Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl1 |
G |
A |
4: 86,150,810 (GRCm39) |
E151K |
|
Het |
Ap3b1 |
T |
C |
13: 94,587,581 (GRCm39) |
S452P |
probably damaging |
Het |
Cacna2d4 |
A |
G |
6: 119,251,200 (GRCm39) |
I463V |
probably benign |
Het |
Calhm4 |
A |
T |
10: 33,920,045 (GRCm39) |
M74K |
possibly damaging |
Het |
Ccdc142 |
T |
C |
6: 83,078,677 (GRCm39) |
S5P |
probably benign |
Het |
Cd300ld |
C |
T |
11: 114,875,038 (GRCm39) |
V199M |
probably damaging |
Het |
Cep162 |
T |
C |
9: 87,114,172 (GRCm39) |
Y300C |
probably damaging |
Het |
Ces2h |
C |
T |
8: 105,727,497 (GRCm39) |
Q5* |
probably null |
Het |
Col9a3 |
C |
T |
2: 180,251,158 (GRCm39) |
L310F |
probably damaging |
Het |
Copa |
A |
G |
1: 171,937,411 (GRCm39) |
D454G |
possibly damaging |
Het |
Ctnnbip1 |
A |
C |
4: 149,630,277 (GRCm39) |
M29L |
probably benign |
Het |
Ctnnbl1 |
A |
G |
2: 157,616,491 (GRCm39) |
D64G |
probably benign |
Het |
Dcxr |
T |
A |
11: 120,617,908 (GRCm39) |
T23S |
probably benign |
Het |
Dennd1b |
T |
A |
1: 138,990,670 (GRCm39) |
H211Q |
probably damaging |
Het |
Ercc8 |
G |
A |
13: 108,320,397 (GRCm39) |
A328T |
probably benign |
Het |
Fam217a |
T |
C |
13: 35,095,111 (GRCm39) |
D216G |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,201,589 (GRCm39) |
Y495F |
probably benign |
Het |
Fbxw13 |
G |
A |
9: 109,024,968 (GRCm39) |
S15F |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,792,962 (GRCm39) |
C964* |
probably null |
Het |
Fshr |
T |
A |
17: 89,292,683 (GRCm39) |
H665L |
probably benign |
Het |
Gm10447 |
A |
T |
11: 53,347,437 (GRCm39) |
C31S |
unknown |
Het |
Gm13272 |
A |
T |
4: 88,698,586 (GRCm39) |
Q167L |
probably benign |
Het |
Gtpbp2 |
T |
C |
17: 46,478,713 (GRCm39) |
I510T |
possibly damaging |
Het |
Hps6 |
G |
A |
19: 45,993,007 (GRCm39) |
A315T |
probably benign |
Het |
Igfbp6 |
A |
C |
15: 102,056,285 (GRCm39) |
T115P |
probably damaging |
Het |
Il11ra1 |
T |
C |
4: 41,764,846 (GRCm39) |
V100A |
probably benign |
Het |
Ints1 |
T |
C |
5: 139,756,840 (GRCm39) |
T493A |
probably benign |
Het |
Itgax |
C |
T |
7: 127,735,028 (GRCm39) |
T453I |
probably benign |
Het |
Kras |
T |
C |
6: 145,166,354 (GRCm39) |
T183A |
probably benign |
Het |
Lhcgr |
T |
C |
17: 89,050,210 (GRCm39) |
T439A |
probably damaging |
Het |
Lrrn4 |
T |
C |
2: 132,721,451 (GRCm39) |
H122R |
probably benign |
Het |
Muc2 |
A |
T |
7: 141,287,452 (GRCm39) |
R210S |
possibly damaging |
Het |
Myh7 |
C |
G |
14: 55,226,258 (GRCm39) |
D461H |
probably damaging |
Het |
Myo18b |
T |
C |
5: 113,022,891 (GRCm39) |
D167G |
unknown |
Het |
Nedd8 |
G |
A |
14: 55,909,446 (GRCm39) |
|
probably benign |
Het |
Or5b94 |
A |
C |
19: 12,652,340 (GRCm39) |
Y257S |
probably damaging |
Het |
Pars2 |
T |
A |
4: 106,511,276 (GRCm39) |
Y353N |
probably damaging |
Het |
Pbxip1 |
T |
A |
3: 89,355,408 (GRCm39) |
D642E |
probably damaging |
Het |
Pcdhb10 |
A |
T |
18: 37,546,654 (GRCm39) |
R577* |
probably null |
Het |
Pcna-ps2 |
T |
A |
19: 9,261,489 (GRCm39) |
Y249* |
probably null |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pla2g6 |
A |
T |
15: 79,171,358 (GRCm39) |
V744E |
probably damaging |
Het |
Ppfibp1 |
A |
G |
6: 146,897,903 (GRCm39) |
I207V |
probably benign |
Het |
Prr11 |
T |
C |
11: 86,994,433 (GRCm39) |
D71G |
probably benign |
Het |
Rnf150 |
A |
C |
8: 83,590,781 (GRCm39) |
Y48S |
probably damaging |
Het |
Rsf1 |
G |
A |
7: 97,331,041 (GRCm39) |
G1237D |
|
Het |
Rusc2 |
C |
T |
4: 43,416,119 (GRCm39) |
T475I |
probably benign |
Het |
Scgb1b20 |
T |
A |
7: 33,072,867 (GRCm39) |
I25N |
probably damaging |
Het |
Sdr39u1 |
T |
C |
14: 56,137,116 (GRCm39) |
N65S |
probably benign |
Het |
Sh3gl3 |
T |
C |
7: 81,933,294 (GRCm39) |
V219A |
possibly damaging |
Het |
Shcbp1 |
A |
G |
8: 4,814,965 (GRCm39) |
F171S |
probably benign |
Het |
Shq1 |
A |
G |
6: 100,648,006 (GRCm39) |
F6S |
probably damaging |
Het |
Slc12a4 |
C |
T |
8: 106,672,203 (GRCm39) |
R868H |
possibly damaging |
Het |
Smg6 |
T |
C |
11: 74,821,445 (GRCm39) |
V572A |
probably benign |
Het |
Syn3 |
A |
G |
10: 86,243,534 (GRCm39) |
V135A |
probably damaging |
Het |
Tars3 |
A |
T |
7: 65,314,717 (GRCm39) |
D425V |
probably benign |
Het |
Tmem253 |
A |
T |
14: 52,254,608 (GRCm39) |
Q21L |
possibly damaging |
Het |
Trpm3 |
G |
T |
19: 22,896,154 (GRCm39) |
R997L |
probably damaging |
Het |
Ubr5 |
G |
A |
15: 37,980,076 (GRCm39) |
A2434V |
probably null |
Het |
Ugt1a9 |
A |
G |
1: 87,998,831 (GRCm39) |
T94A |
probably benign |
Het |
Vmn1r62 |
A |
G |
7: 5,678,182 (GRCm39) |
|
probably benign |
Het |
Vmn2r61 |
T |
C |
7: 41,916,472 (GRCm39) |
C362R |
probably damaging |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
Zfp94 |
T |
C |
7: 24,003,107 (GRCm39) |
K112E |
probably benign |
Het |
Zfp954 |
A |
T |
7: 7,120,889 (GRCm39) |
V47E |
probably damaging |
Het |
|
Other mutations in Ikzf4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00162:Ikzf4
|
APN |
10 |
128,470,416 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01649:Ikzf4
|
APN |
10 |
128,471,689 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02261:Ikzf4
|
APN |
10 |
128,472,591 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02315:Ikzf4
|
APN |
10 |
128,470,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R0099:Ikzf4
|
UTSW |
10 |
128,470,066 (GRCm39) |
missense |
probably damaging |
0.97 |
R0200:Ikzf4
|
UTSW |
10 |
128,470,545 (GRCm39) |
missense |
probably damaging |
0.96 |
R0365:Ikzf4
|
UTSW |
10 |
128,470,276 (GRCm39) |
missense |
probably benign |
|
R0376:Ikzf4
|
UTSW |
10 |
128,468,625 (GRCm39) |
missense |
probably benign |
|
R0456:Ikzf4
|
UTSW |
10 |
128,471,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R0536:Ikzf4
|
UTSW |
10 |
128,477,118 (GRCm39) |
missense |
probably benign |
0.09 |
R1731:Ikzf4
|
UTSW |
10 |
128,470,401 (GRCm39) |
missense |
probably benign |
0.03 |
R2017:Ikzf4
|
UTSW |
10 |
128,470,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R4158:Ikzf4
|
UTSW |
10 |
128,479,605 (GRCm39) |
intron |
probably benign |
|
R4160:Ikzf4
|
UTSW |
10 |
128,479,605 (GRCm39) |
intron |
probably benign |
|
R4623:Ikzf4
|
UTSW |
10 |
128,476,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Ikzf4
|
UTSW |
10 |
128,468,575 (GRCm39) |
missense |
probably benign |
0.00 |
R5008:Ikzf4
|
UTSW |
10 |
128,477,119 (GRCm39) |
missense |
probably benign |
0.03 |
R5432:Ikzf4
|
UTSW |
10 |
128,470,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Ikzf4
|
UTSW |
10 |
128,470,542 (GRCm39) |
missense |
probably benign |
0.15 |
R6445:Ikzf4
|
UTSW |
10 |
128,472,424 (GRCm39) |
splice site |
probably null |
|
R7204:Ikzf4
|
UTSW |
10 |
128,479,759 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7219:Ikzf4
|
UTSW |
10 |
128,470,252 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7239:Ikzf4
|
UTSW |
10 |
128,477,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Ikzf4
|
UTSW |
10 |
128,468,451 (GRCm39) |
missense |
unknown |
|
R7988:Ikzf4
|
UTSW |
10 |
128,470,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Ikzf4
|
UTSW |
10 |
128,468,487 (GRCm39) |
missense |
unknown |
|
R9352:Ikzf4
|
UTSW |
10 |
128,472,623 (GRCm39) |
missense |
probably benign |
0.22 |
Z1176:Ikzf4
|
UTSW |
10 |
128,470,099 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1177:Ikzf4
|
UTSW |
10 |
128,478,509 (GRCm39) |
missense |
possibly damaging |
0.94 |
|