Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
A |
T |
1: 11,588,818 (GRCm39) |
R78S |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,618,780 (GRCm39) |
I791T |
probably damaging |
Het |
Aldh1b1 |
A |
G |
4: 45,803,359 (GRCm39) |
D299G |
probably damaging |
Het |
Aoah |
A |
G |
13: 21,000,764 (GRCm39) |
E66G |
probably damaging |
Het |
Atl2 |
G |
T |
17: 80,160,334 (GRCm39) |
H418N |
probably damaging |
Het |
Atp6v1d |
A |
G |
12: 78,908,214 (GRCm39) |
I7T |
possibly damaging |
Het |
Calhm3 |
C |
T |
19: 47,143,839 (GRCm39) |
V155M |
probably damaging |
Het |
Carmil1 |
A |
T |
13: 24,282,989 (GRCm39) |
I105K |
probably damaging |
Het |
Csrp3 |
C |
A |
7: 48,489,278 (GRCm39) |
M1I |
probably null |
Het |
Dnah10 |
T |
A |
5: 124,837,078 (GRCm39) |
|
probably null |
Het |
Dnah11 |
T |
C |
12: 117,897,547 (GRCm39) |
N3561S |
possibly damaging |
Het |
Dzip3 |
A |
T |
16: 48,772,180 (GRCm39) |
D496E |
probably damaging |
Het |
Eif2ak1 |
T |
C |
5: 143,820,797 (GRCm39) |
V246A |
probably benign |
Het |
Fam171b |
T |
A |
2: 83,643,313 (GRCm39) |
V74E |
probably benign |
Het |
Gm14137 |
C |
T |
2: 119,005,605 (GRCm39) |
R55W |
probably damaging |
Het |
Gm4950 |
T |
C |
18: 51,998,830 (GRCm39) |
I42V |
probably benign |
Het |
Gpr35 |
T |
C |
1: 92,910,870 (GRCm39) |
V194A |
probably damaging |
Het |
Kdm5d |
C |
T |
Y: 941,011 (GRCm39) |
S1132F |
probably damaging |
Het |
Muc4 |
C |
A |
16: 32,754,529 (GRCm38) |
H1468N |
probably benign |
Het |
Ncln |
A |
G |
10: 81,332,027 (GRCm39) |
V24A |
possibly damaging |
Het |
Nphp4 |
A |
G |
4: 152,573,289 (GRCm39) |
K76E |
probably damaging |
Het |
Nsf |
CAATAATAATAATAATA |
CAATAATAATAATAATAATA |
11: 103,816,952 (GRCm39) |
|
probably benign |
Het |
Nup155 |
A |
T |
15: 8,187,244 (GRCm39) |
H1391L |
probably damaging |
Het |
Or52h2 |
A |
T |
7: 103,839,060 (GRCm39) |
L118* |
probably null |
Het |
Pabpc1l |
G |
T |
2: 163,879,091 (GRCm39) |
V313F |
possibly damaging |
Het |
Pcbd2 |
G |
A |
13: 55,880,881 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
T |
A |
11: 54,582,525 (GRCm39) |
V1479D |
probably benign |
Het |
Rnf43 |
T |
C |
11: 87,618,301 (GRCm39) |
|
probably benign |
Het |
Robo3 |
A |
G |
9: 37,329,978 (GRCm39) |
W1113R |
probably damaging |
Het |
Sall1 |
A |
T |
8: 89,758,562 (GRCm39) |
V514E |
probably damaging |
Het |
Sgpp1 |
A |
G |
12: 75,763,056 (GRCm39) |
I375T |
probably benign |
Het |
Strc |
T |
C |
2: 121,202,604 (GRCm39) |
N1187S |
possibly damaging |
Het |
Tbc1d17 |
G |
A |
7: 44,492,895 (GRCm39) |
R363W |
probably damaging |
Het |
Tbcd |
A |
G |
11: 121,366,451 (GRCm39) |
Q242R |
probably benign |
Het |
Tbcel |
A |
C |
9: 42,362,947 (GRCm39) |
V50G |
probably damaging |
Het |
Tead3 |
C |
T |
17: 28,560,536 (GRCm39) |
A23T |
probably benign |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tlcd5 |
A |
G |
9: 43,022,775 (GRCm39) |
V193A |
probably benign |
Het |
Tmem241 |
G |
T |
18: 12,217,035 (GRCm39) |
|
probably benign |
Het |
Tmtc3 |
G |
T |
10: 100,312,606 (GRCm39) |
T79K |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,362,281 (GRCm39) |
V241A |
probably damaging |
Het |
Vps8 |
A |
T |
16: 21,330,307 (GRCm39) |
I729F |
probably damaging |
Het |
Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
|
Other mutations in Aadacl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01293:Aadacl3
|
APN |
4 |
144,190,226 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02590:Aadacl3
|
APN |
4 |
144,184,404 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02629:Aadacl3
|
APN |
4 |
144,190,199 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03308:Aadacl3
|
APN |
4 |
144,182,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R0521:Aadacl3
|
UTSW |
4 |
144,182,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:Aadacl3
|
UTSW |
4 |
144,190,130 (GRCm39) |
nonsense |
probably null |
|
R1701:Aadacl3
|
UTSW |
4 |
144,190,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R2033:Aadacl3
|
UTSW |
4 |
144,182,953 (GRCm39) |
missense |
probably benign |
0.00 |
R2077:Aadacl3
|
UTSW |
4 |
144,183,604 (GRCm39) |
unclassified |
probably benign |
|
R2226:Aadacl3
|
UTSW |
4 |
144,190,295 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2328:Aadacl3
|
UTSW |
4 |
144,182,502 (GRCm39) |
missense |
probably benign |
0.00 |
R4801:Aadacl3
|
UTSW |
4 |
144,182,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Aadacl3
|
UTSW |
4 |
144,182,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Aadacl3
|
UTSW |
4 |
144,184,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R4959:Aadacl3
|
UTSW |
4 |
144,183,656 (GRCm39) |
missense |
probably benign |
0.37 |
R5076:Aadacl3
|
UTSW |
4 |
144,182,640 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5766:Aadacl3
|
UTSW |
4 |
144,182,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6643:Aadacl3
|
UTSW |
4 |
144,183,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Aadacl3
|
UTSW |
4 |
144,182,760 (GRCm39) |
missense |
probably benign |
0.05 |
R7563:Aadacl3
|
UTSW |
4 |
144,184,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R8254:Aadacl3
|
UTSW |
4 |
144,182,760 (GRCm39) |
missense |
probably benign |
0.05 |
R8717:Aadacl3
|
UTSW |
4 |
144,182,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Aadacl3
|
UTSW |
4 |
144,182,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R9642:Aadacl3
|
UTSW |
4 |
144,182,512 (GRCm39) |
missense |
probably benign |
0.05 |
|