Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
C |
T |
19: 57,056,618 (GRCm39) |
A359T |
probably damaging |
Het |
Adam34l |
A |
G |
8: 44,079,388 (GRCm39) |
F279L |
probably damaging |
Het |
Ajuba |
A |
T |
14: 54,809,226 (GRCm39) |
Y400* |
probably null |
Het |
Cckar |
T |
A |
5: 53,857,171 (GRCm39) |
D342V |
possibly damaging |
Het |
Cdc123 |
A |
G |
2: 5,803,260 (GRCm39) |
V253A |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,109,220 (GRCm39) |
D461G |
probably benign |
Het |
Chd7 |
G |
A |
4: 8,859,106 (GRCm39) |
E2399K |
probably damaging |
Het |
Cln8 |
G |
A |
8: 14,946,637 (GRCm39) |
C217Y |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,407,236 (GRCm39) |
V2119A |
possibly damaging |
Het |
Dhx33 |
T |
C |
11: 70,892,446 (GRCm39) |
S108G |
probably benign |
Het |
Dip2a |
T |
A |
10: 76,149,070 (GRCm39) |
M194L |
probably benign |
Het |
Dnah11 |
T |
C |
12: 118,031,831 (GRCm39) |
K1779R |
probably damaging |
Het |
Fads3 |
T |
G |
19: 10,033,045 (GRCm39) |
F328V |
possibly damaging |
Het |
Flad1 |
A |
G |
3: 89,313,160 (GRCm39) |
|
probably null |
Het |
Gnpat |
A |
G |
8: 125,611,752 (GRCm39) |
E513G |
probably damaging |
Het |
H2-M5 |
A |
G |
17: 37,298,732 (GRCm39) |
I238T |
probably damaging |
Het |
Hoxd12 |
G |
A |
2: 74,505,771 (GRCm39) |
R114Q |
probably damaging |
Het |
Ide |
T |
C |
19: 37,253,931 (GRCm39) |
I903V |
unknown |
Het |
Ifi209 |
T |
G |
1: 173,466,529 (GRCm39) |
D120E |
possibly damaging |
Het |
Map3k10 |
T |
C |
7: 27,367,894 (GRCm39) |
D248G |
probably damaging |
Het |
Mat2b |
C |
A |
11: 40,578,565 (GRCm39) |
G41C |
probably damaging |
Het |
Mfsd4a |
T |
C |
1: 131,968,332 (GRCm39) |
I369V |
probably benign |
Het |
Myom1 |
T |
A |
17: 71,433,093 (GRCm39) |
V1480E |
probably damaging |
Het |
Myom2 |
A |
T |
8: 15,119,490 (GRCm39) |
D127V |
probably damaging |
Het |
Olfml2b |
T |
A |
1: 170,496,635 (GRCm39) |
V422E |
probably damaging |
Het |
Pkn3 |
G |
A |
2: 29,971,116 (GRCm39) |
A228T |
probably damaging |
Het |
Rad17 |
A |
T |
13: 100,766,033 (GRCm39) |
I365K |
probably benign |
Het |
Rad17 |
A |
T |
13: 100,766,031 (GRCm39) |
S366T |
probably damaging |
Het |
Rpp14 |
G |
A |
14: 8,083,934 (GRCm38) |
G30E |
possibly damaging |
Het |
Slco1a6 |
A |
C |
6: 142,106,743 (GRCm39) |
C15G |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,988,692 (GRCm39) |
F571I |
probably benign |
Het |
Ttc27 |
T |
A |
17: 75,087,811 (GRCm39) |
C459S |
probably damaging |
Het |
Washc2 |
A |
G |
6: 116,233,637 (GRCm39) |
T888A |
probably benign |
Het |
Zcchc7 |
A |
T |
4: 44,931,318 (GRCm39) |
H490L |
possibly damaging |
Het |
|
Other mutations in Gm7535 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01663:Gm7535
|
APN |
17 |
18,131,619 (GRCm39) |
intron |
probably benign |
|
R0165:Gm7535
|
UTSW |
17 |
18,131,437 (GRCm39) |
intron |
probably benign |
|
R0335:Gm7535
|
UTSW |
17 |
18,131,374 (GRCm39) |
intron |
probably benign |
|
R1985:Gm7535
|
UTSW |
17 |
18,131,800 (GRCm39) |
intron |
probably benign |
|
R2217:Gm7535
|
UTSW |
17 |
18,131,936 (GRCm39) |
intron |
probably benign |
|
R2218:Gm7535
|
UTSW |
17 |
18,131,936 (GRCm39) |
intron |
probably benign |
|
R4464:Gm7535
|
UTSW |
17 |
18,131,924 (GRCm39) |
intron |
probably benign |
|
R4581:Gm7535
|
UTSW |
17 |
18,131,345 (GRCm39) |
intron |
probably benign |
|
R4887:Gm7535
|
UTSW |
17 |
18,131,333 (GRCm39) |
intron |
probably benign |
|
R5225:Gm7535
|
UTSW |
17 |
18,131,809 (GRCm39) |
intron |
probably benign |
|
R5305:Gm7535
|
UTSW |
17 |
18,132,061 (GRCm39) |
intron |
probably benign |
|
R5641:Gm7535
|
UTSW |
17 |
18,131,788 (GRCm39) |
intron |
probably benign |
|
R5658:Gm7535
|
UTSW |
17 |
18,131,582 (GRCm39) |
intron |
probably benign |
|
R5760:Gm7535
|
UTSW |
17 |
18,132,080 (GRCm39) |
intron |
probably benign |
|
|