Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310079G19Rik |
A |
G |
16: 88,424,273 (GRCm39) |
C73R |
probably damaging |
Het |
Ambn |
C |
A |
5: 88,613,201 (GRCm39) |
|
probably benign |
Het |
Ankrd34a |
T |
C |
3: 96,506,247 (GRCm39) |
F484L |
possibly damaging |
Het |
Bcl11a |
A |
G |
11: 24,114,568 (GRCm39) |
K637R |
probably damaging |
Het |
Cenpe |
T |
C |
3: 134,962,337 (GRCm39) |
S1968P |
possibly damaging |
Het |
Cfap61 |
T |
C |
2: 145,792,714 (GRCm39) |
I52T |
probably damaging |
Het |
Cit |
A |
T |
5: 115,997,400 (GRCm39) |
M128L |
probably benign |
Het |
Cnga1 |
G |
T |
5: 72,762,126 (GRCm39) |
L463I |
probably damaging |
Het |
Dnah11 |
C |
T |
12: 118,094,448 (GRCm39) |
|
probably benign |
Het |
Elovl4 |
ACT |
A |
9: 83,667,201 (GRCm39) |
|
probably null |
Het |
Ep400 |
A |
G |
5: 110,839,515 (GRCm39) |
I1853T |
unknown |
Het |
Flg2 |
C |
T |
3: 93,109,730 (GRCm39) |
S586L |
unknown |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably benign |
Het |
Gm21886 |
G |
T |
18: 80,132,649 (GRCm39) |
Q170K |
possibly damaging |
Het |
Gm5819 |
A |
G |
18: 8,694,429 (GRCm39) |
E118G |
probably damaging |
Het |
Gm9376 |
T |
C |
14: 118,504,727 (GRCm39) |
V53A |
probably benign |
Het |
H2-T3 |
T |
C |
17: 36,500,574 (GRCm39) |
T90A |
probably damaging |
Het |
Hif1an |
A |
G |
19: 44,557,847 (GRCm39) |
D243G |
probably damaging |
Het |
Hmgcs2 |
C |
T |
3: 98,206,428 (GRCm39) |
|
probably benign |
Het |
Ighv1-72 |
A |
T |
12: 115,721,636 (GRCm39) |
S107T |
probably damaging |
Het |
Jak1 |
G |
A |
4: 101,013,687 (GRCm39) |
H1014Y |
probably benign |
Het |
Klrb1c |
T |
C |
6: 128,757,306 (GRCm39) |
D253G |
probably damaging |
Het |
Lpin1 |
G |
A |
12: 16,614,569 (GRCm39) |
T404M |
probably damaging |
Het |
Map3k9 |
A |
T |
12: 81,790,565 (GRCm39) |
|
probably benign |
Het |
Mtrex |
A |
T |
13: 113,039,926 (GRCm39) |
|
probably benign |
Het |
Myl12a |
G |
T |
17: 71,301,631 (GRCm39) |
H165Q |
possibly damaging |
Het |
Or6c38 |
A |
G |
10: 128,929,165 (GRCm39) |
F226S |
possibly damaging |
Het |
Pdgfrb |
T |
A |
18: 61,205,738 (GRCm39) |
S575T |
probably damaging |
Het |
Phldb2 |
T |
C |
16: 45,569,118 (GRCm39) |
Y1247C |
probably damaging |
Het |
Pinlyp |
T |
A |
7: 24,241,260 (GRCm39) |
T181S |
probably benign |
Het |
Pkn2 |
A |
G |
3: 142,499,741 (GRCm39) |
V928A |
possibly damaging |
Het |
Skint5 |
C |
T |
4: 113,636,237 (GRCm39) |
|
probably benign |
Het |
Slc24a1 |
A |
G |
9: 64,855,579 (GRCm39) |
Y443H |
unknown |
Het |
Sp8 |
G |
T |
12: 118,812,750 (GRCm39) |
V202L |
possibly damaging |
Het |
Svil |
A |
G |
18: 5,090,855 (GRCm39) |
N915S |
probably damaging |
Het |
Syncrip |
A |
C |
9: 88,358,992 (GRCm39) |
D172E |
probably damaging |
Het |
Tex26 |
T |
C |
5: 149,369,316 (GRCm39) |
I48T |
probably damaging |
Het |
Trpm6 |
A |
C |
19: 18,853,403 (GRCm39) |
I1808L |
possibly damaging |
Het |
Uba2 |
T |
C |
7: 33,854,071 (GRCm39) |
|
probably null |
Het |
Vwa8 |
T |
A |
14: 79,339,762 (GRCm39) |
|
probably benign |
Het |
Wfs1 |
C |
A |
5: 37,125,968 (GRCm39) |
V308L |
probably benign |
Het |
Wrn |
T |
A |
8: 33,731,048 (GRCm39) |
R1095W |
probably damaging |
Het |
Zfp808 |
T |
A |
13: 62,319,717 (GRCm39) |
N315K |
probably damaging |
Het |
|
Other mutations in Acot10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01306:Acot10
|
APN |
15 |
20,666,051 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01610:Acot10
|
APN |
15 |
20,665,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02457:Acot10
|
APN |
15 |
20,666,229 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02587:Acot10
|
APN |
15 |
20,665,883 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02951:Acot10
|
APN |
15 |
20,665,868 (GRCm39) |
missense |
probably benign |
0.36 |
ANU23:Acot10
|
UTSW |
15 |
20,666,051 (GRCm39) |
missense |
probably benign |
0.11 |
PIT4151001:Acot10
|
UTSW |
15 |
20,666,684 (GRCm39) |
missense |
probably damaging |
0.98 |
R0026:Acot10
|
UTSW |
15 |
20,666,322 (GRCm39) |
missense |
probably benign |
0.10 |
R0026:Acot10
|
UTSW |
15 |
20,666,322 (GRCm39) |
missense |
probably benign |
0.10 |
R0462:Acot10
|
UTSW |
15 |
20,666,712 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1312:Acot10
|
UTSW |
15 |
20,666,585 (GRCm39) |
missense |
probably benign |
0.00 |
R1495:Acot10
|
UTSW |
15 |
20,665,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R2128:Acot10
|
UTSW |
15 |
20,666,712 (GRCm39) |
missense |
probably benign |
0.00 |
R4110:Acot10
|
UTSW |
15 |
20,666,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4111:Acot10
|
UTSW |
15 |
20,666,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4464:Acot10
|
UTSW |
15 |
20,665,830 (GRCm39) |
nonsense |
probably null |
|
R4668:Acot10
|
UTSW |
15 |
20,666,028 (GRCm39) |
missense |
probably benign |
|
R4933:Acot10
|
UTSW |
15 |
20,666,416 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5255:Acot10
|
UTSW |
15 |
20,666,018 (GRCm39) |
missense |
probably benign |
0.01 |
R5885:Acot10
|
UTSW |
15 |
20,666,190 (GRCm39) |
missense |
probably benign |
0.01 |
R6190:Acot10
|
UTSW |
15 |
20,665,871 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6301:Acot10
|
UTSW |
15 |
20,666,348 (GRCm39) |
missense |
probably benign |
0.05 |
R6805:Acot10
|
UTSW |
15 |
20,665,452 (GRCm39) |
missense |
probably benign |
0.42 |
R7334:Acot10
|
UTSW |
15 |
20,665,629 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7601:Acot10
|
UTSW |
15 |
20,665,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R8400:Acot10
|
UTSW |
15 |
20,666,258 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9195:Acot10
|
UTSW |
15 |
20,665,517 (GRCm39) |
missense |
probably damaging |
1.00 |
|