Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12b |
G |
A |
12: 70,215,822 (GRCm39) |
G88S |
probably damaging |
Het |
Akap12 |
G |
T |
10: 4,303,273 (GRCm39) |
A28S |
probably benign |
Het |
Anks1 |
C |
A |
17: 28,205,227 (GRCm39) |
T262K |
probably damaging |
Het |
Arfgap3 |
A |
G |
15: 83,197,710 (GRCm39) |
Y349H |
possibly damaging |
Het |
Cacna1g |
G |
A |
11: 94,357,054 (GRCm39) |
|
probably benign |
Het |
Camsap2 |
T |
A |
1: 136,225,528 (GRCm39) |
E199D |
probably benign |
Het |
Ccdc13 |
A |
T |
9: 121,656,429 (GRCm39) |
M128K |
probably benign |
Het |
Ccdc38 |
T |
C |
10: 93,405,797 (GRCm39) |
|
probably null |
Het |
Cep95 |
G |
A |
11: 106,704,641 (GRCm39) |
V499I |
probably benign |
Het |
Cpne6 |
G |
C |
14: 55,749,459 (GRCm39) |
M6I |
probably benign |
Het |
Cpne6 |
A |
T |
14: 55,752,706 (GRCm39) |
I299F |
probably damaging |
Het |
Cse1l |
T |
A |
2: 166,769,428 (GRCm39) |
Y278* |
probably null |
Het |
Dip2c |
A |
G |
13: 9,625,179 (GRCm39) |
N558D |
possibly damaging |
Het |
Edar |
A |
T |
10: 58,464,460 (GRCm39) |
C60S |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,201,698 (GRCm39) |
N459D |
probably benign |
Het |
Fbxw8 |
C |
T |
5: 118,251,785 (GRCm39) |
V243M |
possibly damaging |
Het |
Fem1b |
G |
A |
9: 62,704,810 (GRCm39) |
A150V |
possibly damaging |
Het |
Gm5422 |
A |
T |
10: 31,125,432 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch3 |
CAGGAGGAGGAGGAGGAG |
CAGGAGGAGGAGGAG |
4: 133,305,613 (GRCm39) |
|
probably benign |
Het |
Grin2c |
T |
C |
11: 115,147,020 (GRCm39) |
T392A |
probably benign |
Het |
Idh3a |
T |
A |
9: 54,493,829 (GRCm39) |
|
probably null |
Het |
Itpk1 |
T |
C |
12: 102,572,362 (GRCm39) |
E117G |
probably damaging |
Het |
Kif12 |
G |
T |
4: 63,084,121 (GRCm39) |
P627Q |
probably damaging |
Het |
Krtap15-1 |
T |
A |
16: 88,626,255 (GRCm39) |
F88L |
probably benign |
Het |
Mcm7 |
C |
T |
5: 138,168,653 (GRCm39) |
V13I |
probably benign |
Het |
Mlh1 |
T |
C |
9: 111,081,980 (GRCm39) |
N248D |
possibly damaging |
Het |
Or2i1 |
T |
C |
17: 37,507,833 (GRCm39) |
N342S |
probably benign |
Het |
Or4k15 |
A |
G |
14: 50,364,039 (GRCm39) |
N2D |
probably benign |
Het |
Or52z12 |
T |
C |
7: 103,233,900 (GRCm39) |
Y224H |
probably damaging |
Het |
Per2 |
T |
C |
1: 91,376,555 (GRCm39) |
H106R |
probably damaging |
Het |
Pfkl |
T |
A |
10: 77,827,229 (GRCm39) |
T486S |
probably benign |
Het |
Prkdc |
T |
C |
16: 15,485,595 (GRCm39) |
V474A |
possibly damaging |
Het |
Scamp4 |
C |
A |
10: 80,445,256 (GRCm39) |
Q34K |
probably damaging |
Het |
Serpinb3b |
A |
G |
1: 107,082,395 (GRCm39) |
Y290H |
probably damaging |
Het |
Sft2d2 |
G |
T |
1: 165,011,564 (GRCm39) |
A110E |
probably benign |
Het |
Siglecf |
T |
A |
7: 43,001,377 (GRCm39) |
L115* |
probably null |
Het |
Slc6a11 |
C |
T |
6: 114,111,626 (GRCm39) |
T103M |
probably damaging |
Het |
Slco1a1 |
T |
A |
6: 141,892,313 (GRCm39) |
K18* |
probably null |
Het |
Spata1 |
A |
T |
3: 146,193,154 (GRCm39) |
Y112* |
probably null |
Het |
Tbc1d32 |
G |
A |
10: 56,056,620 (GRCm39) |
T440I |
probably benign |
Het |
Vmn1r159 |
A |
G |
7: 22,542,588 (GRCm39) |
V148A |
probably damaging |
Het |
Wnt16 |
C |
T |
6: 22,297,934 (GRCm39) |
R267C |
probably damaging |
Het |
Xylt1 |
A |
C |
7: 117,148,125 (GRCm39) |
S230R |
probably benign |
Het |
Zfp334 |
T |
C |
2: 165,223,017 (GRCm39) |
H342R |
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 |
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 |
R3779:Acot10
|
UTSW |
15 |
20,665,628 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|