Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre1 |
A |
G |
17: 57,709,811 (GRCm39) |
Y156C |
unknown |
Het |
Ankrd13b |
G |
A |
11: 77,367,201 (GRCm39) |
A21V |
probably damaging |
Het |
Atf7ip |
T |
C |
6: 136,564,499 (GRCm39) |
V914A |
probably damaging |
Het |
C230029F24Rik |
AGAAAG |
A |
1: 49,350,088 (GRCm39) |
|
noncoding transcript |
Het |
Calcr |
T |
A |
6: 3,717,106 (GRCm39) |
D118V |
possibly damaging |
Het |
Cdc42bpg |
T |
C |
19: 6,371,711 (GRCm39) |
V1330A |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,720,885 (GRCm39) |
E2567G |
unknown |
Het |
Ctse |
T |
A |
1: 131,590,479 (GRCm39) |
V67D |
probably benign |
Het |
Ddx19b |
A |
T |
8: 111,737,980 (GRCm39) |
L256Q |
probably damaging |
Het |
Dipk1b |
T |
C |
2: 26,526,193 (GRCm39) |
Y376H |
probably damaging |
Het |
Fahd2a |
C |
T |
2: 127,280,486 (GRCm39) |
V156I |
probably benign |
Het |
Fam185a |
T |
A |
5: 21,630,122 (GRCm39) |
|
probably benign |
Het |
Fam234a |
A |
T |
17: 26,432,834 (GRCm39) |
L467Q |
probably damaging |
Het |
Gabra2 |
G |
A |
5: 71,165,341 (GRCm39) |
P210S |
probably benign |
Het |
Heatr3 |
T |
C |
8: 88,864,888 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
C |
7: 55,772,196 (GRCm39) |
V1125A |
probably benign |
Het |
Itga11 |
T |
A |
9: 62,639,391 (GRCm39) |
C129S |
probably damaging |
Het |
Lama2 |
A |
G |
10: 27,142,660 (GRCm39) |
L606P |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,366,835 (GRCm39) |
F1077S |
possibly damaging |
Het |
Mtmr10 |
G |
T |
7: 63,963,934 (GRCm39) |
W223L |
probably benign |
Het |
Nlgn1 |
T |
A |
3: 25,488,062 (GRCm39) |
T758S |
probably benign |
Het |
Nr4a1 |
T |
C |
15: 101,171,993 (GRCm39) |
S556P |
probably damaging |
Het |
Or4c126 |
C |
A |
2: 89,823,918 (GRCm39) |
Y60* |
probably null |
Het |
Or5p64 |
T |
C |
7: 107,855,330 (GRCm39) |
D5G |
probably benign |
Het |
Or6c201 |
T |
C |
10: 128,968,836 (GRCm39) |
N267S |
possibly damaging |
Het |
Or6c33 |
A |
T |
10: 129,853,847 (GRCm39) |
I206F |
probably damaging |
Het |
Pcdhgb8 |
G |
C |
18: 37,896,594 (GRCm39) |
D555H |
probably damaging |
Het |
Plscr5 |
T |
C |
9: 92,080,651 (GRCm39) |
S46P |
probably benign |
Het |
Ppp2r3d |
T |
C |
9: 124,424,123 (GRCm38) |
|
probably benign |
Het |
Prodh |
C |
T |
16: 17,891,504 (GRCm39) |
V480I |
probably benign |
Het |
Senp2 |
G |
T |
16: 21,865,417 (GRCm39) |
W580L |
probably damaging |
Het |
Sorcs3 |
T |
C |
19: 48,737,812 (GRCm39) |
V743A |
possibly damaging |
Het |
Sp110 |
C |
G |
1: 85,516,839 (GRCm39) |
E219D |
probably damaging |
Het |
Stab2 |
G |
T |
10: 86,714,808 (GRCm39) |
N119K |
probably damaging |
Het |
Telo2 |
T |
C |
17: 25,320,987 (GRCm39) |
T743A |
probably benign |
Het |
Trav6-1 |
A |
G |
14: 52,875,976 (GRCm39) |
N2S |
probably benign |
Het |
Trmt44 |
C |
A |
5: 35,732,314 (GRCm39) |
V26L |
possibly damaging |
Het |
Ttbk1 |
A |
T |
17: 46,790,173 (GRCm39) |
C91S |
probably damaging |
Het |
Vit |
A |
G |
17: 78,894,255 (GRCm39) |
H219R |
probably benign |
Het |
Vmn2r84 |
A |
T |
10: 130,227,163 (GRCm39) |
L225* |
probably null |
Het |
Vmn2r87 |
A |
G |
10: 130,308,556 (GRCm39) |
Y561H |
probably damaging |
Het |
Yars1 |
T |
A |
4: 129,093,820 (GRCm39) |
C60* |
probably null |
Het |
Zfp202 |
T |
C |
9: 40,122,633 (GRCm39) |
V465A |
probably benign |
Het |
|
Other mutations in Acot4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02255:Acot4
|
APN |
12 |
84,088,799 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02806:Acot4
|
APN |
12 |
84,088,737 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02967:Acot4
|
APN |
12 |
84,090,235 (GRCm39) |
missense |
probably benign |
|
R1827:Acot4
|
UTSW |
12 |
84,088,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Acot4
|
UTSW |
12 |
84,085,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Acot4
|
UTSW |
12 |
84,088,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R2904:Acot4
|
UTSW |
12 |
84,090,377 (GRCm39) |
missense |
probably benign |
0.31 |
R3859:Acot4
|
UTSW |
12 |
84,090,218 (GRCm39) |
missense |
probably benign |
0.17 |
R3904:Acot4
|
UTSW |
12 |
84,090,101 (GRCm39) |
splice site |
probably null |
|
R4192:Acot4
|
UTSW |
12 |
84,089,948 (GRCm39) |
intron |
probably benign |
|
R4541:Acot4
|
UTSW |
12 |
84,090,022 (GRCm39) |
missense |
probably benign |
0.38 |
R5061:Acot4
|
UTSW |
12 |
84,085,475 (GRCm39) |
missense |
probably benign |
0.03 |
R5682:Acot4
|
UTSW |
12 |
84,085,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Acot4
|
UTSW |
12 |
84,090,178 (GRCm39) |
missense |
probably benign |
0.04 |
R6818:Acot4
|
UTSW |
12 |
84,088,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Acot4
|
UTSW |
12 |
84,090,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Acot4
|
UTSW |
12 |
84,090,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Acot4
|
UTSW |
12 |
84,088,809 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8974:Acot4
|
UTSW |
12 |
84,090,515 (GRCm39) |
missense |
probably benign |
|
R9003:Acot4
|
UTSW |
12 |
84,089,969 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9246:Acot4
|
UTSW |
12 |
84,090,097 (GRCm39) |
missense |
probably benign |
|
|