Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931428L18Rik |
T |
C |
1: 31,261,588 (GRCm39) |
|
probably benign |
Het |
Aadacl2fm3 |
T |
C |
3: 59,768,478 (GRCm39) |
Y3H |
probably benign |
Het |
Abca9 |
G |
A |
11: 110,056,788 (GRCm39) |
Q11* |
probably null |
Het |
Abcc9 |
A |
T |
6: 142,550,621 (GRCm39) |
M1273K |
probably damaging |
Het |
Abi2 |
A |
G |
1: 60,478,098 (GRCm39) |
|
probably null |
Het |
Acsm5 |
A |
G |
7: 119,134,104 (GRCm39) |
E295G |
probably benign |
Het |
Anapc5 |
T |
C |
5: 122,938,607 (GRCm39) |
D389G |
probably benign |
Het |
Ano3 |
A |
T |
2: 110,625,372 (GRCm39) |
D159E |
probably benign |
Het |
Arhgap26 |
T |
A |
18: 39,283,110 (GRCm39) |
M349K |
probably damaging |
Het |
Arhgef39 |
A |
G |
4: 43,498,580 (GRCm39) |
|
probably null |
Het |
Astn1 |
T |
C |
1: 158,440,032 (GRCm39) |
S867P |
probably benign |
Het |
Atad3a |
A |
T |
4: 155,838,098 (GRCm39) |
|
probably null |
Het |
Cadm1 |
A |
T |
9: 47,699,407 (GRCm39) |
D91V |
probably damaging |
Het |
Cc2d2b |
T |
C |
19: 40,790,839 (GRCm39) |
I933T |
possibly damaging |
Het |
Cdcp3 |
A |
T |
7: 130,858,530 (GRCm39) |
D1066V |
probably benign |
Het |
Celsr3 |
C |
G |
9: 108,714,283 (GRCm39) |
N1937K |
possibly damaging |
Het |
Cic |
A |
C |
7: 24,987,706 (GRCm39) |
T558P |
possibly damaging |
Het |
Cntln |
A |
G |
4: 84,985,747 (GRCm39) |
M933V |
probably benign |
Het |
Coch |
T |
C |
12: 51,644,956 (GRCm39) |
F170S |
probably damaging |
Het |
Col1a2 |
A |
G |
6: 4,538,680 (GRCm39) |
Y1200C |
unknown |
Het |
Col26a1 |
T |
C |
5: 136,773,032 (GRCm39) |
M383V |
probably benign |
Het |
Col4a4 |
A |
T |
1: 82,431,499 (GRCm39) |
M1595K |
unknown |
Het |
Crh |
T |
C |
3: 19,748,501 (GRCm39) |
E47G |
probably benign |
Het |
D930020B18Rik |
T |
C |
10: 121,497,053 (GRCm39) |
|
probably null |
Het |
Def6 |
G |
A |
17: 28,445,137 (GRCm39) |
R482H |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dpagt1 |
T |
C |
9: 44,242,487 (GRCm39) |
L241P |
probably damaging |
Het |
E2f7 |
A |
G |
10: 110,610,542 (GRCm39) |
E389G |
probably damaging |
Het |
Eif2b1 |
T |
C |
5: 124,715,174 (GRCm39) |
I53V |
probably benign |
Het |
Fgfr2 |
A |
G |
7: 129,787,008 (GRCm39) |
S352P |
possibly damaging |
Het |
Fkbpl |
C |
A |
17: 34,864,388 (GRCm39) |
P52Q |
possibly damaging |
Het |
Fry |
G |
A |
5: 150,309,479 (GRCm39) |
R641H |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,820,430 (GRCm39) |
T5388A |
possibly damaging |
Het |
Gm12728 |
A |
G |
4: 105,651,546 (GRCm39) |
K52R |
probably damaging |
Het |
Gtf2a1l |
A |
G |
17: 89,019,053 (GRCm39) |
D379G |
probably benign |
Het |
Gys1 |
A |
T |
7: 45,092,393 (GRCm39) |
Y332F |
possibly damaging |
Het |
Hoxa7 |
T |
A |
6: 52,193,594 (GRCm39) |
|
probably benign |
Het |
Ifitm1 |
G |
A |
7: 140,549,519 (GRCm39) |
V101I |
probably benign |
Het |
Kalrn |
T |
A |
16: 34,181,354 (GRCm39) |
T95S |
probably damaging |
Het |
Leng8 |
A |
G |
7: 4,148,412 (GRCm39) |
Y728C |
probably damaging |
Het |
Lonp2 |
G |
T |
8: 87,361,536 (GRCm39) |
D238Y |
possibly damaging |
Het |
Ltn1 |
A |
C |
16: 87,175,868 (GRCm39) |
S1757A |
probably damaging |
Het |
Man2a2 |
A |
T |
7: 80,013,819 (GRCm39) |
S411T |
probably damaging |
Het |
Mrps33 |
C |
A |
6: 39,782,304 (GRCm39) |
|
probably null |
Het |
Muc16 |
C |
T |
9: 18,461,973 (GRCm39) |
|
probably null |
Het |
Muc5ac |
A |
G |
7: 141,362,808 (GRCm39) |
|
probably benign |
Het |
Naip2 |
A |
C |
13: 100,298,549 (GRCm39) |
S496A |
probably benign |
Het |
Or10al6 |
T |
G |
17: 38,083,194 (GRCm39) |
F217V |
probably damaging |
Het |
Or13p8 |
A |
G |
4: 118,583,930 (GRCm39) |
Y162C |
probably damaging |
Het |
Or1j21 |
T |
A |
2: 36,683,789 (GRCm39) |
D180E |
possibly damaging |
Het |
Or4c106 |
A |
T |
2: 88,682,863 (GRCm39) |
T190S |
probably damaging |
Het |
Or55b10 |
A |
T |
7: 102,143,346 (GRCm39) |
V212D |
probably damaging |
Het |
Or5w17 |
T |
C |
2: 87,583,812 (GRCm39) |
N175S |
probably damaging |
Het |
Pag1 |
T |
A |
3: 9,764,396 (GRCm39) |
E252D |
possibly damaging |
Het |
Plcd3 |
T |
C |
11: 102,968,593 (GRCm39) |
Y366C |
probably damaging |
Het |
Psg17 |
A |
C |
7: 18,548,375 (GRCm39) |
S465R |
probably damaging |
Het |
Ptpn9 |
G |
T |
9: 56,930,324 (GRCm39) |
V50L |
probably damaging |
Het |
Rab17 |
T |
G |
1: 90,886,683 (GRCm39) |
S190R |
probably benign |
Het |
Samd11 |
A |
G |
4: 156,333,535 (GRCm39) |
|
probably null |
Het |
Slc17a5 |
A |
G |
9: 78,445,553 (GRCm39) |
F434S |
possibly damaging |
Het |
Slc22a15 |
A |
G |
3: 101,790,899 (GRCm39) |
I202T |
possibly damaging |
Het |
Slc8a1 |
G |
T |
17: 81,696,347 (GRCm39) |
Q896K |
probably benign |
Het |
Slc9a5 |
A |
T |
8: 106,085,025 (GRCm39) |
K509* |
probably null |
Het |
Slf2 |
A |
C |
19: 44,961,603 (GRCm39) |
M1041L |
probably benign |
Het |
Smn1 |
A |
G |
13: 100,265,008 (GRCm39) |
|
probably null |
Het |
Snx9 |
T |
C |
17: 5,972,484 (GRCm39) |
|
probably null |
Het |
Soat2 |
T |
A |
15: 102,070,490 (GRCm39) |
L431Q |
probably damaging |
Het |
Spam1 |
T |
A |
6: 24,796,929 (GRCm39) |
N293K |
probably benign |
Het |
Tatdn1 |
T |
C |
15: 58,795,760 (GRCm39) |
T66A |
possibly damaging |
Het |
Tmprss11g |
A |
T |
5: 86,640,015 (GRCm39) |
S205T |
probably benign |
Het |
Tnpo3 |
G |
T |
6: 29,571,100 (GRCm39) |
N431K |
possibly damaging |
Het |
Trim39 |
T |
C |
17: 36,579,554 (GRCm39) |
T31A |
probably benign |
Het |
Trmt9b |
T |
C |
8: 36,965,637 (GRCm39) |
|
probably null |
Het |
Tshz3 |
A |
G |
7: 36,451,764 (GRCm39) |
|
probably null |
Het |
Ttll11 |
G |
A |
2: 35,792,766 (GRCm39) |
T359M |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,571,843 (GRCm39) |
D26350A |
probably damaging |
Het |
Ubr4 |
G |
T |
4: 139,159,062 (GRCm39) |
V2472F |
probably damaging |
Het |
Vsx2 |
C |
T |
12: 84,639,878 (GRCm39) |
P265S |
probably benign |
Het |
Wdr90 |
C |
T |
17: 26,064,885 (GRCm39) |
G1708R |
probably damaging |
Het |
Wnt11 |
A |
G |
7: 98,502,481 (GRCm39) |
Y351C |
probably damaging |
Het |
Xpo6 |
A |
C |
7: 125,712,057 (GRCm39) |
N3K |
probably damaging |
Het |
Zfp445 |
A |
G |
9: 122,686,631 (GRCm39) |
S165P |
probably benign |
Het |
Zfp953 |
A |
T |
13: 67,496,001 (GRCm39) |
Y13* |
probably null |
Het |
Zftraf1 |
T |
C |
15: 76,542,908 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Fbxo4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01747:Fbxo4
|
APN |
15 |
3,995,237 (GRCm39) |
nonsense |
probably null |
|
IGL01879:Fbxo4
|
APN |
15 |
4,005,436 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03070:Fbxo4
|
APN |
15 |
4,007,344 (GRCm39) |
missense |
possibly damaging |
0.63 |
PIT1430001:Fbxo4
|
UTSW |
15 |
4,008,782 (GRCm39) |
missense |
probably benign |
0.07 |
R1601:Fbxo4
|
UTSW |
15 |
3,998,447 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4556:Fbxo4
|
UTSW |
15 |
3,995,187 (GRCm39) |
makesense |
probably null |
|
R4557:Fbxo4
|
UTSW |
15 |
3,995,187 (GRCm39) |
makesense |
probably null |
|
R4783:Fbxo4
|
UTSW |
15 |
3,998,523 (GRCm39) |
missense |
probably benign |
0.11 |
R4784:Fbxo4
|
UTSW |
15 |
3,998,523 (GRCm39) |
missense |
probably benign |
0.11 |
R4785:Fbxo4
|
UTSW |
15 |
3,998,523 (GRCm39) |
missense |
probably benign |
0.11 |
R4871:Fbxo4
|
UTSW |
15 |
4,005,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Fbxo4
|
UTSW |
15 |
4,007,238 (GRCm39) |
splice site |
probably null |
|
R5435:Fbxo4
|
UTSW |
15 |
3,995,274 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5876:Fbxo4
|
UTSW |
15 |
4,007,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6423:Fbxo4
|
UTSW |
15 |
3,995,274 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6656:Fbxo4
|
UTSW |
15 |
4,005,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R6999:Fbxo4
|
UTSW |
15 |
4,007,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7505:Fbxo4
|
UTSW |
15 |
4,000,903 (GRCm39) |
missense |
probably benign |
0.09 |
R7543:Fbxo4
|
UTSW |
15 |
4,007,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R8182:Fbxo4
|
UTSW |
15 |
3,998,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Fbxo4
|
UTSW |
15 |
3,995,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R9079:Fbxo4
|
UTSW |
15 |
3,998,388 (GRCm39) |
critical splice donor site |
probably null |
|
R9333:Fbxo4
|
UTSW |
15 |
3,998,502 (GRCm39) |
missense |
probably benign |
0.00 |
R9546:Fbxo4
|
UTSW |
15 |
3,998,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R9547:Fbxo4
|
UTSW |
15 |
3,998,493 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Fbxo4
|
UTSW |
15 |
4,000,933 (GRCm39) |
nonsense |
probably null |
|
|