GRCm39) |
G442S |
probably benign |
Het |
Slc15a4 |
A |
G |
5: 127,681,600 (GRCm39) |
|
probably null |
Het |
Smarcc1 |
A |
G |
9: 110,025,324 (GRCm39) |
D667G |
probably damaging |
Het |
Sned1 |
A |
T |
1: 93,193,113 (GRCm39) |
|
probably null |
Het |
Spsb1 |
T |
C |
4: 149,991,232 (GRCm39) |
H112R |
probably damaging |
Het |
Sun3 |
A |
G |
11: 8,966,328 (GRCm39) |
V231A |
probably damaging |
Het |
Vmn2r106 |
A |
T |
17: 20,499,910 (GRCm39) |
D108E |
probably benign |
Het |
Xdh |
A |
G |
17: 74,222,685 (GRCm39) |
V560A |
probably benign |
Het |
Zfp352 |
T |
A |
4: 90,112,071 (GRCm39) |
H70Q |
possibly damaging |
Het |
Zfp40 |
C |
A |
17: 23,396,164 (GRCm39) |
C73F |
probably benign |
Het |
Zfp975 |
A |
C |
7: 42,311,251 (GRCm39) |
L454R |
probably damaging |
Het |
Zik1 |
A |
T |
7: 10,224,268 (GRCm39) |
C276* |
probably null |
Het |
|
Other mutations in Fbxw25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03330:Fbxw25
|
APN |
9 |
109,474,307 (GRCm39) |
missense |
probably benign |
0.00 |
doughnuts
|
UTSW |
9 |
109,479,132 (GRCm39) |
missense |
|
|
goodtimes
|
UTSW |
9 |
109,492,442 (GRCm39) |
critical splice donor site |
probably null |
|
shakeys
|
UTSW |
9 |
109,483,651 (GRCm39) |
missense |
|
|
R0158:Fbxw25
|
UTSW |
9 |
109,483,720 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0850:Fbxw25
|
UTSW |
9 |
109,478,685 (GRCm39) |
missense |
probably benign |
|
R1109:Fbxw25
|
UTSW |
9 |
109,479,128 (GRCm39) |
missense |
probably benign |
0.00 |
R1386:Fbxw25
|
UTSW |
9 |
109,483,709 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1609:Fbxw25
|
UTSW |
9 |
109,492,578 (GRCm39) |
missense |
probably benign |
0.11 |
R1750:Fbxw25
|
UTSW |
9 |
109,479,141 (GRCm39) |
missense |
probably benign |
0.23 |
R1977:Fbxw25
|
UTSW |
9 |
109,481,924 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2427:Fbxw25
|
UTSW |
9 |
109,481,928 (GRCm39) |
missense |
probably benign |
0.09 |
R3841:Fbxw25
|
UTSW |
9 |
109,491,202 (GRCm39) |
nonsense |
probably null |
|
R4934:Fbxw25
|
UTSW |
9 |
109,480,705 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5024:Fbxw25
|
UTSW |
9 |
109,492,442 (GRCm39) |
critical splice donor site |
probably null |
|
R5175:Fbxw25
|
UTSW |
9 |
109,493,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Fbxw25
|
UTSW |
9 |
109,492,573 (GRCm39) |
missense |
probably benign |
0.04 |
R5389:Fbxw25
|
UTSW |
9 |
109,481,954 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5493:Fbxw25
|
UTSW |
9 |
109,481,984 (GRCm39) |
missense |
probably benign |
0.01 |
R6268:Fbxw25
|
UTSW |
9 |
109,483,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Fbxw25
|
UTSW |
9 |
109,480,699 (GRCm39) |
missense |
probably benign |
0.29 |
R7275:Fbxw25
|
UTSW |
9 |
109,483,660 (GRCm39) |
missense |
|
|
R7492:Fbxw25
|
UTSW |
9 |
109,493,598 (GRCm39) |
critical splice donor site |
probably null |
|
R7623:Fbxw25
|
UTSW |
9 |
109,483,651 (GRCm39) |
missense |
|
|
R7784:Fbxw25
|
UTSW |
9 |
109,479,187 (GRCm39) |
missense |
|
|
R7861:Fbxw25
|
UTSW |
9 |
109,493,625 (GRCm39) |
nonsense |
probably null |
|
R7887:Fbxw25
|
UTSW |
9 |
109,478,662 (GRCm39) |
critical splice donor site |
probably null |
|
R8973:Fbxw25
|
UTSW |
9 |
109,479,132 (GRCm39) |
missense |
|
|
R9517:Fbxw25
|
UTSW |
9 |
109,480,892 (GRCm39) |
missense |
|
|
R9563:Fbxw25
|
UTSW |
9 |
109,483,676 (GRCm39) |
missense |
|
|
R9565:Fbxw25
|
UTSW |
9 |
109,483,676 (GRCm39) |
missense |
|
|
X0023:Fbxw25
|
UTSW |
9 |
109,480,843 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Fbxw25
|
UTSW |
9 |
109,480,806 (GRCm39) |
missense |
|
|
|