Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700037C18Rik |
T |
A |
16: 3,724,146 (GRCm39) |
D130V |
probably damaging |
Het |
4930596D02Rik |
T |
C |
14: 35,533,880 (GRCm39) |
T9A |
probably benign |
Het |
Anapc1 |
C |
A |
2: 128,501,772 (GRCm39) |
A757S |
probably benign |
Het |
Bpifa6 |
A |
T |
2: 153,834,192 (GRCm39) |
D328V |
probably benign |
Het |
Cdh19 |
T |
A |
1: 110,853,616 (GRCm39) |
K275I |
probably benign |
Het |
Col18a1 |
A |
G |
10: 76,895,217 (GRCm39) |
I1148T |
possibly damaging |
Het |
Commd1 |
A |
T |
11: 22,850,017 (GRCm39) |
V222D |
probably damaging |
Het |
Crim1 |
T |
A |
17: 78,677,427 (GRCm39) |
M876K |
possibly damaging |
Het |
Dennd1b |
C |
A |
1: 139,008,992 (GRCm39) |
H232N |
probably damaging |
Het |
Dhx57 |
T |
C |
17: 80,582,268 (GRCm39) |
T393A |
probably benign |
Het |
Dnai7 |
T |
C |
6: 145,123,090 (GRCm39) |
Y592C |
probably damaging |
Het |
Gabrb2 |
G |
T |
11: 42,482,721 (GRCm39) |
R193L |
probably benign |
Het |
Gm6483 |
C |
T |
8: 19,741,629 (GRCm39) |
P55S |
probably damaging |
Het |
Hsp90ab1 |
T |
C |
17: 45,879,364 (GRCm39) |
Y619C |
possibly damaging |
Het |
Kctd19 |
A |
G |
8: 106,123,006 (GRCm39) |
I136T |
probably damaging |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or2w6 |
A |
C |
13: 21,843,170 (GRCm39) |
F108V |
probably benign |
Het |
Sel1l |
T |
C |
12: 91,781,789 (GRCm39) |
Y532C |
probably damaging |
Het |
Sirpb1a |
A |
G |
3: 15,475,469 (GRCm39) |
|
probably null |
Het |
Ush2a |
C |
T |
1: 187,995,466 (GRCm39) |
T79M |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,244,690 (GRCm39) |
V1215A |
probably damaging |
Het |
Vdac3-ps1 |
T |
C |
13: 18,205,379 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r75 |
T |
C |
7: 85,814,348 (GRCm39) |
T382A |
probably benign |
Het |
Vps53 |
T |
C |
11: 75,937,949 (GRCm39) |
Y728C |
probably benign |
Het |
|
Other mutations in Gm5828 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01143:Gm5828
|
APN |
1 |
16,840,172 (GRCm39) |
exon |
noncoding transcript |
|
IGL01751:Gm5828
|
APN |
1 |
16,840,208 (GRCm39) |
exon |
noncoding transcript |
|
IGL02400:Gm5828
|
APN |
1 |
16,840,042 (GRCm39) |
exon |
noncoding transcript |
|
IGL02480:Gm5828
|
APN |
1 |
16,839,766 (GRCm39) |
exon |
noncoding transcript |
|
R0143:Gm5828
|
UTSW |
1 |
16,838,579 (GRCm39) |
exon |
noncoding transcript |
|
R1245:Gm5828
|
UTSW |
1 |
16,839,353 (GRCm39) |
exon |
noncoding transcript |
|
R1405:Gm5828
|
UTSW |
1 |
16,839,768 (GRCm39) |
exon |
noncoding transcript |
|
R1514:Gm5828
|
UTSW |
1 |
16,839,583 (GRCm39) |
exon |
noncoding transcript |
|
R1644:Gm5828
|
UTSW |
1 |
16,839,485 (GRCm39) |
exon |
noncoding transcript |
|
R2118:Gm5828
|
UTSW |
1 |
16,840,199 (GRCm39) |
exon |
noncoding transcript |
|
R2290:Gm5828
|
UTSW |
1 |
16,838,568 (GRCm39) |
exon |
noncoding transcript |
|
R3428:Gm5828
|
UTSW |
1 |
16,838,838 (GRCm39) |
exon |
noncoding transcript |
|
R3962:Gm5828
|
UTSW |
1 |
16,838,868 (GRCm39) |
exon |
noncoding transcript |
|
R4657:Gm5828
|
UTSW |
1 |
16,839,642 (GRCm39) |
exon |
noncoding transcript |
|
R5067:Gm5828
|
UTSW |
1 |
16,839,516 (GRCm39) |
exon |
noncoding transcript |
|
|