Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
A |
G |
2: 35,254,776 (GRCm39) |
Y36H |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,567,750 (GRCm39) |
D5141G |
possibly damaging |
Het |
Adk |
G |
A |
14: 21,153,922 (GRCm39) |
E42K |
probably damaging |
Het |
Akap1 |
C |
A |
11: 88,735,958 (GRCm39) |
V268L |
probably benign |
Het |
Atrx |
A |
G |
X: 104,874,526 (GRCm39) |
S1945P |
probably damaging |
Het |
Clec5a |
G |
A |
6: 40,559,160 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
T |
C |
15: 8,232,741 (GRCm39) |
|
probably benign |
Het |
Cul3 |
G |
T |
1: 80,255,140 (GRCm39) |
H6Q |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,669,012 (GRCm39) |
|
probably benign |
Het |
Furin |
C |
A |
7: 80,042,240 (GRCm39) |
V452F |
probably benign |
Het |
Furin |
T |
A |
7: 80,040,507 (GRCm39) |
D777V |
probably benign |
Het |
Gm57859 |
T |
C |
11: 113,579,927 (GRCm39) |
F441L |
probably benign |
Het |
Hmgb4 |
G |
A |
4: 128,154,166 (GRCm39) |
T134I |
probably benign |
Het |
Ift74 |
A |
T |
4: 94,550,895 (GRCm39) |
E349V |
possibly damaging |
Het |
Igkv6-23 |
A |
T |
6: 70,237,880 (GRCm39) |
L13Q |
probably damaging |
Het |
Lekr1 |
A |
T |
3: 65,591,425 (GRCm39) |
Y54F |
probably damaging |
Het |
Lman1 |
A |
T |
18: 66,127,921 (GRCm39) |
V241E |
possibly damaging |
Het |
Mat1a |
T |
A |
14: 40,836,772 (GRCm39) |
D167E |
probably benign |
Het |
Myl6 |
G |
A |
10: 128,327,966 (GRCm39) |
A130V |
probably damaging |
Het |
Myo9a |
T |
C |
9: 59,791,877 (GRCm39) |
|
probably null |
Het |
Nlrp4f |
A |
T |
13: 65,347,223 (GRCm39) |
W12R |
probably damaging |
Het |
Nr1h4 |
T |
C |
10: 89,314,669 (GRCm39) |
R276G |
probably benign |
Het |
Or4f61 |
T |
C |
2: 111,922,851 (GRCm39) |
N65S |
possibly damaging |
Het |
Or5m13b |
C |
A |
2: 85,754,421 (GRCm39) |
Q270K |
possibly damaging |
Het |
Pag1 |
C |
T |
3: 9,758,886 (GRCm39) |
E411K |
probably damaging |
Het |
Prorp |
T |
G |
12: 55,355,660 (GRCm39) |
|
probably benign |
Het |
Rttn |
A |
G |
18: 89,082,339 (GRCm39) |
N1422D |
probably damaging |
Het |
Ryr1 |
C |
T |
7: 28,759,235 (GRCm39) |
R3345Q |
probably damaging |
Het |
Slc12a8 |
T |
C |
16: 33,361,280 (GRCm39) |
L85P |
probably damaging |
Het |
Slc22a17 |
T |
C |
14: 55,144,718 (GRCm39) |
H565R |
probably damaging |
Het |
Slc46a3 |
T |
C |
5: 147,823,108 (GRCm39) |
T245A |
probably benign |
Het |
Thsd7b |
A |
G |
1: 129,358,665 (GRCm39) |
H33R |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,847,318 (GRCm39) |
V1260A |
probably benign |
Het |
Tmem30a |
A |
T |
9: 79,681,461 (GRCm39) |
F236Y |
probably damaging |
Het |
Trim30b |
A |
C |
7: 104,015,258 (GRCm39) |
Y43* |
probably null |
Het |
Trpc3 |
T |
C |
3: 36,725,743 (GRCm39) |
K78E |
possibly damaging |
Het |
Twist2 |
A |
T |
1: 91,729,736 (GRCm39) |
M130L |
probably benign |
Het |
Ube2q2l |
T |
A |
6: 136,377,804 (GRCm39) |
Y342F |
probably damaging |
Het |
|
Other mutations in Arl6ip5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Arl6ip5
|
APN |
6 |
97,209,501 (GRCm39) |
missense |
probably benign |
|
IGL01530:Arl6ip5
|
APN |
6 |
97,187,785 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02028:Arl6ip5
|
APN |
6 |
97,206,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02724:Arl6ip5
|
APN |
6 |
97,209,365 (GRCm39) |
missense |
probably benign |
0.00 |
R0355:Arl6ip5
|
UTSW |
6 |
97,209,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Arl6ip5
|
UTSW |
6 |
97,209,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Arl6ip5
|
UTSW |
6 |
97,187,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Arl6ip5
|
UTSW |
6 |
97,187,838 (GRCm39) |
missense |
probably benign |
0.00 |
R9586:Arl6ip5
|
UTSW |
6 |
97,206,572 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1176:Arl6ip5
|
UTSW |
6 |
97,206,516 (GRCm39) |
missense |
probably benign |
0.00 |
|