Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
T |
C |
19: 8,987,416 (GRCm39) |
V2900A |
probably damaging |
Het |
Akip1 |
A |
G |
7: 109,306,684 (GRCm39) |
H127R |
probably benign |
Het |
Alad |
A |
T |
4: 62,431,203 (GRCm39) |
Y56N |
probably damaging |
Het |
Ap1g1 |
C |
T |
8: 110,545,614 (GRCm39) |
A89V |
probably damaging |
Het |
Ascc3 |
C |
T |
10: 50,718,279 (GRCm39) |
R1991* |
probably null |
Het |
Cd209b |
T |
C |
8: 3,974,246 (GRCm39) |
I89V |
possibly damaging |
Het |
Cd36 |
T |
C |
5: 17,990,733 (GRCm39) |
K469R |
probably benign |
Het |
Cdh20 |
T |
A |
1: 109,976,581 (GRCm39) |
I82N |
probably damaging |
Het |
Clmn |
G |
T |
12: 104,748,014 (GRCm39) |
P511H |
probably damaging |
Het |
Cyfip1 |
A |
C |
7: 55,576,061 (GRCm39) |
D1077A |
probably damaging |
Het |
Cyp2a5 |
T |
C |
7: 26,542,383 (GRCm39) |
F462L |
probably benign |
Het |
Dclk2 |
A |
G |
3: 86,699,166 (GRCm39) |
*709Q |
probably null |
Het |
Drd1 |
T |
C |
13: 54,208,182 (GRCm39) |
T4A |
probably benign |
Het |
Ephb2 |
C |
T |
4: 136,402,733 (GRCm39) |
V513I |
possibly damaging |
Het |
Fam43a |
T |
A |
16: 30,420,277 (GRCm39) |
V287E |
probably benign |
Het |
Gm5134 |
A |
G |
10: 75,844,450 (GRCm39) |
E602G |
probably benign |
Het |
Gtsf2 |
C |
T |
15: 103,348,063 (GRCm39) |
G149E |
probably benign |
Het |
Kif20a |
G |
A |
18: 34,765,468 (GRCm39) |
A822T |
probably benign |
Het |
Klhl6 |
T |
C |
16: 19,801,570 (GRCm39) |
T62A |
probably benign |
Het |
Lamb1 |
T |
A |
12: 31,348,954 (GRCm39) |
I662N |
possibly damaging |
Het |
Lmod3 |
A |
G |
6: 97,224,963 (GRCm39) |
V286A |
probably damaging |
Het |
Mefv |
T |
C |
16: 3,533,797 (GRCm39) |
D158G |
probably damaging |
Het |
Mff |
T |
C |
1: 82,728,327 (GRCm39) |
|
probably null |
Het |
Mfsd6l |
G |
T |
11: 68,448,036 (GRCm39) |
V296L |
possibly damaging |
Het |
Neu2 |
G |
T |
1: 87,524,478 (GRCm39) |
Q154H |
probably damaging |
Het |
Or5m3b |
A |
G |
2: 85,871,795 (GRCm39) |
I45M |
probably benign |
Het |
Pdk4 |
T |
A |
6: 5,487,452 (GRCm39) |
H266L |
probably benign |
Het |
Pdrg1 |
T |
C |
2: 152,855,975 (GRCm39) |
N40D |
probably damaging |
Het |
Pi4k2a |
T |
C |
19: 42,093,924 (GRCm39) |
|
probably null |
Het |
Pkd1l2 |
T |
A |
8: 117,781,750 (GRCm39) |
D765V |
probably damaging |
Het |
Pspc1 |
A |
T |
14: 56,999,498 (GRCm39) |
|
probably null |
Het |
Ptprm |
T |
C |
17: 67,352,976 (GRCm39) |
|
probably null |
Het |
Spata31d1d |
T |
C |
13: 59,875,054 (GRCm39) |
K827R |
possibly damaging |
Het |
Srebf2 |
T |
A |
15: 82,053,987 (GRCm39) |
F46Y |
probably damaging |
Het |
Tfrc |
T |
A |
16: 32,439,230 (GRCm39) |
C365S |
possibly damaging |
Het |
Ttc7 |
A |
G |
17: 87,629,900 (GRCm39) |
H294R |
possibly damaging |
Het |
Ubr7 |
T |
A |
12: 102,727,753 (GRCm39) |
Y92N |
probably damaging |
Het |
Vmn1r42 |
A |
C |
6: 89,821,761 (GRCm39) |
Y269* |
probably null |
Het |
Vmn2r1 |
A |
G |
3: 64,011,990 (GRCm39) |
E617G |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,889,904 (GRCm39) |
|
probably null |
Het |
Vps50 |
T |
C |
6: 3,536,965 (GRCm39) |
L312P |
probably damaging |
Het |
Wdr82 |
A |
G |
9: 106,062,503 (GRCm39) |
Q252R |
probably benign |
Het |
Zcchc3 |
A |
G |
2: 152,256,444 (GRCm39) |
F85S |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,520,078 (GRCm39) |
L400P |
probably damaging |
Het |
|
Other mutations in Aldoart1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02499:Aldoart1
|
APN |
4 |
72,770,476 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03067:Aldoart1
|
APN |
4 |
72,770,194 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03273:Aldoart1
|
APN |
4 |
72,770,346 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03493:Aldoart1
|
APN |
4 |
72,769,884 (GRCm39) |
missense |
probably damaging |
0.98 |
R0145:Aldoart1
|
UTSW |
4 |
72,769,576 (GRCm39) |
missense |
probably benign |
0.06 |
R0478:Aldoart1
|
UTSW |
4 |
72,770,580 (GRCm39) |
missense |
probably benign |
|
R1770:Aldoart1
|
UTSW |
4 |
72,770,173 (GRCm39) |
missense |
probably benign |
0.00 |
R2044:Aldoart1
|
UTSW |
4 |
72,770,779 (GRCm39) |
missense |
probably benign |
0.00 |
R4627:Aldoart1
|
UTSW |
4 |
72,770,680 (GRCm39) |
missense |
probably benign |
|
R5344:Aldoart1
|
UTSW |
4 |
72,770,352 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6234:Aldoart1
|
UTSW |
4 |
72,770,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Aldoart1
|
UTSW |
4 |
72,769,678 (GRCm39) |
nonsense |
probably null |
|
R7672:Aldoart1
|
UTSW |
4 |
72,770,747 (GRCm39) |
missense |
probably benign |
|
R7847:Aldoart1
|
UTSW |
4 |
72,770,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9259:Aldoart1
|
UTSW |
4 |
72,770,680 (GRCm39) |
missense |
probably benign |
|
R9333:Aldoart1
|
UTSW |
4 |
72,770,367 (GRCm39) |
missense |
probably benign |
0.00 |
R9572:Aldoart1
|
UTSW |
4 |
72,770,770 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Aldoart1
|
UTSW |
4 |
72,770,241 (GRCm39) |
missense |
probably benign |
0.03 |
|