Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921528I07Rik |
G |
A |
9: 114,129,077 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl2 |
T |
A |
3: 59,932,143 (GRCm39) |
Y219* |
probably null |
Het |
Adamts13 |
C |
A |
2: 26,895,198 (GRCm39) |
D1096E |
probably benign |
Het |
Adamts16 |
T |
G |
13: 70,927,671 (GRCm39) |
K523Q |
possibly damaging |
Het |
Adcy2 |
A |
G |
13: 68,820,019 (GRCm39) |
F740S |
probably benign |
Het |
Carmil1 |
T |
A |
13: 24,266,003 (GRCm39) |
N253I |
probably damaging |
Het |
Ccdc97 |
T |
C |
7: 25,413,833 (GRCm39) |
T283A |
probably damaging |
Het |
Cmpk2 |
G |
T |
12: 26,527,150 (GRCm39) |
E380* |
probably null |
Het |
Csmd3 |
A |
G |
15: 47,833,543 (GRCm39) |
I911T |
probably damaging |
Het |
Cyp2c39 |
T |
C |
19: 39,502,079 (GRCm39) |
L156P |
probably damaging |
Het |
D7Ertd443e |
T |
C |
7: 133,899,866 (GRCm39) |
I499V |
possibly damaging |
Het |
Dhx58 |
A |
C |
11: 100,592,374 (GRCm39) |
|
probably null |
Het |
Dip2a |
C |
T |
10: 76,134,621 (GRCm39) |
G390S |
probably damaging |
Het |
Dusp10 |
A |
G |
1: 183,801,253 (GRCm39) |
D340G |
probably damaging |
Het |
Epha1 |
A |
T |
6: 42,342,407 (GRCm39) |
C314S |
probably damaging |
Het |
Exph5 |
A |
T |
9: 53,284,602 (GRCm39) |
H561L |
probably benign |
Het |
Foxc1 |
A |
C |
13: 31,991,495 (GRCm39) |
N102T |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,814,908 (GRCm39) |
I3547T |
probably benign |
Het |
Gm5464 |
G |
T |
14: 67,106,774 (GRCm39) |
|
probably benign |
Het |
Gnptab |
C |
T |
10: 88,269,456 (GRCm39) |
R720C |
possibly damaging |
Het |
Greb1l |
T |
C |
18: 10,469,375 (GRCm39) |
V130A |
possibly damaging |
Het |
Hmg20a |
A |
T |
9: 56,394,934 (GRCm39) |
D216V |
probably damaging |
Het |
Hnrnpul2 |
C |
A |
19: 8,801,777 (GRCm39) |
D328E |
probably damaging |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Ift172 |
T |
C |
5: 31,410,985 (GRCm39) |
Y1691C |
probably damaging |
Het |
Kremen2 |
T |
C |
17: 23,961,784 (GRCm39) |
D241G |
probably benign |
Het |
Meis2 |
T |
C |
2: 115,893,897 (GRCm39) |
D5G |
possibly damaging |
Het |
Mrps5 |
G |
A |
2: 127,433,749 (GRCm39) |
R46K |
probably benign |
Het |
Myh14 |
C |
T |
7: 44,310,374 (GRCm39) |
V170M |
probably damaging |
Het |
Nexn |
T |
C |
3: 151,953,894 (GRCm39) |
N123D |
probably benign |
Het |
Or11g26 |
T |
A |
14: 50,753,282 (GRCm39) |
M207K |
probably benign |
Het |
Or4d11 |
A |
T |
19: 12,013,765 (GRCm39) |
S114T |
probably benign |
Het |
Or51l14 |
T |
A |
7: 103,101,423 (GRCm39) |
I293N |
probably damaging |
Het |
Pacs1 |
C |
T |
19: 5,191,726 (GRCm39) |
V704M |
probably damaging |
Het |
Papolg |
A |
G |
11: 23,822,425 (GRCm39) |
|
probably null |
Het |
Pdlim3 |
T |
C |
8: 46,370,543 (GRCm39) |
V281A |
probably benign |
Het |
Plpp4 |
T |
G |
7: 128,925,190 (GRCm39) |
F142V |
probably damaging |
Het |
Prb1a |
G |
A |
6: 132,184,620 (GRCm39) |
Q338* |
probably null |
Het |
Psg26 |
G |
T |
7: 18,216,481 (GRCm39) |
Y119* |
probably null |
Het |
Ptger4 |
A |
G |
15: 5,272,491 (GRCm39) |
C68R |
probably benign |
Het |
Ptpre |
T |
A |
7: 135,272,444 (GRCm39) |
I399N |
probably damaging |
Het |
Ripply2 |
A |
G |
9: 86,898,372 (GRCm39) |
Y72C |
probably damaging |
Het |
Rp1l1 |
T |
A |
14: 64,266,837 (GRCm39) |
S808T |
possibly damaging |
Het |
Scn5a |
G |
A |
9: 119,362,838 (GRCm39) |
T594I |
probably damaging |
Het |
Sf3b1 |
T |
C |
1: 55,037,267 (GRCm39) |
D883G |
probably benign |
Het |
Skint5 |
A |
T |
4: 113,369,220 (GRCm39) |
|
probably null |
Het |
Terf1 |
A |
G |
1: 15,889,207 (GRCm39) |
H212R |
probably damaging |
Het |
Tmco5 |
T |
G |
2: 116,711,269 (GRCm39) |
|
probably null |
Het |
Tnfaip3 |
A |
T |
10: 18,882,660 (GRCm39) |
Y252* |
probably null |
Het |
Tnrc6a |
T |
A |
7: 122,770,083 (GRCm39) |
N624K |
probably damaging |
Het |
Top3a |
C |
A |
11: 60,633,615 (GRCm39) |
R827L |
probably damaging |
Het |
Unc79 |
G |
A |
12: 103,055,031 (GRCm39) |
|
probably null |
Het |
Usp20 |
T |
C |
2: 30,901,116 (GRCm39) |
S422P |
probably benign |
Het |
Utrn |
T |
C |
10: 12,509,766 (GRCm39) |
E2402G |
probably benign |
Het |
Wdr3 |
G |
A |
3: 100,063,734 (GRCm39) |
Q181* |
probably null |
Het |
Zfp536 |
T |
C |
7: 37,267,373 (GRCm39) |
E681G |
probably damaging |
Het |
Zfp91 |
C |
T |
19: 12,747,438 (GRCm39) |
V562I |
possibly damaging |
Het |
Zfp942 |
A |
T |
17: 22,148,017 (GRCm39) |
I204N |
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 |
|
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 |
R3615:Fbxw26
|
UTSW |
9 |
109,572,828 (GRCm39) |
nonsense |
probably null |
|
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 |
|