Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402N03Rik |
T |
A |
7: 131,139,196 (GRCm38) |
H97L |
possibly damaging |
Het |
Abca9 |
T |
A |
11: 110,145,546 (GRCm38) |
N579I |
probably damaging |
Het |
Acbd3 |
A |
T |
1: 180,722,095 (GRCm38) |
|
probably benign |
Het |
Ankrd50 |
A |
T |
3: 38,455,050 (GRCm38) |
I1056N |
probably damaging |
Het |
Ceacam18 |
T |
C |
7: 43,642,034 (GRCm38) |
V300A |
probably benign |
Het |
Cfap46 |
C |
A |
7: 139,627,473 (GRCm38) |
R1843S |
possibly damaging |
Het |
D430041D05Rik |
A |
G |
2: 104,248,284 (GRCm38) |
V1229A |
probably damaging |
Het |
Dbx2 |
G |
A |
15: 95,640,641 (GRCm38) |
S206L |
probably benign |
Het |
Dnah11 |
A |
T |
12: 117,954,893 (GRCm38) |
D1530E |
probably damaging |
Het |
Ecm2 |
A |
C |
13: 49,520,943 (GRCm38) |
T280P |
probably benign |
Het |
Emc2 |
G |
A |
15: 43,511,811 (GRCm38) |
|
probably null |
Het |
Epb42 |
C |
T |
2: 121,019,462 (GRCm38) |
V689I |
probably benign |
Het |
Fam114a1 |
T |
A |
5: 65,006,109 (GRCm38) |
M209K |
possibly damaging |
Het |
Fam117a |
C |
T |
11: 95,375,633 (GRCm38) |
S193F |
probably damaging |
Het |
Foxp2 |
A |
T |
6: 15,377,914 (GRCm38) |
|
probably benign |
Het |
Frmd6 |
T |
A |
12: 70,864,100 (GRCm38) |
C19* |
probably null |
Het |
Fyb |
A |
G |
15: 6,580,678 (GRCm38) |
|
probably null |
Het |
Gata6 |
C |
A |
18: 11,063,059 (GRCm38) |
H442Q |
possibly damaging |
Het |
Gldc |
A |
G |
19: 30,158,521 (GRCm38) |
S160P |
probably benign |
Het |
Gm3952 |
A |
G |
8: 128,745,974 (GRCm38) |
S1626P |
possibly damaging |
Het |
Gm9762 |
T |
A |
3: 78,966,435 (GRCm38) |
|
noncoding transcript |
Het |
Gtpbp2 |
T |
C |
17: 46,166,304 (GRCm38) |
|
probably benign |
Het |
Hgd |
A |
T |
16: 37,589,751 (GRCm38) |
T50S |
probably benign |
Het |
Itpr1 |
C |
T |
6: 108,387,498 (GRCm38) |
T22M |
probably damaging |
Het |
Kif26b |
G |
A |
1: 178,915,884 (GRCm38) |
E1182K |
probably damaging |
Het |
Kirrel3 |
A |
G |
9: 35,007,738 (GRCm38) |
E230G |
probably damaging |
Het |
Leng8 |
A |
G |
7: 4,139,988 (GRCm38) |
Y88C |
probably damaging |
Het |
Lypd2 |
G |
T |
15: 74,733,059 (GRCm38) |
A29E |
probably benign |
Het |
Mdn1 |
C |
T |
4: 32,723,690 (GRCm38) |
P2542L |
probably damaging |
Het |
Mical3 |
T |
C |
6: 120,959,473 (GRCm38) |
Y1364C |
probably damaging |
Het |
Mroh2b |
A |
G |
15: 4,905,572 (GRCm38) |
N163S |
probably damaging |
Het |
Mtf1 |
G |
A |
4: 124,825,079 (GRCm38) |
C295Y |
probably damaging |
Het |
Nbn |
T |
A |
4: 15,969,391 (GRCm38) |
L212Q |
probably damaging |
Het |
Obscn |
A |
T |
11: 59,069,026 (GRCm38) |
|
probably null |
Het |
Olfr1118 |
T |
A |
2: 87,308,782 (GRCm38) |
|
probably null |
Het |
Olfr1215 |
A |
G |
2: 89,002,091 (GRCm38) |
S66P |
probably damaging |
Het |
Peli1 |
A |
G |
11: 21,148,389 (GRCm38) |
T375A |
probably damaging |
Het |
Picalm |
T |
C |
7: 90,207,595 (GRCm38) |
*611Q |
probably null |
Het |
Plch1 |
G |
T |
3: 63,701,973 (GRCm38) |
Q938K |
possibly damaging |
Het |
Plxnb2 |
A |
G |
15: 89,159,593 (GRCm38) |
V1352A |
possibly damaging |
Het |
Pmepa1 |
G |
A |
2: 173,228,322 (GRCm38) |
R147W |
probably damaging |
Het |
Prdm16 |
T |
G |
4: 154,345,391 (GRCm38) |
K373Q |
probably damaging |
Het |
Qk |
T |
G |
17: 10,239,035 (GRCm38) |
E135A |
probably damaging |
Het |
Rad50 |
T |
C |
11: 53,684,246 (GRCm38) |
K556E |
probably benign |
Het |
Scara5 |
CG |
C |
14: 65,759,662 (GRCm38) |
|
probably null |
Het |
Sin3a |
T |
A |
9: 57,110,800 (GRCm38) |
D834E |
possibly damaging |
Het |
Smg8 |
G |
A |
11: 87,080,260 (GRCm38) |
S895L |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,979,390 (GRCm38) |
I1944M |
probably benign |
Het |
Stam2 |
G |
A |
2: 52,736,293 (GRCm38) |
|
probably benign |
Het |
Tmprss7 |
A |
T |
16: 45,660,889 (GRCm38) |
W645R |
probably damaging |
Het |
Tns1 |
T |
C |
1: 73,941,017 (GRCm38) |
M1111V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,811,243 (GRCm38) |
L5176Q |
possibly damaging |
Het |
Ttn |
A |
C |
2: 76,778,382 (GRCm38) |
D17763E |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,397,528 (GRCm38) |
|
probably benign |
Het |
Usp31 |
T |
C |
7: 121,661,365 (GRCm38) |
H637R |
probably damaging |
Het |
Vps50 |
A |
C |
6: 3,567,739 (GRCm38) |
E545A |
possibly damaging |
Het |
Wdfy3 |
G |
T |
5: 101,872,858 (GRCm38) |
L2527M |
probably damaging |
Het |
Wfdc2 |
T |
C |
2: 164,563,434 (GRCm38) |
V85A |
possibly damaging |
Het |
|
Other mutations in Lpo |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01483:Lpo
|
APN |
11 |
87,821,138 (GRCm38) |
missense |
probably benign |
0.43 |
IGL01833:Lpo
|
APN |
11 |
87,807,333 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL02413:Lpo
|
APN |
11 |
87,806,906 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL02706:Lpo
|
APN |
11 |
87,817,773 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02865:Lpo
|
APN |
11 |
87,806,977 (GRCm38) |
missense |
possibly damaging |
0.80 |
IGL02939:Lpo
|
APN |
11 |
87,815,178 (GRCm38) |
missense |
possibly damaging |
0.85 |
R1072:Lpo
|
UTSW |
11 |
87,818,434 (GRCm38) |
missense |
probably damaging |
1.00 |
R1169:Lpo
|
UTSW |
11 |
87,817,317 (GRCm38) |
missense |
possibly damaging |
0.58 |
R1667:Lpo
|
UTSW |
11 |
87,807,241 (GRCm38) |
unclassified |
probably benign |
|
R1719:Lpo
|
UTSW |
11 |
87,809,192 (GRCm38) |
splice site |
probably null |
|
R2133:Lpo
|
UTSW |
11 |
87,821,130 (GRCm38) |
missense |
probably benign |
0.17 |
R2871:Lpo
|
UTSW |
11 |
87,816,524 (GRCm38) |
missense |
possibly damaging |
0.51 |
R2871:Lpo
|
UTSW |
11 |
87,816,524 (GRCm38) |
missense |
possibly damaging |
0.51 |
R4382:Lpo
|
UTSW |
11 |
87,822,201 (GRCm38) |
missense |
probably benign |
0.14 |
R4657:Lpo
|
UTSW |
11 |
87,814,347 (GRCm38) |
missense |
probably damaging |
1.00 |
R4936:Lpo
|
UTSW |
11 |
87,810,340 (GRCm38) |
missense |
probably benign |
0.02 |
R4969:Lpo
|
UTSW |
11 |
87,806,925 (GRCm38) |
missense |
probably benign |
0.09 |
R5536:Lpo
|
UTSW |
11 |
87,816,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R6246:Lpo
|
UTSW |
11 |
87,822,232 (GRCm38) |
missense |
unknown |
|
R6556:Lpo
|
UTSW |
11 |
87,817,763 (GRCm38) |
nonsense |
probably null |
|
R6817:Lpo
|
UTSW |
11 |
87,809,241 (GRCm38) |
missense |
probably benign |
|
R7024:Lpo
|
UTSW |
11 |
87,816,443 (GRCm38) |
missense |
probably damaging |
1.00 |
R7203:Lpo
|
UTSW |
11 |
87,809,251 (GRCm38) |
missense |
possibly damaging |
0.75 |
R7206:Lpo
|
UTSW |
11 |
87,807,423 (GRCm38) |
missense |
probably damaging |
1.00 |
R8355:Lpo
|
UTSW |
11 |
87,814,288 (GRCm38) |
missense |
probably damaging |
1.00 |
R8455:Lpo
|
UTSW |
11 |
87,814,288 (GRCm38) |
missense |
probably damaging |
1.00 |
R8693:Lpo
|
UTSW |
11 |
87,809,240 (GRCm38) |
missense |
probably benign |
0.04 |
R8848:Lpo
|
UTSW |
11 |
87,817,777 (GRCm38) |
missense |
probably benign |
0.00 |
R8891:Lpo
|
UTSW |
11 |
87,807,022 (GRCm38) |
missense |
probably benign |
0.08 |
R8989:Lpo
|
UTSW |
11 |
87,817,834 (GRCm38) |
missense |
probably benign |
0.00 |
RF010:Lpo
|
UTSW |
11 |
87,821,102 (GRCm38) |
missense |
probably benign |
0.00 |
|