Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
G |
11: 109,837,081 (GRCm39) |
V1138A |
possibly damaging |
Het |
Adgrv1 |
A |
T |
13: 81,567,594 (GRCm39) |
I5193K |
probably benign |
Het |
Adnp |
A |
T |
2: 168,026,743 (GRCm39) |
I184N |
probably damaging |
Het |
Ahnak |
T |
G |
19: 8,985,262 (GRCm39) |
V2182G |
probably benign |
Het |
Aif1l |
T |
A |
2: 31,859,763 (GRCm39) |
F94L |
probably damaging |
Het |
Aspm |
G |
A |
1: 139,385,838 (GRCm39) |
G494D |
probably benign |
Het |
Atic |
T |
A |
1: 71,617,738 (GRCm39) |
S563T |
probably benign |
Het |
Bahcc1 |
A |
T |
11: 120,165,923 (GRCm39) |
I1060F |
probably benign |
Het |
Cd27 |
A |
G |
6: 125,210,281 (GRCm39) |
Y189H |
probably damaging |
Het |
Dnm2 |
C |
A |
9: 21,417,669 (GRCm39) |
|
probably benign |
Het |
Exo1 |
A |
G |
1: 175,721,395 (GRCm39) |
T345A |
probably benign |
Het |
Fbf1 |
T |
C |
11: 116,052,299 (GRCm39) |
H53R |
possibly damaging |
Het |
Fbf1 |
A |
G |
11: 116,054,179 (GRCm39) |
I29T |
probably damaging |
Het |
Gm14399 |
G |
A |
2: 174,973,303 (GRCm39) |
R151* |
probably null |
Het |
Gsdma |
T |
A |
11: 98,557,045 (GRCm39) |
Y53* |
probably null |
Het |
Hid1 |
A |
T |
11: 115,249,601 (GRCm39) |
L208Q |
probably damaging |
Het |
Kif4-ps |
A |
G |
12: 101,112,312 (GRCm39) |
E147G |
probably damaging |
Het |
Kif7 |
A |
T |
7: 79,360,640 (GRCm39) |
V245D |
probably benign |
Het |
Klhdc4 |
A |
G |
8: 122,524,794 (GRCm39) |
V378A |
probably benign |
Het |
Lrfn2 |
A |
G |
17: 49,378,188 (GRCm39) |
E423G |
possibly damaging |
Het |
Lrp4 |
T |
A |
2: 91,332,299 (GRCm39) |
N1665K |
probably benign |
Het |
Mast3 |
C |
A |
8: 71,232,251 (GRCm39) |
R1242L |
probably benign |
Het |
Mon1b |
T |
C |
8: 114,365,779 (GRCm39) |
M369T |
possibly damaging |
Het |
Mta3 |
A |
G |
17: 84,070,417 (GRCm39) |
I193V |
probably damaging |
Het |
Narf |
G |
T |
11: 121,137,764 (GRCm39) |
E224* |
probably null |
Het |
Nedd4l |
G |
A |
18: 65,342,790 (GRCm39) |
V909I |
possibly damaging |
Het |
Nmnat3 |
T |
A |
9: 98,292,276 (GRCm39) |
Y108N |
probably damaging |
Het |
Npr2 |
A |
T |
4: 43,643,378 (GRCm39) |
Y534F |
probably benign |
Het |
Obox5 |
A |
T |
7: 15,492,713 (GRCm39) |
M223L |
probably benign |
Het |
Optc |
A |
T |
1: 133,832,819 (GRCm39) |
S94T |
probably benign |
Het |
Or10al5 |
T |
A |
17: 38,063,271 (GRCm39) |
C175* |
probably null |
Het |
Or1l4 |
A |
G |
2: 37,091,285 (GRCm39) |
T11A |
probably benign |
Het |
Or5d47 |
A |
T |
2: 87,804,066 (GRCm39) |
N314K |
probably benign |
Het |
Or6c206 |
A |
T |
10: 129,097,093 (GRCm39) |
K88* |
probably null |
Het |
Or8w1 |
T |
C |
2: 87,466,025 (GRCm39) |
D22G |
probably benign |
Het |
Rbm27 |
T |
C |
18: 42,425,177 (GRCm39) |
|
probably benign |
Het |
Stab2 |
A |
G |
10: 86,702,572 (GRCm39) |
L423P |
probably damaging |
Het |
Sun5 |
A |
G |
2: 153,709,468 (GRCm39) |
V74A |
probably benign |
Het |
Tanc2 |
A |
G |
11: 105,689,516 (GRCm39) |
Y226C |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,111,152 (GRCm39) |
D585G |
possibly damaging |
Het |
Tmt1a3 |
A |
T |
15: 100,232,961 (GRCm39) |
M51L |
probably benign |
Het |
Tnrc6c |
A |
G |
11: 117,613,950 (GRCm39) |
T863A |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,542,489 (GRCm39) |
G3352S |
probably benign |
Het |
Wt1 |
G |
A |
2: 104,993,773 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
C |
T |
18: 44,966,240 (GRCm39) |
L159F |
probably damaging |
Het |
Zc3h6 |
A |
G |
2: 128,859,251 (GRCm39) |
N1094S |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,347,830 (GRCm39) |
S2070P |
possibly damaging |
Het |
Zfp648 |
T |
A |
1: 154,080,304 (GRCm39) |
S154R |
probably benign |
Het |
Zfp748 |
A |
G |
13: 67,688,915 (GRCm39) |
C782R |
probably damaging |
Het |
Zfp992 |
C |
T |
4: 146,551,976 (GRCm39) |
H566Y |
probably damaging |
Het |
|
Other mutations in Spopl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Spopl
|
APN |
2 |
23,427,643 (GRCm39) |
missense |
possibly damaging |
0.88 |
P4748:Spopl
|
UTSW |
2 |
23,401,455 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4453001:Spopl
|
UTSW |
2 |
23,435,461 (GRCm39) |
missense |
probably damaging |
0.99 |
R0738:Spopl
|
UTSW |
2 |
23,427,533 (GRCm39) |
missense |
probably benign |
0.04 |
R2358:Spopl
|
UTSW |
2 |
23,427,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R3712:Spopl
|
UTSW |
2 |
23,427,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R4097:Spopl
|
UTSW |
2 |
23,401,413 (GRCm39) |
missense |
probably benign |
0.01 |
R4400:Spopl
|
UTSW |
2 |
23,407,957 (GRCm39) |
missense |
probably damaging |
0.97 |
R4421:Spopl
|
UTSW |
2 |
23,407,957 (GRCm39) |
missense |
probably damaging |
0.97 |
R4497:Spopl
|
UTSW |
2 |
23,407,957 (GRCm39) |
missense |
probably damaging |
0.97 |
R4498:Spopl
|
UTSW |
2 |
23,407,957 (GRCm39) |
missense |
probably damaging |
0.97 |
R4570:Spopl
|
UTSW |
2 |
23,427,497 (GRCm39) |
nonsense |
probably null |
|
R4702:Spopl
|
UTSW |
2 |
23,405,309 (GRCm39) |
splice site |
probably null |
|
R6919:Spopl
|
UTSW |
2 |
23,407,873 (GRCm39) |
missense |
probably benign |
0.06 |
R7387:Spopl
|
UTSW |
2 |
23,427,521 (GRCm39) |
missense |
probably benign |
|
R7921:Spopl
|
UTSW |
2 |
23,435,490 (GRCm39) |
missense |
probably benign |
|
X0067:Spopl
|
UTSW |
2 |
23,434,879 (GRCm39) |
missense |
possibly damaging |
0.94 |
|