Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg3 |
T |
C |
5: 105,117,318 (GRCm39) |
D204G |
possibly damaging |
Het |
Acox3 |
C |
A |
5: 35,765,710 (GRCm39) |
L588I |
probably damaging |
Het |
Adamts9 |
G |
T |
6: 92,857,828 (GRCm39) |
L849I |
probably benign |
Het |
Alkbh3 |
T |
G |
2: 93,826,692 (GRCm39) |
T170P |
probably damaging |
Het |
Anks1b |
A |
T |
10: 90,757,240 (GRCm39) |
H300L |
probably damaging |
Het |
Arhgap29 |
T |
C |
3: 121,786,173 (GRCm39) |
|
probably benign |
Het |
Brd8dc |
A |
G |
18: 34,726,068 (GRCm39) |
S112P |
probably benign |
Het |
Cd86 |
C |
T |
16: 36,438,847 (GRCm39) |
G181D |
probably benign |
Het |
Cep68 |
A |
T |
11: 20,190,096 (GRCm39) |
H305Q |
possibly damaging |
Het |
Cimip4 |
A |
G |
15: 78,262,736 (GRCm39) |
M245T |
possibly damaging |
Het |
Clptm1l |
A |
T |
13: 73,755,879 (GRCm39) |
D165V |
probably benign |
Het |
Dctn1 |
T |
C |
6: 83,159,704 (GRCm39) |
Y61H |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,657,205 (GRCm39) |
M857K |
possibly damaging |
Het |
Gpr158 |
A |
G |
2: 21,831,407 (GRCm39) |
M836V |
probably benign |
Het |
Gria1 |
G |
T |
11: 57,180,314 (GRCm39) |
A755S |
possibly damaging |
Het |
Helb |
G |
A |
10: 119,925,617 (GRCm39) |
T920M |
probably damaging |
Het |
Hr |
T |
C |
14: 70,797,306 (GRCm39) |
|
probably benign |
Het |
Igf2bp1 |
A |
G |
11: 95,864,994 (GRCm39) |
S152P |
probably damaging |
Het |
Iqsec1 |
T |
C |
6: 90,646,327 (GRCm39) |
Y784C |
probably damaging |
Het |
Ldah |
T |
A |
12: 8,333,935 (GRCm39) |
C275* |
probably null |
Het |
Lpin3 |
T |
C |
2: 160,738,707 (GRCm39) |
S220P |
probably damaging |
Het |
Med23 |
T |
C |
10: 24,774,473 (GRCm39) |
|
probably null |
Het |
Mllt1 |
T |
C |
17: 57,206,806 (GRCm39) |
D346G |
probably benign |
Het |
Myef2 |
A |
C |
2: 124,942,345 (GRCm39) |
|
probably null |
Het |
Myh2 |
A |
G |
11: 67,079,991 (GRCm39) |
S1095G |
probably benign |
Het |
Nav1 |
A |
G |
1: 135,512,651 (GRCm39) |
|
silent |
Het |
Or10a3m |
A |
G |
7: 108,312,949 (GRCm39) |
M118V |
possibly damaging |
Het |
Piwil2 |
G |
A |
14: 70,628,935 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,441,896 (GRCm39) |
F3612I |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,264,764 (GRCm39) |
S764N |
probably damaging |
Het |
S100pbp |
A |
T |
4: 129,075,644 (GRCm39) |
|
probably null |
Het |
Scnn1b |
T |
C |
7: 121,516,746 (GRCm39) |
I495T |
probably damaging |
Het |
Sgo2b |
A |
C |
8: 64,379,571 (GRCm39) |
V1087G |
probably damaging |
Het |
Sil1 |
A |
T |
18: 35,481,786 (GRCm39) |
V91E |
probably damaging |
Het |
Slc5a4b |
A |
G |
10: 75,946,685 (GRCm39) |
I29T |
possibly damaging |
Het |
Spink5 |
A |
T |
18: 44,148,661 (GRCm39) |
N908I |
probably benign |
Het |
Svopl |
A |
C |
6: 37,993,978 (GRCm39) |
I351S |
probably damaging |
Het |
Syngr3 |
A |
G |
17: 24,905,302 (GRCm39) |
V198A |
probably benign |
Het |
Tbck |
C |
A |
3: 132,456,953 (GRCm39) |
Y622* |
probably null |
Het |
Tkt |
T |
A |
14: 30,280,737 (GRCm39) |
M56K |
probably damaging |
Het |
Trip10 |
T |
C |
17: 57,570,135 (GRCm39) |
V544A |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,409,995 (GRCm39) |
E195G |
probably damaging |
Het |
Vmn2r69 |
G |
A |
7: 85,059,014 (GRCm39) |
P516S |
probably damaging |
Het |
Vmn2r74 |
T |
C |
7: 85,606,581 (GRCm39) |
N255S |
probably benign |
Het |
Xpo4 |
T |
C |
14: 57,827,545 (GRCm39) |
T884A |
probably benign |
Het |
Zdhhc2 |
A |
G |
8: 40,915,155 (GRCm39) |
N167S |
probably damaging |
Het |
|
Other mutations in 9930111J21Rik1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:9930111J21Rik1
|
APN |
11 |
48,839,039 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02189:9930111J21Rik1
|
APN |
11 |
48,838,248 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03172:9930111J21Rik1
|
APN |
11 |
48,839,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03334:9930111J21Rik1
|
APN |
11 |
48,838,302 (GRCm39) |
missense |
probably benign |
0.09 |
R0502:9930111J21Rik1
|
UTSW |
11 |
48,838,322 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0503:9930111J21Rik1
|
UTSW |
11 |
48,838,322 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2023:9930111J21Rik1
|
UTSW |
11 |
48,839,247 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3704:9930111J21Rik1
|
UTSW |
11 |
48,838,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3705:9930111J21Rik1
|
UTSW |
11 |
48,838,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3714:9930111J21Rik1
|
UTSW |
11 |
48,838,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3715:9930111J21Rik1
|
UTSW |
11 |
48,838,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3961:9930111J21Rik1
|
UTSW |
11 |
48,838,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3962:9930111J21Rik1
|
UTSW |
11 |
48,838,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4867:9930111J21Rik1
|
UTSW |
11 |
48,839,375 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5033:9930111J21Rik1
|
UTSW |
11 |
48,838,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:9930111J21Rik1
|
UTSW |
11 |
48,839,352 (GRCm39) |
missense |
probably benign |
0.06 |
R6567:9930111J21Rik1
|
UTSW |
11 |
48,838,950 (GRCm39) |
missense |
probably benign |
0.26 |
R6774:9930111J21Rik1
|
UTSW |
11 |
48,838,143 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7730:9930111J21Rik1
|
UTSW |
11 |
48,838,703 (GRCm39) |
missense |
probably benign |
0.19 |
R7863:9930111J21Rik1
|
UTSW |
11 |
48,838,101 (GRCm39) |
missense |
probably benign |
0.18 |
R8408:9930111J21Rik1
|
UTSW |
11 |
48,838,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R9381:9930111J21Rik1
|
UTSW |
11 |
48,839,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9400:9930111J21Rik1
|
UTSW |
11 |
48,839,244 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9493:9930111J21Rik1
|
UTSW |
11 |
48,838,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R9560:9930111J21Rik1
|
UTSW |
11 |
48,839,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R9574:9930111J21Rik1
|
UTSW |
11 |
48,838,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R9687:9930111J21Rik1
|
UTSW |
11 |
48,839,249 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:9930111J21Rik1
|
UTSW |
11 |
48,838,869 (GRCm39) |
missense |
probably damaging |
1.00 |
|