Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg2 |
C |
A |
17: 57,152,443 (GRCm39) |
L666F |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,588,344 (GRCm39) |
V4414E |
possibly damaging |
Het |
Apoc3 |
T |
G |
9: 46,144,585 (GRCm39) |
D79A |
probably damaging |
Het |
Arfgap1 |
T |
A |
2: 180,621,022 (GRCm39) |
|
probably null |
Het |
Ascc1 |
T |
C |
10: 59,843,551 (GRCm39) |
S38P |
probably benign |
Het |
Asl |
C |
T |
5: 130,040,791 (GRCm39) |
E389K |
probably benign |
Het |
Atat1 |
A |
T |
17: 36,215,008 (GRCm39) |
I215K |
probably benign |
Het |
Bod1l |
A |
T |
5: 41,991,075 (GRCm39) |
L160* |
probably null |
Het |
Cbl |
C |
A |
9: 44,069,836 (GRCm39) |
S637I |
possibly damaging |
Het |
Ccdc112 |
A |
C |
18: 46,420,720 (GRCm39) |
S343R |
probably benign |
Het |
Cr1l |
A |
G |
1: 194,799,925 (GRCm39) |
S250P |
possibly damaging |
Het |
Cspg4b |
T |
A |
13: 113,456,263 (GRCm39) |
F770I |
|
Het |
Dlgap3 |
A |
G |
4: 127,129,947 (GRCm39) |
E907G |
probably damaging |
Het |
Dsp |
A |
T |
13: 38,352,600 (GRCm39) |
E159D |
probably benign |
Het |
Ech1 |
G |
A |
7: 28,524,728 (GRCm39) |
|
probably benign |
Het |
Erbin |
G |
T |
13: 103,971,485 (GRCm39) |
N710K |
possibly damaging |
Het |
Gm4871 |
G |
C |
5: 144,969,012 (GRCm39) |
D100E |
probably damaging |
Het |
Got1l1 |
A |
G |
8: 27,687,619 (GRCm39) |
I388T |
probably damaging |
Het |
Ing5 |
T |
A |
1: 93,744,166 (GRCm39) |
N184K |
probably damaging |
Het |
Izumo3 |
A |
T |
4: 92,035,145 (GRCm39) |
L24* |
probably null |
Het |
Lig1 |
T |
C |
7: 13,020,491 (GRCm39) |
V99A |
possibly damaging |
Het |
Mbtps1 |
A |
G |
8: 120,255,794 (GRCm39) |
Y488H |
possibly damaging |
Het |
Muc5ac |
A |
G |
7: 141,358,520 (GRCm39) |
Y1240C |
possibly damaging |
Het |
Nav3 |
T |
C |
10: 109,594,828 (GRCm39) |
T1458A |
probably damaging |
Het |
Nedd1 |
T |
C |
10: 92,527,778 (GRCm39) |
E472G |
probably damaging |
Het |
Nod2 |
A |
T |
8: 89,391,685 (GRCm39) |
H664L |
possibly damaging |
Het |
Ntrk3 |
A |
G |
7: 78,227,450 (GRCm39) |
S28P |
probably damaging |
Het |
Or14a257 |
A |
G |
7: 86,138,231 (GRCm39) |
F176S |
probably damaging |
Het |
Or1i2 |
C |
T |
10: 78,448,242 (GRCm39) |
V78I |
probably benign |
Het |
Or2ag17 |
T |
A |
7: 106,390,338 (GRCm39) |
|
probably benign |
Het |
Or2ag17 |
C |
A |
7: 106,390,337 (GRCm39) |
|
probably benign |
Het |
Or6c66b |
T |
A |
10: 129,376,826 (GRCm39) |
M140K |
probably benign |
Het |
Pcdha4 |
G |
T |
18: 37,087,106 (GRCm39) |
G430W |
probably damaging |
Het |
Pcnx1 |
T |
A |
12: 82,030,385 (GRCm39) |
Y1114* |
probably null |
Het |
Pde6a |
T |
A |
18: 61,364,566 (GRCm39) |
D207E |
probably damaging |
Het |
Plekhg1 |
T |
A |
10: 3,902,326 (GRCm39) |
I540N |
|
Het |
Pnp2 |
A |
T |
14: 51,197,099 (GRCm39) |
I62F |
probably benign |
Het |
Rarg |
C |
A |
15: 102,148,334 (GRCm39) |
D258Y |
probably damaging |
Het |
Rnps1 |
T |
A |
17: 24,643,484 (GRCm39) |
M262K |
unknown |
Het |
Scaf11 |
T |
C |
15: 96,316,483 (GRCm39) |
D1027G |
probably benign |
Het |
Serpina3a |
A |
T |
12: 104,079,110 (GRCm39) |
|
probably benign |
Het |
Slc25a1 |
A |
G |
16: 17,744,297 (GRCm39) |
|
probably null |
Het |
Slc44a3 |
A |
C |
3: 121,291,521 (GRCm39) |
V365G |
probably benign |
Het |
Slc45a3 |
T |
C |
1: 131,904,754 (GRCm39) |
F26L |
probably benign |
Het |
Slc9a2 |
T |
A |
1: 40,757,809 (GRCm39) |
I116K |
probably damaging |
Het |
Stk36 |
T |
A |
1: 74,665,756 (GRCm39) |
S700T |
probably benign |
Het |
Tekt3 |
A |
G |
11: 62,968,945 (GRCm39) |
D224G |
probably benign |
Het |
Tgtp1 |
A |
T |
11: 48,877,841 (GRCm39) |
I288N |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,710,567 (GRCm39) |
V8485M |
unknown |
Het |
Tubg1 |
G |
T |
11: 101,014,854 (GRCm39) |
A199S |
probably benign |
Het |
Uso1 |
T |
A |
5: 92,306,280 (GRCm39) |
I79K |
probably damaging |
Het |
Utp20 |
C |
T |
10: 88,593,766 (GRCm39) |
D2215N |
probably damaging |
Het |
Wdr43 |
C |
T |
17: 71,923,350 (GRCm39) |
A32V |
probably benign |
Het |
Zfp704 |
T |
C |
3: 9,630,301 (GRCm39) |
D170G |
probably benign |
Het |
|
Other mutations in Fbxw28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01883:Fbxw28
|
APN |
9 |
109,157,393 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02080:Fbxw28
|
APN |
9 |
109,168,641 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02313:Fbxw28
|
APN |
9 |
109,166,420 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0029:Fbxw28
|
UTSW |
9 |
109,157,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Fbxw28
|
UTSW |
9 |
109,167,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Fbxw28
|
UTSW |
9 |
109,157,279 (GRCm39) |
missense |
probably benign |
0.22 |
R1288:Fbxw28
|
UTSW |
9 |
109,166,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R1898:Fbxw28
|
UTSW |
9 |
109,152,452 (GRCm39) |
missense |
probably benign |
0.32 |
R2065:Fbxw28
|
UTSW |
9 |
109,157,292 (GRCm39) |
missense |
probably benign |
0.03 |
R2117:Fbxw28
|
UTSW |
9 |
109,159,985 (GRCm39) |
missense |
probably benign |
0.04 |
R3410:Fbxw28
|
UTSW |
9 |
109,167,472 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3812:Fbxw28
|
UTSW |
9 |
109,167,598 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4400:Fbxw28
|
UTSW |
9 |
109,157,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R4840:Fbxw28
|
UTSW |
9 |
109,168,602 (GRCm39) |
missense |
probably null |
1.00 |
R4899:Fbxw28
|
UTSW |
9 |
109,159,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R5129:Fbxw28
|
UTSW |
9 |
109,155,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R5613:Fbxw28
|
UTSW |
9 |
109,167,601 (GRCm39) |
missense |
probably benign |
0.02 |
R5777:Fbxw28
|
UTSW |
9 |
109,167,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R6029:Fbxw28
|
UTSW |
9 |
109,158,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Fbxw28
|
UTSW |
9 |
109,155,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R6367:Fbxw28
|
UTSW |
9 |
109,168,599 (GRCm39) |
critical splice donor site |
probably null |
|
R6820:Fbxw28
|
UTSW |
9 |
109,167,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Fbxw28
|
UTSW |
9 |
109,159,856 (GRCm39) |
missense |
probably benign |
0.00 |
R7763:Fbxw28
|
UTSW |
9 |
109,155,701 (GRCm39) |
missense |
probably damaging |
0.96 |
R8407:Fbxw28
|
UTSW |
9 |
109,155,269 (GRCm39) |
missense |
probably benign |
|
R8414:Fbxw28
|
UTSW |
9 |
109,155,604 (GRCm39) |
nonsense |
probably null |
|
R8721:Fbxw28
|
UTSW |
9 |
109,157,382 (GRCm39) |
missense |
probably benign |
0.15 |
R8766:Fbxw28
|
UTSW |
9 |
109,155,749 (GRCm39) |
missense |
probably benign |
0.15 |
R8955:Fbxw28
|
UTSW |
9 |
109,167,857 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9609:Fbxw28
|
UTSW |
9 |
109,167,515 (GRCm39) |
missense |
probably benign |
0.06 |
RF024:Fbxw28
|
UTSW |
9 |
109,167,594 (GRCm39) |
nonsense |
probably null |
|
|