Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1c |
T |
A |
2: 58,173,561 (GRCm39) |
|
probably benign |
Het |
Alb |
G |
A |
5: 90,618,698 (GRCm39) |
|
probably null |
Het |
Ankrd9 |
A |
G |
12: 110,943,797 (GRCm39) |
V46A |
probably damaging |
Het |
Ccdc158 |
T |
C |
5: 92,810,598 (GRCm39) |
N97D |
possibly damaging |
Het |
Cobl |
T |
G |
11: 12,203,987 (GRCm39) |
H823P |
probably benign |
Het |
Dnaja2 |
A |
T |
8: 86,279,908 (GRCm39) |
H90Q |
probably benign |
Het |
Dpagt1 |
T |
C |
9: 44,238,899 (GRCm39) |
F73S |
possibly damaging |
Het |
Dph3 |
C |
T |
14: 31,807,417 (GRCm39) |
E20K |
possibly damaging |
Het |
Fbxl13 |
G |
T |
5: 21,695,412 (GRCm39) |
T660K |
possibly damaging |
Het |
Gask1a |
G |
A |
9: 121,794,149 (GRCm39) |
S101N |
possibly damaging |
Het |
Glt6d1 |
T |
C |
2: 25,684,431 (GRCm39) |
T192A |
probably benign |
Het |
Mroh7 |
C |
T |
4: 106,560,358 (GRCm39) |
V649I |
probably benign |
Het |
Mta3 |
T |
C |
17: 84,063,072 (GRCm39) |
Y4H |
possibly damaging |
Het |
Myh14 |
A |
G |
7: 44,292,956 (GRCm39) |
L369P |
probably damaging |
Het |
Or2y1 |
G |
T |
11: 49,385,793 (GRCm39) |
L144F |
probably damaging |
Het |
Or4c52 |
T |
C |
2: 89,845,351 (GRCm39) |
C26R |
probably benign |
Het |
Paxx |
T |
C |
2: 25,350,277 (GRCm39) |
D110G |
probably damaging |
Het |
Pcyox1 |
T |
G |
6: 86,365,735 (GRCm39) |
D493A |
probably damaging |
Het |
Plk2 |
A |
G |
13: 110,535,976 (GRCm39) |
E560G |
probably benign |
Het |
Rnf6 |
A |
G |
5: 146,147,036 (GRCm39) |
F661L |
probably benign |
Het |
Sema4a |
T |
C |
3: 88,345,491 (GRCm39) |
K531E |
probably benign |
Het |
Svs5 |
T |
C |
2: 164,079,446 (GRCm39) |
K154E |
possibly damaging |
Het |
Tbx4 |
A |
T |
11: 85,802,769 (GRCm39) |
Q242L |
probably damaging |
Het |
Tgm3 |
A |
T |
2: 129,886,488 (GRCm39) |
I570F |
probably damaging |
Het |
Thrap3 |
A |
T |
4: 126,059,322 (GRCm39) |
M908K |
possibly damaging |
Het |
Trmo |
A |
G |
4: 46,386,092 (GRCm39) |
|
probably null |
Het |
Usp8 |
T |
A |
2: 126,600,072 (GRCm39) |
L997Q |
probably damaging |
Het |
Vmn1r202 |
T |
C |
13: 22,685,890 (GRCm39) |
R176G |
probably benign |
Het |
Vps52 |
T |
A |
17: 34,180,589 (GRCm39) |
Y308* |
probably null |
Het |
|
Other mutations in Apol11a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03112:Apol11a
|
APN |
15 |
77,401,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R1296:Apol11a
|
UTSW |
15 |
77,395,219 (GRCm39) |
splice site |
probably benign |
|
R1576:Apol11a
|
UTSW |
15 |
77,401,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Apol11a
|
UTSW |
15 |
77,397,766 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2517:Apol11a
|
UTSW |
15 |
77,401,395 (GRCm39) |
missense |
probably benign |
0.00 |
R4614:Apol11a
|
UTSW |
15 |
77,400,772 (GRCm39) |
missense |
probably benign |
0.08 |
R4892:Apol11a
|
UTSW |
15 |
77,401,190 (GRCm39) |
nonsense |
probably null |
|
R5027:Apol11a
|
UTSW |
15 |
77,401,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Apol11a
|
UTSW |
15 |
77,400,953 (GRCm39) |
missense |
probably benign |
0.14 |
R6208:Apol11a
|
UTSW |
15 |
77,401,241 (GRCm39) |
missense |
probably damaging |
0.99 |
R7883:Apol11a
|
UTSW |
15 |
77,400,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8868:Apol11a
|
UTSW |
15 |
77,401,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:Apol11a
|
UTSW |
15 |
77,397,778 (GRCm39) |
missense |
probably benign |
0.03 |
R9674:Apol11a
|
UTSW |
15 |
77,401,347 (GRCm39) |
missense |
possibly damaging |
0.85 |
|