Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9230009I02Rik |
T |
C |
11: 50,982,645 (GRCm39) |
|
noncoding transcript |
Het |
Aip |
A |
G |
19: 4,171,397 (GRCm39) |
I13T |
probably damaging |
Het |
Cacna2d1 |
C |
T |
5: 16,417,895 (GRCm39) |
P140S |
probably benign |
Het |
Cald1 |
A |
G |
6: 34,730,403 (GRCm39) |
D40G |
probably damaging |
Het |
Cep250 |
T |
A |
2: 155,825,279 (GRCm39) |
V1052E |
possibly damaging |
Het |
Chd1 |
A |
G |
17: 15,962,435 (GRCm39) |
N731D |
probably damaging |
Het |
Chml |
C |
T |
1: 175,515,166 (GRCm39) |
V252I |
probably benign |
Het |
Cog8 |
T |
C |
8: 107,783,010 (GRCm39) |
Y93C |
probably damaging |
Het |
Creld1 |
G |
A |
6: 113,469,794 (GRCm39) |
A399T |
probably damaging |
Het |
Cyp2a4 |
T |
A |
7: 26,007,133 (GRCm39) |
V80E |
probably damaging |
Het |
Cyp2c37 |
T |
A |
19: 39,984,277 (GRCm39) |
L255* |
probably null |
Het |
Cyp2d12 |
C |
A |
15: 82,439,545 (GRCm39) |
|
probably benign |
Het |
Dimt1 |
A |
G |
13: 107,089,963 (GRCm39) |
I229V |
probably benign |
Het |
Dsc1 |
G |
A |
18: 20,230,282 (GRCm39) |
T341I |
probably damaging |
Het |
Ercc3 |
T |
A |
18: 32,390,411 (GRCm39) |
F567I |
probably damaging |
Het |
Espl1 |
C |
A |
15: 102,214,097 (GRCm39) |
|
probably benign |
Het |
Fcrl2 |
T |
C |
3: 87,166,939 (GRCm39) |
D18G |
probably damaging |
Het |
Fnip1 |
T |
A |
11: 54,381,738 (GRCm39) |
S296R |
possibly damaging |
Het |
Fzd5 |
C |
A |
1: 64,775,105 (GRCm39) |
A219S |
possibly damaging |
Het |
Gbp7 |
A |
G |
3: 142,247,108 (GRCm39) |
|
probably benign |
Het |
Gm3298 |
T |
C |
14: 5,018,731 (GRCm38) |
L162S |
probably damaging |
Het |
Hspa1l |
A |
G |
17: 35,196,111 (GRCm39) |
E50G |
probably damaging |
Het |
Ipo9 |
T |
C |
1: 135,348,093 (GRCm39) |
|
probably null |
Het |
Kazn |
A |
G |
4: 141,878,195 (GRCm39) |
L185P |
probably damaging |
Het |
Kcnh8 |
T |
C |
17: 53,141,635 (GRCm39) |
S293P |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,202,539 (GRCm39) |
T1191A |
probably damaging |
Het |
Mnat1 |
A |
G |
12: 73,228,705 (GRCm39) |
|
probably benign |
Het |
Msx2 |
C |
T |
13: 53,622,638 (GRCm39) |
|
probably benign |
Het |
Ndufs2 |
T |
G |
1: 171,064,798 (GRCm39) |
I317L |
probably benign |
Het |
Nms |
T |
C |
1: 38,981,006 (GRCm39) |
|
probably benign |
Het |
Pask |
A |
G |
1: 93,262,329 (GRCm39) |
V177A |
probably benign |
Het |
Poldip2 |
G |
T |
11: 78,403,133 (GRCm39) |
|
probably benign |
Het |
Prr14l |
A |
T |
5: 32,987,549 (GRCm39) |
S649T |
possibly damaging |
Het |
Slc6a18 |
T |
A |
13: 73,825,984 (GRCm39) |
N22I |
probably damaging |
Het |
Smco2 |
T |
A |
6: 146,763,208 (GRCm39) |
S228T |
probably benign |
Het |
Speer4a1 |
G |
A |
5: 26,240,902 (GRCm39) |
Q197* |
probably null |
Het |
Speg |
A |
G |
1: 75,367,734 (GRCm39) |
K641R |
probably damaging |
Het |
Strip2 |
G |
A |
6: 29,928,553 (GRCm39) |
V286M |
probably damaging |
Het |
Tnfrsf22 |
C |
T |
7: 143,197,012 (GRCm39) |
|
probably null |
Het |
Tnpo3 |
A |
G |
6: 29,589,019 (GRCm39) |
|
probably benign |
Het |
Top2b |
T |
A |
14: 16,422,695 (GRCm38) |
N1377K |
probably benign |
Het |
Trmt1 |
T |
A |
8: 85,418,005 (GRCm39) |
|
probably null |
Het |
Trpm1 |
A |
G |
7: 63,858,723 (GRCm39) |
M266V |
possibly damaging |
Het |
Vmn1r199 |
A |
G |
13: 22,567,290 (GRCm39) |
T195A |
probably benign |
Het |
Vmn2r10 |
A |
G |
5: 109,145,571 (GRCm39) |
V512A |
probably benign |
Het |
Zfp777 |
A |
G |
6: 48,021,275 (GRCm39) |
F116L |
probably benign |
Het |
Zp3r |
T |
A |
1: 130,519,188 (GRCm39) |
K253* |
probably null |
Het |
|
Other mutations in Oosp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00861:Oosp3
|
APN |
19 |
11,689,004 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02006:Oosp3
|
APN |
19 |
11,676,784 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02231:Oosp3
|
APN |
19 |
11,676,803 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02836:Oosp3
|
APN |
19 |
11,678,332 (GRCm39) |
missense |
probably benign |
0.03 |
R1669:Oosp3
|
UTSW |
19 |
11,678,378 (GRCm39) |
splice site |
probably benign |
|
R2045:Oosp3
|
UTSW |
19 |
11,676,733 (GRCm39) |
missense |
probably benign |
0.03 |
R2852:Oosp3
|
UTSW |
19 |
11,676,896 (GRCm39) |
critical splice donor site |
probably null |
|
R4820:Oosp3
|
UTSW |
19 |
11,688,997 (GRCm39) |
missense |
probably damaging |
0.97 |
R5030:Oosp3
|
UTSW |
19 |
11,678,308 (GRCm39) |
missense |
probably benign |
0.02 |
R5524:Oosp3
|
UTSW |
19 |
11,682,794 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5641:Oosp3
|
UTSW |
19 |
11,674,537 (GRCm39) |
critical splice donor site |
probably null |
|
R5933:Oosp3
|
UTSW |
19 |
11,682,753 (GRCm39) |
missense |
probably benign |
0.07 |
R7018:Oosp3
|
UTSW |
19 |
11,676,783 (GRCm39) |
missense |
probably benign |
0.00 |
R7585:Oosp3
|
UTSW |
19 |
11,678,322 (GRCm39) |
missense |
probably benign |
0.00 |
R7958:Oosp3
|
UTSW |
19 |
11,682,820 (GRCm39) |
missense |
probably benign |
0.07 |
R9238:Oosp3
|
UTSW |
19 |
11,676,753 (GRCm39) |
missense |
probably damaging |
0.97 |
R9684:Oosp3
|
UTSW |
19 |
11,682,806 (GRCm39) |
missense |
probably benign |
0.31 |
|