Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
A |
G |
17: 48,349,049 (GRCm39) |
V11A |
possibly damaging |
Het |
6030452D12Rik |
T |
C |
8: 107,230,979 (GRCm39) |
I55T |
unknown |
Het |
Aadacl2 |
A |
G |
3: 59,932,460 (GRCm39) |
D325G |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,988,274 (GRCm39) |
S113G |
probably benign |
Het |
Agxt2 |
T |
C |
15: 10,392,130 (GRCm39) |
|
probably null |
Het |
Aicda |
C |
T |
6: 122,530,847 (GRCm39) |
|
probably benign |
Het |
Aifm2 |
T |
C |
10: 61,563,535 (GRCm39) |
M135T |
probably benign |
Het |
Asah2 |
T |
C |
19: 32,031,871 (GRCm39) |
|
probably null |
Het |
Btbd17 |
T |
C |
11: 114,682,543 (GRCm39) |
R390G |
probably damaging |
Het |
Cadps |
T |
C |
14: 12,705,654 (GRCm38) |
E247G |
possibly damaging |
Het |
Cds2 |
T |
C |
2: 132,146,873 (GRCm39) |
I383T |
probably damaging |
Het |
Celf3 |
T |
A |
3: 94,392,174 (GRCm39) |
|
probably null |
Het |
Crhr2 |
T |
C |
6: 55,079,852 (GRCm39) |
S162G |
possibly damaging |
Het |
Dapl1 |
A |
T |
2: 59,335,118 (GRCm39) |
K91* |
probably null |
Het |
Ddx60 |
A |
C |
8: 62,465,458 (GRCm39) |
M1372L |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,389,358 (GRCm39) |
F845I |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,411,524 (GRCm39) |
D1784G |
probably damaging |
Het |
Ech1 |
T |
C |
7: 28,531,478 (GRCm39) |
V310A |
probably benign |
Het |
Eef1g |
A |
G |
19: 8,955,330 (GRCm39) |
D393G |
possibly damaging |
Het |
Eif3k |
T |
C |
7: 28,671,969 (GRCm39) |
I172V |
possibly damaging |
Het |
Foxd4 |
A |
G |
19: 24,877,625 (GRCm39) |
F192L |
probably damaging |
Het |
Gpr153 |
T |
A |
4: 152,366,240 (GRCm39) |
S268R |
probably damaging |
Het |
H3c13 |
C |
A |
3: 96,176,394 (GRCm39) |
R129S |
probably damaging |
Het |
Ivl |
T |
C |
3: 92,478,698 (GRCm39) |
K456E |
unknown |
Het |
Kif20b |
A |
T |
19: 34,928,944 (GRCm39) |
D1190V |
probably damaging |
Het |
Kif21a |
T |
A |
15: 90,840,508 (GRCm39) |
I1223L |
possibly damaging |
Het |
Lmf1 |
T |
C |
17: 25,798,324 (GRCm39) |
V55A |
probably damaging |
Het |
Loxhd1 |
A |
G |
18: 77,459,987 (GRCm39) |
E659G |
possibly damaging |
Het |
Lrrc37a |
T |
C |
11: 103,394,930 (GRCm39) |
E165G |
possibly damaging |
Het |
Mios |
T |
C |
6: 8,228,113 (GRCm39) |
Y677H |
possibly damaging |
Het |
Mtpap |
A |
T |
18: 4,375,724 (GRCm39) |
T35S |
possibly damaging |
Het |
Ndc1 |
C |
G |
4: 107,268,334 (GRCm39) |
D623E |
probably benign |
Het |
Nedd4l |
A |
G |
18: 65,336,951 (GRCm39) |
Y666C |
probably damaging |
Het |
Or52s6 |
T |
A |
7: 103,091,842 (GRCm39) |
I163F |
possibly damaging |
Het |
Or5ac22 |
T |
C |
16: 59,135,720 (GRCm39) |
T17A |
probably damaging |
Het |
Or5b12b |
T |
G |
19: 12,861,985 (GRCm39) |
F247V |
probably benign |
Het |
Or5m10b |
A |
G |
2: 85,699,596 (GRCm39) |
Y220C |
possibly damaging |
Het |
Papss1 |
G |
T |
3: 131,313,092 (GRCm39) |
V369F |
probably damaging |
Het |
Pcdhac2 |
T |
A |
18: 37,278,822 (GRCm39) |
Y601N |
probably damaging |
Het |
Pde7a |
C |
T |
3: 19,365,095 (GRCm39) |
R24Q |
probably damaging |
Het |
Phf21a |
A |
G |
2: 92,187,297 (GRCm39) |
D445G |
probably damaging |
Het |
Plekho1 |
T |
A |
3: 95,902,964 (GRCm39) |
N15I |
possibly damaging |
Het |
Pprc1 |
T |
C |
19: 46,057,634 (GRCm39) |
|
probably benign |
Het |
Ralgapa1 |
A |
T |
12: 55,724,061 (GRCm39) |
|
probably null |
Het |
Rrp12 |
T |
C |
19: 41,861,481 (GRCm39) |
E942G |
probably benign |
Het |
Skor1 |
T |
C |
9: 63,051,830 (GRCm39) |
D685G |
probably benign |
Het |
Smim23 |
A |
T |
11: 32,774,510 (GRCm39) |
I3N |
possibly damaging |
Het |
Spata7 |
A |
T |
12: 98,630,536 (GRCm39) |
I333F |
probably damaging |
Het |
Sppl2c |
T |
C |
11: 104,079,141 (GRCm39) |
I647T |
probably benign |
Het |
Srgap1 |
C |
A |
10: 121,628,392 (GRCm39) |
R837L |
probably benign |
Het |
Stpg2 |
C |
A |
3: 139,014,990 (GRCm39) |
P385H |
probably damaging |
Het |
Tmem238 |
C |
A |
7: 4,792,016 (GRCm39) |
E19* |
probably null |
Het |
Top2b |
A |
T |
14: 16,387,331 (GRCm38) |
K140* |
probably null |
Het |
Trp53 |
T |
A |
11: 69,479,248 (GRCm39) |
L142* |
probably null |
Het |
Tyro3 |
A |
T |
2: 119,633,751 (GRCm39) |
D133V |
probably damaging |
Het |
Virma |
T |
A |
4: 11,528,636 (GRCm39) |
I1291N |
probably damaging |
Het |
Vmn1r213 |
A |
G |
13: 23,195,507 (GRCm39) |
|
probably benign |
Het |
Zbtb10 |
T |
C |
3: 9,329,610 (GRCm39) |
S323P |
possibly damaging |
Het |
Zfp521 |
A |
T |
18: 13,978,660 (GRCm39) |
N584K |
probably damaging |
Het |
Zfp944 |
A |
G |
17: 22,558,180 (GRCm39) |
C356R |
probably damaging |
Het |
|
Other mutations in Mnx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01602:Mnx1
|
APN |
5 |
29,682,591 (GRCm39) |
missense |
unknown |
|
IGL01605:Mnx1
|
APN |
5 |
29,682,591 (GRCm39) |
missense |
unknown |
|
3370:Mnx1
|
UTSW |
5 |
29,679,885 (GRCm39) |
missense |
unknown |
|
PIT4472001:Mnx1
|
UTSW |
5 |
29,679,105 (GRCm39) |
missense |
unknown |
|
R1752:Mnx1
|
UTSW |
5 |
29,682,727 (GRCm39) |
missense |
unknown |
|
R1785:Mnx1
|
UTSW |
5 |
29,679,187 (GRCm39) |
missense |
unknown |
|
R1786:Mnx1
|
UTSW |
5 |
29,679,187 (GRCm39) |
missense |
unknown |
|
R1854:Mnx1
|
UTSW |
5 |
29,682,780 (GRCm39) |
missense |
unknown |
|
R1866:Mnx1
|
UTSW |
5 |
29,679,043 (GRCm39) |
missense |
unknown |
|
R1893:Mnx1
|
UTSW |
5 |
29,682,828 (GRCm39) |
missense |
unknown |
|
R1899:Mnx1
|
UTSW |
5 |
29,678,955 (GRCm39) |
missense |
unknown |
|
R2131:Mnx1
|
UTSW |
5 |
29,679,187 (GRCm39) |
missense |
unknown |
|
R4713:Mnx1
|
UTSW |
5 |
29,683,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R5171:Mnx1
|
UTSW |
5 |
29,679,851 (GRCm39) |
missense |
unknown |
|
R6126:Mnx1
|
UTSW |
5 |
29,683,110 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7427:Mnx1
|
UTSW |
5 |
29,679,211 (GRCm39) |
missense |
unknown |
|
R8792:Mnx1
|
UTSW |
5 |
29,683,372 (GRCm39) |
start gained |
probably benign |
|
Z1176:Mnx1
|
UTSW |
5 |
29,679,172 (GRCm39) |
nonsense |
probably null |
|
Z1176:Mnx1
|
UTSW |
5 |
29,679,086 (GRCm39) |
missense |
unknown |
|
|