Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
C |
6: 128,535,257 (GRCm39) |
T818A |
probably benign |
Het |
Aasdh |
A |
G |
5: 77,036,629 (GRCm39) |
V304A |
probably benign |
Het |
Angptl3 |
G |
A |
4: 98,922,702 (GRCm39) |
A248T |
probably benign |
Het |
Ap2b1 |
T |
A |
11: 83,215,391 (GRCm39) |
C112S |
possibly damaging |
Het |
Aqr |
A |
T |
2: 113,967,368 (GRCm39) |
I549N |
probably damaging |
Het |
Barhl1 |
C |
T |
2: 28,801,562 (GRCm39) |
D161N |
possibly damaging |
Het |
Col28a1 |
A |
G |
6: 8,014,942 (GRCm39) |
V821A |
probably damaging |
Het |
Dclk2 |
G |
A |
3: 86,827,342 (GRCm39) |
P46S |
probably damaging |
Het |
Dnah1 |
A |
G |
14: 31,037,105 (GRCm39) |
L247P |
possibly damaging |
Het |
Dpysl2 |
T |
A |
14: 67,071,819 (GRCm39) |
H107L |
probably damaging |
Het |
Dzip3 |
A |
G |
16: 48,757,426 (GRCm39) |
L869S |
probably damaging |
Het |
Efs |
T |
C |
14: 55,157,552 (GRCm39) |
Y160C |
probably damaging |
Het |
Enam |
A |
T |
5: 88,652,306 (GRCm39) |
N1197Y |
possibly damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fam184b |
A |
G |
5: 45,740,157 (GRCm39) |
V343A |
possibly damaging |
Het |
Fiz1 |
A |
G |
7: 5,011,171 (GRCm39) |
L449P |
probably benign |
Het |
Foxi2 |
T |
A |
7: 135,012,180 (GRCm39) |
C23S |
possibly damaging |
Het |
Gdf2 |
G |
A |
14: 33,666,914 (GRCm39) |
R212Q |
probably damaging |
Het |
Gm5105 |
C |
A |
3: 137,755,449 (GRCm39) |
A46S |
unknown |
Het |
Grik5 |
C |
T |
7: 24,721,996 (GRCm39) |
A581T |
probably benign |
Het |
Gse1 |
C |
G |
8: 121,299,481 (GRCm39) |
|
probably benign |
Het |
Hsp90aa1 |
T |
A |
12: 110,662,114 (GRCm39) |
M1L |
possibly damaging |
Het |
Hsp90aa1 |
C |
A |
12: 110,662,115 (GRCm39) |
|
probably null |
Het |
Krt25 |
A |
C |
11: 99,208,124 (GRCm39) |
V368G |
possibly damaging |
Het |
Lacc1 |
A |
G |
14: 77,270,727 (GRCm39) |
V269A |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,126,896 (GRCm39) |
K417E |
probably damaging |
Het |
Miip |
A |
G |
4: 147,950,371 (GRCm39) |
M75T |
probably benign |
Het |
Nlrp10 |
A |
G |
7: 108,523,683 (GRCm39) |
F599S |
probably benign |
Het |
Nlrp12 |
T |
A |
7: 3,289,205 (GRCm39) |
M436L |
probably benign |
Het |
Or4b13 |
T |
C |
2: 90,082,753 (GRCm39) |
E193G |
possibly damaging |
Het |
Pafah1b1 |
G |
A |
11: 74,581,058 (GRCm39) |
S57F |
probably damaging |
Het |
Pla2g2e |
G |
A |
4: 138,607,685 (GRCm39) |
V22I |
probably benign |
Het |
Plekhd1 |
A |
G |
12: 80,764,044 (GRCm39) |
E202G |
probably damaging |
Het |
Prss21 |
A |
G |
17: 24,091,805 (GRCm39) |
T258A |
probably benign |
Het |
Prss34 |
A |
G |
17: 25,517,820 (GRCm39) |
E65G |
probably benign |
Het |
Psap |
A |
G |
10: 60,130,383 (GRCm39) |
N149S |
probably benign |
Het |
Ptprf |
C |
T |
4: 118,095,080 (GRCm39) |
A275T |
probably benign |
Het |
Sem1 |
A |
G |
6: 6,578,520 (GRCm39) |
L12P |
probably damaging |
Het |
Sf3b3 |
A |
G |
8: 111,571,155 (GRCm39) |
Y4H |
probably damaging |
Het |
Sh3bp4 |
G |
T |
1: 89,065,427 (GRCm39) |
R7L |
probably damaging |
Het |
Slc16a1 |
T |
A |
3: 104,560,886 (GRCm39) |
L397Q |
probably damaging |
Het |
Smg5 |
A |
G |
3: 88,243,758 (GRCm39) |
S10G |
possibly damaging |
Het |
Spata31e5 |
T |
C |
1: 28,815,656 (GRCm39) |
D792G |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,971,864 (GRCm39) |
N399S |
probably benign |
Het |
Tas2r102 |
C |
T |
6: 132,739,781 (GRCm39) |
Q230* |
probably null |
Het |
Tdo2 |
A |
G |
3: 81,882,735 (GRCm39) |
Y13H |
possibly damaging |
Het |
Tmem231 |
C |
T |
8: 112,644,945 (GRCm39) |
R187H |
possibly damaging |
Het |
Tmem30b |
A |
G |
12: 73,592,353 (GRCm39) |
M254T |
probably damaging |
Het |
Trpm1 |
G |
A |
7: 63,893,318 (GRCm39) |
G1057R |
probably damaging |
Het |
Tusc3 |
A |
T |
8: 39,617,879 (GRCm39) |
K347N |
probably damaging |
Het |
Usp36 |
C |
T |
11: 118,167,585 (GRCm39) |
|
probably null |
Het |
Vash2 |
T |
C |
1: 190,702,616 (GRCm39) |
Y117C |
probably damaging |
Het |
Vrk2 |
A |
G |
11: 26,439,866 (GRCm39) |
I235T |
possibly damaging |
Het |
Wdr20 |
A |
G |
12: 110,760,373 (GRCm39) |
T420A |
probably benign |
Het |
|
Other mutations in Fbxw26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00589:Fbxw26
|
APN |
9 |
109,547,016 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01072:Fbxw26
|
APN |
9 |
109,552,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01151:Fbxw26
|
APN |
9 |
109,550,848 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01394:Fbxw26
|
APN |
9 |
109,547,057 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01432:Fbxw26
|
APN |
9 |
109,547,043 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02559:Fbxw26
|
APN |
9 |
109,551,232 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02981:Fbxw26
|
APN |
9 |
109,573,862 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03370:Fbxw26
|
APN |
9 |
109,575,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Fbxw26
|
UTSW |
9 |
109,547,079 (GRCm39) |
missense |
probably benign |
0.01 |
R0087:Fbxw26
|
UTSW |
9 |
109,554,006 (GRCm39) |
missense |
probably benign |
|
R0369:Fbxw26
|
UTSW |
9 |
109,552,780 (GRCm39) |
critical splice donor site |
probably null |
|
R0446:Fbxw26
|
UTSW |
9 |
109,572,788 (GRCm39) |
missense |
probably benign |
0.03 |
R1844:Fbxw26
|
UTSW |
9 |
109,553,946 (GRCm39) |
missense |
probably benign |
0.42 |
R1891:Fbxw26
|
UTSW |
9 |
109,551,232 (GRCm39) |
missense |
probably benign |
0.34 |
R2042:Fbxw26
|
UTSW |
9 |
109,561,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R3616:Fbxw26
|
UTSW |
9 |
109,572,828 (GRCm39) |
nonsense |
probably null |
|
R4659:Fbxw26
|
UTSW |
9 |
109,573,939 (GRCm39) |
missense |
probably damaging |
0.97 |
R4785:Fbxw26
|
UTSW |
9 |
109,553,868 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4898:Fbxw26
|
UTSW |
9 |
109,547,037 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5791:Fbxw26
|
UTSW |
9 |
109,574,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5818:Fbxw26
|
UTSW |
9 |
109,561,634 (GRCm39) |
missense |
probably benign |
|
R5921:Fbxw26
|
UTSW |
9 |
109,575,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R5983:Fbxw26
|
UTSW |
9 |
109,547,033 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6145:Fbxw26
|
UTSW |
9 |
109,561,691 (GRCm39) |
missense |
probably benign |
0.09 |
R6209:Fbxw26
|
UTSW |
9 |
109,547,033 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6412:Fbxw26
|
UTSW |
9 |
109,561,715 (GRCm39) |
missense |
probably damaging |
0.97 |
R6842:Fbxw26
|
UTSW |
9 |
109,553,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7228:Fbxw26
|
UTSW |
9 |
109,554,012 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7451:Fbxw26
|
UTSW |
9 |
109,561,691 (GRCm39) |
missense |
probably benign |
0.03 |
R7467:Fbxw26
|
UTSW |
9 |
109,561,765 (GRCm39) |
missense |
probably benign |
0.00 |
R8397:Fbxw26
|
UTSW |
9 |
109,561,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R8912:Fbxw26
|
UTSW |
9 |
109,561,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R9284:Fbxw26
|
UTSW |
9 |
109,550,962 (GRCm39) |
intron |
probably benign |
|
R9479:Fbxw26
|
UTSW |
9 |
109,561,625 (GRCm39) |
missense |
probably damaging |
0.99 |
R9694:Fbxw26
|
UTSW |
9 |
109,575,135 (GRCm39) |
start gained |
probably benign |
|
X0020:Fbxw26
|
UTSW |
9 |
109,561,700 (GRCm39) |
missense |
probably damaging |
1.00 |
|